Patent application title: Method of elevating photosynthesis speed of plant by improving pyruvate phosphate dikinase

Inventors: Satoru Usami (Shizuoka, JP) Shozo Ohta (Kanagawa, JP) Yuji Ishida (Shizuoka, JP)
IPC8 Class: AC12N1582FI
USPC Class: 4353201
Class name: VECTOR, PER SE (E.G., PLASMID, HYBRID PLASMID, COSMID, VIRAL VECTOR, BACTERIOPHAGE VECTOR, ETC.) BACTERIOPHAGE VECTOR, ETC.)
Publication date: 10/16/2008
Patent application number: 20080254536

Abstract:

The present invention relates to the transformation of C4 plants. It also relates to the high-level expression of foreign genes in C4 plants. More specifically, the present invention relates to the creation of C4 plants retaining an excellent photosynthetic capacity at low temperature by achieving high-level expression of an enzyme constituting the C4 photosynthetic pathway. In the present invention, C4 plants are transformed using an expression cassette that comprises a promoter, a C4 plant genomic gene, under control of said promoter, encoding an enzyme constituting a photosynthetic pathway, and a terminator. The C4 plant genomic gene encoding an enzyme constituting a photosynthetic pathway is preferably a C4 plant genome-derived PPDK gene or a modified form thereof. The present invention is particularly useful in improving the production of C4 plants having PPDK (especially, in improving the production of maize under low temperature conditions).

Claims:

1. An expression cassette that comprises a promoter, a C4 plant genomic gene under control of said promoter, and a terminator, wherein the C4 plant genomic gene consists of any DNA selected from:(a) a DNA molecule consisting of a partial nucleotide sequence of SEQ ID NO: 16 which corresponds to the C-terminal 1/6 region of PPDK;(b) a DNA molecule consisting of a nucleotide sequence derived from a partial nucleotide sequence of SEQ ID NO: 16 which corresponds to the C-terminal 1/6 region of PPDK by deletion, substitution, addition or insertion of one or more nucleotides, and encoding a protein possessing an activity in increasing the expression level of PPDK in a C4 plant;(c) a DNA molecule being hybridizable under stringent conditions to the DNA molecule complementary to the DNA molecule consisting of a partial nucleotide sequence of SEQ ID NO: 16 which corresponds to the C-terminal 1/6 region of PPDK, and encoding a protein possessing an activity in increasing the expression level of PPDK in a C4 plant; and(d) a DNA molecule consisting of a nucleotide sequence being at least 50% homologous to a partial nucleotide sequence of SEQ ID NO: 16 which corresponds to the C-terminal 1/6 region of PPDK, and encoding a protein possessing an activity in increasing the expression level of PPDK in a C4 plant.

2. The expression cassette according to claim 1, for enhancing photosynthesis rate in a C4 plant under low temperature conditions.

3. The expression cassette according to claim 1, wherein the PPDK activity is a cold-tolerant PPDK activity.

4. A recombinant vector containing the expression cassette according to claims 1, 2 or 3.

Description:

[0001]This application is a Divisional of co-pending application Ser. No. 10/493,537 filed on Apr. 22, 2004, which is the National Phase of PCT/JPO2/10993 filed on Oct. 23, 2002, and for which priority is claimed under 35 U.S.C. § 120; and this application claims priority of Application No. 2001-324899 filed in Japan on Oct. 23, 2001 under 35 U.S.C. § 119; the entire contents of which are all hereby incorporated by reference.

FIELD OF THE INVENTION

[0002]The present invention relates to the transformation of C4 plants. It also relates to the high-level expression of foreign genes in C4 plants. More specifically, the present invention relates to the creation of C4 plants retaining an excellent photosynthetic capacity at low temperature by achieving high-level expression of an enzyme constituting the C4 photosynthetic pathway. The present invention is particularly useful in improving the production of C4 plants having PPDK (especially, in improving the production of maize under low temperature conditions).

BACKGROUND OF THE INVENTION

[0003]Plant pyruvate, orthophosphate dikinase (PPDK; EC2.7.9.1) is one of the important enzymes constituting the C4 cycle and it has been believed that there is a high correlation between PPDK activity and photosynthesis rate in C4 plants. Further, PPDK has the lowest activity among enzymes constituting the C4 cycle; the PPDK reaction has been regarded as a rate-limiting stage of C4 photosynthesis. Also, PPDK is a tetramer composed of four subunits which are weakly associated with each other. When exposed to low temperature conditions (at or below 12° C.), PPDK is known to be dissociated into dimers or monomers, thus rapidly losing its activity. In general, maize PPDK will lose approximately 70% of its activity when treated at 0° C. for 20 minutes. Meanwhile, the activity of maize PPDK was measured at various temperatures to prepare an Arrhenius plot, indicating that there was an inflection point at 11.7° C., which was found to match the critical temperature for maize growth. In view of these points, a decrease in PPDK activity has been regarded as the main factor responsible for slowdown of photosynthesis in C4 plants at low temperature.

[0004]Flayeria brownii (F. brownii), an Asteraceae plant, is categorized as a C3/C4 intermediate type and its PPDK is known to be hardly deactivated even when treated at a temperature as low as 0° C. (Burnell J N, A comparative sturdy of the cold-sensitivity of pyruvate, Pi dikinese in Flayeria species, Plant Cell Physiol., 31:295-297 (1990)). Hence, it was expected that this cold-tolerant PPDK gene could be used to create C4 plants capable of C4 photosynthesis at a lower temperature, i.e., C4 plants more resistant to cold.

[0005]In the previous studies, the inventors of the present invention succeeded in determining a region important for cold tolerance of PPDK by isolation and DNA sequencing of the F. brownii PPDK gene. They also demonstrated that the sequence of this region could be used to convert cold-sensitive PPDK into a cold-tolerant form through recombination between this sequence and the DNA of cold-sensitive PPDK derived from other plant (WO95/15385; Usami S, Ohta S, Komari T, Burnell J N, Cold stability of pyruvate, orthophosphate dikinase of Flayeria brownii, Plant Mol Biol, 27:969-80 (1995); Ohta S, Usami S, Ueki J, Kumashiro T, Komari T, Burnell J N, Identification of the amino acid residues responsible for cold tolerance in Flayeria brownii pyruvate, orthophosphate dikinase, FEBS Lett, 396:152-6 (1996)).

[0006]Through many studies of maize transformants, however, the inventors of the present invention found that effects of the artificially introduced PPDK (introduced PPDK) were masked by naturally-occurring PPDK in C4 plants (endogenous PPDK). This would be attributed to an abundance of endogenous PPDK constituting several percent of soluble proteins in C4 plants. Further, the inventors of the present invention found that heterotetramers could be formed between introduced PPDK subunits and endogenous PPDK subunits.

[0007]To overcome the phenomenon where effects of the introduced PPDK are masked by the endogenous PPDK, two techniques are available, one of which involves increasing the expression level of the introduced PPDK and the other is inhibition of the endogenous PPDK. The former involves integrating a sequence (e.g., intron) into a gene construct for transformation (in most cases, an intron(s) being integrated between a promoter and a structural gene) to increase the expression level of an externally introduced gene (WO96/30510: PLD intron, WO97/47755: double-ligated introns). The latter is an antisense technique for inhibiting the expression level of an object gene by introduction of a gene whose mRNA has a sequence complementary to mRNA from the object gene to be inhibited from expression (Japanese Patent No. 2651442 and its divisional patent No. 2694924). The inventors of the present invention have tried these techniques.

[0008]In increasing the expression level of the introduced PPDK by integration of an intron(s) etc., a gene construct used for transformation was constructed in a general manner through ligation between a maize PPDK promoter (Glackin C A, Grula J W, Organ-specific transcripts of different size and abundance derive from the same pyruvate, orthophosphate dikinase gene in maize, PNAS, 87:3004-3008 (1990)) and a cDNA molecule of the PPDK gene derived from F. brownii, F. bidentis (Usami S, Ohta S, Komari T, Burnell J N, Cold stability of pyruvate, orthophosphate dikinase of Flayeria brownii, Plant Mol Biol, 27:969-80 (1995)) or maize (Matsuoka M, Structure, genetic mapping, and expression of the gene for pyruvate, orthophosphate dikinase from maize, J. Biol. Chem., 265:16772-16777 (1990)). At the same time, the inventors of the present invention attempted to increase the expression level of the introduced PPDK by inserting any one of the following introns between the promoter and the structural gene: Intron 1 of the Castor bean catalase gene (Ohta S, Mita S, Hattori T, Nakamura K, Construction and expression in tobacco of a β-glucuronidase (GUS) reporter gene containing an intron within the coding sequence, Plant Cell Physiol, 31:805-813 (1990)), Intron 1 of the rice phospholipase D gene (Ueki J, Morioka S, Komari T, Kumashiro T, Purification and characterization of phospholipase D from rice and maize (Zea mays L.), Plant Cell Physiol, 36:903-914 (1995)), Intron 1 of maize ubiquitin (Christensen et al., (1992)) and Intron 1 of maize Shrunken-1 (Vasil V, Clancy M, Ferl R J, Vasil I K, Hannah L C, Increased gene expression by the first intron of maize Shrunken-1 locus in grass species, Plant Physiol, 91:1575-1579 (1989)). Further, based upon a report suggesting that repeated introns resulted in an increased expression level (Ueki J, Ohta S, Morioka S, Komari T, Kuwata S, Kubo T, Imaseki H, The synergistic effects of two-intron insertions on heterologous gene expression and advantages of the first intron of a rice gene for phospholipase D, Plant Cell Physiol, 40:618-623 (1999)), the inventors of the present invention also attempted to insert multiple repeated introns.

DISCLOSURE OF THE INVENTION

[0009]The studies of the present inventors indicated that these introns resulted in an increased expression level in the order: Intron 1 of Shrunken-1<Intron 1 of the Castor bean catalase gene<Intron 1 of the rice phospholipase D gene and that these introns, when inserted in combination, resulted in a greater increase in expression level than when inserted alone, for example, Intron 1 of the rice phospholipase D gene resulted in an increased expression level when combined with Intron 1 of the Castor bean catalase gene or Intron 1 of maize ubiquitin.

[0010]However, even the most improved transformants expressed the introduced PPDK at a level as low as around 700 μg/g of fresh green leaves, which was only about half that of the endogenous PPDK; there was no remarkable effect resulting from the introduced PPDK. Although the expression level of the introduced PPDK is regarded as high compared to other artificially introduced genes, it would be impossible to clarify effects of the introduced gene in a case where there are abundant products of the endogenous gene (i.e., where the endogenous gene is highly expressed) unless the endogenous gene is inhibited.

[0011]In contrast, an antisense gene for inhibition of the endogenous PPDK was constructed based on a 395 bp sequence of the maize PPDK gene covering from SacI in the 5'-untranslated region to EcoRI in Intron 1, 6 repeated copies of this sequence, or a cDNA-derived PstI fragment (2.4 kb) covering almost all segments of the maize PPDK mature enzyme. The constructed antisense gene was used to transform maize. The reason why attention was directed to the 395 bp sequence was because this sequence corresponded to a transit peptide segment, for which low homology was shared between maize PPDK and F. brownii PPDK, and hence it would be able to selectively inhibit the maize PPDK alone.

[0012]As a consequence, there was no inhibitory effect on expression levels was observed in simple introduction of the antisense gene for the 395 bp sequence. With low frequency, some transformants modified to inhibit their endogenous PPDK appeared in a case where maize was transformed with an antisense gene for the 6 repeated copies of the 395 bp sequence or the cDNA-derived PstI fragment (2.4 kb). However, such transformants modified to inhibit their endogenous PPDK also had a reduced level of the introduced PPDK and therefore did not achieve specific inhibition of the endogenous PPDK alone. Further, such transformants were too weak to grow and most of them withered and died before maturation because inhibition occurred on PPDK essential for C4 plants, including both the endogenous PPDK and the introduced PPDK. Also, no seed production was seen in even those transformants that came into flower. It was theoretically impossible to selectively control the expression of genes sharing a very similar sequence by the antisense technique in view of its mechanism, thus indicating that such a technique could not be adapted in this case.

[0013]There is an attempt to introduce a genomic gene instead of cDNA to achieve high-level expression, in C3 plants, of a gene for an enzyme constituting the C4 photosynthetic pathway (JP 10-248419 A). In this attempt, however, a gene that is not present in C3 plants (or, if any, expressed at a very low level) is merely introduced from C4 plants. It would be much more difficult to achieve further expression, in C4 plants, of genes naturally occurring in C4 plants or high-level expression, in C4 plants, of genes encoding proteins which are already expressed in abundance in C4 plants, like photosynthesis-related enzymes, than to achieve expression of C4 plants-derived genes in C3 plants.

