Abstract
Light-shade adaptation of the chlorophyll a/b containing procaryote Prochlorothrix hollandica was studied in semicontinuous cultures adapted to 8, 80 and 200 μmole quanta per square meter per second. Chlorophyll a contents based on dry weight differed by a factor of 6 and chlorophyll b by a factor of 2.5 between the two extreme light conditions. Light utilization efficiencies determined from photosynthesis response curves were found to decrease in low light grown cultures due to lower light harvesting efficiencies; quantum requirements were constant at limiting and saturating irradiances for growth. At saturating growth irradiances, changes in light saturated oxygen evolution rate originated from changes in chlorophyll a antenna relative to the number of reaction centers II. At light-limiting conditions both the number of reaction centers II and the antenna size changed. The amount of chlorophyll b relative to reaction center II remained constant. As in cyanobacteria, the ratio of reaction center I to reaction center II was modulated during light-shade adaptation. On the other hand, time constants for photosynthetic electron transport (4 milliseconds) were low as observed in green algae and diatoms. The occurrence of state one to two and state two to one transitions is reported here. Another feature linking photosynthetic electron transport in P. hollandica to that in the eucaryotic photosynthetic apparatus was blockage of the state one to two transition by 3-(3,4-dichlorophenyl)-1,1-dimethylurea. Although chlorophyll b was reported in association with photosystem I, the 630 nanometer light effect does not exclude that chlorophyll b is the photoreceptor for the state one to two transition.
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- Batschauer A., Mösinger E., Kreuz K., Dörr I., Apel K. The implication of a plastid-derived factor in the transcriptional control of nuclear genes encoding the light-harvesting chlorophyll a/b protein. Eur J Biochem. 1986 Feb 3;154(3):625–634. doi: 10.1111/j.1432-1033.1986.tb09444.x. [DOI] [PubMed] [Google Scholar]
- Bennett J. Regulation of photosynthesis by reversible phosphorylation of the light-harvesting chlorophyll a/b protein. Biochem J. 1983 Apr 15;212(1):1–13. doi: 10.1042/bj2120001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bullerjahn G. S., Matthijs H. C., Mur L. R., Sherman L. A. Chlorophyll-protein composition of the thylakoid membrane from Prochlorothrix hollandica, a prokaryote containing chlorophyll b. Eur J Biochem. 1987 Oct 15;168(2):295–300. doi: 10.1111/j.1432-1033.1987.tb13420.x. [DOI] [PubMed] [Google Scholar]
- Falkowski P. G., Owens T. G. Light-Shade Adaptation : TWO STRATEGIES IN MARINE PHYTOPLANKTON. Plant Physiol. 1980 Oct;66(4):592–595. doi: 10.1104/pp.66.4.592. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Göbel F. Direct measurement of pure absorbance spectra of living phototrophic microorganisms. Biochim Biophys Acta. 1978 Feb 1;538(3):593–602. doi: 10.1016/0304-4165(78)90420-8. [DOI] [PubMed] [Google Scholar]
- Lewin R. A. Prochlorophyta as a proposed new division of algae. Nature. 1976 Jun 24;261(5562):697–698. doi: 10.1038/261697b0. [DOI] [PubMed] [Google Scholar]
- Myers J., Graham J. R. The photosynthetic unit in chlorella measured by repetitive short flashes. Plant Physiol. 1971 Sep;48(3):282–286. doi: 10.1104/pp.48.3.282. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Withers N. W., Alberte R. S., Lewin R. A., Thornber J. P., Britton G., Goodwin T. W. Photosynthetic unit size, carotenoids, and chlorophyll-protein composition of Prochloron sp., a prokaryotic green alga. Proc Natl Acad Sci U S A. 1978 May;75(5):2301–2305. doi: 10.1073/pnas.75.5.2301. [DOI] [PMC free article] [PubMed] [Google Scholar]