EP1002118A1 - Procedes pour augmenter le rendement de plantes - Google Patents

Procedes pour augmenter le rendement de plantes

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Publication number
EP1002118A1
EP1002118A1 EP98945149A EP98945149A EP1002118A1 EP 1002118 A1 EP1002118 A1 EP 1002118A1 EP 98945149 A EP98945149 A EP 98945149A EP 98945149 A EP98945149 A EP 98945149A EP 1002118 A1 EP1002118 A1 EP 1002118A1
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Prior art keywords
plant
plants
sucrose
nucleotide sequence
cells
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EP98945149A
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German (de)
English (en)
Inventor
Marion Kwart
Jörg Riesmeier
Lothar Willmitzer
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Max Planck Gesellschaft zur Foerderung der Wissenschaften eV
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Max Planck Gesellschaft zur Foerderung der Wissenschaften eV
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/10—Transferases (2.)
    • C12N9/1048—Glycosyltransferases (2.4)
    • C12N9/1051—Hexosyltransferases (2.4.1)
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    • C12N9/10—Transferases (2.)
    • C12N9/1048—Glycosyltransferases (2.4)
    • C12N9/1051—Hexosyltransferases (2.4.1)
    • C12N9/1062—Sucrose synthase (2.4.1.13)
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8216—Methods for controlling, regulating or enhancing expression of transgenes in plant cells
    • C12N15/8222—Developmentally regulated expression systems, tissue, organ specific, temporal or spatial regulation
    • C12N15/8223—Vegetative tissue-specific promoters
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8242—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits
    • C12N15/8243—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine
    • C12N15/8245—Phenotypically and genetically modified plants via recombinant DNA technology with non-agronomic quality (output) traits, e.g. for industrial processing; Value added, non-agronomic traits involving biosynthetic or metabolic pathways, i.e. metabolic engineering, e.g. nicotine, caffeine involving modified carbohydrate or sugar alcohol metabolism, e.g. starch biosynthesis
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09—Recombinant DNA-technology
    • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
    • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
    • C12N15/82—Vectors or expression systems specially adapted for eukaryotic hosts for plant cells, e.g. plant artificial chromosomes (PACs)
    • C12N15/8241—Phenotypically and genetically modified plants via recombinant DNA technology
    • C12N15/8261—Phenotypically and genetically modified plants via recombinant DNA technology with agronomic (input) traits, e.g. crop yield
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C—CHEMISTRY; METALLURGY
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14—Hydrolases (3)
    • C12N9/24—Hydrolases (3) acting on glycosyl compounds (3.2)
    • C12N9/2402—Hydrolases (3) acting on glycosyl compounds (3.2) hydrolysing O- and S- glycosyl compounds (3.2.1)
    • C12N9/2405—Glucanases
    • C12N9/2408—Glucanases acting on alpha -1,4-glucosidic bonds
    • C12N9/2431—Beta-fructofuranosidase (3.2.1.26), i.e. invertase
    • C—CHEMISTRY; METALLURGY
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    • C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/88—Lyases (4.)
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Y—ENZYMES
    • C12Y302/00—Hydrolases acting on glycosyl compounds, i.e. glycosylases (3.2)
    • C12Y302/01—Glycosidases, i.e. enzymes hydrolysing O- and S-glycosyl compounds (3.2.1)
    • C12Y302/01026—Beta-fructofuranosidase (3.2.1.26), i.e. invertase
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
    • Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
    • Y02A40/146—Genetically Modified [GMO] plants, e.g. transgenic plants

Definitions

  • the present invention relates to processes for increasing the yield in plants, recombinant nucleic acid molecules used for these processes, their uses as well as to plants with an increased yield.
  • the problem underlying the present invention is to provide further processes for increasing the yield in plants.
  • This problem is solved according to the invention by providing the embodiments characterized in the claims.
  • the present invention relates to a process for increasing the yield in plants, characterized in that recombinant DNA molecules stably integrated into the genome of plants are expressed, comprising
  • the term "increase in yield” preferably relates to an increase of the biomass production, in particular when determined as the fresh weight of the plant.