[0014]A variety of previous biochemical studies have estimated that PPDK might be a rate-limiting factor of C4 photosynthesis. However, no conclusive evidence has been established that these previous studies were correct because there was no report showing actual high-level expression of PPDK in C4 plants or artificial introduction of PPDK with new properties.

[0015]As stated above, the cDNA-based technique could not increase expression of the introduced gene to a sufficient level even in combination with an intron(s) etc., while the antisense technique was unable to selectively inhibit the endogenous gene alone. For this reason, the inventors of the present invention tried to introduce a genomic gene.

[0016]Meanwhile, the studies of the present inventors indicated that when a cold-tolerant F. brownii PPDK cDNA was introduced as such into maize, the introduced gene was expressed at a very low level. This would be because F. brownii is a C3/C4 intermediate plant and inherently produces a smaller amount of PPDK than C4 plants. Further, the inventors of the present invention have found that expression of F. brownii PPDK in C4 plants was improved by constructing a chimeric gene between a pure C4 plant F. bidentis or maize and F. brownii.

[0017]In turn, the inventors of the present invention made a variety of studies on genomic gene introduction based on the maize PPDK genomic gene, instead of the genomic gene for C3/C4 intermediate F. brownii PPDK. As a result, they found that the expression level of PPDK in maize was increased by simple introduction of the maize PPDK genomic gene into maize and that the expression level of maize PPDK under cold cultivation was increased using a gene that was modified into a cold-tolerant type by mutagenesis in a certain region of the maize PPDK genomic gene. These findings led to the completion of the present invention.

[0018]The present invention provides a method for increasing the expression level of an enzyme constituting a photosynthetic pathway in a C4 plant, comprising transforming the C4 plant using an expression cassette that comprises a promoter, a C4 plant genomic gene, under control of said promoter, encoding the enzyme, and a terminator. It also provides a transgenic C4 plant obtainable by the method.

BRIEF DESCRIPTION OF THE DRAWINGS

[0019]FIG. 1 shows procedures for construction of #2706 in Example 1.

[0020]FIG. 2A shows the amount of PPDK present in progeny plants of transformants modified with a maize genomic gene (#2706), compared between individuals homozygous or heterozygous for the introduced PPDK gene (homo or hetero) and individuals null for the gene (null). The vertical axis represents the expression level (μg/gfwt) of PPDK contained per g of fresh green leaves, and each bar represents standard error. There was a significant difference between homo or hetero individuals and null individuals at a significance level of 1%.

[0021]FIG. 2B shows the photosynthesis rate at various leaf surface temperatures in progeny plants of transformants modified with a maize genomic gene (#2706), compared between homo or hetero individuals and null individuals. The vertical axis represents the photosynthesis rate (μmol CO₂m^-2s^-1), and each bar represents standard error. At a leaf surface temperature of 8° C., there was a significant difference between homo or hetero individuals and null individuals at a significance level of 5%.

[0022]FIG. 3 shows procedures for introduction of F. brownii-type mutations into the PPDK genome.

[0023]FIG. 4 shows procedures for construction of #2838 in Example 2.

[0024]FIG. 5A shows the maize PPDK amino acid sequence (SEQ ID NO: 17).

[0025]FIG. 5B shows the F. brownii PPDK amino acid sequence (SEQ ID NO: 18). The line-encircled amino acid sequence is an approximately 1/6 region from the C-terminal, which is important for cold tolerance.

[0026]FIG. 5C shows a comparison of the C-terminal 1/6 region between maize PPDK (residues 824-947 of SEQ ID NO: 17) and F. brownii PPDK (residues 833-955 of SEQ ID NO: 18) amino acid sequences. The line-encircled amino acid residues are different between them.

[0027]FIG. 6A shows the amount of PPDK present in progeny plants of transformants modified with a mutated maize genomic gene (#2838), compared between homo or hetero individuals and null individuals. The vertical axis represents the expression level (μg/gfwt) of PPDK contained per g of fresh green leaves, and each bar represents standard error.

[0028]FIG. 6B shows the photosynthesis rate at various leaf surface temperatures in progeny plants of transformants modified with #2838, compared between homo or hetero individuals and null individuals. The vertical axis represents the photosynthesis rate (μmol CO₂m^-2s^-1), and each bar represents standard error.

[0029]FIG. 7A shows the amount of PPDK present at various leaf surface temperatures in progeny plants of transformants modified with a mutated maize genomic gene (#2838), compared between homo or hetero individuals and null individuals. The vertical axis represents the expression level (μg/gfwt) of PPDK contained per g of fresh green leaves, and each bar represents standard error.

[0030]FIG. 7B shows the photosynthesis rate at various leaf surface temperatures in progeny plants of transformants modified with #2838, compared between homo or hetero individuals and null individuals. The vertical axis represents the photosynthesis rate (μmol CO₂m^-2s^-1), and each bar represents standard error. At leaf surface temperatures of 20° C. and 13° C., there was a significant difference between homo or hetero individuals and null individuals at a significance level of 5%. At a leaf surface temperature of 8° C., there was a significant difference at a significance level of 1%.

[0031]FIG. 8 shows a cold inactivation pattern of PPDK in transformants with a mutated maize genomic gene. The horizontal axis represents time on ice (min), while the vertical axis represents PPDK activity (%). Open triangle (Δ), open square (quadrature), solid triangle (.tangle-solidup.), solid circle ( ) and open circle (◯) represents transformants with PPDK contents of 4152.3 μg/gfwt, 9122.4 μg/gfwt, 1390.6 μg/gfwt, 9802.8 μg/gfwt and 1292.1 μg/gfwt, respectively, relative to 1 g of desalted fresh green leaves. Cross (x) represents F. brownii and plus (+) represents the maize inbred line A188 (1495.2 μg/gfwt). Transformants with high PPDK contents could retain their PPDK activity, even on ice, at almost the same level as F. brownii.

DETAILED DESCRIPTION OF THE INVENTION

[0032]Various types of enzymes are known to be included in the "enzyme constituting the C4 photosynthetic pathway" as used herein. Among these enzymes, the method of the present invention can be used to increase the expression levels of enzymes that are expressed at relatively low levels, easily deactivated, and/or involved in the rate-limiting stage of the photosynthetic pathway. In particular, the method of the present invention can be used to increase the expression levels of enzymes that have the properties as mentioned above under low temperature conditions (e.g., at or below about 12° C.). PPDK is known as an example of such enzymes. Also, the method of the present invention can be used to enhance the photosynthetic capacity at low temperature in C4 plants having a limit for growth under low temperature conditions (e.g., at or below about 12° C.).

[0033]In a case where the method of the present invention is used to create transgenic C4 plants, a gene consisting of any one of the following DNA molecules may be used as a "C4 plant genomic gene encoding an enzyme constituting a photosynthetic pathway." The method using such a gene is particularly preferred to obtain maize plants modified to enhance their photosynthesis rate under low temperature conditions:

[0034](a) the maize PPDK genomic gene, i.e., a DNA molecule consisting of the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 15;

[0035](b) a DNA molecule consisting of a nucleotide sequence derived from the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 15 by deletion, substitution, addition or insertion of one or more nucleotides, and encoding a protein possessing PPDK activity;

[0036](c) a DNA molecule being hybridizable under stringent conditions to the DNA molecule being complementary to the DNA molecule consisting of the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 15, and encoding a protein possessing PPDK activity; and

[0037](d) a DNA molecule consisting of a nucleotide sequence being at least 50% (preferably at least 60%, more preferably at least 70%, even more preferably at least 80%, still more preferably at least 90%, particularly preferably at least 95%, and most preferably at least 98%) homologous to the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 15, and encoding a protein possessing PPDK activity. To calculate a homology between nucleotide sequences, a commercially available software package may be used. As used herein, the term "stringent conditions" refers to hybridization conditions of a temperature of at least about 40° C., a salt concentration of about 6×SSC (1×SSC=15 mM sodium citrate buffer; pH7.0; 0.15 M sodium chloride) and 0.1% SDS, preferably at least about 50° C., more preferably at least about 65° C.

[0038]Alternatively, a gene encoding any one of the following proteins may be used:

[0039](a) a protein consisting of the amino acid sequence of SEQ ID NO: 17;

[0040](b) a protein consisting of an amino acid sequence derived from the amino acid sequence of SEQ ID NO: 17 by deletion, substitution, addition or insertion of one or more amino acids, and possessing PPDK activity;

[0041](c) PPDK derived from a C4 plant; and

[0042](d) a protein consisting of an amino acid sequence being at least 50% (preferably at least 60%, more preferably at least 70%, even more preferably at least 80%, still more preferably at least 90%, particularly preferably at least 95%, and most preferably at least 98%) homologous to the amino acid sequence of SEQ ID NO: 17, and possessing PPDK activity. The term "homology" when used herein for amino acid sequences generally means that the extent of the similarity between amino acid residues constituting the respective sequences to be compared. In this sense, the presence of gaps and the nature of amino acids are taken into account. To calculate a homology, a commercially available software package may be used.

[0043]As used herein, the term "genomic gene" encompasses a genome-derived gene per se and a modified form thereof, unless otherwise specified. Also as used herein, the term "C4 plant genomic gene encoding an enzyme constituting a photosynthetic pathway" encompasses a C4 plant genome-derived gene per se and a modified form thereof. Such a modified gene is preferably modified to have one or more nucleotide substitutions such that the amino acid sequence of the enzyme encoded by the gene is equivalent to the amino acid sequence of the corresponding enzyme in plants with desired characteristics (e.g., cold tolerance), preferably in C4 plants or plants of an intermediate nature between C3 and C4, more preferably in plants belonging to Flayeria, even more preferably in F. brownii or F. bidentis. Preferably, such a substitution is allowed to occur exclusively in exon segments, with as many intron segments as possible being retained intact. The number of bases to be substituted is not particularly limited, but it is preferably about 1 to 50, more preferably about 1 to 40, and most preferably about 1 to 30 (e.g., 29) when the enzyme constituting a photosynthetic pathway is PPDK. Likewise, the number of amino acids to be substituted is preferably about 1 to 40, more preferably about 1 to 30, and most preferably about 1 to 20 (e.g., 17 as shown in FIG. 5) when the enzyme constituting a photosynthetic pathway is PPDK.

[0044]In one preferred embodiment of the present invention for creation of cold-tolerant C4 plants, a PPDK gene that is modified into a cold-tolerant type and capable of high-level expression in target plants is used as a C4 plant genomic gene encoding an enzyme constituting a photosynthetic pathway.

[0045]Such a modification into a cold-tolerant type is accomplished, for example, by establishing "equivalence" between the amino acid sequence of PPDK to be expressed and the corresponding PPDK amino acid sequence found in plants expressing cold-tolerant PPDK (preferably at a high level). Specifically, this modification is accomplished, e.g., by introducing a mutation(s) such that the amino acid sequence is equivalent to F. brownii PPDK. More specifically, it is accomplished, for example, by introducing 17 point mutations into or downstream of Exon 15 of the maize PPDK genome-derived gene such that an amino acid sequence covering an approximately 1/6 region from the C-terminal of the maize PPDK (said amino acid sequence corresponding to the sequence downstream of No. 7682 in SEQ ID NO: 15) is identical with an amino acid sequence covering an approximately 1/6 region from the C-terminal of F. brownii PPDK, which is important for cold tolerance (said amino acid sequence corresponding to the sequence downstream of No. 7682 in SEQ ID NO: 16). For this purpose, it is desirable to use codons that occur frequently in maize. Introduction of point mutations may be carried out in a general manner well known to those skilled in the art, e.g., by PCR using a primer set(s) carrying mutations.

[0046]When used herein for amino acid sequences, the term "equivalent" or "equivalence" encompasses both the meanings that an amino acid sequence is "identical" with a target sequence and that an amino acid sequence is modified to include substitution of amino acids by other qualitatively similar amino acids, with consideration given to the nature of amino acids. Likewise, for the case where the amino acid sequence of a certain enzyme is "equivalent to the amino acid sequence of the corresponding enzyme in plants with desired characteristics," the meaning is that the former amino acid sequence is exactly identical with the latter amino acid sequence, and that the former amino acid sequence is not exactly identical with the latter amino acid sequence, but is modified to include substitution of one or more (preferably about 1 to 40, more preferably about 1 to 30, most preferably about 1 to 20) amino acids different from those of the latter amino acid sequence so as to establish equivalence.

