The Method for Enhancement of Photosynthesis and Biomass of Plant by Plastid Transformation of Malate Dehydrogenase

• US 20100043096A1
• Filed: 11/02/2007
• Published: 02/18/2010
• Est. Priority Date: 11/07/2006
• Status: Abandoned Application

• Current Assignee: Korea Research Institute of Bioscience & Biotechnology
• Original Assignee: Korea Research Institute of Bioscience & Biotechnology
• Inventors: Kim, Hyun Tae, Hur, Jung He, Jeong, Won Joong, Min, Sung Ran, Liu, Jang Ryol, Chung, Hwa-Jee, Park, Ju Young
• Application Number:
  US12/447,901
• Publication Number:
  US 20100043096A1
• Time in Patent Office: Days
• US Class Current: 800/278
• CPC Class Codes: C12N 15/8214 Plastid transformation
• CPC Class Codes: C12N 15/8261 with agronomic (input) traits, e.g. crop yield
• CPC Class Codes: C12N 9/0004 Oxidoreductases (1.)
• CPC Class Codes: Y02A 40/146 Genetically Modified [GMO] plants, e.g. transgenic plants

Abstract

The present invention relates to a method for enhancement of photosynthesis and biomass of a plant by plastid transformation with MDH gene, more precisely a method for enhancement of photosynthesis and biomass of C3 plant by plastid transformation system with MDH gene. The MDH plastid transgenic plant prepared by the method of the present invention exhibits not only increased photosynthesis efficiency but also increased growth rate, leaf area, stem diameter and biomass of the plant, compared with the control plant. Therefore, the plastid transformed C3 plant prepared by C4 type gene introduction can be effectively used for enhancing photosynthesis and biomass of the plant.

Claims

1. A transgenic plant prepared by inserting MDH (malate dehydrogenase) gene originated from a bacteria into the plastid genome of a target plant.

2. The transgenic plant according to claim 1, wherein the bacteria is selected from the group consisting of Corynebacterium glutamicum, Rhodococcus, Oceanobacillus, Aspergillus, Methanothermus, Chaetomium, Methanopyrus, Bacillus, Methanocaldococcus, Magnaporthe, Phaeosphaeria, Gibberella, Desulfitobacterium, coccidioides, Thermus, Candidatus, Pyrococcus, Solibacter, Aurantimonas, Syntrophus, Enterococcus, Methanosphaera, Anopheles, Entamoeba, Yersinia, Mesorhizobium, Tribolium, Salmonella, Aurantimonas, Amycolatopsis, Escherichia coli, Apis, Burkhoderia, Bordetella, Pseudomonas and Aedes.

3. The transgenic plant according to claim 1, wherein the bacteria is Corynebacterium glutamicum.

4. The transgenic plant according to claim 1, wherein the target plant is C3 plant.

5. The transgenic plant according to claim 4, wherein the C3 plant is selected from the group consisting of tobacco;

cereals including rice;

beans including mung bean, kidney bean and pea;

starch-storing plants including potato, cassava and sweet potato;

oil-storing plants including soybean, rape, sunflower and cotton plant;

vegetables including tomato, eggplant, carrot, hot pepper, Chinese cabbage, radish, water melon, cucumber, melon, crown daisy, spinach, cabbage and strawberry;

garden plants including chrysanthemum, rose, carnation and petunia; and

Arabidopsis.

17. A method for enhancing photosynthesis and biomass of a plant, which includes the step of cultivating the transgenic plant of claim 1 in outdoors or greenhouse under the high luminosity condition.

6. A method for preparing a transgenic plant with the insertion of MDH gene originated from a bacteria in its plastid genome, comprising the following steps:

1) constructing a vector for MDH plastid transformation by inserting MDH (malate dehydrogenase) gene sequence which is active in plastid into a vector for plastid transformation;

2) preparing a transformant by introducing the vector for MDH plastid transformation into C3 plant or C3 plant culture cell;

3) culturing the transformant of step

     2); and

4) re-differentiating the cultured transformant of step

     3) by tissue culture.

7. The method for preparing a transgenic plant according to claim 6, wherein the bacteria of step 1) is selected from the group consisting of Corynebacterium glutamicum, Rhodococcus, Oceanobacillus, Aspergillus, Methanothermus, Chaetomium, Methanopyrus, Bacillus, Methanocaldococcus, Magnaporthe, Phaeosphaeria, Gibberella, Desulfitobacterium, coccidioides, Thermus, Candidatus, Pyrococcus, Solibacter, Aurantimonas, Syntrophus, Enterococcus, Methanosphaera, Anopheles, Entamoeba, Yersinia, Mesorhizobium, Tribolium, Salmonella, Aurantimonas, Amycolatopsis, Escherichia coli, Apis, Burkhoderia, Bordetella, Pseudomonas and Aedes.

8. The method for preparing a transgenic plant according to claim 6, wherein the bacteria of step 1) is Corynebacterium glutamicum.

9. The method for preparing a transgenic plant according to claim 8, wherein the MDH gene is represented by SEQ. ID.

10. The method for preparing a transgenic plant according to claim 6, wherein the expression vector for plastid transformation of step 1) contains the gene construct composed of a plant plastid originated promoter that has low homology with the polynucleotide of the genome of a target plant plastid, rbs sequence, and a terminator that has low homology with the polynucleotide of the genome of a target plant plastid in that order.

11. The method for preparing a transgenic plant according to claim 10, wherein the target plant is C3 plant.

12. The method for preparing a transgenic plant according to claim 11, wherein the C3 plant is selected from the group consisting of tobacco;

cereals including rice;

beans including mung bean, kidney bean and pea;

starch-storing plants including potato, cassava and sweet potato;

oil-storing plants including soybean, rape, sunflower and cotton plant;

vegetables including tomato, eggplant, carrot, hot pepper, Chinese cabbage, radish, water melon, cucumber, melon, crown daisy, spinach, cabbage and strawberry;

garden plants including chrysanthemum, rose, carnation and petunia; and

Arabidopsis.

13. The method for preparing a transgenic plant according to claim 10, wherein the plastid originated promoter is clp promoter originated from Oryza sativa.

14. The method for preparing a transgenic plant according to claim 10, wherein the terminator is rrnB1/B2 terminator originated from Escherichia coli pHCE19 vector.

15. The method for preparing a transgenic plant according to claim 10, wherein the vector for plastid transformation additionally includes a selection gene.

16. The method for preparing a transgenic plant according to claim 15, wherein the selection gene is aadA or gfp.