  • Such an increase in yield preferably refers to the so-called “sink” organs of the plant, which are the organs that take up the photoassimilates produced during photosynthesis.
  • Particularly preferred are parts of plants which can be harvested, such as seeds, fruits, storage roots, roots, tubers, flowers, buds, shoots, stems or wood.
  • the increase in yield according to the invention is at least 3 % with regard to the biomass in comparison to non-transformed plants of the same genotype when cultivated under the same conditions, preferably at least 10 % and particularly preferred at least 20 %.
  • photoassimilates are understood to be sugars and/or amino acids.
  • the nucleotide sequence mentioned in (b) can usually encode a plant protein or a bacterial protein or a protein originating from fungi or animal organisms.
  • the nucleotide sequence encodes a sucrose synthase (E.C. 2.4.1.13), preferably a plant sucrose synthase, in particular from Solanum tuberosum, and particularly preferred the type expressed in the tubers of S. tuberosum.
  • sucrose synthase E.C. 2.4.1.13
  • Such sequences are, for example, described in Salanoubat and Belliard (Gene 60 (1987), 47-56) and are available in the EMBL gene bank under accession number X67125.
  • nucleotide sequence encodes a sucrose phosphorylase (E.C. 2.4.1.7).
  • sucrose phosphorylase sequences encoding sucrose phosphorylase are, for example, known from WO 96/24679.
  • the nucleotide sequence encodes an invertase (E.C. 3.2.1.26), preferably an invertase from a microorganism, in particular from a fungus of the genus Saccharomyces, preferably from S. cerevisiae.
  • an invertase E.C. 3.2.1.26
  • a microorganism in particular from a fungus of the genus Saccharomyces, preferably from S. cerevisiae.
  • sequences encoding a cytosolic invertase (Sonnewald et al., Plant J. 1 (1991 ), 95-106).
  • a sucrose transporter is understood to be a transporter transporting sucrose in plant systems across a membrane.
  • a transporter preferably is of plant origin (for example EMBL gene bank accession number G21319).
  • sequence described in (b) encodes a sucrose transporter from spinach (Spinacia oleracea), in particular with the sequence of the clone SoSUTI , as, e.g., described in Riesmeier et al. (EMBO J. 11 (1992), 4705- 4713).
  • the protein that stimulates the proton gradient located at the plasma membrane is a proton ATPase.
  • sequence described in (b) preferably encodes a protein from a microorganism, in particular a fungus of the genus Saccharomyces, preferably from
  • the nucleotide sequence can also encode a proton ATPase from plants, preferably a proton ATPase from Solanum tuberosum.
  • the citrate synthase can be any citrate synthase, for example those from bacteria, fungi, animals or plants.
  • DNA sequences encoding citrate synthase are known, for example, from the following organisms: Bacillus subtilis (U05256 and U05257), E. coli (V01501 ), R. prowazekii (M17149), P. aeruginosa (M29728), A. anitratum (M33037) (see Schendel et al., Appl. Environ. Microbiol. 58 (1992), 335-345 and references cited therein), Haloferax volcanii (James et al., Biochem. Soc. Trans.
  • the numbers in brackets are the corresponding accession numbers in the GenEMBL data base.
  • the nucleotide sequences according to the invention can generally encode any appropriate proteins from any organism, in particular from plants, fungi, bacteria or animals.
  • the sequences preferably encode proteins from plants or fungi.
  • the plants are higher plants, in particular starch or oil storing useful plants, for example potato or cereals such as rice, maize, wheat, barley, rye, triticale, oat, millet, etc., as well as spinach, tobacco, sugar beet, soya, cotton etc.
  • the fungi preferably are of the genus Saccharomyces, Schizosaccharomyces, Aspergillus or Neurospora, in particular Saccharomyces cerevisiae, Schizosaccharomyces pombe, Aspergillus flavus, Aspergillus niger or Neurospora crassa.