[0047]To obtain a PPDK gene modified into a cold-tolerant type and capable of high-level expression in target plants, for example, the above-mentioned mutations are allowed to occur exclusively in exon segments, with as many intron segments of the C4 plant genome-derived PPDK gene as possible being retained intact.

[0048]As a mutated "C4 plant genomic gene encoding an enzyme constituting a photosynthetic pathway," a gene consisting of any one of the following DNA molecules may be used. Such a gene is particularly preferred to obtain maize plants modified to enhance their photosynthetic rate under low temperature conditions:

[0049](a) a nucleotide sequence derived from the region downstream of Exon 15 of the maize PPDK genomic gene, whose amino acid sequence is mutated to be equivalent to the F. brownii PPDK amino acid sequence, i.e., a DNA molecule consisting of the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 16;

[0050](b) a DNA molecule consisting of a nucleotide sequence derived from the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 16 by deletion, substitution, addition or insertion of one or more nucleotides, and encoding a protein possessing PPDK activity;

[0051](c) a DNA molecule being hybridizable under stringent conditions to the DNA molecule being complementary to the DNA molecule consisting of the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 16, and encoding a protein possessing PPDK activity; and

[0052](d) a DNA molecule consisting of a nucleotide sequence being at least 50% (preferably at least 60%, more preferably at least 70%, even more preferably at least 80%, still more preferably at least 90%, particularly preferably at least 95%, and most preferably at least 98%) homologous to the nucleotide sequence of Nos. 1732-8508 of SEQ ID NO: 16, and encoding a protein possessing PPDK activity.

[0053]Alternatively, a gene encoding any one of the following proteins may be used:

[0054](a) F. brownii PPDK, i.e., a protein consisting of the amino acid sequence of SEQ ID NO: 18;

[0055](b) a protein consisting of an amino acid sequence derived from the amino acid sequence of SEQ ID NO: 18 by deletion, substitution, addition or insertion of one or more amino acids, and possessing PPDK activity;

[0056](c) PPDK derived from a C4 plant being cold-tolerant, or PPDK derived from a C3/C4 intermediate plant being cold-tolerant (preferably Flayeria brownii); and

[0057](d) a protein consisting of an amino acid sequence being at least 50% (preferably at least 60%, more preferably at least 70%, even more preferably at least 80%, still more preferably at least 90%, particularly preferably at least 95%, and most preferably at least 98%) homologous to the amino acid sequence of SEQ ID NO: 18, and possessing PPDK activity.

[0058]The present invention also provides an expression cassette that comprises an expression control region such as a promoter, a downstream C4 plant genomic gene (either of the genome-derived type or the modified type), under control of said region, encoding an enzyme constituting a photosynthetic pathway, and a terminator.

[0059]Any promoter may be used in the expression cassette of the present invention as long as it is operable in plants to be transformed. Examples of a promoter available for use include promoters driving high-level expression, in green organs, of photosynthesis-related genes including PPDK (Matsuoka et al., Proc Natl Acad Sci USA, 90:9586-9590 (1993)), PEPC (Yanagisawa and Izui, J Biochem, 106:982-987 (1989) and Matsuoka et al., Plant J, 6:311-319 (1994)) and Rubisco (Matsuoka et al., Plant J, 6:311-319 (1994)); cauliflower mosaic virus 35S promoter; ubiquitin promoter (Cornejo et al., Plant Mol Biol, 23:567-581 (1993)); actin promote (McElroy et al., Plant Cell, 2:163-171 (1990)); α-tubulin promoter (Carpenter et al., Plant Mol Biol, 21:937-942 (1993)); Sc promoter (Schenk et al., Plant Mol Biol, 39:1221-1230 (1999)); pea PAL promoter; Prp1 promoter (JP 10-500312 A); hsr203J promoter (Pontier et al., Plant J, 5:507-521 (1994)); EAS4 promoter (Yin et al., Plant Physiol, 115:437-451 (1997)); PR1b1 promoter (Tornero et al., Mol Plant Microbe Interact, 10:624-634 (1997)); tap1 promoter (Mohan et al., Plant Mol Biol, 22:475-490 (1993)); and AoPR1 promoter (Warner et al., Plant J, 3:191-201 (1993)).

[0060]Any terminator may be used in the expression cassette of the present invention as long as it is operable in plants to be transformed. Examples of a terminator available for use include nos terminator, CaMV 35S terminator, gene7 terminator and protease inhibitor II terminator.

[0061]Expression cassettes comprising the following DNA molecules may be presented by way of example for the expression cassette of the present invention:

[0062](a) a DNA molecule consisting of the nucleotide sequence of SEQ ID NO: 15;

[0063](b) a DNA molecule consisting of a nucleotide sequence derived from the nucleotide sequence of SEQ ID NO: 15 by deletion, substitution, addition or insertion of one or more nucleotides, and encoding a protein possessing PPDK activity;

[0064](c) a DNA molecule being hybridizable under stringent conditions to the DNA molecule being complementary to the DNA molecule consisting of the nucleotide sequence of SEQ ID NO: 15, and encoding a protein possessing PPDK activity; and

[0065](d) a DNA molecule consisting of a nucleotide sequence being at least 50% (preferably at least 60%, more preferably at least 70%, even more preferably at least 80%, still more preferably at least 90%, particularly preferably at least 95%, and most preferably at least 98%) homologous to the nucleotide sequence of SEQ ID NO: 15, and encoding a protein possessing PPDK activity; or

[0066](a) a DNA molecule consisting of the nucleotide sequence of SEQ ID NO: 16;

[0067](b) a DNA molecule consisting of a nucleotide sequence derived from the nucleotide sequence of SEQ ID NO: 16 by deletion, substitution, addition or insertion of one or more nucleotides, and encoding a protein possessing PPDK activity;

[0068](c) a DNA molecule being hybridizable under stringent conditions to the DNA molecule complementary to the DNA molecule consisting of the nucleotide sequence of SEQ ID NO: 16, and encoding a protein possessing PPDK activity; and

[0069](d) a DNA molecule consisting of a nucleotide sequence being at least 50% (preferably at least 60%, more preferably at least 70%, even more preferably at least 80%, still more preferably at least 90%, particularly preferably at least 95%, and most preferably at least 98%) homologous to the nucleotide sequence of SEQ ID NO: 16, and encoding a protein possessing PPDK activity.

[0070]The expression cassette of the present invention is particularly useful in creating C4 plants modified to enhance their photosynthesis rate under low temperature conditions. The present invention also provides a recombinant vector containing such an expression cassette.

[0071]A vector used for subcloning of each DNA fragment constituting the expression cassette of the present invention may be conveniently prepared by ligating a desired gene to a recombination vector (plasmid DNA) available in the art in a general manner. Specific examples of a vector available for use include pCR2.1, pBluescript, pUC18, pUC19 and pBR322, by way of example for E. coli-derived plasmids.

[0072]A plant transformation vector is useful in introducing the expression cassette of the present invention into target plants. Any plant transformation vector may be used as long as it is capable of expressing the gene of interest in plant cells and thus producing the protein of interest. Examples include pBI221, pBI121 (both available form Clontech) and vectors derived therefrom. In particular, for transformation of monocotyledonous plants, the following vectors may be exemplified: pIG121Hm, pTOK233 (both found in Hiei et al., Plant J., 6:271-282 (1994)), pSB424 (Komari et al., Plant J., 10:165-174 (1996)), pSB11, pSB21 and vectors derived therefrom.

[0073]Preferably, a plant transformation vector at least comprises a promoter, an initiation codon, a C4 plant genomic gene (either of the genome-derived type or the modified type) encoding an enzyme constituting a photosynthetic pathway, a termination codon and a terminator. It may also comprise, as appropriate, a DNA sequence encoding a signal peptide, an enhancer sequence, 5'- and 3'-untranslated regions of the desired gene, a selective marker region and the like. Examples of a marker gene include genes resistant to antibiotics such as tetracycline, ampicillin, kanamycin, neomycin, hygromycin and spectinomycin, as well as luciferase gene, β-galactosidase gene, β-glucuronidase (GUS) gene, green fluorescent protein (GFP) gene, β-lactamase gene and chloramphenicol acetyltransferase (CAT) gene.

[0074]Techniques for plant transformation have already been established, among which the Agrobacterium method can be employed. This method is well known and can be used to transform both dicotyledonous and monocotyledonous plants (WO94/00977, WO95/06722). Gene introduction may also be accomplished, e.g., by electroporation which is a standard technique for protoplasts or by using a particle gun in a general manner. When used herein for genes, the term "introduce" or "introduction" means that a gene is put into a target plant (usually, plant cells) from outside, unless otherwise specified. The introduced gene is preferably integrated into the genome of the target plant.

[0075]Transformed cells may be selected by screening using an appropriate marker as an indicator. Transformed cells may be differentiated into transgenic plants of interest using conventional techniques.

[0076]Analysis of transformants may be carried out according to various procedures well known to those skilled in the art. For example, oligonucleotide primers are synthesized based on the DNA sequence of the introduced gene and then used in PCR to analyze the chromosomal DNAs of the transgenic plants. Alternatively, the analysis may also be accomplished by determining the presence or absence of mRNA or protein expression corresponding to the introduced gene. Further, the analysis may be accomplished by testing the resulting plants for their characteristics including cold tolerance. In a case where a genomic gene for PPDK is introduced, transformants may be analyzed for the expression level of PPDK. To determine whether transformants are cold-tolerant or not, the transformants themselves or PPDK collected therefrom may be analyzed for a decrease in PPDK activity when treated at low temperature. Procedures for these analyses are well known to those skilled in the art.

[0077]The transgenic plant of the present invention allows more expression of an enzyme constituting a photosynthetic pathway, when compared with a non-transgenic plant. The expression level is preferably an effective amount to enhance photosynthesis rate in the transgenic plant. The "effective amount to enhance photosynthesis rate" means that at a certain temperature, preferably at low temperature (e.g., at around 12° C., at around 0° C.), the transgenic plant allows more expression of the enzyme constituting a photosynthetic pathway when compared with a non-transgenic plant, so that the transgenic plant has a greater photosynthesis rate and/or it grows better or produces a desired product in a higher yield.

[0078]Further, in the transgenic plant of the present invention created using a modified genomic gene, an enzyme constituting a photosynthetic pathway is more highly expressed and/or is more resistant to deactivation, when compared with a non-transgenic plant. In this case, the level of expression/deactivation is preferably an effective amount/level to enhance photosynthesis rate in the transgenic plant. The "effective amount to enhance photosynthesis rate" is as stated previously. The "effective level to enhance photosynthesis rate" used for deactivation means that at a certain temperature, preferably at low temperature (e.g., at around 12° C., at around 0° C.), the enzyme in the transgenic plant is more resistant to deactivation when compared with a non-transgenic plant, so that the transgenic plant has a greater photosynthesis rate and/or it grows better or produces a desired product in a higher yield.

[0079]In addition to maize shown below in the Examples, the present invention can also be applied to other C4 plants including sugarcane, green amaranth, Japanese millet, foxtail millet, sorgum, millet and proso millet.

[0080]As used herein, the term "transgenic plant" encompasses not only transgenic plants (T₀ generation) regenerated from recombinant plant cells created according to the method of the present invention, but also progeny plants (e.g., T₁ generation) obtained from such transgenic plants as long as the progeny plants retain the introduced characteristics. Also, the term "plant" as used herein encompasses plant individuals as well as seeds (including germinated seeds, immature seeds), organs or portions thereof (including leaves, roots, stems, flowers, stamens, pistils, pieces thereof), cultured plant cells, calluses and protoplasts, unless otherwise specified.

[0081]The method of the present invention achieves more expression of an enzyme constituting a photosynthetic pathway (e.g., PPDK as an important enzyme in the C4 cycle, or a modified form thereof) in C4 plants. The method of the present invention further achieves enhancement of photosynthesis rate in C4 plants, enabling the C4 plants to attain cold tolerance. This in turn achieves increased production of C4 plants having PPDK, particularly increased production of maize or the like under low temperature conditions.

[0082]To date, there were some examples where a C4 plant genomic gene was expressed in C3 plants, but there was no case where a C4 plant genomic gene was introduced into C4 plants to achieve high-level expression of the gene. Since C3 plants are essentially free from genes involved in the C4 photosynthesis (or, if any, in very low amounts), C3 plants readily show effects of the introduced gene. According to the present invention, high-level expression of a C4 plant genomic gene can be achieved in C4 plants and effects of the introduced gene can be obtained without being masked by the corresponding endogenous gene. Also, in another embodiment of the present invention, the nature of a gene may be modified using point mutagenesis procedures to give greater effects under specific conditions (e.g., low temperature conditions), unlike simply improving the expression level. The present invention enables the PPDK gene involved in the C4 photosynthesis to be expressed in C4 plants at high level, thus achieving for the first time enhancement of photosynthesis rate in C4 plants, which has not been realized.

