Patent application title: Downy Mildew Resistance Providing Genes in Sunflower
Inventors:
Chirstianus Cornelis Nicolaas Van Schie (Amsterdam, NL)
Tieme Zeilmaker (Amersfoort, NL)
IPC8 Class: AC12N1582FI
USPC Class:
800279
Class name: Multicellular living organisms and unmodified parts thereof and related processes method of introducing a polynucleotide molecule into or rearrangement of genetic material within a plant or plant part the polynucleotide confers pathogen or pest resistance
Publication date: 2016-06-09
Patent application number: 20160160233
Abstract:
Described herein are downy mildew resistant genes in sunflower and downy
mildew resistance sunflower plants. Specifically, the present invention
relates to sunflower plants being resistant to the plant pathogen downy
mildew, wherein the plant comprises a downy mildew resistance conferring
gene encoding a protein including the amino acid sequence as shown in SEQ
ID No. 2 or SEQ ID No. 4 and wherein the expression of the resistance
conferring gene is reduced as compared to the expression of said
resistance conferring gene in a sunflower plant not being resistant to
the plant pathogen downy mildew or the enzymatic activity of said protein
is reduced as compared to the enzymatic activity of said protein in a
sunflower plant not being resistant to the plant pathogen downy mildew.Claims:
1. A sunflower plant resistant to the plant pathogen downy mildew,
comprising a downy mildew resistance conferring gene encoding a protein
comprising the amino acid sequence as shown in SEQ ID No. 2 or SEQ ID No.
4 or a downy mildew resistance conferring gene encoding a protein with
more than 90% sequence identity, to SEQ ID No. 2 or SEQ ID No. 4 and
wherein the expression of said resistance conferring gene is reduced as
compared to the expression of said resistance conferring gene in a
sunflower plant not being resistant to the plant pathogen downy mildew or
the enzymatic activity of said protein is reduced as compared to the
enzymatic activity of said protein in a sunflower plant not being
resistant to the plant pathogen downy mildew.
2. The sunflower plant according to claim 1, wherein the downy mildew plant pathogen is Plasmopara halstedii or Plasmopara helianthi.
3. The sunflower plant according to claim 1, wherein said reduced enzymatic activity is provided by one or more mutations in the coding sequence of said gene resulting in a truncated or non-functional protein.
4. The sunflower plant according to claim 3, wherein said one or more mutations are amino acid substitutions, frame-shifts or pre-mature stop codons.
5. The sunflower plant according to claim 4, wherein said one or more mutations result in one or more amino acid substitutions in the sequence motif "WRDYLR" (SEQ ID No. 5) of the coding sequence of said resistance providing gene.
6. The sunflower plant according to claim 1, wherein said reduced expression is providing by one or more mutations in the regulatory regions or non-coding sequences of said gene.
7. Seeds, plant tissue or plants parts of a sunflower plant as defined in claim 1 comprising a downy mildew resistance conferring gene encoding a protein comprising the amino acid sequence as shown in SEQ ID No. 2 or SEQ ID No. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity, to SEQ ID No. 2 or SEQ ID No. 4 and wherein the expression of said resistance conferring gene is reduced as compared to the expression of said resistance conferring gene in a sunflower plant not being resistant to the plant pathogen downy mildew or the enzymatic activity of said protein is reduced as compared to the enzymatic activity of said protein in a sunflower plant not being resistant to the plant pathogen downy mildew.
8. Seeds, plant tissue or plants parts obtainable from a sunflower plant as defined in claim 1 comprising a downy mildew resistance conferring gene encoding a protein comprising the amino acid sequence as shown in SEQ ID No. 2 or SEQ ID No. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity, to SEQ ID No. 2 or SEQ ID No. 4 and wherein the expression of said resistance conferring gene is reduced as compared to the expression of said resistance conferring gene in a sunflower plant not being resistant to the plant pathogen downy mildew or the enzymatic activity of said protein is reduced as compared to the enzymatic activity of said protein in a sunflower plant not being resistant to the plant pathogen downy mildew.
9. A method for providing a sunflower plant resistant to the plant pathogen downy mildew comprising the step of introducing in a sunflower plant a downy mildew resistance conferring gene encoding a protein comprising the amino acid sequence as shown in SEQ ID No. 2 or SEQ ID No. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity to SEQ ID No. 2 or SEQ ID No. 4 and wherein the expression of said resistance conferring gene is reduced as compared to the expression of said resistance conferring gene in a sunflower plant not being resistant to the plant pathogen downy mildew or the enzymatic activity of said protein is reduced as compared to the enzymatic activity of said protein in a sunflower plant not being resistant to the plant pathogen downy mildew.