  • the region mentioned in (a), which guarantees a companion cell specific transcription is the promoter of the rolC gene from Agrobacterium rhizogenes.
  • This promoter is, for example, described in Schm ⁇ lling et al. (Plant Cell (1989), 665- 671 ) and K ⁇ hn (Characterization and localization of the sucrose carrier SUT1 in Solanaceae, Doctoral Thesis (1991 ), Freie Universitat Berlin, biology department).
  • the region of the promoter is used that has the nucleotide sequence described in Seq ID No. 1.
  • rolC promoter Apart from the rolC promoter mentioned above the person skilled in the art can without further ado use other promoters for a companion cell specific expression. Further companion cell specific promoters are described in the literature, such as the promoter of the sucrose transporter from Arabidopsis thaliana (Truernit and Sauer, Planta 196 (1995), 564-570.
  • RNAs and proteins their specific occurrence in the companion cells has been described in the literature (see, for example, Foley et al., Plant Mol. Biol. 30 (1996), 687-695; DeWitt, Plant J. 1 (1991 ), 121-128; Stadler et al., Plant Cell 7 (1995), 1545-1554).
  • Starting from a known protein it is possible for the person skilled in the art without further ado to isolate the cDNA by means of antibodies or by using oligonucleotides derived from the amino acid sequence (cf., e.g., Sambrook et al, Molecular Cloning, A Laboratory Manual, Cold Spring Harbor Laboratory Press (1989), Cold Spring Harbor, NY.).
  • the position of the promoter can be roughly determined.
  • the specificity of the promoter can be verified in a transgenic situation by using chimeric genes consisting of the promoter and indicator genes, such as the ⁇ -glucuronidase (cf., e.g., Kertbundit et al., Proc. Natl. Acad. Sci. USA 88 (1991 ), 5212-5216).
  • the process according to the invention can in principle be applied to any plant.
  • monocotyledonous as well as dicotyledonous plant species are particularly suitable.
  • the process is preferably used with plants that are interesting for agriculture, horticulture and/or forestry.
  • Examples thereof are vegetable plants such as, for example, cucumber, melon, pumpkin, egg plant, zucchini, tomato, spinach, cabbage species, peas, beans, etc., as well as fruits such as, for example, pears, apples, etc.
  • oil storing plants are suitable such as, for example, rape, sunflower, soya.
  • starch storing plants are suitable, in particular such as cereals (rice, maize, wheat, rye, oats, triticale, millet, barley), potato, cassava, sweet potato, etc.
  • sucrose storing plants such as, for example, sugar beet and sugar cane, but also for other useful plants such as, for example, cotton, tobacco, types of wood, wine, hops etc.
  • the invention further relates to recombinant nucleic acid molecules, containing
  • sucrose transporters (iii) sucrose transporters; (iv) proteins the activity of which leads to the stimulation of the proton gradient located at the plasma membrane of plant cells; and (v) citrate synthases.
  • the invention also relates to vectors containing nucleic acid molecules of the invention, in particular those which are suitable for the transformation of plant cells as well as for the integration of foreign DNA into the plant genome.
  • the present invention further relates to plant cells transformed with a nucleic acid molecule of the invention and containing it stably integrated into the genome. These cells differ from naturally occurring plant cells for example in that a nucleic acid molecule of the invention is integrated into the genome of the cell at a location where it does not naturally occur.
  • the invention further relates to transgenic plants containing plant cells of the invention and, due to the expression of the recombinant nucleic acid molecule integrated into the genome in the companion cells of the plants, showing an increased yield in comparison with corresponding non-transformed plants that were cultivated under the same conditions.
  • the present invention further relates to propagation material of plants of the invention containing the above-described plant cells of the invention.
  • propagation material in particular comprises seeds, fruits, tubers, rhizomes, cuttings, calli, cell cultures, etc.