[0083]Although, as stated above, the method of the present invention is useful for transformation of an enzyme constituting the C4 photosynthetic pathway, the same procedures may also be adapted to provide C4 plants with other desired characteristics. Namely, the present invention also provides a method for highly expressing an object protein in a plant using an expression cassette that comprises a promoter, a plant genomic gene, under control of said promoter, encoding the object protein, and a terminator. The genomic gene as used here will preferably comprise a nucleotide sequence derived from the nucleotide sequence of the plant genome-derived gene encoding the object protein, by deletion, substitution, addition or insertion of one or more nucleotides in the exon(s) of the gene, with the introns of the gene retained. Although the method of the present invention is useful for transformation of C4 plants, the same procedures may also be adapted to transformation of other plants.

EXAMPLES

Example 1

Construction of #2706

[0084]In order to introduce the unmodified maize PPDK genomic gene into maize, a gene used for transformation (#2706) was constructed as follows.

[0085]A 4.5 kb BamHI fragment covering from the latter half of Intron 1 to the first half of Intron 6 was cleaved from the maize PPDK genome cloned in λongC (Matsuoka M, 1990) and then inserted into a BamHI site of pSB11 (Komari T, Hiei Y, Saito Y, Murai N, Kumashiro T, Vectors carrying two separate T-DNAs for co-transformation of higher plants mediated by Agrobacterium tumefaciens and segregation of transformants free from selection marker, Plant J, 10:165-175, 1996). This plasmid was digested with XbaI to remove the λ arm segment and then blunt-ended with Klenow enzyme. The resulting fragment was ligated to a similarly blunt-ended 2 kb EcoRI fragment (covering from the promoter region to the middle of Intron 1) cleaved from the PPDK genome cloned in λEMBL3 (Matsuoka M, 1990). Subsequently, a 3.3 kb BamHI fragment covering from the latter half of Intron 6 to the transcription termination region was cleaved from the λongC clone and then inserted into a BamHI site of the vector prepared above, covering from the promoter to the first half of Intron 6. Finally, the bar gene ligated to the maize ubiquitin promoter, maize introns and the nos terminator was inserted into a KpnI site (FIG. 1). The DNA sequence (promoter to terminator) of the finally constructed clone #2706 is shown in SEQ ID NO: 15.

(Creation and Evaluation of Transgenic Plants)

[0086]According to the Agrobacterium method, the gene for transformation (#2706) was introduced into a maize inbred line (A188) to create a transgenic plant. At that time, a gene resistant to the herbicide Basta was used as a selective marker. The resulting transgenic plant was inbred to produce its progeny of the next generation, which were then cultivated. Cut leaves were sampled at the young-seedling stage and put into a Basta-containing medium to classify the progeny plants between individuals homozygous or heterozygous for the introduced PPDK gene (homo or hetero) and individuals null for the gene (null) (Ming-Bo Wang, Peter M. Waterhouse, A rapid and simple method of assaying plants transformed with hygromycin or PPT resistance, Plant Molecular Biology Reporter, 15:209-215 (1997)).

[0087]Subsequently, a green leaf extract was collected from leaves of each plant and subjected to Western analysis to estimate the amount of PPDK present in each progeny plant.

[0088]Further, from knee-height stage to de-tasselling stage, the photosynthesis rate was determined using photosynthesis-measuring devices (Model LI-6400, LI-COR). Two devices were always used for determination to perform simultaneous measurement on a pair of the same transformant-derived homo or hetero individual and null individual (25 pairs). Conditions under the photosynthesis rate was determined were set as follows: light level in a chamber: constant at 1000 μmolm^-2s^-1 (LED source of artificial light); CO₂ level in a chamber: constant at 350 μmolCO₂ mol^-1; humidity in a chamber: not controlled in principle (loosely controlled within a range where measurement was not affected); and air stream (flow rate) in a chamber: constant at 500 μmols^-1. The photosynthesis rate was determined at leaf surface temperatures of 30° C., 20° C., 13° C. and 8° C. For determination under low temperature conditions, the photosynthesis-measuring devices and plants (leaves only) were transferred into a refrigerating room where the determination was performed. Data analysis was made by paired t-test.

(Results)

[0089]The amount of PPDK contained per g of fresh green leaves is, on average, 2484.0 μg/gfwt in the homo or hetero group and 1179.6 μg/gfwt in the null group. There was a significant difference between them at a significance level of 1%, as analyzed by paired t-test. This indicated that the introduction of the maize PPDK genomic gene resulted in an increase in the expression level of PPDK (FIG. 2A).

[0090]This increase in the expression level of PPDK was also as much as sufficient to clarify effects of the introduced gene. At a leaf surface temperature of 8° C., the photosynthesis rate was found to be improved in the homo or hetero individuals when compared with null individuals (at a significance level of 5%) (FIG. 2B).

Example 2

[0091]Next, the inventors of the present invention attempted to modify the maize PPDK genomic gene into a cold-tolerant type. In the previous studies, the inventors of the present invention had already succeeded in artificially creating a cold-tolerant PPDK gene by forming a chimeric gene between cDNAs (WO95/15385). They in turn created a modified maize PPDK genomic gene whose sequence was partially replaced with the F. brownii PPDK cDNA such that the resulting spliced mRNA was identical with mRNA prepared from the cold-tolerant chimeric gene between cDNAs. This chimeric gene was then introduced into maize, but resulting in low level expression. This result would be brought about by elimination of introns naturally occurring in the genomic gene due to partial replacement of the genomic gene with the cDNA.

[0092]For this reason, with the aim of modifying the maize PPDK genomic gene into a cold-tolerant type while leaving its structure as intact as possible, point mutations were introduced to construct a cold-tolerant modified maize PPDK genomic gene (#2838) as follows.

(Construction of #2838)

[0093]Introduction of these mutations into the genomic clone was carried out by PCR (Ho S N, Hunt H D, Horton R M, Pullen J K, Pease L R, Site-directed mutagenesis by overlap extension using the polymerase chain reaction, Gene 77:51-59 (1989)). As a PCR polymerase, ExTaq or Pyrobest (both available from Takara Shuzo Co., Ltd.) was used in order to minimize amplification errors and each fragment was subcloned every step into the plasmid vector pCR2.1 or pUC19 to confirm that there was no error in its nucleotide sequence. The mutations were introduced such that the amino acid sequence was equivalent to F. brownii PPDK, and codons used for this purpose were selected from those which occurred frequently in the maize PPDK gene. First, an approximately 1/6 region from the C-terminal of PPDK, which was important for cold tolerance (Ohta S et al., (1996); corresponding to Exon 15 and its downstream region) was divided into 6 fragments and these separate fragments were amplified using primer sets carrying mutations: F1 & R1, F2 & R2, F3 & R3, F4 & R4, F5 & R5 and F6 & R6 (SEQ ID NOs: 1 to 6 and 8 to 13). Flanking two fragments were successively ligated together by PCR and Fragments 1 to 4 were then ligated into one fragment. Finally, all fragments were ligated together to complete a XhoI-BamHI fragment (FIG. 3).

[0094]Meanwhile, a SmaI-EcoRI fragment covering from the latter half of Exon 14 to the first half of Exon 16 of the maize PPDK genomic clone was subsloned into pUC18, followed by introduction of a XhoI site into Exon 15 by PCR using the primer set M4 (SEQ ID NO: 7) and mXho (SEQ ID NO: 14). This fragment was ligated to the XhoI-BamHI fragment prepared above to replace the corresponding region in the 3.3 kb BamHI fragment. This fragment was inserted into a BamHI site of the vector covering from the promoter to the first half of Intron 6. Finally, the bar gene ligated to the maize ubiquitin promoter, maize introns and the nos terminator was inserted into a KpnI site (FIG. 4). The DNA sequence (promoter to terminator) of the finally constructed clone #2838 is shown in SEQ ID NO: 16.

[0095]The amino acid sequence covering an approximately 1/6 region from the C-terminal of F. brownii PPDK, which is important for cold tolerance (said amino acid sequence corresponding to the sequence downstream of No. 7682 in SEQ ID NO: 16) is shown in FIG. 5 along with the amino acid sequence covering the same region of the maize PPDK gene (said amino acid sequence corresponding to the sequence downstream of No. 7682 in SEQ ID NO: 15).

(Creation and Evaluation of Transgenic Plants)

[0096]In the same manner as shown in Example 1, the point-mutated cold-tolerant maize PPDK genomic gene (#2838) was introduced into a maize inbred line (A188) to create a transgenic plant.

[0097]Subsequently, in the same manner as shown in Example 1, the progeny plants were classified between homo or hetero individuals and null individuals, followed by Western analysis to estimate the amount of PPDK and determination of the photosynthesis rate. As in Example 1, two devices were always used for determination of the photosynthesis rate to perform simultaneous measurement on a pair of the same transformant-derived homo or hetero individual and null individual. Data analysis was also made by paired t-test.

(Result 1)

[0098]The amount of PPDK is, on average, 2742.2 μg/gfwt in the homo or hetero group and 1471.8 μg/gfwt in the null group (FIG. 6A). This indicated that the introduction of the point-mutated cold-tolerant maize PPDK genomic gene resulted in an increase in the expression level of PPDK.

[0099]Also, the photosynthesis rate was found to be improved in the homo or hetero individuals when compared with null individuals (analysis on 15 pairs) (FIG. 6B).

(Result 2)

[0100]The number of plants used for determination of the photosynthesis rate was 15 pairs at 30° C., 19 pairs at 20° C. and 21 pairs at 8° C. The amount of PPDK is shown for the respective temperatures (FIG. 7A). The homo or hetero individuals far exceeded the null individuals (at a significance level of 1%).

[0101]Also, the photosynthesis rate was found to be improved in the homo or hetero individuals when compared with null individuals (FIG. 7B).

[0102]These results indicated that the introduction of the point-mutated cold-tolerant maize PPDK genomic gene resulted in an extremely large increase in the expression level of PPDK and a further improvement in photosynthesis rate, as compared with simple introduction of the unmodified genomic PPDK. Namely, the inventors of the present invention found that the photosynthesis rate was improved even in a temperature range where no difference was observed by simply improving the expression level.

Example 3

[0103]Further, the inventors of the present invention examined PPDK activity in the transgenic maize plants having the cold tolerance-improved genomic gene introduced thereinto. In the experiment, several maize plants with different expression levels of PPDK were used along with F. brownii and a maize inbred line (A188) as controls. A green leaf extract collected from leaves of each plant was desalted on a Sephadex G25 column and then allowed to stand at 0° C. (on ice), followed by periodical verification of PPDK activity to monitor the time course of the change in PPDK activity under low temperature conditions. PPDK activity was determined in a general manner (Jenkins C L, Hatch M D, Properties and reaction mechanism of C4 leaf pyruvate, Pi dikinase, Arch Biochem Biophys, 239:53-62, 1985).

[0104]The results are shown in FIG. 8. It could be confirmed that transformants with high expression levels of PPDK were resistant to deactivation, even on ice, as in the case of F. brownii.

