Abstract
The possibility of HCO3− transport in the blue-green alga (cyanobacterium) Coccochloris peniocystis has been investigated. Coccochloris photosynthesized most rapidly in the pH range 8 to 10, where most of the inorganic C exists as HCO3−. If photosynthesis used only CO2 from the external solution the rate of photosynthesis would be limited by the rate of HCO3− dehydration to CO2. Observed rates of photosynthesis at alkaline pH were as much as 48-fold higher than could be supported by spontaneous dehydration of HCO3− in the external solution. Assays for extracellular carbonic anhydrase were negative. The evidence strongly suggests that HCO3− was a direct C source for photosynthesis.
Weakly buffered solutions became alkaline during photosynthesis with a one-to-one stoichiometry between OH− appearance in the medium and HCO3− initially added. Alkalization occurred only during photosynthesis and was blocked by 3-(3,4-dichlorophenyl)-1, 1-dimethylurea, diuron. It is suggested that HCO3− was transported into cells of Coccochloris in exchange for OH− produced as a result of HCO3− fixation in photosynthesis.
The inorganic C concentration required to support a rate of photosynthesis of half the maximum rate (Km) was 6 micromolar at pH 8.0 or, in terms of available CO2, a Km of 0.16 micromolar. This value is two orders of magnitude lower than reported Km values for the d-ribulose-1,5-bisphosphate carboxylase for blue-green algae. It is suggested that the putative HCO3− transport by Coccochloris serves to raise the CO2 concentration around the carboxylase to levels high enough for effective fixation.
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- Birmingham B. C., Colman B. Measurement of carbon dioxide compensation points of freshwater algae. Plant Physiol. 1979 Nov;64(5):892–895. doi: 10.1104/pp.64.5.892. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Falkner G., Horner F. pH Changes in the Cytoplasm of the Blue-Green Alga Anacystis nidulans Caused by Light-dependent Proton Flux into the Thylakoid Space. Plant Physiol. 1976 Dec;58(6):717–718. doi: 10.1104/pp.58.6.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lucas W. J. Alkaline Band Formation in Chara corallina: Due to OH Efflux or H Influx? Plant Physiol. 1979 Feb;63(2):248–254. doi: 10.1104/pp.63.2.248. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Masamoto K., Nishimura M. Estimation of internal pH in cells of blue-green algae in the dark and under illumination. J Biochem. 1977 Aug;82(2):483–487. [PubMed] [Google Scholar]
- Padan E., Schuldiner S. Energy transduction in the photosynthetic membranes of the cyanobacterium (blue-green alga) P-lectonema boryanum. J Biol Chem. 1978 May 10;253(9):3281–3286. [PubMed] [Google Scholar]
- Scholes P., Mitchell P., Moyle J. The polarity of proton translocation in some photosynthetic microorganisms. Eur J Biochem. 1969 Apr;8(3):450–454. doi: 10.1111/j.1432-1033.1969.tb00548.x. [DOI] [PubMed] [Google Scholar]
- Stanier R. Y., Kunisawa R., Mandel M., Cohen-Bazire G. Purification and properties of unicellular blue-green algae (order Chroococcales). Bacteriol Rev. 1971 Jun;35(2):171–205. doi: 10.1128/br.35.2.171-205.1971. [DOI] [PMC free article] [PubMed] [Google Scholar]