  • the present invention relates to the use of recombinant nucleic acid molecules containing a region allowing the transcription specifically in the companion cells of plants and, operatively linked thereto, a nucleotide sequence encoding a polypeptide selected from the group consisting of: (i) proteins with sucrose cleaving enzymatic activity;
  • proteins the activity of which leads to the stimulation of the proton gradient located at the plasma membrane and (iv) citrate synthases for the expression in transgenic plants for increasing the yield.
  • the encoded proteins preferably are the proteins further described above.
  • the DNA to the plant cell plant explants can be co-cultivated with Agrobacterium tumefaciens or Agrobacterium rhizogenes.
  • Agrobacterium tumefaciens or Agrobacterium rhizogenes From the infected plant material (for example leaf explants, segments of stems, roots but also protoplasts or suspension cultivated plant cells) whole plants can be regenerated in a suitable medium which may contain antibiotics or biozides for the selection of transformed cells.
  • the plants obtained that way can then be examined for the presence of the introduced DNA.
  • Other possibilities for the introduction of foreign DNA using the biolistic method or by protoplast transformation are known (cf., e.g., Willmitzer, L., 1993 Transgenic plants. In: Biotechnology, A Multi-Volume Comprehensive Treatise (H.J.
  • the introduced DNA Once the introduced DNA has been integrated into the genome of the plant cell, it usually is stable there and is also contained in the progenies of the originally transformed cell. It usually contains a selection marker which makes the transformed plant cells resistant to a biozide or an antibiotic such as kanamycin, G 418, bleomycin, hygromycin or phosphinotricin and others. Therefore, the individually chosen marker should allow the selection of transformed cells from cells lacking the introduced DNA.
  • the transformed cells grow within the plant in the usual way (see also McCormick et al., Plant Cell Reports 5 (1986), 81-84). The resulting plants can be cultured normally. Seeds can be obtained from the plants.
  • Two or more generations should be cultivated to make sure that the phenotypic feature is maintained stably and is transmitted. Seeds should be harvested to make sure that the corresponding phenotype or other properties are maintained.
  • Figure 1 schematically shows the construction of the plasmid pBinRolC-SS.
  • Figure 2a shows the analysis of the sucrose synthase (SS) activity in leaves of transgenic potato plants which had been transformed with the RolC-SS construct.
  • the enzyme activity was determined according to Zrenner et al. (Plant J. 7 (1995), 97-107). The activity is indicated in ⁇ mol hexose equivalents/(min x g fresh weight).
  • the columns represent the average values of three samples per genotype. The standard deviation is also indicated.
  • Figure 2b shows the analysis of the tuber yield of transgenic potato plants which had been transformed with the RolC-SS construct.
  • the columns represent average values of ten to fifteen plants per genotype. The standard deviation is also indicated.
  • the tuber yield is indicated in g per fresh weight.
  • Figure 2c shows the analysis of the tuber starch of transgenic potato plants that had been transformed with the RolC-SS construct.
  • tubers harvested from ten to fifteen plants per genotype were collected and the starch content of the tubers was determined according to Von Scheele et al. (Landw. Vers. Sta. 127 (1937), 67-96).
  • Figure 3 schematically shows the construction of the plasmid pBinRolC-Suc2.
  • Figure 4 schematically shows the construction of the plasmid pBinRolC- ⁇ PMA1
  • Figure 5 schematically shows the cloning strategy of ⁇ PMA1 .
  • the H + -ATPase ⁇ PMA1 which was truncated at the 3' end, was amplified via PCR with the PMA1 cDNA as the matrix and complementary internal primers (A).
  • the flanking cleavage sites of the PCR product (B) were introduced via the correspondingly synthesized primers.
  • Figure 6 shows the results of the polymerase chain reaction with specific oligonucleotides indicating the stable integration of ⁇ PMA1 in the genome of transgenic plants which had been obtained by transformation with the rolC- ⁇ PMA2 construct.
  • Figure 7 schematically shows the construction of the plasmid pBinRolC- ⁇ PHA2.