10. (canceled)
11. A protein comprising an amino acid sequence of SEQ ID No. 2 or SEQ ID No. 4.
12. A nucleic acid comprising a nucleotide sequence of SEQ ID No. 1 or SEQ ID NO. No. 3.
13. (canceled)
Description:
[0001] The present invention relates to downy mildew resistant genes in
sunflower and especially to downy mildew resistance sunflower plants. The
present invention further relates to methods for obtaining the present
downy mildew resistant sunflower plants and the use of the present genes
for providing downy mildew resistance in sunflower.
[0002] Helianthus L. is a genus of plants comprising about 52 species in the Asteraceae family. The common designation "sunflower" is generally used to indicate the annual species Helianthus annuus. Helianthus annuus and other species such as Jerusalem artichoke (Helianthus tuberoses), are cultivated in temperate regions as food crops and ornamental plants. The domesticated sunflower, Helianthus annuus, is the most familiar species of the Helianthus L. genus. Helianthus annuus is cultivated both for ornamental purposes as for providing vegetable oil from seeds.
[0003] Downy mildew, a common and destructive disease in sunflowers, is capable of killing or stunting plants, reducing stand and causing significant yield loss (up to 50 to 95%). Sunflowers are most susceptible to downy mildew in fields where heavy rain has fallen within 2-3 weeks after planting.
[0004] Downy mildew refers to any of several types of oomycete plant pathogens that are obligate parasites of plants. Downy mildews exclusively belong to Peronosporaceae. The downy mildew pathogen generally causing downy mildew disease in cultivated sunflowers is designated Plasmopara halstedii or Plasmopara helianthi.
[0005] In the technical field of sunflower cultivation and breeding, there is a constant need to identify new resistance genes against downy mildew. However, most resistance gene identified are monogenic dominant resistance genes and the resistance provided by these genes is generally rapidly broken because downy mildew pathogens evolve and adapt at a high frequency thereby regaining the ability to successfully infect a host plant. Accordingly, there is a continuous need in de art for new resistance genes, preferably resistance genes of which the resistance is not readily broken by adaptation of the pathogen.
[0006] A disadvantage of known sunflower resistance genes is that, besides providing pathogen resistance, these genes often are accompanied by undesired phenotypes such as stunted growth or spontaneous occurrence cell death. Accordingly, there is a continuous need in the art for new resistance genes not providing, besides the resistance, undesirable phenotypes. It is an object of the present invention, amongst other objects, to meet, at least partially if not fully, the above needs of the art.
[0007] This object of the present invention, amongst other objects, is met by providing a sunflower plants and resistance genes as outlined in the appended claims.
[0008] Specifically, this object of the present invention, amongst other objects, is met, according to a first aspect, by sunflower plants being resistant to the plant pathogen downy mildew, wherein the present plant comprises a downy mildew resistance conferring gene encoding (a) protein(s) comprising the amino acid sequence as shown in SEQ ID No. 2 and/or SEQ ID NO. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity, preferably more than 94% sequence identity, more preferably more than 96% sequence identity with identity SEQ ID No. 2 and/or SEQ ID NO. 4 and wherein the expression of the present resistance conferring gene is reduced as compared to the expression of the present resistance conferring gene in a sunflower plant not being resistant to the plant pathogen downy mildew or the enzymatic activity of the present protein is reduced as compared to the enzymatic activity of the present protein in a sunflower plant not being resistant to the plant pathogen downy mildew.
[0009] In the research that led to the present invention, it was surprisingly found that a reduced expression of the present genes or a reduced enzymatic activity of the present proteins provided a broad and durable resistance to downy mildew in sunflower plants.
[0010] According to the present invention, an expression is reduced in comparison with the expression of the present resistance conferring gene in a sunflower plant not being resistant to the plant pathogen downy mildew. The term "not being resistant" indicates a resistance level, determined in an appropriate disease test and using an appropriate reference plant such as a parent plant, being less than the resistance level observed in the present plants. Accordingly, the present resistance can also be designated as an increased resistance to downy mildew. Suitable reference plants according to the invention, besides parent plants, can also be plants generally designated in the art as downy mildew susceptible plants.