Sequence CWU 1

19127DNAArtificial SequenceSynthetic PCR forward primer (F1) 1ctcgagcagc tctgatcgct gatgagg 27220DNAArtificial SequenceSynthetic PCR forward primer (F2) 2gatagcgaag gaggctgaat 20325DNAArtificial SequenceSynthetic PCR forward primer (F3) 3cccatctatc tttcccaggg cattc 25444DNAArtificial SequenceSynthetic PCR forward primer (F4) 4tcaagatggc tacagagaag ggccgcgccg ctaaccctaa cttg 44521DNAArtificial SequenceSynthetic PCR forward primer (F5) 5ttcgacgggg ttgggctgga t 21617DNAArtificial SequenceSynthetic PCR forward primer (F6) 6ctcaggtggt tgtctga 17717DNAArtificial SequenceSynthetic PCR forward primer (M4) 7gttttcccag tcacgac 17817DNAArtificial SequenceSynthetic PCR reverse primer (R1) 8cctccttcgc tatctgc 17925DNAArtificial SequenceSynthetic PCR reverse primer (R2) 9aagatagatg ggaaggaact ttccc 251043DNAArtificial SequenceSynthetic PCR reverse primer (R3) 10ctctgtagcc atcttgatca gctggcccac tcccttctgg tcc 431121DNAArtificial SequenceSynthetic PCR reverse primer (R4) 11cccaaccccg tcgaagaagg c 211217DNAArtificial SequenceSynthetic PCR reverse primer (R5) 12tcagacaacc acctgag 171317DNAArtificial SequenceSynthetic PCR reverse primer (R6) 13ggatcctagc gacatgc 171421DNAArtificial SequenceSynthetic PCR reverse primer (mXho) 14ctcgagggat ctcaatcatt g 21158820DNAmaizeDNA sequence of clone #2706 (promoter to terminator). Maize genomic DNA. 15gaattcccat tttttgttgt ttgtcaaaat aatcattgtt tggtcagtgg ttgttaggaa 60ggaggtggat agaaagttaa atttagattt tccctggggt ggaggacatg aaagagtggg 120aaaggttgct ggacattttg gaaggagtga taattactaa acgagaatat atgttatctt 180cgtcgttaga gaaatctaga cagtatacaa caagatccac gtactatagg taaactttta 240ggggtattgt gaacaagagg atgagtaaac tctaaaagaa caaagctcca atgaaaattt 300aggtttttat gtggttagtc atagggcaag ttgcaaacag gtgttgatct aaaaaggaag 360tagtagggaa atgtgaagtg tctttgcgag gaattggaaa atgaagatca cattttcttt 420gggtgcatca tgggaagaac catttgggac tcttttaagg aggcctaaga atgccataaa 480gtttgcaaga tctttttgaa gagtgtctac ctataaacaa tagtaaatat catgtcaaat 540ttttcatctt cgccattatt ctttaggaga atttagaatg ttccgaataa aatatggata 600gaaaagaagt tcccaaagtc atccaatttt ctacaaaatc ttcaacttta agattgagag 660tgagtgttgt aaagttcttg gaagatgagt tgaaccccat ggaggcgttg gctaaagtac 720tgaaagcaat ctaaagacat ggaggtggaa ggcctgacgt agatagagaa gatgctctta 780gctttcattg tctttctttt gtagtcatct gatttacctc tctcgtttat acaactggtt 840ttttaaacac tccttaactt ttcaaattgt ctctttcttt accctagact agataatttt 900aatggtgatt ttgctaatgt ggcgccatgt tagatagagg taaaatgaac tagttaaaag 960ctcagagtga taaatcaggc tctcaaaaat tcataaactg ttttttaaat atccaaatat 1020ttttacatgg aaaataataa aatttagttt agtattaaaa attcagttga atatagtttt 1080gtcttcaaaa attatgaaac tgatcttaat tatttttcct taaaaccgtg ctctatcttt 1140gatgtctagt ttgagacgat tgtataattt ttttgtgctt atctacgacg agctgaagta 1200cgtagaaata ctagtggagt cgtgccgcgt gtgcctgtag ccactcgtac gctacagccc 1260aagcgctaga gcccaagagg ccggaggtgg aaggcgtcgc ggcactatag ccactcgccg 1320caagagccca agaggccgga gctggaagga tgagggtctg ggtgttcacg aattgcctgg 1380aggcaggagg ctcgtcgtcc ggagccacag gcgtggagac gtccgggata aggtgagcag 1440ccgctgcgat aggggcgcgt gtgaaccccg tcgcgcccca cggatggtat aagaataaag 1500gcattccgcg tgcaggattc acccgttcgc ctctcacctt ttcgctgtac tcactcgcca 1560cacacacccc ctctccagct ccgttggagc tccggacagc agcaggcgcg gggcggtcac 1620gtagtaagca gctctcggct ccctctcccc ttgctccata tgatcgtgca acccatcgag 1680ctacgcgcgt ggactgcctt ccctgggtcg gcgcaggagg ggatcggaag gatgacggca 1740tcggtttcca gggccatctg cgtacagaag ccgggctcaa aatgcaccag ggacagggaa 1800gcgacctcct tcgcccgccg atcggtcgca gcgccgaggc ccccgcacgc caaagccgcc 1860ggcgtcatcc gctccgactc cggcgcggga cggggccagc attgctcgcc gctgagggcc 1920gtcgttgacg ccgcgccgat acagacgacc aaaaaggtat cccttgcagc tcttagaaac 1980tgaattctag aggttcaggg ttgtatatcc acaatctagt ttatccacca ttaataagat 2040ataatttgtt acggcgtggc aatgcacttc cacgaactcc tgaggcagcg gataatgttt 2100aaaaacgcat ttttgtcaac caggattaag aagctcattt tgagtttgcc cccatttggt 2160tagaacatgg aacacgttct gcatatagtt ttcctctggg taagattgcg tagcgatcag 2220gttttcggat cttccactcc gttttcccgt cgtcatacgt aggcgtagcg gtccacctca 2280ttcgttcact tgtagttgta gctaggaagc tctctcccaa cggcgtgccg cacactcttt 2340tgccggcccg acgcaaaaat ggcatgaatt tgctccaccg tgtttacata tgtaggagaa 2400cttggataaa actgtgtaaa tactgcaaca catggatatg ggcactgtag tttaccctac 2460cttaattaag caccaagctg cggcagagcg gctcggagtg cgtgcaaaaa cgacagccat 2520ccgtgcgctc tccttgtggc ttctgcaggc tgcagcagct gccacccgcc cgcgccatgg 2580acgcacggtg gacggtgctc tgcgcctctg cctatctccc gggaacgccg tgaccgggta 2640ctagctagct tgaacgggat accaggcgga gacgcccgcg gatttgcgga agcgtatcgc 2700cggccgtgct gcgatctata tcccatcgtc taacaggcga cccatccagc tgacgcgacg 2760aattaacaac gctatccgcg cgcatgcatg gccatgactt ggctattttg cactgtgcaa 2820atgtctgccc agtagttcat ctcacgaaca caaatgccgg tggtcagtag gagagagaag 2880aactaactcc agcgtccgat cgggacgcca ctcgctcgct cacaagcaaa gacactagct 2940agtctcaact ctcaactaca acaacgctag taaagcctaa aacacacaca cgcacgcaca 3000cacaagcaaa gcgagcaacg tacgttcgtc agtgcgtcct tgtgaaacag aaagcgcgcg 3060ctctagctat agctgcaccg tgtctgcatg cgtgctgaca cgacagggtg agtcacacag 3120aagcggcgct tggacgctag cagcacgatc agttcagttt ttcagcgttt cttttttttt 3180ctggctggat atgcatcacg catggaacaa gagggtgtga catgcacgcc cagtggtggt 3240cgttcttgca ttgcatttgg gctctgtatg atttaagatg gagggagtag cacaagtgta 3300gttggcaggc tatttaccga tgatcaattt ttattaccag gtactctatc aaacaagtag 3360tagctctact gtttaattag tctaacaagt gtagttggca cgtagggaag caagcccatg 3420ttgatctgag gtggccgcgg gcgtccggaa ctccggatat gtatgctcgc tgctaccggc 3480cagtaagctg gggcatgcgt gcgttcactt gcttgagacc gtttctaact ttgcaaacaa 3540aaaaaaaaca accagcacca gactacgtga cgtgtaaagc tcatcctgac tgtttattgc 3600tgcctgtttg tgaagaaaga aagaaaaaaa aaaagagaga gtcggccggg ctgctgcaca 3660cgcacatcac tcgcggccgc cgctgctata aatagagccc ggggcaggcc ctgcttaatt 3720catcaccagc cacggctgca tttatttgtc actgatcgtt gatcagccta gctagctagc 3780gctgttttcc tgtgtgctaa tggcgcccgt tcaatgtgcg cgttcgcaga gggtgttcca 3840cttcggcaag ggcaagagcg agggcaacaa gaccatgaag gaactggtga gaggtttctt 3900ctttctgtat tctcgcttaa tctgcatgca tgcatgcata catactaatg aagtaataac 3960gatgctgtcg atgaatgatg acgcatgcag ctgggcggca agggcgcgaa cctggcggag 4020atggcgagca tcgggctgtc ggtgccgcca gggttcacgg tgtcgacgga ggcgtgccag 4080cagtaccagg acgccgggtg cgccctcccc gcggggctct gggccgagat cgtcgacggc 4140ctgcagtggg tggaggagta catgggcgcc accctgggcg atccgcagcg cccgctcctg 4200ctctccgtcc gctccggcgc cgccgtgtcc atgcccggca tgatggacac ggtgctcaac 4260ctggggctca acgacgaagt ggccgccggg ctggcggcca agagcgggga gcgcttcgcc 4320tacgactcct tccgccgctt cctcgacatg ttcggcaacg tcgtgagtat cccccgcgcc 4380gtagcatgcg tcttcgattc cgcgccctga ctcagctcct cgcttccatt cccgtccgcc 4440ggttgttgtt actgctagct tgtcccacta gctaggtgca gtaggtgcct agttttgcgc 4500gcatcgcgtc gcgtcgacga cgacccatcc tccaccgcgc tgccgtggcc gcaaccaagg 4560ctggatggag cttttgtctg tttgccaggc cagccgttgc tttgggttaa aagtgcaaaa 4620aaaaaatgat gaaggtcacg ctacgaacta aacagaccat atacgtacgg catcggcatg 4680taaacttggc ttgtcggact cgagaaacga aagaacgatg actcaaactg ctctcagatt 4740ttgtttcatt gtttgtgttt accaggtcat ggacatcccc cgctcactgt tcgaagagaa 4800gcttgagcac atgaaggaat ccaaggggct gaagaacgac accgacctca cggcctctga 4860cctcaaagag ctcgtgggtc agtacaagga ggtctacctc tcagccaagg gagagccatt 4920cccctcaggt acataccggc ccgtcgatcg tcctcagctc tactgatcga tggagctagc 4980ggtcagtttc cctgtgcacc gaaatcatgt gcttgcctgc cttgcagacc ccaagaagca 5040gctggagcta gcagtgctgg ctgtgttcaa ctcgtgggag agccccaggg ccaagaagta 5100caggagcatc aaccagatca ctggcctcag gggcaccgcc gtgaacgtgc agtgcatggt 5160gttcggcaac atggggaaca cttctggcac cggcgtgctc ttcaccagga accccaacac 5220cggagagaag aagctgtatg gcgagttcct ggtgaacgct caggtatgag tcggccctca 5280ggcttccatt gcgcgcctgt tcgtgcatgg atacacgtac gtacgttact tgacgccatg 5340catgcaattc gtttcctgct cagggtgagg atgtggttgc cggaataaga accccagagg 5400accttgacgc catgaagaac ctcatgccac aggcctacga cgagcttgtt gagaactgca 5460acatcctgga gagccactac aaggaaatgc aggtacagtt taattttcac cttctaattt 5520aaacaccaca ccaccgtctc tctctctctc tctggatcct gatgtttctt ctccagatga 5580tgtgagctca ggctgagact tggtttttct ttggcgtgtg tgatcatgca ggatatcgag 5640ttcactgtcc aggaaaacag gctgtggatg ttgcagtgca ggacagggaa acgtacgggc 5700aaaagtgccg tgaagatcgc cgtggacatg gttaacgagg gccttgttga gccccgctca 5760gcgatcaaga tggtagagcc aggccacctg gaccagcttc tccatcctca ggtaatctat 5820cgatcaagaa ccatggacgt acgtactaag ggcttaccaa atcaatcctt actaatgccg 5880ttatgcattg atgccgttat ggaaacccac agtttgagaa cccgtcggcg tacaaggatc 5940aagtcattgc cactggtctg ccagcctcac ctggggctgc tgtgggccag gttgtgttca 6000ctgctgagga tgctgaagca tggcattccc aagggaaagc tgctattctg gtaatattca 