  • Figure 8 schematically shows the cloning strategy of ⁇ PHA2. Step from A to B:
  • the H + -ATPase ⁇ PHA2 which was truncated at the 3' end, was amplified via PCR with the PHA2 cDNA as the matrix and complementary internal primers (A).
  • the flanking cleavage sites of the PCR product (B) were introduced via the correspondingly synthesized primers.
  • Figure 9 shows the results of the polyermase chain reaction with specific oligonucleotides indicating the stable integration of ⁇ PHA2 in the genome of transgenic plants which had been obtained by transformation with the rolC- ⁇ PHA2 construct.
  • Figure 10 schematically shows the construction of the plasmid pBinRolC-SoSUTI .
  • Figure 11 schematically shows the construction of the plasmid pBinRolC-CiSy.
  • Figure 12 shows the results of the determination of the sucrose content in parenchymatic samples of tubers of engrafted potato plants enriched with vascular tissue.
  • the genotypes used for engrafting are the lines RolC-Suc2-#25 (cytosolic invertase) and wildtype Solanum tuberosum var. Desiree.
  • the sucrose content was determined according to Stitt et al. (Methods Enzymol. 174 (1989), 518-522). The columns represent the average values of 12 samples per engrafted type. The standard deviation is indicated.
  • the sucrose content is indicated as ⁇ mol hexose equivalents/g fresh weight.
  • Figure 13 shows the analysis of phloem exudates of ⁇ PMA1 leaves which were kept under light for six hours in a 14CO 2 atmosphere.
  • the sucrose content was determined according to Stitt et al. (loc. cit).
  • the columns represent the average values of four to five samples per genotype.
  • the standard deviation is indicated.
  • Figure 14 shows the tuber yield (in gram fresh weight) of ⁇ PMA1 plants.
  • the columns represent the average values of six plants per genotype.
  • the standard deviation is indicated.
  • the tuber yield is indicated in g fresh weight.
  • Figure 15 shows the tuber yield (in gram fresh weight) of ⁇ PHA2 plants.
  • the columns represent average values of four to five plants per genotype. The standard deviation is indicated.
  • the tuber yield is indicated in g fresh weight.
  • the plasmid pBinRolC-SS contains the three fragments A, B and C in the binary vector pBin19 (Bevan, Nucl. Acids Res. 12 (1984), 8711 ) (cf. Fig.1 ).
  • the fragment A comprises the rolC promoter from Agrobacterium rhizogenes.
  • the rolC promoter contains as an EcoRI/Asp718 DNA fragment of 1138 bp (Lerchl et al., Plant Cell 7 (1995), 259-270) the DNA region (position: 11306 to position 12432) of the TL-DNA of the Ri-agropin-type plasmid from A. rhizogenes (Slightom et al., J. Biol. Chem. 261 (1986), 108-121 ).
  • the fragment A is inserted into the EcoRI and Asp718 cleavage sites of the polylinker of pBin19.
  • the fragment B contains the coding region (position: 76 to position 2493) of the cDNA of the sucrose synthase (SS) from Solanum tuberosum (Salanoubat and Belliard, Gene 60 (1987), 47-56).
  • the fragment B was obtained as BamHI fragment of 2427 bp from the vector pBluescript SK " , in which it is inserted into the BamHI cleavage site of the polylinker.
  • the fragment B was inserted in sense orientation in the vector pBin19 into the BamHI cleavage site, that is downstream of the rolC promoter in an orientation allowing the transcription of a translatable RNA.
  • the fragment C contains the polyadenylation signal of the Gene 3 of the T-DNA of the Ti plasmid pTi ACH 5 (Gielen et al., EMBO J. 3 (1984), 835-846), in particular the nucleotides 11749-11939, which was isolated as a Pvull/Hindlll fragment from the plasmid pAGV 40 (Herrera-Estrella et al., Nature 303 (1983), 209-213) and which upon addition of Sphl linkers was cloned into the Pvull cleavage site between the Sphl and the Hindlll cleavage site of the polylinker of pBinl 9.
