Depletion of Vipp1 in Synechocystis sp PCC 6803 affects photosynthetic activity before the loss of thylakoid membranes
Gao, Hong; Xu, Xudong
刊名FEMS MICROBIOLOGY LETTERS
2009-03-01
卷号292期号:1页码:63-70
关键词Vipp1 P(petE) photosynthesis thylakoid membranes viability Synechocystis
ISSN号0378-1097
通讯作者Xu, XD, Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Hubei, Peoples R China
中文摘要A vipp1 mutant of Synechocystis sp. PCC 6803 could not be completely segregated under either mixotrophic or heterotrophic conditions. A vipp1 gene with a copper-regulated promoter (P-petE-vipp1) was integrated into a neutral platform in the genome of the merodiploid mutant. The copper-induced expression of P-petE-vipp1 allowed a complete segregation of the vipp1 mutant and observation of the phenotype of Synechocystis 6803 with different levels of vesicle-inducing protein in plastids 1 (Vipp1). When P-petE-vipp1 was turned off by copper deprivation, Synechocystis lost Vipp1 and photosynthetic activity almost simultaneously, and at a later stage, thylakoid membranes and cell viability. The photosystem II (PSII)-mediated electron transfer was much more rapidly reduced than the PSI-mediated electron transfer. By testing a series of concentrations, we found that P-petE-vipp1 cells grown in medium with 0.025 mu M Cu2+ showed no reduction of thylakoid membranes, but greatly reduced photosynthetic activity and viability. These results suggested that in contrast to a previous report, the loss of photosynthetic activity may not have been due to the loss of thylakoid membranes, but may have been caused more directly by the loss of Vipp1 in Synechocystis 6803.
英文摘要A vipp1 mutant of Synechocystis sp. PCC 6803 could not be completely segregated under either mixotrophic or heterotrophic conditions. A vipp1 gene with a copper-regulated promoter (P(petE)-vipp1) was integrated into a neutral platform in the genome of the merodiploid mutant. The copper-induced expression of P(petE)-vipp1 allowed a complete segregation of the vipp1 mutant and observation of the phenotype of Synechocystis 6803 with different levels of vesicle-inducing protein in plastids 1 (Vipp1). When P(petE)-vipp1 was turned off by copper deprivation, Synechocystis lost Vipp1 and photosynthetic activity almost simultaneously, and at a later stage, thylakoid membranes and cell viability. The photosystem II (PSII)-mediated electron transfer was much more rapidly reduced than the PSI-mediated electron transfer. By testing a series of concentrations, we found that P(petE)-vipp1 cells grown in medium with 0.025 mu M Cu(2+) showed no reduction of thylakoid membranes, but greatly reduced photosynthetic activity and viability. These results suggested that in contrast to a previous report, the loss of photosynthetic activity may not have been due to the loss of thylakoid membranes, but may have been caused more directly by the loss of Vipp1 in Synechocystis 6803.
学科主题Microbiology
WOS标题词Science & Technology ; Life Sciences & Biomedicine
类目[WOS]Microbiology
研究领域[WOS]Microbiology
关键词[WOS]SP STRAIN PCC-6803 ; CHILL-LIGHT TOLERANCE ; PHOTOSYSTEM-II ; MOLECULAR-CLONING ; GENE ; BIOGENESIS ; EXPRESSION ; PLASMA ; GROWTH ; MUTANT
收录类别SCI
资助信息National Natural Science Foundation of China [30330030]; Chinese Academy of Sciences [KSCX2-SW-332]
语种英语
WOS记录号WOS:000263036900010
公开日期2010-10-13
内容类型期刊论文
源URL[http://ir.ihb.ac.cn/handle/152342/7876]  
专题水生生物研究所_中科院水生所知识产出(2009年前)_期刊论文
作者单位Chinese Acad Sci, Inst Hydrobiol, State Key Lab Freshwater Ecol & Biotechnol, Wuhan 430072, Hubei, Peoples R China
推荐引用方式
GB/T 7714
Gao, Hong,Xu, Xudong. Depletion of Vipp1 in Synechocystis sp PCC 6803 affects photosynthetic activity before the loss of thylakoid membranes[J]. FEMS MICROBIOLOGY LETTERS,2009,292(1):63-70.
APA Gao, Hong,&Xu, Xudong.(2009).Depletion of Vipp1 in Synechocystis sp PCC 6803 affects photosynthetic activity before the loss of thylakoid membranes.FEMS MICROBIOLOGY LETTERS,292(1),63-70.
MLA Gao, Hong,et al."Depletion of Vipp1 in Synechocystis sp PCC 6803 affects photosynthetic activity before the loss of thylakoid membranes".FEMS MICROBIOLOGY LETTERS 292.1(2009):63-70.
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