[0011] A suitable disease test is inoculating plants with a downy mildew pathogen and subsequently observing the occurrence of disease symptoms such as large, angular or blocky, yellow areas visible on the upper surface of leaves or destroyed leaf tissue.
[0012] Expression levels in the present plants and the reference plants can be determined using any suitable and generally known Molecular Biology technique such as a quantitative Polymerase Chain Reaction (PCR) or mRNA hybridization.
[0013] According to the present invention, an enzymatic activity is reduced in comparison with the activity of the present protein in a sunflower plant not being resistant to the plant pathogen downy mildew. The term "not being resistant" indicates a resistance level, determined in an appropriate disease test and using an appropriate reference plant, such as a parent plant, being less than the resistance level observed in the present plants. Accordingly, the present resistance can also be designated as an increased resistance to downy mildew. Suitable reference plants according to the invention can, besides parent plants, also be plants generally designated in the art as downy mildew susceptible plants. A suitable disease test is inoculating plants with downy mildew and subsequently observing the occurrence of disease symptoms such as large, angular or blocky, yellow areas visible on the upper surface of leaves or destroyed leaf tissue.
[0014] The present proteins have a 2-oxoglutarate FE(II)-dependent oxygenase activity. The enzyme has an absolute requirement for Fe(II) and catalyzes two-electron oxidations, including hydroxylation, desaturation and oxidative ring closure reactions. The oxidation of the `prime` substrate is coupled to the conversion of 2OG into succinate and CO.sub.2. One of the oxygens of the dioxygen molecule is incorporated into succinate. In the case of desaturation reactions, the other dioxygen-derived oxygen is presumably converted to water. In hydroxylation reactions, the partial incorporation of oxygen from dioxygen into the alcohol product occurs with significant levels of exchange of oxygen from water being observed. Accordingly, the present reduced activity can be determined using an assay measuring compounds being either the starting compounds or the resulting compounds of the enzymatic reaction. As a suitable alternative, protein levels, being inherently indicative of a reduced activity, of the present proteins can be determined by, for example, ELISA or protein hybridization both being techniques commonly known to the skilled person.
[0015] Within the context of the present invention, resistance to downy mildew is individually or in combination provided, through reduced expression or activity, to the present sunflower plants by the present proteins or genes encoding the present proteins.
[0016] The present sunflower plants can be obtained by mutagenesis of downy mildew susceptible plant or downy mildew resistant plants thereby increasing the resistance thereof. For example, mutations, either at the expression level or the protein level, can be introduced in these plants by using mutagenic chemicals such as ethyl methane sul2fonate (EMS) or by irradiation of plant material with gamma rays or fast neutrons. The resulting mutations can be directed or random. In the latter case, mutagenized plants carrying mutations in the present resistance conferring genes can be readily identified by using the TILLING (Targeting Induced Local Lesions IN Genomes) method (McCallum et al. (2000) Targeted screening for induced mutations. Nat. Biotechnol. 18, 455-457, and Henikoff et al. (2004) TILLING. Traditional mutagenesis meets functional genomics. Plant Physiol. 135, 630-636). Briefly, this method is based on the PCR amplification of a gene of interest from genomic DNA of a large collection of mutagenized plants in the M2 generation. By DNA sequencing or by scanning for point mutations using a single-strand specific nuclease, such as the CEL-I nuclease (Till et al. (2004) Mismatch cleavage by single-strand specific nucleases. Nucleic Acids Res. 32, 2632-2641) individual plants having a mutation in the present genes are identified.
[0017] According to a preferred embodiment of this first aspect of the present invention, the present downy mildew pathogens are Plasmopara halstedii and/or Plasmopara helianthi. However, other pathogens belonging to the Peronosporaceae and capable of causing downy mildew disease in sunflower are contemplated within the context of the present invention. According to another preferred embodiment of this first aspect of the present invention, the present reduced enzymatic activity is provided by one or more mutations in the coding sequence of the present genes resulting in a truncated or non-functional protein. Truncated proteins can be readily determined by analyzing gene transcripts at the mRNA or cDNA level and non-functional proteins can be determined in enzyme assays or using conformation-dependent antibodies. Mutations which can be assayed at the transcript level are, for example, amino acid substitutions, frame-shifts or pre-mature stop codons.