  • the resulting plasmid pBinRolC-SS was introduced into potato plant cells via the gene transfer mediated by Agrobacterium tumefaciens.
  • Agrobacterium tumefaciens For this purpose ten small leaves of a potato sterile culture (Solanum tuberosum L. cv. Desiree) wounded with the scalpel were put into 10 ml MS medium (Murashige and Skoog, Physiol. Plant. 15 (1962)), 473 with 2% of sucrose containing 50 ⁇ l of a Agrobacterium tumefaciens overnight culture grown under selection. After 3 to 5 minutes of gentle shaking a further incubation followed for two days in the dark.
  • the leaves were put on MS medium with 1.6 % glucose, 5 mg/l naphtyl acetic acid, 0.2 mg/l benzylaminopurin, 250 mg/l claforan, 50 mg/l kanamycin and 0.8 % bacto-agar for callus induction.
  • MS medium with 1.6 % glucose, 1.4 mg/l zeatin ribose, 20 ⁇ g/l naphtyl acetic acid, 20 ⁇ g/l giberellic acid, 250 mg/l claforan, 50 mg/l kanamycin and 0.8 % bacto-agar.
  • tuber yield (tuber fresh weight in gram) of plants transformed with this vector system and showing an increased sucrose synthase activity unambiguously showed an increased tuber yield. This is also a result of the expression of the sucrose synthase gene from potato contained in pBinRolC-SS (cf. Figure 2b).
  • the starch content of potato tubers is linearly dependent on the density of the tubers (von Scheele et al., Landw. Vers. Sta. 127 (1937), 67-96).
  • the plasmid pBinRolC-Suc2 contains the three fragments A, B and C in the binary vector pBin19 (Bevan, loc. cit.) and is illustrated in Figure 3.
  • the fragments A and C correspond to the fragments A and C as described in Example 1.
  • the fragment B contains the coding region (position: 845 to position: 2384) of the gene of the cytosolic invertase from yeast (Saccharomyces cerevisiae).
  • the fragment B was obtained as a BamHI fragment with a length of 1548 bp from the vector pBluescript SK " in which it is inserted in the BamHI cleavage site of the polylinker.
  • the fragment B is inserted in sense orientation into pBin19 in the BamHI cleavage site.
  • the plasmid pBinRolC-Suc2 was introduced into potato plant cells via gene transfer mediated by Agrobacterium. From transformed cells whole plants were regenerated. Such plants show in comparison to non-transformed plants an increased yield (increased biomass).
  • the plasmid pBinRolC- ⁇ PMA1 contains the three fragments A, B and C in the binary vector pBin19 (Bevan, loc. cit.) and is schematically illustrated in Figure 4.
  • the fragments A and C correspond to the fragments A and C as described in
  • the fragment B contains the coding region (position: 937 to position: 3666) of the gene of the proton ATPase PMA1 from the yeast Saccharomyces cerevisiae
  • the fragment B was obtained by means of polymerase chain reaction (PCR). For this purpopse the 3' end of the coding region of the gene PMA1 was truncated on purpose by 27 bp and at the same time a necessary new stop codon was introduced. The DNA fragment modified this way was called ⁇ PMA1.
  • the fragment B was inserted, as a Bcll/Spel fragment with a length of 2739 bp, in sense orientation into the BamHI (compatible insertion site for
  • the fragment B was obtained as Bcll/Spel fragment from the vector pBluescript SK " in which it is inserted via the cleavage sites Notl and Pstl of the polylinker (cf. Fig. 5).
  • the plasmid pBinRolC- ⁇ PMA1 was introduced into potato plant cells via the gene transfer mediated by Agrobacterium. Whole plants were regenerated from transformed cells.
  • the transformed plants show an increased yield (increased biomass) in comparison to non-transformed plants (see Figures 13 and 14).
  • the plasmid pBinRolC- ⁇ PHA2 contains the three fragments A, B and C in the binary vector pBin19 (Bevan, loc. cit.) and is schematically illustrated in Figure 7.