6060tcgcaaaaca ctttttattt ggactgcttt tccatacaac attttcacca gtttttgtaa 6120atatatatac tgtatactgt atgcaggtaa gggcagagac cagccctgag gacgttggtg 6180gcatgcacgc tgctgtgggg attcttacag agaggggtgg catgacttcc cacgctgctg 6240tggtcgcacg tgggtggggg aaatgctgcg tctcgggatg ctcaggcatt cgcgtaaacg 6300atgcggagaa ggtgacttga aatcctctgt tacgcaagga agctccagca tgtctcgtga 6360tttaccttgc tgtttattta tatgaattag ctcgtgacga tcggaggcca tgtgctgcgc 6420gaaggtgagt ggctgtcgct gaatgggtcg actggtgagg tgatccttgg gaagcagccg 6480ctttccccac cagcccttag tggtgatctg ggaactttca tggcctgggt ggatgatgtt 6540agaaagctca aggtaaaaat cccagacata ttccaatctt tctttttttc aagttcaaac 6600aagctaaaag ggtttccatc ggcaatgact aaattatttg catatgttct tctaggtcct 6660ggctaacgcc gatacccctg atgatgcatt gactgcgcga aacaatgggg cacaaggaat 6720tggattatgc cggacagagc acatggtacg tccgatccta catagttttt ggctagggat 6780acttggacat tttactcttc ctttagtttc tttgtcctag acaagaaaaa cagtttcatg 6840ttttttctcc ccacctgtac ttggggcagt tctttgcttc agacgagagg attaaggctg 6900tcaggcagat gattatggct cccacgcttg agctgaggca gcaggcgctc gaccgtctct 6960tgccgtatca gaggtctgac ttcgaaggca ttttccgtgc tatggatggt aagtgaaaaa 7020aacacagtgc atcccattta catgcaggac tgcatggtct gaacattctc ttggtatctt 7080gcgtttcagg actcccggtg accatccgac tcctggaccc tcccctccac gagttccttc 7140cagaagggaa catcgaggac attgtaagtg aattatgtgc tgagacggga gccaaccagg 7200aggatgccct cgcgcgaatt gaaaagcttt cagaagtaaa cccgatgctt ggcttccgtg 7260ggtgcaggtt ggatttctgc tactctatca cagcaaaaga aaaaaaaatc actggtgatg 7320cctgattgac tgattttgga actgccgaaa tttccaggct tggtatatcg taccctgaat 7380tgacagagat gcaagcccgg gccatttttg aagctgctat agcaatgacc aaccagggtg 7440ttcaagtgtt cccagagata atggttcctc ttgttggaac accacaggca tgtgtcttta 7500ctttttatat attaatgtat gtacatactg tctctgcagt tcaaaaaaag tgagcaaata 7560aatccagttg atgcagaaac aagcagctaa ttaatagctg acgtttggta tttccaggaa 7620ctggggcatc aagtgactct tatccgccaa gttgctgaga aagtgttcgc caatgtgggc 7680aagactatcg ggtacaaagt tggaacaatg attgagatcc ccagggcagc tctggtggct 7740gatgaggtag ggaaaactac caagttcaga atcgcccaga actttgccaa caagtttgtt 7800tatctgtgca ttcctacgct ggtctgaaat ctgtggctgt tgttgttgtt tttttggttt 7860cgtcaacctg gcagatagcg gagcaggctg aattcttctc cttcggaacg aacgacctga 7920cgcagatgac ctttgggtac agcagggatg atgtgggaaa gttcattccc gtctatcttg 7980ctcagggcat tctccaacat gaccccttcg aggtaactgt tgcaactctg cctgccaccc 8040tcgcatgtcg catctgatgt gacatgagca tctcatgtcg cgatcgcctt tcatttggat 8100gcccgtacac ctaccaggtc ctggaccaga ggggagtggg cgagctggtg aagcttgcta 8160cagagagggg ccgcaaagct aggcctaact tgaaggttgg ttttgggaca ctgcttcgta 8220cgtctcctta gaaaaccacg gtttgattgt tgtttggttt tgtgtgcaaa caggtgggca 8280tttgtggaga acacggtgga gagccttcct ctgtggcctt cttcgcgaag gctgggctgg 8340attacgtttc ttgctcccct ttcaggtcgg ttcagtcact gataaactcg tgattgaatc 8400caataagcgt atcctcttat gttaacggta gcaaaatgtt cactgttttc tttgaatgct 8460ttctgcaggg ttccgattgc taggctagct gcagctcagg tgcttgtctg aggctgcctc 8520ctcattggca accggattgc ctgctgctgg tggatgtggt gatcaacagt attattacag 8580agccatgcta tgtgaacatt actagtagca gtgctcataa aagctacaat cccatgtcct 8640ttttttcccc agtcatgtaa aacttccaaa ctgctccatg gttcaaaact ctgttcttca 8700atacatcatc aattatcgat tatatacgtg gcaagttttt ttctttgttt gctttttttc 8760ctttctggca tgtgtttttt ggttttcttg gtgtgtgagg tgtgcatgtc gctaggatcc 8820168820DNAmaizeDNA sequence of mutated clone #2838 (promoter to terminator). Amino acid substituted maize genomic DNA 16gaattcccat tttttgttgt ttgtcaaaat aatcattgtt tggtcagtgg ttgttaggaa 60ggaggtggat agaaagttaa atttagattt tccctggggt ggaggacatg aaagagtggg 120aaaggttgct ggacattttg gaaggagtga taattactaa acgagaatat atgttatctt 180cgtcgttaga gaaatctaga cagtatacaa caagatccac gtactatagg taaactttta 240ggggtattgt gaacaagagg atgagtaaac tctaaaagaa caaagctcca atgaaaattt 300aggtttttat gtggttagtc atagggcaag ttgcaaacag gtgttgatct aaaaaggaag 360tagtagggaa atgtgaagtg tctttgcgag gaattggaaa atgaagatca cattttcttt 420gggtgcatca tgggaagaac catttgggac tcttttaagg aggcctaaga atgccataaa 480gtttgcaaga tctttttgaa gagtgtctac ctataaacaa tagtaaatat catgtcaaat 540ttttcatctt cgccattatt ctttaggaga atttagaatg ttccgaataa aatatggata 600gaaaagaagt tcccaaagtc atccaatttt ctacaaaatc ttcaacttta agattgagag 660tgagtgttgt aaagttcttg gaagatgagt tgaaccccat ggaggcgttg gctaaagtac 720tgaaagcaat ctaaagacat ggaggtggaa ggcctgacgt agatagagaa gatgctctta 780gctttcattg tctttctttt gtagtcatct gatttacctc tctcgtttat acaactggtt 840ttttaaacac tccttaactt ttcaaattgt ctctttcttt accctagact agataatttt 900aatggtgatt ttgctaatgt ggcgccatgt tagatagagg taaaatgaac tagttaaaag 960ctcagagtga taaatcaggc tctcaaaaat tcataaactg ttttttaaat atccaaatat 1020ttttacatgg aaaataataa aatttagttt agtattaaaa attcagttga atatagtttt 1080gtcttcaaaa attatgaaac tgatcttaat tatttttcct taaaaccgtg ctctatcttt 1140gatgtctagt ttgagacgat tgtataattt ttttgtgctt atctacgacg agctgaagta 1200cgtagaaata ctagtggagt cgtgccgcgt gtgcctgtag ccactcgtac gctacagccc 1260aagcgctaga gcccaagagg ccggaggtgg aaggcgtcgc ggcactatag ccactcgccg 1320caagagccca agaggccgga gctggaagga tgagggtctg ggtgttcacg aattgcctgg 1380aggcaggagg ctcgtcgtcc ggagccacag gcgtggagac gtccgggata aggtgagcag 1440ccgctgcgat aggggcgcgt gtgaaccccg tcgcgcccca cggatggtat aagaataaag 1500gcattccgcg tgcaggattc acccgttcgc ctctcacctt ttcgctgtac tcactcgcca 1560cacacacccc ctctccagct ccgttggagc tccggacagc agcaggcgcg gggcggtcac 1620gtagtaagca gctctcggct ccctctcccc ttgctccata tgatcgtgca acccatcgag 1680ctacgcgcgt ggactgcctt ccctgggtcg gcgcaggagg ggatcggaag gatgacggca 1740tcggtttcca gggccatctg cgtacagaag ccgggctcaa aatgcaccag ggacagggaa 1800gcgacctcct tcgcccgccg atcggtcgca gcgccgaggc ccccgcacgc caaagccgcc 1860ggcgtcatcc gctccgactc cggcgcggga cggggccagc attgctcgcc gctgagggcc 1920gtcgttgacg ccgcgccgat acagacgacc aaaaaggtat cccttgcagc tcttagaaac 1980tgaattctag aggttcaggg ttgtatatcc acaatctagt ttatccacca ttaataagat 2040ataatttgtt acggcgtggc aatgcacttc cacgaactcc tgaggcagcg gataatgttt 2100aaaaacgcat ttttgtcaac caggattaag aagctcattt tgagtttgcc cccatttggt 2160tagaacatgg aacacgttct gcatatagtt ttcctctggg taagattgcg tagcgatcag 2220gttttcggat cttccactcc gttttcccgt cgtcatacgt aggcgtagcg gtccacctca 2280ttcgttcact tgtagttgta gctaggaagc tctctcccaa cggcgtgccg cacactcttt 2340tgccggcccg acgcaaaaat ggcatgaatt tgctccaccg tgtttacata tgtaggagaa 2400cttggataaa actgtgtaaa tactgcaaca catggatatg ggcactgtag tttaccctac 2460cttaattaag caccaagctg cggcagagcg gctcggagtg cgtgcaaaaa cgacagccat 2520ccgtgcgctc tccttgtggc ttctgcaggc tgcagcagct gccacccgcc cgcgccatgg 2580acgcacggtg gacggtgctc tgcgcctctg cctatctccc gggaacgccg tgaccgggta 2640ctagctagct tgaacgggat accaggcgga gacgcccgcg gatttgcgga agcgtatcgc 2700cggccgtgct gcgatctata tcccatcgtc taacaggcga cccatccagc tgacgcgacg 2760aattaacaac gctatccgcg cgcatgcatg gccatgactt ggctattttg cactgtgcaa 2820atgtctgccc agtagttcat ctcacgaaca caaatgccgg tggtcagtag gagagagaag 2880aactaactcc agcgtccgat cgggacgcca ctcgctcgct cacaagcaaa gacactagct 2940agtctcaact ctcaactaca acaacgctag taaagcctaa aacacacaca cgcacgcaca 3000cacaagcaaa gcgagcaacg tacgttcgtc agtgcgtcct tgtgaaacag aaagcgcgcg 3060ctctagctat agctgcaccg tgtctgcatg cgtgctgaca cgacagggtg agtcacacag 3120aagcggcgct tggacgctag cagcacgatc agttcagttt ttcagcgttt cttttttttt 3180ctggctggat atgcatcacg catggaacaa gagggtgtga catgcacgcc cagtggtggt 3240cgttcttgca ttgcatttgg gctctgtatg atttaagatg gagggagtag cacaagtgta 3300gttggcaggc tatttaccga tgatcaattt ttattaccag gtactctatc aaacaagtag 3360tagctctact gtttaattag tctaacaagt gtagttggca cgtagggaag caagcccatg 3420ttgatctgag gtggccgcgg gcgtccggaa ctccggatat gtatgctcgc tgctaccggc 3480cagtaagctg gggcatgcgt gcgttcactt gcttgagacc gtttctaact ttgcaaacaa 3540aaaaaaaaca accagcacca gactacgtga cgtgtaaagc tcatcctgac tgtttattgc 3600tgcctgtttg tgaagaaaga aagaaaaaaa aaaagagaga gtcggccggg ctgctgcaca 3660cgcacatcac tcgcggccgc cgctgctata aatagagccc ggggcaggcc ctgcttaatt 3720catcaccagc cacggctgca tttatttgtc actgatcgtt gatcagccta gctagctagc 3780gctgttttcc tgtgtgctaa tggcgcccgt tcaatgtgcg cgttcgcaga gggtgttcca 3840cttcggcaag ggcaagagcg agggcaacaa gaccatgaag gaactggtga gaggtttctt 3900ctttctgtat tctcgcttaa tctgcatgca tgcatgcata catactaatg aagtaataac 3960gatgctgtcg atgaatgatg acgcatgcag ctgggcggca agggcgcgaa cctggcggag 4020atggcgagca tcgggctgtc ggtgccgcca gggttcacgg tgtcgacgga ggcgtgccag 4080cagtaccagg acgccgggtg cgccctcccc gcggggctct gggccgagat cgtcgacggc 4140ctgcagtggg tggaggagta catgggcgcc accctgggcg atccgcagcg cccgctcctg 4200ctctccgtcc gctccggcgc cgccgtgtcc atgcccggca tgatggacac ggtgctcaac 4260ctggggctca acgacgaagt ggccgccggg ctggcggcca agagcgggga gcgcttcgcc 4320tacgactcct tccgccgctt cctcgacatg

