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. 1996 Dec;112(4):1573–1584. doi: 10.1104/pp.112.4.1573

Driving Forces for Bicarbonate Transport in the Cyanobacterium Synechococcus R-2 (PCC 7942).

R J Ritchie 1, C Nadolny 1, AWD Larkum 1
PMCID: PMC158090  PMID: 12226464

Abstract

Air-grown Synechococcus R-2 (PCC 7942) cultures grown in BG-11 medium are very alkaline (outside pH is 10.0) and use HCO3- as their inorganic carbon source. The cells showed a dependence on Na+ for photosynthesis, but low Na+ conditions (1 mol m-3) were sufficient to support saturating photosynthesis. The intracellular dissolved inorganic carbon in the light was greater than 20 mol m-3 in both low-Na+ conditions and in BG-11 medium containing the usual [Na+] (24 mol m-3, designated high-Na+ conditions). The electrochemical potential for HCO3- in the light was in excess of 25 kJ mol-1, even in high-Na+ conditions. The Na+-motive force was greater than -12 kJ mol-1 under both Na+ conditions. On thermodynamic grounds, an Na+-driven co-port process would need to have a stoichiometry of 2 or greater ([greater than or equal to]2Na+ in/HCO3-1 in), but we show that Na+ or K+ fluxes cannot be linked to HCO3- transport. Na+ and K+ fluxes were unaffected by the presence or absence of dissolved inorganic carbon. In low-Na+ conditions, Na+ fluxes are too low to support the observed net 14C-carbon fixation rate. Active transport of HCO3- hyperpolarizes (not depolarizes) the membrane potential.

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Selected References

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  1. Badger M. R., Bassett M., Comins H. N. A Model for HCO(3) Accumulation and Photosynthesis in the Cyanobacterium Synechococcus sp: Theoretical Predictions and Experimental Observations. Plant Physiol. 1985 Feb;77(2):465–471. doi: 10.1104/pp.77.2.465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Cleland W. W. Statistical analysis of enzyme kinetic data. Methods Enzymol. 1979;63:103–138. doi: 10.1016/0076-6879(79)63008-2. [DOI] [PubMed] [Google Scholar]
  3. Espie G. S., Canvin D. T. Evidence for Na-Independent HCO(3) Uptake by the Cyanobacterium Synechococcus leopoliensis. Plant Physiol. 1987 May;84(1):125–130. doi: 10.1104/pp.84.1.125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Espie G. S., Kandasamy R. A. Monensin Inhibition of Na+-Dependent HCO3- Transport Distinguishes It from Na+-Independent HCO3- Transport and Provides Evidence for Na+/HCO3- Symport in the Cyanobacterium Synechococcus UTEX 625. Plant Physiol. 1994 Apr;104(4):1419–1428. doi: 10.1104/pp.104.4.1419. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Espie G. S., Kandasamy R. A. Na-Independent HCO(3) Transport and Accumulation in the Cyanobacterium Synechococcus UTEX 625. Plant Physiol. 1992 Feb;98(2):560–568. doi: 10.1104/pp.98.2.560. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Espie G. S., Miller A. G., Birch D. G., Canvin D. T. Simultaneous Transport of CO(2) and HCO(3) by the Cyanobacterium Synechococcus UTEX 625. Plant Physiol. 1988 Jul;87(3):551–554. doi: 10.1104/pp.87.3.551. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Espie G. S., Miller A. G., Canvin D. T. Characterization of the na-requirement in cyanobacterial photosynthesis. Plant Physiol. 1988 Nov;88(3):757–763. doi: 10.1104/pp.88.3.757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. FOGG G. E. The comparative physiology and biochemistry of the blue-green algae. Bacteriol Rev. 1956 Sep;20(3):148–165. doi: 10.1128/br.20.3.148-165.1956. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Johnson M. L., Faunt L. M. Parameter estimation by least-squares methods. Methods Enzymol. 1992;210:1–37. doi: 10.1016/0076-6879(92)10003-v. [DOI] [PubMed] [Google Scholar]
  10. Miller A. G., Colman B. Evidence for HCO(3) Transport by the Blue-Green Alga (Cyanobacterium) Coccochloris peniocystis. Plant Physiol. 1980 Feb;65(2):397–402. doi: 10.1104/pp.65.2.397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Miller A. G., Espie G. S., Canvin D. T. Chlorophyll a Fluorescence Yield as a Monitor of Both Active CO(2) and HCO(3) Transport by the Cyanobacterium Synechococcus UTEX 625. Plant Physiol. 1988 Mar;86(3):655–658. doi: 10.1104/pp.86.3.655. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Miller A. G., Turpin D. H., Canvin D. T. Na+ requirement for growth, photosynthesis, and pH regulation in the alkalotolerant cyanobacterium Synechococcus leopoliensis. J Bacteriol. 1984 Jul;159(1):100–106. doi: 10.1128/jb.159.1.100-106.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Price G. D., Badger M. R. Expression of Human Carbonic Anhydrase in the Cyanobacterium Synechococcus PCC7942 Creates a High CO(2)-Requiring Phenotype : Evidence for a Central Role for Carboxysomes in the CO(2) Concentrating Mechanism. Plant Physiol. 1989 Oct;91(2):505–513. doi: 10.1104/pp.91.2.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Reinhold L., Volokita M., Zenvirth D., Kaplan A. Is HCO(3) Transport in Anabaena a Na Symport? Plant Physiol. 1984 Dec;76(4):1090–1092. doi: 10.1104/pp.76.4.1090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Volokita M., Zenvirth D., Kaplan A., Reinhold L. Nature of the Inorganic Carbon Species Actively Taken Up by the Cyanobacterium Anabaena variabilis. Plant Physiol. 1984 Nov;76(3):599–602. doi: 10.1104/pp.76.3.599. [DOI] [PMC free article] [PubMed] [Google Scholar]

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