  • the fragments A and C correspond to the fragments A and C as described in Example 1.
  • the fragment B contains the coding region (position: 64 to position: 2672) of the cDNA of the proton-ATPase PHA2 (Harms et al., Plant Mol. Biol. 26 (1994), 979- 988).
  • the fragment B was obtained by means of polymerase chain reaction (PCR).
  • PCR polymerase chain reaction
  • the 3' end of the coding region of the gene PHA2 was on purpose truncated by 249 bp, and at the same time two new stop codons were introduced.
  • the DNA fragment modified that way was called ⁇ PHA2.
  • the fragment B was inserted in sense orientation as a Bglll/Spel fragment with a length of 2631 bp into the BamHI (compatible insertion site for Bglll restriction sites) and Xbal (compatible insertion site for Spel restriction sites) cleavage sites of the vector pBin19.
  • the fragment B was obtained as Bglll/Spel fragment from the vector pBluescript SK " , in which it is inserted into the EcoRI and Pstl cleavage sites of the polylinker sequence (cf. Fig. 8: cloning strategy ⁇ PHA2).
  • the plasmid pBinRolC- ⁇ PHA2 was introduced into potato plant cells via the gene transfer mediated by Agrobacterium. Whole plants were regenerated from transformed cells.
  • the transformed plants show an increased yield (increased biomass) in comparison to non-transformed plants (see Figure 15).
  • the plasmid pBinRolC-SoSUTI contains the three fragments A, B and C in the binary vector pBin19 (Bevan, loc. cit.) and is schematically illustrated in Figure 10.
  • the fragments A and C correspond to the fragments A and C as described in Example 1.
  • the fragment B contains the cDNA (position: 1 to position: 1969) encoding a sucrose transporter from spinach (Spinacia oleracea) (Riesmeier et al., EMBO J. 11 (1992), 4705-4713; accession number X67125 and S51273).
  • the fragment B was obtained as a Notl fragment from the vector pBluescript SK " , in which it is inserted via a Notl linker sequence.
  • the plasmid pBinRolC-CiSy contains the three fragments A, B and C in the binary vector pBin19 (Bevan, Nucl. Acids Res. 12 (1984), 8711 ) modified according to Becker (Nucl. Acids Res. 18 (1990), 203) (cf. Fig. 11 ).
  • the fragment A comprises the rolC promoter from Agrobacterium rhizogenes.
  • the rolC promoter contains as an EcoRI/Asp718 DNA fragment with a length of 1143 bp (Lerchl et al., The Plant Cell 7 (1995), 259-270) the DNA region (position: 11306 to position 12432) of the TL-DNA of the Ri-agropin type plasmid from A. rhizogenes (Slightom et al., J. Biol. Chem. 261 (1986), 108-121 ).
  • the fragment A is inserted in the EcoRI and Asp718 cleavage sites of the polylinker of pBin19.
  • the fragment B contains the coding region of the cDNA of the citrate synthase (CiSy) from the fission yeast Saccharomyces cerevisiae.
  • the fragment B was obtained as a BamHI fragment with a length of 1400 bp from the vector pBluescript SK-, in which it is inserted in the BamHI cleavage site of the polylinker (Landsch ⁇ tze, Studies on the influence of the acetyl-CoA synthesis and use in transgenic plants, Doctoral Thesis, Freie Universitat Berlin, (1985) D83/FB15 No. 028).
  • the fragment C contains the polyadenylation signal of the gene 3 of the T-DNA of the
  • the plasmid pBinRolC-CiSy has a length of about 13 kb.
  • the plasmid pBinRolC-CiSy was inserted into potato plants via the gene transfer mediated by Agrobacterium tumefaciens. Whole plants were regenerated from transformed cells.
  • the shoot of a transgenic plant (RolC-Suc2 #25) is grafted onto the stock of a wildtype plant (Solanum tuberosum, var. Desiree).
  • a wildtype shoot is grafted onto a wildtype stock in order to rule out culturing differences in the experiments (autografting).