ttcggcaacg tcgtgagtat cccccgcgcc 4380gtagcatgcg tcttcgattc cgcgccctga ctcagctcct cgcttccatt cccgtccgcc 4440ggttgttgtt actgctagct tgtcccacta gctaggtgca gtaggtgcct agttttgcgc 4500gcatcgcgtc gcgtcgacga cgacccatcc tccaccgcgc tgccgtggcc gcaaccaagg 4560ctggatggag cttttgtctg tttgccaggc cagccgttgc tttgggttaa aagtgcaaaa 4620aaaaaatgat gaaggtcacg ctacgaacta aacagaccat atacgtacgg catcggcatg 4680taaacttggc ttgtcggact cgagaaacga aagaacgatg actcaaactg ctctcagatt 4740ttgtttcatt gtttgtgttt accaggtcat ggacatcccc cgctcactgt tcgaagagaa 4800gcttgagcac atgaaggaat ccaaggggct gaagaacgac accgacctca cggcctctga 4860cctcaaagag ctcgtgggtc agtacaagga ggtctacctc tcagccaagg gagagccatt 4920cccctcaggt acataccggc ccgtcgatcg tcctcagctc tactgatcga tggagctagc 4980ggtcagtttc cctgtgcacc gaaatcatgt gcttgcctgc cttgcagacc ccaagaagca 5040gctggagcta gcagtgctgg ctgtgttcaa ctcgtgggag agccccaggg ccaagaagta 5100caggagcatc aaccagatca ctggcctcag gggcaccgcc gtgaacgtgc agtgcatggt 5160gttcggcaac atggggaaca cttctggcac cggcgtgctc ttcaccagga accccaacac 5220cggagagaag aagctgtatg gcgagttcct ggtgaacgct caggtatgag tcggccctca 5280ggcttccatt gcgcgcctgt tcgtgcatgg atacacgtac gtacgttact tgacgccatg 5340catgcaattc gtttcctgct cagggtgagg atgtggttgc cggaataaga accccagagg 5400accttgacgc catgaagaac ctcatgccac aggcctacga cgagcttgtt gagaactgca 5460acatcctgga gagccactac aaggaaatgc aggtacagtt taattttcac cttctaattt 5520aaacaccaca ccaccgtctc tctctctctc tctggatcct gatgtttctt ctccagatga 5580tgtgagctca ggctgagact tggtttttct ttggcgtgtg tgatcatgca ggatatcgag 5640ttcactgtcc aggaaaacag gctgtggatg ttgcagtgca ggacagggaa acgtacgggc 5700aaaagtgccg tgaagatcgc cgtggacatg gttaacgagg gccttgttga gccccgctca 5760gcgatcaaga tggtagagcc aggccacctg gaccagcttc tccatcctca ggtaatctat 5820cgatcaagaa ccatggacgt acgtactaag ggcttaccaa atcaatcctt actaatgccg 5880ttatgcattg atgccgttat ggaaacccac agtttgagaa cccgtcggcg tacaaggatc 5940aagtcattgc cactggtctg ccagcctcac ctggggctgc tgtgggccag gttgtgttca 6000ctgctgagga tgctgaagca tggcattccc aagggaaagc tgctattctg gtaatattca 6060tcgcaaaaca ctttttattt ggactgcttt tccatacaac attttcacca gtttttgtaa 6120atatatatac tgtatactgt atgcaggtaa gggcagagac cagccctgag gacgttggtg 6180gcatgcacgc tgctgtgggg attcttacag agaggggtgg catgacttcc cacgctgctg 6240tggtcgcacg tgggtggggg aaatgctgcg tctcgggatg ctcaggcatt cgcgtaaacg 6300atgcggagaa ggtgacttga aatcctctgt tacgcaagga agctccagca tgtctcgtga 6360tttaccttgc tgtttattta tatgaattag ctcgtgacga tcggaggcca tgtgctgcgc 6420gaaggtgagt ggctgtcgct gaatgggtcg actggtgagg tgatccttgg gaagcagccg 6480ctttccccac cagcccttag tggtgatctg ggaactttca tggcctgggt ggatgatgtt 6540agaaagctca aggtaaaaat cccagacata ttccaatctt tctttttttc aagttcaaac 6600aagctaaaag ggtttccatc ggcaatgact aaattatttg catatgttct tctaggtcct 6660ggctaacgcc gatacccctg atgatgcatt gactgcgcga aacaatgggg cacaaggaat 6720tggattatgc cggacagagc acatggtacg tccgatccta catagttttt ggctagggat 6780acttggacat tttactcttc ctttagtttc tttgtcctag acaagaaaaa cagtttcatg 6840ttttttctcc ccacctgtac ttggggcagt tctttgcttc agacgagagg attaaggctg 6900tcaggcagat gattatggct cccacgcttg agctgaggca gcaggcgctc gaccgtctct 6960tgccgtatca gaggtctgac ttcgaaggca ttttccgtgc tatggatggt aagtgaaaaa 7020aacacagtgc atcccattta catgcaggac tgcatggtct gaacattctc ttggtatctt 7080gcgtttcagg actcccggtg accatccgac tcctggaccc tcccctccac gagttccttc 7140cagaagggaa catcgaggac attgtaagtg aattatgtgc tgagacggga gccaaccagg 7200aggatgccct cgcgcgaatt gaaaagcttt cagaagtaaa cccgatgctt ggcttccgtg 7260ggtgcaggtt ggatttctgc tactctatca cagcaaaaga aaaaaaaatc actggtgatg 7320cctgattgac tgattttgga actgccgaaa tttccaggct tggtatatcg taccctgaat 7380tgacagagat gcaagcccgg gccatttttg aagctgctat agcaatgacc aaccagggtg 7440ttcaagtgtt cccagagata atggttcctc ttgttggaac accacaggca tgtgtcttta 7500ctttttatat attaatgtat gtacatactg tctctgcagt tcaaaaaaag tgagcaaata 7560aatccagttg atgcagaaac aagcagctaa ttaatagctg acgtttggta tttccaggaa 7620ctggggcatc aagtgactct tatccgccaa gttgctgaga aagtgttcgc caatgtgggc 7680aagactatcg ggtacaaagt tggaacaatg attgagatcc ctcgagcagc tctgatcgct 7740gatgaggtag ggaaaactac caagttcaga atcgcccaga actttgccaa caagtttgtt 7800tatctgtgca ttcctacgct ggtctgaaat ctgtggctgt tgttgttgtt tttttggttt 7860cgtcaacctg gcagatagcg aaggaggctg aattcttctc cttcggaacg aacgacctga 7920cgcagatgac ctttgggtac agcagggatg atgtgggaaa gttccttccc atctatcttt 7980cccagggcat tctccaacat gaccccttcg aggtaactgt tgcaactctg cctgccaccc 8040tcgcatgtcg catctgatgt gacatgagca tctcatgtcg cgatcgcctt tcatttggat 8100gcccgtacac ctaccaggtc ctggaccaga agggagtggg ccagctgatc aagatggcta 8160cagagaaggg ccgcgccgct aaccctaact tgaaggttgg ttttgggaca ctgcttcgta 8220cgtctcctta gaaaaccacg gtttgattgt tgtttggttt tgtgtgcaaa caggtgggca 8280tttgtggaga acacggtgga gagccttcct ctgtggcctt cttcgacggg gttgggctgg 8340attacgtttc ttgctcccct ttcaggtcgg ttcagtcact gataaactcg tgattgaatc 8400caataagcgt atcctcttat gttaacggta gcaaaatgtt cactgttttc tttgaatgct 8460ttctgcaggg ttccgattgc taggctagct gcagctcagg tggttgtctg aggctgcctc 8520ctcattggca accggattgc ctgctgctgg tggatgtggt gatcaacagt attattacag 8580agccatgcta tgtgaacatt actagtagca gtgctcataa aagctacaat cccatgtcct 8640ttttttcccc agtcatgtaa aacttccaaa ctgctccatg gttcaaaact ctgttcttca 8700atacatcatc aattatcgat tatatacgtg gcaagttttt ttctttgttt gctttttttc 8760ctttctggca tgtgtttttt ggttttcttg gtgtgtgagg tgtgcatgtc gctaggatcc 882017947PRTmaizePPDK 17Met Thr Ala Ser Val Ser Arg Ala Ile Cys Val Gln Lys Pro Gly Ser1 5 10 15Lys Cys Thr Arg Asp Arg Glu Ala Thr Ser Phe Ala Arg Arg Ser Val 20 25 30Ala Ala Pro Arg Pro Pro His Ala Lys Ala Ala Gly Val Ile Arg Ser 35 40 45Asp Ser Gly Ala Gly Arg Gly Gln His Cys Ser Pro Leu Arg Ala Val 50 55 60Val Asp Ala Ala Pro Ile Gln Thr Thr Lys Lys Arg Val Phe His Phe65 70 75 80Gly Lys Gly Lys Ser Glu Gly Asn Lys Thr Met Lys Glu Leu Leu Gly 85 90 95Gly Lys Gly Ala Asn Leu Ala Glu Met Ala Ser Ile Gly Leu Ser Val 100 105 110Pro Pro Gly Phe Thr Val Ser Thr Glu Ala Cys Gln Gln Tyr Gln Asp 115 120 125Ala Gly Cys Ala Leu Pro Ala Gly Leu Trp Ala Glu Ile Val Asp Gly 130 135 140Leu Gln Trp Val Glu Glu Tyr Met Gly Ala Thr Leu Gly Asp Pro Gln145 150 155 160Arg Pro Leu Leu Leu Ser Val Arg Ser Gly Ala Ala Val Ser Met Pro 165 170 175Gly Met Met Asp Thr Val Leu Asn Leu Gly Leu Asn Asp Glu Val Ala 180 185 190Ala Gly Leu Ala Ala Lys Ser Gly Glu Arg Phe Ala Tyr Asp Ser Phe 195 200 205Arg Arg Phe Leu Asp Met Phe Gly Asn Val Val Met Asp Ile Pro Arg 210 215 220Ser Leu Phe Glu Glu Lys Leu Glu His Met Lys Glu Ser Lys Gly Leu225 230 235 240Lys Asn Asp Thr Asp Leu Thr Ala Ser Asp Leu Lys Glu Leu Val Gly 245 250 255Gln Tyr Lys Glu Val Tyr Leu Ser Ala Lys Gly Glu Pro Phe Pro Ser 260 265 270Asp Pro Lys Lys Gln Leu Glu Leu Ala Val Leu Ala Val Phe Asn Ser 275 280 285Trp Glu Ser Pro Arg Ala Lys Lys Tyr Arg Ser Ile Asn Gln Ile Thr 290 295 300Gly Leu Arg Gly Thr Ala Val Asn Val Gln Cys Met Val Phe Gly Asn305 310 315 320Met Gly Asn Thr Ser Gly Thr Gly Val Leu Phe Thr Arg Asn Pro Asn 325 330 335Thr Gly Glu Lys Lys Leu Tyr Gly Glu Phe Leu Val Asn Ala Gln Gly 340 345 350Glu Asp Val Val Ala Gly Ile Arg Thr Pro Glu Asp Leu Asp Ala Met 355 360 365Lys Asn Leu Met Pro Gln Ala Tyr Asp Glu Leu Val Glu Asn Cys Asn 370 375 380Ile Leu Glu Ser His Tyr Lys Glu Met Gln Asp Ile Glu Phe Thr Val385 390 395 400Gln Glu Asn Arg Leu Trp Met Leu Gln Cys Arg Thr Gly Lys Arg Thr 405 410 415Gly Lys Ser Ala Val Lys Ile Ala Val Asp Met Val Asn Glu Gly Leu 420 425 430Val Glu Pro Arg Ser Ala Ile Lys Met Val Glu Pro Gly His Leu Asp 435 440 445Gln Leu Leu His Pro Gln Phe Glu Asn Pro Ser Ala Tyr Lys Asp Gln 450 455 460Val Ile Ala Thr Gly Leu Pro Ala Ser Pro Gly Ala Ala Val Gly Gln465 470 475 480Val Val Phe Thr Ala Glu Asp Ala Glu Ala Trp His Ser Gln Gly Lys 485 490 495Ala Ala Ile Leu Val Arg Ala Glu Thr Ser Pro Glu Asp Val Gly Gly 500 505 510Met His Ala Ala Val Gly Ile Leu Thr Glu Arg Gly Gly Met Thr Ser 515 520 525His Ala Ala Val Val Ala Arg Gly Trp Gly Lys Cys Cys Val Ser Gly 530 535 540Cys Ser Gly Ile Arg Val Asn Asp Ala Glu Lys Leu Val Thr Ile Gly545 550 555 560Gly His Val Leu Arg Glu Gly Glu Trp Leu Ser Leu Asn Gly Ser Thr 565 570 575Gly Glu Val Ile Leu Gly Lys Gln Pro Leu Ser Pro Pro Ala Leu Ser 580 585 590Gly Asp Leu Gly Thr Phe Met Ala Trp Val Asp Asp Val Arg Lys Leu 595 600 605Lys Val Leu Ala Asn Ala Asp Thr Pro Asp Asp Ala Leu Thr Ala Arg 610 615 620Asn Asn Gly Ala Gln Gly Ile Gly Leu Cys Arg Thr Glu His Met Phe625 630 635 640Phe Ala Ser Asp Glu Arg Ile Lys Ala Val Arg Gln Met Ile Met Ala 645 650 655Pro Thr Leu Glu Leu Arg Gln Gln Ala Leu Asp Arg Leu Leu Pro Tyr 660 665 670Gln Arg Ser Asp Phe Glu Gly Ile Phe Arg Ala Met Asp Gly Leu Pro 675 680 685Val Thr Ile Arg Leu Leu Asp Pro Pro Leu His Glu Phe Leu Pro Glu 690 695 700Gly Asn Ile Glu Asp Ile Val Ser Glu Leu Cys Ala Glu Thr Gly Ala705 710 715 720Asn Gln Glu Asp Ala Leu Ala Arg Ile Glu Lys Leu Ser Glu Val Asn 725 730 735Pro Met Leu Gly Phe Arg Gly Cys Arg Leu Gly Ile Ser Tyr Pro Glu 740 745 750Leu Thr Glu Met Gln Ala Arg Ala Ile Phe Glu Ala Ala Ile Ala Met 755 760 765Thr Asn Gln Gly Val Gln Val Phe Pro Glu Ile Met Val Pro Leu Val 770 775 780Gly Thr Pro Gln Glu Leu Gly His Gln Val Thr Leu Ile Arg Gln Val785 790 795 800Ala Glu Lys Val Phe Ala Asn Val Gly Lys Thr Ile Gly Tyr Lys Val 805 810 815Gly Thr Met Ile Glu Ile Pro Arg Ala Ala Leu Val Ala Asp Glu Ile 820 825 830Ala Glu Gln Ala Glu Phe Phe Ser Phe Gly Thr Asn Asp Leu Thr Gln 835 840 845Met Thr Phe Gly Tyr Ser Arg Asp Asp Val Gly Lys Phe Ile Pro Val 850 855 860Tyr Leu Ala Gln Gly Ile Leu Gln His Asp Pro Phe Glu Val Leu Asp865 870 875 880Gln Arg Gly Val Gly Glu Leu Val Lys Leu Ala Thr Glu Arg Gly Arg 885 890 895Lys Ala Arg Pro Asn Leu Lys Val Gly Ile Cys Gly Glu His Gly Gly 900 905 910Glu Pro Ser Ser Val Ala Phe Phe Ala Lys Ala Gly Leu Asp Tyr Val 915 920 925Ser Cys Ser Pro Phe Arg Val Pro Ile Ala Arg Leu Ala Ala Ala Gln 930 935 940Val Leu Val945 94718955PRTFlaveria browniiPPDK 18Met Ser Ser Leu Phe Val Glu Gly Met Pro Leu Lys Ser Ala Asn Glu1 5 10 15Ser Cys Leu Pro Ala Ser Val Lys Gln Arg Arg Thr Gly Asp Leu Arg 20 25 30Arg Leu Asn His His Arg Gln Pro Ala Phe Val Arg Gly Ile Cys Arg 35 40 45Arg Lys Leu Ser Gly Val Ser Arg Ile Glu Leu Arg Thr Gly Gly Leu 50 55 60Thr Leu Pro Arg Ala Val Leu Asn Pro Val Ser Pro Pro Val Thr Thr65 70 75 80Thr Lys Lys Arg Val Phe Thr Phe Gly Lys Gly Asn Ser Glu Gly Asn 85 90 95Lys Asp Met Lys Ser Leu Leu Gly Gly Lys Gly Ala Asn Leu Ala Glu 100 105 110Met Ala Ser Ile Gly Leu Ser Val Pro Pro Gly Leu Thr Ile Ser Thr 115 120 125Glu Ala Cys Glu Glu Tyr Gln Gln Asn Gly Lys Lys Leu Pro Pro Gly 130 135 140Leu Trp Asp Glu Ile Leu Glu Gly Leu Gln Tyr Val Gln Lys Glu Met145 150 155 160Ser Ala Ser Leu Gly Asp Pro Ser Lys Ala Leu Leu Leu Ser Val Arg 165 170 175Ser Gly Ala Ala Ile Ser Met Pro Gly Met Met Asp Thr Val Leu Asn 180 185 190Leu Gly Leu Asn Asp Glu Val Val Asp Gly Leu Ala Ala Lys Ser Gly 195 200 205Ala Arg Phe Ala Tyr Asp Ser Tyr Arg Arg Phe Leu Asp Met Phe Gly 210 215 220Asn Val Val Met Gly Ile Pro His Ser Leu Phe Asp Glu Lys Leu Glu225 230 235 240Gln Met Lys Ala Glu Lys Gly Ile His Leu Asp Thr Asp Leu Thr Ala 245 250 255Ala Asp Leu Lys Asp Leu Ala Glu Gln Tyr Lys Asn Val Tyr Val Glu 260 265 270Ala Lys Gly Glu Lys Phe Pro Thr Asp Pro Lys Lys Gln Leu Glu Leu 275 280 285Ala Val Asn Ala Val Phe Asp Ser Trp Asp Ser Pro Arg Ala Asn Lys 290 295 300Tyr Arg Ser Ile Asn Gln Ile Thr Gly Leu Lys Gly Thr Ala Val Asn305 310 315 320Ile Gln Cys Met Val Phe Gly Asn Met Gly Asn Thr Ser Gly Thr Gly 325 330 335Val Leu Phe Thr Arg Asn Pro Ser Thr Gly Glu Lys Lys Leu Tyr Gly 340 345 350Glu Phe Leu Val Asn Ala Gln Gly Glu Asp Val Val Ala Gly Ile Arg 355 360 365Thr Pro Glu Asp Leu Val Thr Met Glu Thr Cys Met Pro Glu Ala Tyr 370 375 380Arg Glu Leu Val Glu Asn Cys Val Ile Leu Glu Arg His Tyr Lys Asp385 390 395 400Met Met Asp Ile Glu Phe Thr Val Gln Glu Asn Arg Leu Trp Met Leu 405 410 415Gln Cys Arg Thr Gly Lys Arg Thr Gly Lys Gly Ala Val Arg Ile Ala 420 425 430Val Asp Met Val Asn Glu Gly Leu Ile Asp Thr Arg Thr Ala Ile Lys 435 440 445Arg Val Glu Thr Gln His Leu Asp Gln Leu Leu His Pro Gln Phe Glu 450 455 460Asn Pro Ser Ala Tyr Lys Ser His Val Val Ala Thr Gly Leu Pro Ala465 470 475 480Ser Pro Gly Ala Ala Val Gly Gln Val Val Phe Ser Ala Glu Asp Ala 485 490 495Glu Thr Trp His Ala Gln Gly Lys Ser Ala Ile Leu Val Arg Thr Glu 500 505 510Thr Ser Pro Glu Asp Val Gly Gly Met His Ala Ala Ala Gly Ile Leu 515 520 525Thr Ala Arg Gly Gly Met Thr Ser His Ala Ala Val Val Ala Arg Gly 530 535 540Trp Gly Lys Cys Cys Val Ser Gly Cys Ala Asp Ile Arg Val Asn Asp545 550 555 560Asp Met Lys Val Phe Thr Ile Gly Asp Arg Val Ile Lys Glu Gly Asp 565 570 575Trp Leu Ser Leu Asn Gly Ser Thr Gly Glu Val Ile Leu Gly Lys Gln 580 585 590Leu Leu Ala Pro Pro Ala Met Ser Asn Asp Leu Glu Thr Phe Met Ser 595 600 605Trp Ala Asp Gln Ala Arg Arg Leu Lys Val Met Ala Asn Ala Asp Thr 610 615 620Pro Asn Asp Ala Leu Thr Ala Arg Asn Asn Gly Ala Gln Gly Ile Gly625 630 635 640Leu Cys Arg Thr Glu His Met Phe Phe Ala Ser Asp Glu Arg Ile Lys 645 650 655Ala Val Arg Lys Met Ile Met Ala Val Thr Pro Glu Gln Arg Lys Ala 660 665 670Ala Leu Asp Leu Leu Leu Pro Tyr Gln Arg Ser Asp Phe Glu Gly Ile 675 680 685Phe Arg Ala Met Asp Gly Leu Pro Val Thr Ile Arg Leu Leu Asp Pro 690 695 700Pro Leu His Glu Phe Leu Pro Glu Gly Asp Leu Glu His Ile Val Asn705 710 715 720Glu Leu Thr Ala Asp Thr Gly Met Ser Lys Asp Glu Ile Tyr Ser Arg 725 730 735Ile Glu Lys Leu Ser Glu Val Asn Pro Met Leu Gly Phe Arg Gly Cys 740 745 750Arg Leu Gly Ile Ser Tyr Pro Glu Leu Thr Glu Met Gln Val Arg Ala 755 760 765Ile Phe Gln Ala Ala Val Ser Met Asn Asn Gln Gly Val Thr Val Ile 770 775 780Pro Glu Ile Met Val Pro Leu Val