[0018] According to an especially preferred embodiment of this first aspect of the present invention, the present mutations resulting in a reduced activity of the present proteins are mutations resulting in the absence of or amino acid substitution(s) in the sequence motif "WRDYLR" or Trp-Arg-Asp-Tyr-Leu-Arg of the coding sequence of the present resistance providing gene. The present sequence motif can be found at amino acid positions 107 to 112 of SEQ ID No. 2 and at amino acid positions 116 to 121 of SEQ ID No. 4. The present inventors have found that mutations in this region especially affect the downy mildew resistance phenotype, i.e. level of resistance, observed. Especially mutations involving Y (Tyr) and/or R (Arg) are highly correlated the downy mildew resistance phenotype, i.e. level of resistance, observed.
[0019] According to yet another preferred embodiment this first aspect of the present invention, the present reduced expression is provided by one or more mutations in the regulatory regions or non-coding sequences of the present genes. Examples of regulatory regions of the present genes are promotor and terminator regions and examples of non-coding regions are introns and especially splicing influencing motifs therein.
[0020] According to a second aspect, the present invention provides seeds, plant tissues or plants parts of the sunflower plants as described above or obtainable from the sunflower plants as described above, comprising a downy mildew resistance conferring gene encoding a protein comprising the amino acid sequence as shown in SEQ ID No. 2 and/or SEQ ID NO. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity, preferably more than 94% sequence identity, more preferably more than 96% sequence identity with identity SEQ ID No. 2 and/or SEQ ID NO. 4 and the expression of the resistance conferring gene is reduced as compared to the expression of the resistance conferring gene in a sunflower plant not being resistant to the plant pathogen downy mildew or the enzymatic activity of the protein is reduced as compared to the enzymatic activity of the protein in a sunflower plant not being resistant to the plant pathogen downy mildew.
[0021] According to a third aspect, the present invention relates to methods for providing sunflower plants being resistant, or methods for increasing the resistance of sunflower plants, to the plant pathogen downy mildew wherein the present methods comprise the step of introducing in a sunflower plant a downy mildew resistance conferring gene encoding a protein comprising the amino acid sequence as shown in SEQ ID No. 2 and/or SEQ ID NO. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity, preferably more than 94% sequence identity, more preferably more than 96% sequence identity with identity SEQ ID No. 2 and/or SEQ ID NO. 4 and the expression of the resistance conferring gene is reduced as compared to the expression of the resistance conferring gene in the starting sunflower plant or the enzymatic activity of the protein is reduced as compared to the enzymatic activity of the protein in the starting sunflower plant not being resistant to the plant pathogen downy mildew.
[0022] According to a fourth aspect, the present invention relates to the use of a gene, or the cDNA sequence thereof, encoding a protein comprising the amino acid sequence as shown in SEQ ID No. 2 or SEQ ID NO. 4 or a downy mildew resistance conferring gene encoding a protein with more than 90% sequence identity, preferably more than 94% sequence identity, more preferably more than 96% sequence identity with identity SEQ ID No. 2 or SEQ ID NO. 4 for providing sunflower plants being resistant or having an increased resistance to the plant pathogen downy mildew.
[0023] According to a fifth aspect, the present invention relates to proteins having an amino acid sequence comprising SEQ ID No. 2 or SEQ ID No. 4.
[0024] According to a sixth aspect, the present invention relates to nucleic acid sequences comprising SEQ ID No. 1 or SEQ ID NO. 3.
[0025] According to a seventh aspect, the present invention relates to gene encoding a protein having an amino acid sequence comprising SEQ ID No. 2 or SEQ ID No. 4 or a nucleic acid sequence comprising SEQ ID No. 1 or SEQ ID NO. 3.