  • the aim of the experiment is to examine the exclusive impact of the photosynthetic activity and photoassimilate distribution of a transgenic shoot on organs (in this case tubers) of a wildtype stock.
  • Potato plants were transferred from a tissue culture to soil and placed into a greenhouse. After approx. five weeks (the plants have not yet induced tuber production at this stage) the plants are grafted.
  • the shoot of the receiver plant which is not needed is cut off, and a wedge is cut into the stem of the receiver plant.
  • the donor shoot to be grafted is cut at the stem end in the appropriate way and is inserted into the wedge of the receiver plant.
  • the grafting site is fixed with an adhesive tape. Then the grafted potato plants are kept under increased air humidity and in shadow for approx. one week. Within seven to ten days they are step by step adapted to normal greenhouse conditions. At this stage the plants are seven weeks old.
  • the plants are kept in the greenhouse until the potato tubers are harvested approx. two months after the grafting and approx. three months after the planting into soil.
  • ORGANISM Agrobacterium rhizogenes

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Abstract

L'invention a pour objet des procédés servant à augmenter le rendement de plantes; selon ces procédés, les séquences nucléotidiques sont exprimées sous le contrôle des promoteurs spécifiques de cellules compagnes. Les séquences nucléotidiques codent pour des protéines dont l'expression a un effet stimulant sur le chargement du phloème par des photosynthétats.
EP98945149A 1997-08-07 1998-08-05 Procedes pour augmenter le rendement de plantes Withdrawn EP1002118A1 (fr)

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DE19734218A DE19734218A1 (de) 1997-08-07 1997-08-07 Verfahren zur Ertragssteigerung in Pflanzen
DE19734218 1997-08-07
PCT/EP1998/004878 WO1999007863A1 (fr) 1997-08-07 1998-08-05 Procedes pour augmenter le rendement de plantes

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WO2000023597A2 (fr) * 1998-10-16 2000-04-27 Scottish Crop Research Institute Promoteurs specifiques de tissu pour expression genique
HUP0303806A2 (hu) * 2001-02-22 2004-03-01 Pioneer Hi-Bred International, Inc. Szacharóz-szintetáz gének manipulálása a szár és a mag minőségének javítására
CN101851629B (zh) * 2010-05-24 2013-10-09 中国科学院遗传与发育生物学研究所 转化水稻蔗糖转运蛋白基因OsSUT5Z提高作物产量的方法和用途
EP2431471A1 (fr) 2010-09-17 2012-03-21 Université Catholique De Louvain Procédés pour augmenter la taille des plantes ou organes de plantes
CN103880935B (zh) * 2012-12-19 2017-02-08 中国科学院植物研究所 蔗糖转运蛋白AtSUT2在培育高产转基因植物中的应用
US10494641B2 (en) 2013-12-27 2019-12-03 Toyota Jidosha Kabushiki Kaisha Transformed plant and method for producing exudate containing sugar using transformed plant
AU2014370933A1 (en) * 2013-12-27 2016-07-07 National Agriculture And Food Research Organization Transgenic plant and method for producing sugar-containing exudate that uses transgenic plant
CN105543260B (zh) * 2016-02-06 2019-03-19 中国热带农业科学院橡胶研究所 HbCS4基因在提高原核表达菌生长速率、研究橡胶树产胶能力中的应用
CN105671076B (zh) * 2016-03-31 2019-07-12 西南大学 一种植物表达载体及其在提高棉花产量中的应用
CN106834343B (zh) * 2017-02-21 2019-09-13 中国农业大学 蔗糖合成酶在调控植物果实发育中的应用
CN110818785B (zh) * 2019-11-26 2022-04-19 吉林省农业科学院 一种玉米蔗糖转运蛋白ZmSUT3J及其编码基因和应用

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HUP0004258A3 (en) 2003-06-30
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HUP0004258A2 (hu) 2001-04-28
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CA2299388A1 (fr) 1999-02-18
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