Transformation of phaG and phaC Genes into Tobacco Chloroplast Genome and Genetic Analysis

Acta Agronomica Sinica

Volumn 35, Issue 11, 2009, Pages 1949-1957

  WANG, Yu Hua ^a   WU, Zhong Yi ^b   ZHANG, Xiu Hai ^b   WANG, Yong Qin ^b   HUANG, Cong Lin ^b   JIA, Jing Fen ^a  

^a Key Laboratory of Resource Biology and Biotechnology in Western China   (China)

^b INSTITUTE OF PLANT AND ENVIRONMENT PROTECTION   (China)

Author keywords

chloroplast genetic transformation; genetic analysis; maternally inheritance; phaG and phaC; tobacco

Indexed keywords

BACTERIA (MICROORGANISMS); NICOTIANA OBTUSIFOLIA; NICOTIANA TABACUM; ORYZA SATIVA;

EID: 77953273496     PISSN: 18752780     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1875-2780(08)60113-3     Document Type: Article

References (27)

1. Lee S.Y. Bacterial polyhydroxyalkanoates. Biotechnol Bioeng 49 (1996) 1-14
2. Steinbüchel A., and Byrom D. Polyhydroxyalkanoic acids. Novel Biomaterials from Biological Sources (1991), MacMillan Publishing Company, New York 123-213
3. Rehm B., Krüger N., and Steinbüchel A. A new metabolic link between fatty acid de novo synthesis and polyhydroxyalkanoic acid synthesis. J Biol Chem 273 (1998) 24044-24051
4. Poirier Y., Dennis D.E., Klomparens K., and Somerville C. Polyhydroxybutyrate, a biodegradable thermoplastic, produced in transgenic plants. Science 256 (1992) 520-523
5. Houmiel K.L., Slater S., Broyles D., Casagrande L., Colburn S., Gonzalez K., Mitsky T.A., Reiser S.E., Shah D., Taylor N.B., Tran M., Valentin H.E., and Gruys K.J. Poly (β-hydroxybutyrate) production in oilseed leukoplasts of Brassica napus. Planta 209 (1999) 547-550
6. Hahn J.J., Eschenlauer A.C., Sleytr U.B., Somers D.A., and Srienc F. Peroxisomes as sites for synthesis of polyhydroxyalkanoates in transgenic plants. Biotechnol Prog 15 (1999) 1053-1057
7. Gray M.W. Origin and evolution of organelle genomes. Curr Opin Genet Dev 3 (1993) 884-890
8. Svab Z., and Maliga P. High-frequency plastid transformation in tobacco by selection for a chimeric aadA gene. Proc Natl Acad Sci USA 90 (1993) 913-917
9. Gong X.S., and Yan L.F. Improvement of chloroplast DNA isolation from higher plant. Chin Sci Bull 36 (1991) 467-469 (in Chinese)
10. McBride K.E., Svab Z., Schaaf D.J., Hogan P.S., Stalker D.M., and Maliga P. Amplification of a chimeric Bacillus gene in chloroplasts leads to an extraordinary level of an insecticidal protein in tobacco. Bio/Technology 13 (1995) 362-365
11. Baecker J.J., Sneddon J.C., and Hollingsworth M.J. Efficient translation in chloroplasts requires element(s) upstream of the putative ribosome binding site from atp I. Am J Bot 96 (2009) 627-636
12. Chakrabarti S.K., Lutz K.A., Lertwiriyawong B., Svab Z., and Maliga P. Expression of the cry9Aa2 B. t. gene in tobacco chloroplasts confers resistance to potato tuber moth. Transgenic Res 15 (2006) 481-488
13. Dufourmantel N., Tissot G., Goutorbe F., Garçon F., Muhr C., Jansens S., Pelissier B., Peltier G., and Dubald M. Generation and analysis of soybean plastid transformants expressing Bacillus thuringiensts cry1Ab protoxin. Plant Mol Biol 58 (2005) 659-668
