Photosynthesis

About: Photosynthesis is a research topic. Over the lifetime, 19789 publications have been published within this topic receiving 895197 citations.

Adaptation toHydrogen Sulfide ofOxygenic andAnoxygenic Photosynthesis among Cyanobacteria

Abstract: Four different types of adaptation to sulfide among cyanobacteria are described based on the differential toxicity to sulfide of photosystems I and II and the capacity for the induction of anoxygenic photosynthesis. Most cyanobacteria are highly sensitive to sulfide toxicity, and brief exposures to low concentrations cause complete and irreversible cessation of CO2 photoassimilation. Resistance of photosystem II to sulfide toxicity, allowing for oxygenic photosynthesis under sulfide, is found in cyanobacteria exposed to low H2S concentrations in various hot springs. When H2S levels exceed 200 μM another type of adaptation involving partial induction of anoxygenic photosynthesis, operating in concert with partially inhibited oxygenic photosynthesis, is found in cyanobacterial strains isolated from both hot springs and hypersaline cyanobacterial mats. The fourth type of adaptation to sulfide is found at H2S concentrations higher than 1 mM and involves a complete replacement of oxygenic photosynthesis by an effective sulfide-dependent, photosystem II-independent anoxygenic photosynthesis. The ecophysiology of the various sulfide-adapted cyanobacteria may point to their uniqueness within the division of cyanobacteria.

Adaptation to Hydrogen Sulfide of Oxygenic and Anoxygenic Photosynthesis among Cyanobacteria.

Abstract: Four different types of adaptation to sulfide among cyanobacteria are described based on the differential toxicity to sulfide of photosystems I and II and the capacity for the induction of anoxygenic photosynthesis. Most cyanobacteria are highly sensitive to sulfide toxicity, and brief exposures to low concentrations cause complete and irreversible cessation of CO2 photoassimilation. Resistance of photosystem II to sulfide toxicity, allowing for oxygenic photosynthesis under sulfide, is found in cyanobacteria exposed to low H2S concentrations in various hot springs. When H2S levels exceed 200 μM another type of adaptation involving partial induction of anoxygenic photosynthesis, operating in concert with partially inhibited oxygenic photosynthesis, is found in cyanobacterial strains isolated from both hot springs and hypersaline cyanobacterial mats. The fourth type of adaptation to sulfide is found at H2S concentrations higher than 1 mM and involves a complete replacement of oxygenic photosynthesis by an effective sulfide-dependent, photosystem II-independent anoxygenic photosynthesis. The ecophysiology of the various sulfide-adapted cyanobacteria may point to their uniqueness within the division of cyanobacteria.

Effects of Extracellular pH on the Metabolic Pathways in Sulfur-Deprived, H2-Producing Chlamydomonas reinhardtii Cultures

Abstract: Sustained photoproduction of H(2) by the green alga, Chlamydomonas reinhardtii, can be obtained by incubating cells in sulfur-deprived medium [Ghirardi et al. (2000b) Trends Biotechnol. 18: 506; Melis et al. (2000) Plant Physiol. 122: 127]. The current work focuses on (a) the effects of different initial extracellular pHs on the inactivation of photosystem II (PSII) and O(2)-sensitive H(2)-production activity in sulfur-deprived algal cells and (b) the relationships among H(2)-production, photosynthetic, aerobic and anaerobic metabolisms under different pH regimens. The maximum rate and yield of H(2) production occur when the pH at the start of the sulfur deprivation period is 7.7 and decrease when the initial pH is lowered to 6.5 or increased to 8.2. The pH profile of hydrogen photoproduction correlates with that of the residual PSII activity (optimum pH 7.3-7.9), but not with the pH profiles of photosynthetic electron transport through photosystem I or of starch and protein degradation. In vitro hydrogenase activity over this pH range is much higher than the actual in situ rates of H(2) production, indicating that hydrogenase activity per se is not limiting. Starch and protein catabolisms generate formate, acetate and ethanol; contribute some reductant for H(2) photoproduction, as indicated by 3-(3,4-dichlorophenyl)-1,1-dimethylurea and 2,5-dibromo-6-isopropyl-3-methyl-1,4-benzoquinone inhibition results; and are the primary sources of reductant for respiratory processes that remove photosynthetically generated O(2). Carbon balances demonstrate that alternative metabolic pathways predominate at different pHs, and these depend on whether residual photosynthetic activity is present or not.

Plants and high temperature stress.

Abstract: The effect of high temperature on higher plants is primarily on photosynthetic functions. The heat tolerance limit of leaves of higher plants coincides with (and appears to be determined by) the thermal sensitivity of primary photochemical reactions occurring in the thylakoid membrane system. Tolerance limits vary between genotypes, but are also subject to acclimation. Long-term acclimations can be superimposed upon fast adaptive adjustment of the thermal stability, occurring in the time range of a few hours. Light causes an increase in tolerance to heat, and this stabilization is related to the light-induced proton gradient. In addition to irreversible effects, high temperature may also cause large, reversible effects on the rate of photosynthesis. We report here some studies of photosynthetic gas exchange and chlorophyll fluorescence, designed to examine the energetic balance between photosynthetic carbon metabolism and light reactions during steady state photosynthesis with leaves of cotton plants at different temperatures. At temperatures exceeding the optimum for assimilation, but well below the tolerance limit, the feedback control of light reactions by carbon metabolism declines, as additional dissipative processes become important. Energy dissipated by photorespiration can exceed that consumed by CO2 assimilation, and a reversible, temperature-induced non-photochemical 'quenching' process, related to 'spillover' of excitation energy to photosystem 1, decreases the efficiency of photosystem 2 with increasing temperature. However, despite the overall decline in the 'potential quantum efficiency', our analysis indicates that CO2 assimilation may be limited, in part, at high temperature by an imbalance in the regulation of the carbon metabolism, which is reflected in a 'down-regulation' of the ribulose-1,5-bisphosphate carboxylase/oxygenase.