Journal
JOURNAL OF PLANKTON RESEARCH
Volume 22, Issue 5, Pages 865-885Publisher
OXFORD UNIV PRESS
DOI: 10.1093/plankt/22.5.865
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Recent evidence from algal physiology and molecular biology confirms that photoinhibition is directly related to D1 protein damage and recovery, and D1 protein damage leads to a decrease in electron transfer or an increase in turnover time of the electron transfer chain. In this study, the turnover time of the electron transfer chain is defined as a function of the relative concentration of D1 protein in reaction centre II and the photoinhibition processes due to D1 protein degradation are incorporated into a model of photosynthesis, initiated by Dubinsky et al. (Plant Cell Physiol., 27, 1335-1349. 1986) and developed by Sakshaug et al. (Limnol. Oceanogr., 34, 198-205, 1989). D1 protein damage is assumed to be both Light and D1 protein concentration dependent, and to be proportional to the cross-section of PSII (sigma(PSII)). D1 protein recovery is only D1 protein concentration dependent. Two parameters, the damage constant (k(d)) and recovery rate (k(r)), are introduced to formulate the dynamics of D1 protein concentration. Setting minimal turnover time tau(m) = 3 ms, maximal quantum yield phi(m) = 0.1 mol O-2 E-1, optical cross-section a* = 0.0075 m(2) (mg Chi a)(-1), sigma(PSII) = 2 nm(2), k(d) ranging from 0 to 10(-7) and k(r) = 0.55 h(-1), the dynamic effect of photoinhibition on photosynthesis in natural conditions is simulated. Simulation results are consistent with observations. Some aspects of photosynthesis associated with photoinhibition, e.g. nutrient limitation and the interaction between photoinhibition and photoadaptation, are investigated through this dynamic model.
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