Photosynthetic electron transport involved in PxcA-dependent proton extrusion in Synechocystis sp. strain PCC6803: Effect of pxcA inactivation on CO2, HCO3-, and NO3- uptake

Journal of Bacteriology

Volumn 180, Issue 15, 1998, Pages 3799-3803

  Sonoda, Masatoshi ^a   Katoh, Hirokazu ^a   Vermaas, Wim ^b   Schmetterer, George ^c   Ogawa, Teruo ^a  

^a NAGOYA UNIVERSITY   (Japan)

^b ARIZONA STATE UNIVERSITY   (United States)

^c UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BACTERIAL GENE; BACTERIAL METABOLISM; CYANOBACTERIUM; ELECTRON TRANSPORT; NONHUMAN; PHOTOSYNTHESIS; PRIORITY JOURNAL; PROTON TRANSPORT;

SYNECHOCYSTIS;

EID: 0031830705     PISSN: 00219193     EISSN: None     Source Type: Journal    
DOI: 10.1128/jb.180.15.3799-3803.1998     Document Type: Article

References (25)

1. Elstner, E. F., and H. Zeller. 1978. Bleaching of p-nitrosodimethylaniline by photosystem 1 of spinach lamellae. Plant Sci. Lett. 13:15-20.
2. Hawkesford, M. J., P. Rowell, and W. D. P. Slewart. 1963. Energy transduction in cyanobacteria, p. 199-218. In G. C. Papageorgiou and L. Packer (ed.), Photosynthetic prokaryotes: cell differentiation and function. Elsevier, Amsterdam, The Netherlands.
3. Hinrichs, I., S. Scherer, and P. Boger. 1985. Two different mechanisms of light induced proton efflux in the blue-green alga Anabaena variabilis. Physiol. Veg. 23:717-724.
4. Kaneko, T., S. Sato, H. Kotani, A. Tanaka, E. Asamizu, Y. Nakamura, N. Miyajima, M. Hirosawa, M. Sugiura, S. Sasamoto, T. Kimura, T. Hosouchi, A. Matsuno, A. Muraki, N. Nakazaki, K. Naruo, S. Okumura, S. Shimpo, C. Takeuchi, T. Wada, A. Watanabe, M. Yamada, M. Yasuda, and S. Tabata. 1996. Sequence analysis of the genome of the unicellular cyanobacterium Synechocystis sp. strain PCC6803. II. Sequence determination of the entire genome and assignment of potential protein-coding regions. DNA Res. 3:109-136.
5. Kaplan, A., R. Schwarz, J. Lieman-Hurwitz, M. Ronen-Tarazi, and L. Reinhold. 1994. Physiological and molecular studies on the response of cyanobacteria to changes in the ambient inorganic carbon concentration, p. 469-485. In D. A. Bryant (ed.), The molecular biology of cyanobacteria. Kluwer Academic Publishers, Dordrecht, The Netherlands.
6. + uptake in cyanobacteria. Plant Physiol. 89:1220-1225.
7. 2 transport in the cyanobacterium, Synechocystis PCC6803. Proc. Natl. Acad. Sci. USA 93:4006-4010.
8. Katoh, A., M. Sonoda, H. Katoh, and T. Ogawa. 1996. Absence of light-induced proton extrusion in cotA-less mutant of Synechocystis sp. strain PCC6803. J. Bacteriol. 178:5452-5455.
9. Lockau, W., and S. Pfeffer. 1982. A cyanobactcrial ATPase distinct from the coupling factor of photophosphorylation. Z. Naturforsch. Sect. C 37:658-664.
10. Miller, A. G., and B. Colman. 1980. Active transport and accumulation of bicarbonate by a unicellular cyanobacterium. J. Bacteriol. 143:1253-1259.
11. Ogawa, T. 1991. A gene homologous to the subunit-2 gene of NADH dehydrogenase is essential to inorganic carbon transport of Synechocystis PCC6803. Proc. Natl. Acad. Sci. USA 88:4275-4279.
12. + fluxes involved in the transport of inorganic carbon in cyanobacteria. Plant Physiol. 83:888-891.
13. Omata, T., M. Ohmori, N. Arai, and T. Ogawa. 1989. Genetically engineered mutant of the cyanobacterium Synechococcus PCC7942 defective in nitrate transport. Proc. Natl. Acad. Sci. USA 86:6612-6616.
14. Ritchie, R. J. 1992. Sodium transport and the origin of the membrane potential in the cyanobacterium Synechococcus R-2 (Anacystis nidulans) PCC7942. J. Plant Physiol. 139:320-330.
15. Rolland, N., A.-J. Dorne, G. Amoroso, D. F. Sultemeyer, J. Joyard, and J.-D. Rochaix. 1997. Disruption of the plastid ycflO open reading frame affects uptake of inorganic carbon in the chloroplast of Chlamydomonas. EMBO J. 16:6713-6726.
16. Sasaki, Y., K. Sekiguchi, Y. Nagano, and R. Matsuno. 1993. Chloroplast envelope protein encoded by chloroplast genome. FEBS Lett. 316:93-98.
17. Scherer, S., I. Hinrichs, and P. Boger. 1986. Effect of monochromatic light on proton efflux of the blue-green alga Anabaena variabilis. Plant Physiol. 81:939-941.
18. + . Plant Physiol. 86:769-772.
19. Schmetterer, G., D. Alge, and W. Gregor. 1994. Deletion of cytochrome c oxidase genes from the cyanobacterium Synechocystis sp. PCC6803: evidence for alternative respiratory pathways. Photosynth. Res. 42:43-50.
20. Shen, G., S. Boussiba, and W. F. J. Vermaas. 1993. Synechocystis sp. PCC6803 strains lacking photosystem I and phycobilisome function. Plant Cell 5:1853-1863.
21. Sonoda, M., K. Kitano, A. Katoh, H. Katoh, H. Ohkawa, and T. Ogawa. 1997. Size of cotA and identification of the gene Product in Synechocystis sp. strain PCC6803. J. Bacteriol. 179:3845-3850.
22. Sonoda, M., H. Katoh, H. Ohkawa, and T. Ogawa. 1997b. Cloning of cotA gene of Synechococcus PCC7942 and complementation of a cotA-less mutant of Synechocystis PCC6803 with chimeric genes of the two strains. Photosynth. Res. 54:99-105.
23. Stanier, R. Y., R. Kunisawa, M. Mandel, and G. Cohen-Bazire. 1971. Purification and properties of unicellular blue-green algae (order Chroococcales). Bacteriol. Rev. 35:171-205.
24. Vermaas, W. F. J., J. Charit, and B. Eggers. 1990. System for site-directed mutagenesis in the psbD1/C operon of Synechocystis sp. PCC6803, p. 231-238. In M. Baltscheffsky (ed.). Current research in photosynthesis, vol. 1. Kluwer Academic Publishers, Dordrecht, The Netherlands.
25. Volokita, M., D. Zenvirth, A. Kaplan, and L. Reinhold. 1984. Nature of the inorganic carbon species actively taken up by the cyanobacterium Anabaena variabilis. Plant Physiol. 76:599-602.