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Regulation of electron transport at photosystem II

Regulation of electron transport at photosystem II
光系统 II 电子传输的调节
批准号:
04453167
负责人:
TOYOSHIMA Yoshinori
金额:
$4.74万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1992
资助国家:
日本
项目状态:
已结题
起止时间:
1992 至 1994

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中文摘要
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英文摘要
We examined the two major mechanisms by which balance of photosystem I (PSI) and Photosystem II (PSII) in the photosynthetic electron transport in higher plants was regulated in response to the variation of light environment, focusing on the regulation at PSII.1.Regulation of electron transport at primary quinone acceptor (QA) L protein which is a component of PSII complex and encoded by chloroplast psbL gene was found to be involved in the regulation of electron transport at QA site by in vitro reconstitution experiments. Plastoquinone-9 (PQ-9) depleted PSII reaction center core complex, consisting of CP47/D1/D2/Cytb-559/I proteins was isolated and submitted to the reconstitution with PQ-9. Only when the reconstitution was carried out with the L protein, PQ-9 reinserted in the complex and worked as QA in the resulting complex. Recombinant L protein was successfully over expressed in E.coli.and found to stand for the isolated L protein from PSII particles. Based on these findings, the … More molecular mechanism of the regulation of electron transport at QA site is being examined by the in vitro reconstitution with various types of mutant L protein.2.Regulation of the gene expression of psbC and psbD by light at transcription level There are two light-responsive promoters in chloroplast psbD/C gene cluster which encodes several important proteins of PSII.One (D/C-3 promoter) produces mRNA for D2 protein and the other (D/C-4 promoter) does that for CP43 protein. Upon light illumination, the former is reversibly activated while the latter is inactivated, respectively, suggesting that synthesis of these two proteins responses to light intensity through the regulation of activities of these promoters. We succeeded in the patrial purification of a nuclear-encoded regulatory factor which specifically activates the D/C-3 promoter. This factor seems to be a sequence specific DNA binding protein which recognizes the cis-element residing upstream region of the D/C-3 transcription initiation site. Less
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会议论文
Wada,Takuji: "In vitro analysis of light-induced transcription in wheat psbD/C gene cluster using plastid extracts from dark-grown and short-term illuminated seedlings." Plant Physiology. 104. 1259-1267 (1994)
Wada, Takuji:“使用黑暗生长和短期光照幼苗的质体提取物对小麦 psbD/C 基因簇中的光诱导转录进行体外分析。”
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通讯作者:
Kawaguchi,Hiroshi: "Dynamical behavior of psb gene transcripts in greening wheat seedlings. I.Time course of accumulation of the psbA through psbN gene transcripts during light-induced greening." Plant Molecular Biology. 20. 695-704 (1992)
Kawaguchi, Hiroshi:“psb 基因转录本在绿化小麦幼苗中的动态行为。I.在光诱导绿化过程中通过 psbN 基因转录本积累 psbA 的时间过程。”
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