{"title":"Acyl-turnover of acylplastoquinol enhances recovery of photodamaged PSII in Synechocystis","authors":"Haruhiko Jimbo, Mana Torii, Yuichiro Fujino, Yoshiki Tanase, Kazuki Kurima, Naoki Sato, Hajime Wada","doi":"10.1111/tpj.17051","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Photosynthetic electron transport is carried out by the electron carrier, plastoquinone (PQ). Recently, another form of PQ, acylplastoquinol (APQ), was discovered in <i>Synechocystis</i> sp. PCC 6803 (<i>Synechocystis</i>), but its physiological function in photosynthesis is unclear. In the present study, we identified a lipase encoded in <i>sll0482</i> gene in <i>Synechocystis</i> that deacylates APQ and releases a free fatty acid and a reduced PQ (plastoquinol, PQH<sub>2</sub>), which we named acylplastoquinol lipase (APL). Disruption of <i>apl</i> gene increased APQ content, and recovery of photodamaged PSII under low light (LL) after the exposure to very high light (vHL) at 2500 μmol photons m<sup>−2</sup> sec<sup>−1</sup> without aeration (vHL) for 60 min, was suppressed in the Δ<i>apl</i> cells. Δ<i>apl</i> cells also show the slow rate of <i>de novo</i> synthesis of D1, a reaction center of PSII under such condition. Under high light, the cellular growth of Δ<i>apl</i> was inhibited; however, disruption of <i>apl</i> gene did not affect the photosynthetic activity or photoinhibition of PSII. In wild-type cells, APQ content increased under vHL condition. Also, APQ was converted to PQH<sub>2</sub> after transfer to LL with aeration by ambient air. Such striking changes in APQ were not observed in Δ<i>apl</i> cells. The deacylation of APQ by APL may help repair PSII when PSII cannot drive photosynthetic electron transport efficiently.</p>\n </div>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"120 4","pages":"1317-1325"},"PeriodicalIF":6.2000,"publicationDate":"2024-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.17051","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
Photosynthetic electron transport is carried out by the electron carrier, plastoquinone (PQ). Recently, another form of PQ, acylplastoquinol (APQ), was discovered in Synechocystis sp. PCC 6803 (Synechocystis), but its physiological function in photosynthesis is unclear. In the present study, we identified a lipase encoded in sll0482 gene in Synechocystis that deacylates APQ and releases a free fatty acid and a reduced PQ (plastoquinol, PQH2), which we named acylplastoquinol lipase (APL). Disruption of apl gene increased APQ content, and recovery of photodamaged PSII under low light (LL) after the exposure to very high light (vHL) at 2500 μmol photons m−2 sec−1 without aeration (vHL) for 60 min, was suppressed in the Δapl cells. Δapl cells also show the slow rate of de novo synthesis of D1, a reaction center of PSII under such condition. Under high light, the cellular growth of Δapl was inhibited; however, disruption of apl gene did not affect the photosynthetic activity or photoinhibition of PSII. In wild-type cells, APQ content increased under vHL condition. Also, APQ was converted to PQH2 after transfer to LL with aeration by ambient air. Such striking changes in APQ were not observed in Δapl cells. The deacylation of APQ by APL may help repair PSII when PSII cannot drive photosynthetic electron transport efficiently.
期刊介绍:
Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community.
Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.