Sequence CWU
1
1
511014DNAHelianthus annuus 1atggcgggaa aagtcatctc cagtggcatc caatacacta
ctttacccga cagttacgtc 60cgtccggtca acgacaggcc taacctatcc caagtctccg
aatgcaacga tgttccggtt 120atcgacatcg gtggagctga ccgggagctc ataagccggc
aaatcggcga tgcgtgccgt 180cactacggct ttttccaggt gataaaccac ggtgtggcgg
atgaattggt gaagaagatg 240gagcaggtag ggagagattt cttccagttg ccggttgagg
agaagatgaa gctctactcg 300gaggatccga cgaagacgat gaggctttcg acgagcttca
acgtcaagaa agaacaagtg 360cataactgga gggattatct ccggcttcac tgctatcctt
tggatcagta ctctcctgaa 420tggccttcca atccttgtta tttcaaagaa tatgttggaa
attactgtat agcggtacgc 480gaattaggga tgaggatact tgaattcata tcggaaagtt
taggtttaga aaaagagcga 540ctaaatatga tattaggcga gcaaggacaa catatggcca
tcaaccatta tccagtgtgc 600cctgaacctg agttaactta tgggttgcct ggtcacactg
atcctaatgc actcaccata 660ctccttcaag acacgcttgt ctctggatta caagttcaaa
aagatggcaa atgggtagcg 720gttaaaccac accctaacgc gtttgtcatc aacattggcg
accaactaga ggcgttgagt 780aatggtgaat acaagagtgt gtggcatcga gccgtggtca
actcagacca accaagaatg 840tcaatagctt cgtttttgtg tccctgtaat gactcagtcc
tcagcgctcc taacgaacta 900ataaaagatg gatcgacgcg tgttttcaaa gactttactt
acacagaata ctacaagaag 960ttttggagtc gaaatctaga ccaagaacat tgtttagagt
tcttcaagaa ctag 10142337PRTHelianthus annuus 2Met Ala Gly Lys Val
Ile Ser Ser Gly Ile Gln Tyr Thr Thr Leu Pro 1 5
10 15 Asp Ser Tyr Val Arg Pro Val Asn Asp Arg
Pro Asn Leu Ser Gln Val 20 25
30 Ser Glu Cys Asn Asp Val Pro Val Ile Asp Ile Gly Gly Ala Asp
Arg 35 40 45 Glu
Leu Ile Ser Arg Gln Ile Gly Asp Ala Cys Arg His Tyr Gly Phe 50
55 60 Phe Gln Val Ile Asn His
Gly Val Ala Asp Glu Leu Val Lys Lys Met 65 70
75 80 Glu Gln Val Gly Arg Asp Phe Phe Gln Leu Pro
Val Glu Glu Lys Met 85 90
95 Lys Leu Tyr Ser Glu Asp Pro Thr Lys Thr Met Arg Leu Ser Thr Ser
100 105 110 Phe Asn
Val Lys Lys Glu Gln Val His Asn Trp Arg Asp Tyr Leu Arg 115
120 125 Leu His Cys Tyr Pro Leu Asp
Gln Tyr Ser Pro Glu Trp Pro Ser Asn 130 135
140 Pro Cys Tyr Phe Lys Glu Tyr Val Gly Asn Tyr Cys
Ile Ala Val Arg 145 150 155
160 Glu Leu Gly Met Arg Ile Leu Glu Phe Ile Ser Glu Ser Leu Gly Leu
165 170 175 Glu Lys Glu
Arg Leu Asn Met Ile Leu Gly Glu Gln Gly Gln His Met 180
185 190 Ala Ile Asn His Tyr Pro Val Cys
Pro Glu Pro Glu Leu Thr Tyr Gly 195 200
205 Leu Pro Gly His Thr Asp Pro Asn Ala Leu Thr Ile Leu
Leu Gln Asp 210 215 220
Thr Leu Val Ser Gly Leu Gln Val Gln Lys Asp Gly Lys Trp Val Ala 225
230 235 240 Val Lys Pro His
Pro Asn Ala Phe Val Ile Asn Ile Gly Asp Gln Leu 245
250 255 Glu Ala Leu Ser Asn Gly Glu Tyr Lys
Ser Val Trp His Arg Ala Val 260 265
270 Val Asn Ser Asp Gln Pro Arg Met Ser Ile Ala Ser Phe Leu
Cys Pro 275 280 285
Cys Asn Asp Ser Val Leu Ser Ala Pro Asn Glu Leu Ile Lys Asp Gly 290
295 300 Ser Thr Arg Val Phe
Lys Asp Phe Thr Tyr Thr Glu Tyr Tyr Lys Lys 305 310
315 320 Phe Trp Ser Arg Asn Leu Asp Gln Glu His
Cys Leu Glu Phe Phe Lys 325 330
335 Asn 31035DNAHelianthus annuus 3atggctacca cctcaaaaag
