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The effect of redox potential on the kinetics of fluorescence induction in Photosystem II particles from Phormidium laminosum. Sigmoidicity,energy transfer and the slow phase
Authors:Jane M. Bowes  Peter Horton
Affiliation:1. Department of Biochemistry, University of Cambridge, Tennis Court Road, Cambridge CB2 1QW, U.K.;2. Department of Biochemistry and A.R.C. Research Group on Photosynthesis, University of Sheffield, Sheffield S10 2TN U.K.
Abstract:Fluorescence induction curves in 3-(3,4-dichlorophenyl)-1,1-dimethylurea (DCMU)-inhibited Photosystem (PS) II particles isolated from the blue-green alga Phormidium laminosum have been analysed as a function of redox potential. Redox titration of the initial fluorescence indicated a single component with Em,7.5 = +30 mV (n = 1) (Bowes, J., Horton, P. and Bendall, D.S. (1981) FEBS Lett. 135, 261–264). Despite this simplified electron acceptor system and the small number of chlorophylls per reaction centre, a sigmoidal induction curve was nevertheless seen. Sigmoidicity decreased as Q was reduced potentiometrically prior to induction such that the induction was exponential when the ratio FiFm = 0.64. These particles also showed a slow (β) phase of induction which titrated with an Em value slightly more positive than that of the major quencher. It is concluded that the sigmoidal shape of the fluorescence induction curve observed in Phormidium PS II particles is not a consequence of a requirement for two photons to close the PS II reaction centre, but is generated as a result of energy transfer between photosynthetic units comprising one reaction centre per approx. 50 chlorophylls. Also, the existence of PS II heterogeneity (PS IIα, PS IIβ centres) does not require a structurally differentiated chloroplast, but may only indicate the extent of aggregation of PS II centres.
Keywords:Photosystem II  Fluorescence induction kinetics  Redox Potential  (Blue-green alga)  PS II  Photosystem II  Chl  chlorophyll  Hepes  4-(2-hydroxyethyl)-1-piperazineethanesulphonic acid  DCMU  3-(3,4-dichlorophenyl)-1,1-dimethylurea  minimum fluorescence when Q is oxidised  maximum fluorescence when Q is reduced  initial fluorescence
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