4.5 Article

Dissection of respiratory and cyclic electron transport in Synechocystis sp. PCC 6803

Journal

JOURNAL OF PLANT RESEARCH
Volume 135, Issue 4, Pages 555-564

Publisher

SPRINGER JAPAN KK
DOI: 10.1007/s10265-022-01401-z

Keywords

Cyclic electron transport; P700; Photosynthesis; Photosystem I; Respiratory electron transport

Categories

Funding

  1. Japan Society for the Promotion of Science (JSPS) [21399224]

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Cyclic electron transport (CET) is a hypothesis for regulating photosynthetic electron transport and producing additional ATP, with its activity in cyanobacteria being evaluated through P700 redox state and chlorophyll fluorescence. In cyanobacteria, distinguishing between in vivo electron transport rates in respiratory electron transport (RET) and CET can be complex due to shared intersystem chains.
Cyclic electron transport (CET) is an attractive hypothesis for regulating photosynthetic electron transport and producing the additional ATP in oxygenic phototrophs. The concept of CET has been established in the last decades, and it is proposed to function in the progenitor of oxygenic photosynthesis, cyanobacteria. The in vivo activity of CET is frequently evaluated either from the redox state of the reaction center chlorophyll in photosystem (PS) I, P700, in the absence of PSII activity or by comparing PSI and PSII activities through the P700 redox state and chlorophyll fluorescence, respectively. The evaluation of CET activity, however, is complicated especially in cyanobacteria, where CET shares the intersystem chain, including plastoquinone, cytochrome b(6)/f complex, plastocyanin, and cytochrome c(6), with photosynthetic linear electron transport (LET) and respiratory electron transport (RET). Here we sought to distinguish the in vivo electron transport rates in RET and CET in the cyanobacterium Synechocystis sp. PCC 6803. The reduction rate of oxidized P700 (P700(+)) decreased to less than 10% when PSII was inhibited, indicating that PSII is the dominant electron source to PSI but P700(+) is also reduced by electrons derived from other sources. The oxidative pentose phosphate (OPP) pathway functions as the dominant electron source for RET, which was found to be inhibited by glycolaldehyde (GA). In the condition where the OPP pathway and respiratory terminal oxidases were inhibited by GA and KCN, the P700(+) reduction rate was less than 1% of that without any inhibitors. This study indicate that the electron transport to PSI when PSII is inhibited is dominantly derived from the OPP pathway in Synechocystis sp. PCC 6803.

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