14. Shimizu M., Goto M., Hanai M., Shimizu T., Izawa N., Kanamoto H., Tomizawa K.I., Yokota A., and Kobayashi H. Selectable tolerance to herbicides by mutated acetolactate synthase genes integrated into the chloroplast genome of tobacco. Plant Physiol 147 (2008) 1976-1983
15. Kumar S., Dhingra A., and Daniell H. Plastid-expressed bataine aldehyde dehydrogenase gene in carrot cultured cells roots, and leaves confers enhanced salt tolerance. Plant Physiol 136 (2004) 2843-2854
16. Hussein H.S., Ruiz O.N., Terry N., and Daniell H. Phytoremediation of mercury and organomercurials in chloroplast transgenic plants: enhanced root uptake, translocation to shoots, and volatilization. Environ Sci Technol 41 (2007) 8439-8446
17. Arlen P.A., Falconer R., Cherukumilli S., Cole A., Cole A.M., Oishi K.K., and Daniell H. Field production and functional evaluation of chloroplast-derived interferon-alphα 2b. Plant Biotechnol J 5 (2007) 511-525
18. Fernández-San Millán A., Farran I., Molina A., Mingo-Castel A.M., and Veramendi J. Expression of recombinant proteins lacking methionine as N-terminal amino acid in plastids: human serum albumin as a case study. J Biotechnol 127 (2007) 593-604
19. Arlen P.A., Singleton M., Adamovicz J.J., Ding Y., Davoodi-Semiromi A., and Daniell H. Effective plague vaccination via oral delivery of plant cells expressing F1-V antigens in chloroplasts. Infect Immun 76 (2008) 3640-3650
20. Chebolu S., and Daniell H. Stable expression of Gal/GalNac lectin of Entamoeba histolytica in transgenic chloroplasts and immunogenicity in mice towards vaccine development for amoebiasis. Plant Biotechnol J 5 (2007) 230-239
21. Shao H.B., He D.M., Qian K.X., Shen G.F., and Su Z.L. The expression of classical swine fever virus structural protein E2 gene in tobacco chloroplasts for applying chloroplasts as bioreactors. Mol Biol Genet 331 (2008) 179-184
22. Roh K.H., Shin K.S., Lee Y.H., Seo S.C., Park H.G., Daniell H., and Lee S.B. Accumulation of sweet protein monellin is regulated by the psbA 5′ UTR in tobacco chloroplasts. J Plant Biol 49 (2006) 34-43
23. Nakahira Y., and Shiina T. Plastid transformation in higher plants: application for chloroplast factory. Protein Nucl Acid Enzyme 50 (2005) 1918-1920 (in Japanese)
24. Zhang J.Y., Su N., Zhang Z.L., Zhao H.Y., Zhu S.W., and Song Y.R. Expressing of poly-3-hydroxybutyrate synthetic genes through chloroplast genetic engineering. Chin Sci Bull 47 (2002) 1373-1376
25. Arai Y., Shikanai T., Doi Y., Yoshida S., Yamaguchi I., and Nakashita H. Production of polyhydroxybutyrate by polycistronic expression of bacterial genes in tobacco plastid. Plant Cell Physiol 45 (2004) 1176-1184
26. Romano A., van der Plas L.H.W., Witholt B., Eggink G., and Mooibroek H. Expression of poly-3-(R)-hydrozyalkanoate (PHA) polymerase and acyl-CoA-transacylase in plastids of transgenic potato leads to the synthesis of a hydrophobic polymer, presumably medium-chain-length PHAs. Planta 220 (2005) 455-464
27. Nawrath C., Poirier Y., and Somerville C. Targeting of the polyhydroxybutyrate biosynthetic pathway to the plastids of Arabidopsis thaliana results in high levels of polymer accumulation. Proc Natl Acad Sci USA 91 (1994) 12760-12764