Abstract
The apparent affinity of photosynthesis for inorganic carbon in Anabaena variabilis strain M-3 increased during the course of adaptation from high to low CO2 concentration (5% and 0.03% v/v CO2 in air, respectively). This was attributed to an increased ability of the cells to accumulate inorganic carbon during the course of adaptation to low CO2 conditions. The release of phycobiliproteins was used to evaluate the sensitivity of the cells to lysozyme treatment followed by osmotic shock. High CO2-grown cells were more sensitive to this treatment than were low CO2 ones. The efflux of inorganic carbon from cells preloaded with radioactive bicarbonate is faster in high than it is in low CO2-adapted cells. It is postulated that the cell wall or membrane components undergo changes during the course of adaptation to low CO2 conditions. This is supported by electron micrographs showing differences in the cell wall appearance between high and low CO2-grown cells. The increasing ability to accumulate HCO3− and the lessened sensitivity to lysozyme during adaptation to low CO2 conditions depends on protein synthesis. The increase in affinity for inorganic carbon during the adaptation to low CO2 conditions is severely inhibited by the presence of spectinomycin. Incubation in the light significantly lessens the time required for the adaptation to low CO2 conditions.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Badger M. R., Kaplan A., Berry J. A. Internal Inorganic Carbon Pool of Chlamydomonas reinhardtii: EVIDENCE FOR A CARBON DIOXIDE-CONCENTRATING MECHANISM. Plant Physiol. 1980 Sep;66(3):407–413. doi: 10.1104/pp.66.3.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bennett A., Bogorad L. Complementary chromatic adaptation in a filamentous blue-green alga. J Cell Biol. 1973 Aug;58(2):419–435. doi: 10.1083/jcb.58.2.419. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bruin W. J., Nelson E. B., Tolbert N. E. Glycolate pathway in green algae. Plant Physiol. 1970 Sep;46(3):386–391. doi: 10.1104/pp.46.3.386. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ginzberg D., Padan E. Light effect on the internal osmotic pressure of the blue-green algae Plectonema boryanum and Phormidium luridum. Arch Mikrobiol. 1972;87(2):181–183. doi: 10.1007/BF00424999. [DOI] [PubMed] [Google Scholar]
- Kaplan A. Photosynthetic Response to Alkaline pH in Anabaena variabilis. Plant Physiol. 1981 Feb;67(2):201–204. doi: 10.1104/pp.67.2.201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Miller A. G., Colman B. Active transport and accumulation of bicarbonate by a unicellular cyanobacterium. J Bacteriol. 1980 Sep;143(3):1253–1259. doi: 10.1128/jb.143.3.1253-1259.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simon S. A., Gutknecht J. Solubility of carbon dioxide in lipid bilayer membranes and organic solvents. Biochim Biophys Acta. 1980 Mar 13;596(3):352–358. doi: 10.1016/0005-2736(80)90122-4. [DOI] [PubMed] [Google Scholar]
- Spurr A. R. A low-viscosity epoxy resin embedding medium for electron microscopy. J Ultrastruct Res. 1969 Jan;26(1):31–43. doi: 10.1016/s0022-5320(69)90033-1. [DOI] [PubMed] [Google Scholar]

