期刊名称：Proceedings of the National Academy of Sciences
印刷版ISSN：0027-8424
电子版ISSN：1091-6490
出版年度：2004
卷号：101
期号：15
页码：5530-5535
DOI：10.1073/pnas.0401269101
语种：English
出版社：The National Academy of Sciences of the United States of America
摘要：Energy-dependent exciton quenching, or qE, protects the higher plant photosynthetic apparatus from photodamage. Initiation of qE involves protonation of violaxanthin deepoxidase and PsbS, a component of the photosystem II antenna complex, as a result of lumen acidification driven by photosynthetic electron transfer. It has become clear that the response of qE to linear electron flow, termed "qE sensitivity," must be modulated in response to fluctuating environmental conditions. Previously, three mechanisms have been proposed to account for qE modulation: (i) the sensitivity of qE to the lumen pH is altered; (ii) elevated cyclic electron flow around photosystem I increases proton translocation into the lumen; and (iii) lowering the conductivity of the thylakoid ATP synthase to protons (gH+) allows formation of a larger steady-state proton motive force (pmf). Kinetic analysis of the electrochromic shift of intrinsic thylakoid pigments, a linear indicator of transthylakoid electric field component, suggests that, when CO2 alone was lowered from 350 ppm to 50 ppm CO2, modulation of qE sensitivity could be explained solely by changes in conductivity. Lowering both CO2 (to 50 ppm) and O2 (to 1%) resulted in an additional increase in qE sensitivity that could not be explained by changes in conductivity or cyclic electron flow associated with photosystem I. Evidence is presented for a fourth mechanism, in which changes in qE sensitivity result from variable partitioning of proton motive force into the electric field and pH gradient components. The implications of this mechanism for the storage of proton motive force and the regulation of the light reactions are discussed.