Gly Thr Pro Gln Glu Leu Arg His785 790 795 800Gln Ile Gly Val Ile Arg Gly Val Ala Ala Asn Val Phe Ala Glu Met 805 810 815Gly Leu Thr Leu Glu Tyr Lys Val Gly Thr Met Ile Glu Ile Pro Arg 820 825 830Ala Ala Leu Ile Ala Asp Glu Ile Ala Lys Glu Ala Glu Phe Phe Ser 835 840 845Phe Gly Thr Asn Asp Leu Thr Gln Met Thr Phe Gly Tyr Ser Arg Asp 850 855 860Asp Val Gly Lys Phe Leu Pro Ile Tyr Leu Ser Gln Gly Ile Leu Gln865 870 875 880His Asp Pro Phe Glu Val Leu Asp Gln Lys Gly Val Gly Gln Leu Ile 885 890 895Lys Met Ala Thr Glu Lys Gly Arg Ala Ala Asn Pro Asn Leu Lys Val 900 905 910Gly Ile Cys Gly Glu His Gly Gly Glu Pro Ser Ser Val Ala Phe Phe 915 920 925Asp Gly Val Gly Leu Asp Tyr Val Ser Cys Ser Pro Phe Arg Val Pro 930 935 940Ile Ala Arg Leu Ala Ala Ala Gln Val Val Val945 950 95519827DNAmaizeDNA consisting of a nucleotide sequence corresponding to the 1/6 region of amino acid substituted PPDK (Nos.7682-8508 of SEQ ID NO 16). Amino acid substituted maize genomic DNA. 19agactatcgg gtacaaagtt ggaacaatga ttgagatccc tcgagcagct ctgatcgctg 60atgaggtagg gaaaactacc aagttcagaa tcgcccagaa ctttgccaac aagtttgttt 120atctgtgcat tcctacgctg gtctgaaatc tgtggctgtt gttgttgttt ttttggtttc 180gtcaacctgg cagatagcga aggaggctga attcttctcc ttcggaacga acgacctgac 240gcagatgacc tttgggtaca gcagggatga tgtgggaaag ttccttccca tctatctttc 300ccagggcatt ctccaacatg accccttcga ggtaactgtt gcaactctgc ctgccaccct 360cgcatgtcgc atctgatgtg acatgagcat ctcatgtcgc gatcgccttt catttggatg 420cccgtacacc taccaggtcc tggaccagaa gggagtgggc cagctgatca agatggctac 480agagaagggc cgcgccgcta accctaactt gaaggttggt tttgggacac tgcttcgtac 540gtctccttag aaaaccacgg tttgattgtt gtttggtttt gtgtgcaaac aggtgggcat 600ttgtggagaa cacggtggag agccttcctc tgtggccttc ttcgacgggg ttgggctgga 660ttacgtttct tgctcccctt tcaggtcggt tcagtcactg ataaactcgt gattgaatcc 720aataagcgta tcctcttatg ttaacggtag caaaatgttc actgttttct ttgaatgctt 780tctgcagggt tccgattgct aggctagctg cagctcaggt ggttgtc 827

Patent applications by Satoru Usami, Shizuoka JP

Patent applications by Shozo Ohta, Kanagawa JP

Patent applications by Yuji Ishida, Shizuoka JP

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Patent applications in all subclasses VECTOR, PER SE (E.G., PLASMID, HYBRID PLASMID, COSMID, VIRAL VECTOR, BACTERIOPHAGE VECTOR, ETC.) BACTERIOPHAGE VECTOR, ETC.)

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Patent application title: Method of elevating photosynthesis speed of plant by improving pyruvate phosphate dikinase

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