Abstract
The ability of bicarbonate ion (HCO3-) to stimulate photosynthetic oxygen evolution in maize chloroplast fragments exposed to continuous light depends on light intensity. Stimulation by HCO3- is less at low intensities. In HCO3--depleted chloroplasts exposed to brief saturating light flashes, period 4 oscillations (in O2 yield per flash) are damped within three cycles. Readdition of HCO3- to these preparations restores the oscillatory pattern to higher flash numbers, indicating that HCO3- reduces the probability of “misses” in the photosystem II reaction center. The rate of the dark relaxation reaction Sn′ → Sn+1 (where S refers to the oxidation state of the oxygen-evolving mechanism and n = 0, 1, or 2), after a photoact in the photosystem II reaction center, is retarded in HCO3--depleted chloroplasts compared to the rate for this reaction in depleted chloroplasts to which HCO3- has been resupplied. However, the final oxygen-evolving reaction after the accumulation of four positive charges appears to be independent of HCO3-. Bicarbonate has no effect on the dark deactivation of the higher oxidation states (S2 and S3) of the positive charge-accumulating system. We propose two alternate ways in which the kinetic model of oxygen evolution developed by Kok et al. [(1970) Photochem. Photobiol. 11, 457-475] can be extended to include the action of HCO3-.
Keywords: photosynthesis, Hill reaction, photochemical reactions of system II
Full text
PDF![4679](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bbd/433959/a875e9bb910c/pnas00075-0041.png)
![4680](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bbd/433959/03dc73111be0/pnas00075-0042.png)
![4681](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bbd/433959/9c6cf69e118d/pnas00075-0043.png)
![4682](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bbd/433959/85e44b7e171b/pnas00075-0044.png)
![4683](https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bbd/433959/446c381cc5e4/pnas00075-0045.png)
Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Antoshechkin A. G. Chromosomal damage in Chinese hamster cells grown in U.V.-irradiated medium. Photochem Photobiol. 1970 Jan;11(1):49–52. doi: 10.1111/j.1751-1097.1970.tb05716.x. [DOI] [PubMed] [Google Scholar]
- Bouges-Bocquet B. Limiting steps in photosystem II and water decomposition in Chlorella and spinach chloroplasts. Biochim Biophys Acta. 1973 Apr 5;292(3):772–785. doi: 10.1016/0005-2728(73)90024-8. [DOI] [PubMed] [Google Scholar]
- Good N. E. Carbon Dioxide & the Hill Reaction. Plant Physiol. 1963 May;38(3):298–304. doi: 10.1104/pp.38.3.298. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kok B., Forbush B., McGloin M. Cooperation of charges in photosynthetic O2 evolution-I. A linear four step mechanism. Photochem Photobiol. 1970 Jun;11(6):457–475. doi: 10.1111/j.1751-1097.1970.tb06017.x. [DOI] [PubMed] [Google Scholar]
- Mar T., Govindjee Kinetic models of oxygen evolution in photosynthesis. J Theor Biol. 1972 Sep;36(3):427–446. doi: 10.1016/0022-5193(72)90001-x. [DOI] [PubMed] [Google Scholar]
- Stemler A., Govindjee Bicarbonate ion as a critical factor in photosynthetic oxygen evolution. Plant Physiol. 1973 Aug;52(2):119–123. doi: 10.1104/pp.52.2.119. [DOI] [PMC free article] [PubMed] [Google Scholar]
- West J., Hill R. Carbon dioxide and the reduction of indophenol and ferricyanide by chloroplasts. Plant Physiol. 1967 Jun;42(6):819–826. doi: 10.1104/pp.42.6.819. [DOI] [PMC free article] [PubMed] [Google Scholar]