attactagtt agcgacctcg tatccaccga taaaatcgac 60caagtccctt caaactacat
ccgacccatc acccaacgtc ccaatttcca aaatgttgtt 120cgcgactcca tccctctcat
tgacctcaaa gatctcaacg gccccaatca cgctaacgtg 180atcaaacaaa tcggtcaagc
ttgcgctgat cacggcttct tccaggttaa aaaccatggc 240gtacccgaat ccatcatagc
caacatgatg caaaccgctc gagacttctt caacctaccc 300gaacaagaac gactcaaaaa
ctattcagat gaccccacaa agaccactag actctccacc 360agcttcaaca tacgaaccga
aaaggtcgca aactggagag attacttacg actccattgc 420tacccgatcg ataacttcat
cgacgaatgg ccaaccaatc cggcctcgtt tcgggcccat 480gtagcggagt attgccagag
tacaagaaac ttagcactcc aacttattgc agccatttca 540gaaagcttag gacttcataa
agactacatg aacacacagt tagggaagca tgctcagcat 600atggtcttga actactaccc
accatgccca caacccgatt taacatacgg gttacccgga 660cacactgatc ctaatttcat
caccatcctt cttcaagatg aggttcctgg tcttcaggtc 720ttgaaagatg gtaaatgggt
agcggttgat ccggttccaa acactttcat catcaacatt 780ggtgatcaag ttcaggtgat
gagtaatgat aagtacaaga gtattttgca tcgagctgtg 840gtgaattgtg ataaagaacg
gatatctata ccgactttct actgtccgtc gcctgaggcg 900gttatcgggc ctgctcccga
ggttgtaact gatgatgagc ctgctgtgta tcgacagttt 960acttatgggg agtactatga
gaagttttgg gacaatgggc ttgagaagtg tttggatatg 1020ttcaagacta gttga
10354344PRTHelianthus annuus
4Met Ala Thr Thr Ser Lys Arg Leu Leu Val Ser Asp Leu Val Ser Thr 1
5 10 15 Asp Lys Ile Asp
Gln Val Pro Ser Asn Tyr Ile Arg Pro Ile Thr Gln 20
25 30 Arg Pro Asn Phe Gln Asn Val Val Arg
Asp Ser Ile Pro Leu Ile Asp 35 40
45 Leu Lys Asp Leu Asn Gly Pro Asn His Ala Asn Val Ile Lys
Gln Ile 50 55 60
Gly Gln Ala Cys Ala Asp His Gly Phe Phe Gln Val Lys Asn His Gly 65
70 75 80 Val Pro Glu Ser Ile
Ile Ala Asn Met Met Gln Thr Ala Arg Asp Phe 85
90 95 Phe Asn Leu Pro Glu Gln Glu Arg Leu Lys
Asn Tyr Ser Asp Asp Pro 100 105
110 Thr Lys Thr Thr Arg Leu Ser Thr Ser Phe Asn Ile Arg Thr Glu
Lys 115 120 125 Val
Ala Asn Trp Arg Asp Tyr Leu Arg Leu His Cys Tyr Pro Ile Asp 130
135 140 Asn Phe Ile Asp Glu Trp
Pro Thr Asn Pro Ala Ser Phe Arg Ala His 145 150
155 160 Val Ala Glu Tyr Cys Gln Ser Thr Arg Asn Leu
Ala Leu Gln Leu Ile 165 170
175 Ala Ala Ile Ser Glu Ser Leu Gly Leu His Lys Asp Tyr Met Asn Thr
180 185 190 Gln Leu
Gly Lys His Ala Gln His Met Val Leu Asn Tyr Tyr Pro Pro 195
200 205 Cys Pro Gln Pro Asp Leu Thr
Tyr Gly Leu Pro Gly His Thr Asp Pro 210 215
220 Asn Phe Ile Thr Ile Leu Leu Gln Asp Glu Val Pro
Gly Leu Gln Val 225 230 235
240 Leu Lys Asp Gly Lys Trp Val Ala Val Asp Pro Val Pro Asn Thr Phe
245 250 255 Ile Ile Asn
Ile Gly Asp Gln Val Gln Val Met Ser Asn Asp Lys Tyr 260
265 270 Lys Ser Ile Leu His Arg Ala Val
Val Asn Cys Asp Lys Glu Arg Ile 275 280
285 Ser Ile Pro Thr Phe Tyr Cys Pro Ser Pro Glu Ala Val
Ile Gly Pro 290 295 300
Ala Pro Glu Val Val Thr Asp Asp Glu Pro Ala Val Tyr Arg Gln Phe 305
310 315 320 Thr Tyr Gly Glu
Tyr Tyr Glu Lys Phe Trp Asp Asn Gly Leu Glu Lys 325
330 335 Cys Leu Asp Met Phe Lys Thr Ser
340 56PRTHelianthus annuus 5Trp Arg Asp Tyr Leu
Arg 1 5
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