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本文引用的文献

1
One of two alb3 proteins is essential for the assembly of the photosystems and for cell survival in Chlamydomonas.衣藻中两个alb3蛋白之一对于光系统的组装以及细胞存活至关重要。
Plant Cell. 2006 Jun;18(6):1454-66. doi: 10.1105/tpc.105.038695. Epub 2006 May 5.
2
Evidence for the role of the oxygen-evolving manganese complex in photoinhibition of Photosystem II.放氧锰复合体在光系统II光抑制中作用的证据。
Biochim Biophys Acta. 2005 Jan 7;1706(1-2):68-80. doi: 10.1016/j.bbabio.2004.09.001.
3
Systematic analysis of the relation of electron transport and ATP synthesis to the photodamage and repair of photosystem II in Synechocystis.集胞藻中电子传递和ATP合成与光系统II光损伤及修复关系的系统分析
Plant Physiol. 2005 Jan;137(1):263-73. doi: 10.1104/pp.104.054478. Epub 2004 Dec 23.
4
A homolog of Albino3/OxaI is essential for thylakoid biogenesis in the cyanobacterium Synechocystis sp. PCC6803.白化3/氧化酶I的同源物对集胞藻PCC6803中的类囊体生物合成至关重要。
J Biol Chem. 2004 Dec 31;279(53):55792-800. doi: 10.1074/jbc.M411041200. Epub 2004 Oct 21.
5
Accumulation of the D2 protein is a key regulatory step for assembly of the photosystem II reaction center complex in Synechocystis PCC 6803.D2蛋白的积累是集胞藻PCC 6803中光系统II反应中心复合物组装的关键调控步骤。
J Biol Chem. 2004 Nov 19;279(47):48620-9. doi: 10.1074/jbc.M405725200. Epub 2004 Sep 3.
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PratA, a periplasmic tetratricopeptide repeat protein involved in biogenesis of photosystem II in Synechocystis sp. PCC 6803.PratA，一种参与集胞藻PCC 6803中光系统II生物合成的周质四肽重复蛋白。
J Biol Chem. 2004 Oct 22;279(43):44639-44. doi: 10.1074/jbc.M405393200. Epub 2004 Aug 24.
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Evolution: red algal genome affirms a common origin of all plastids.进化：红藻基因组证实了所有质体的共同起源。
Curr Biol. 2004 Jul 13;14(13):R514-6. doi: 10.1016/j.cub.2004.06.041.
8
Efficient assembly of photosystem II in Chlamydomonas reinhardtii requires Alb3.1p, a homolog of Arabidopsis ALBINO3.莱茵衣藻中光系统II的有效组装需要Alb3.1p，它是拟南芥ALBINO3的同源物。
Plant Cell. 2004 Jul;16(7):1790-800. doi: 10.1105/tpc.023226. Epub 2004 Jun 18.
9
Yeast Oxa1 interacts with mitochondrial ribosomes: the importance of the C-terminal region of Oxa1.酵母Oxa1与线粒体核糖体相互作用：Oxa1 C端区域的重要性。
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集胞藻PCC 6803的oxa1同源物对于反应中心前体蛋白pD1的膜整合至关重要。

The synechocystis sp PCC 6803 oxa1 homolog is essential for membrane integration of reaction center precursor protein pD1.

作者信息

Ossenbühl Friedrich, Inaba-Sulpice Masami, Meurer Jörg, Soll Jürgen, Eichacker Lutz A

机构信息

Department for Molecular Botany, University Ulm, D-89069 Ulm, Germany.

出版信息

Plant Cell. 2006 Sep;18(9):2236-46. doi: 10.1105/tpc.106.043646. Epub 2006 Aug 11.

DOI:10.1105/tpc.106.043646
PMID:16905652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1560907/
Abstract

Synechocystis sp PCC 6803 Slr1471p, an Oxa1p/Alb3/YidC homolog, is an essential protein for cell viability for which functions in thylakoid membrane biogenesis and cell division have been proposed. Using a fusion of green fluorescent protein to the C terminus of Slr1471p, we found that the mutant slr1471-gfp is photochemically inhibited when light intensities increase to 80 micromol x m(-2) x s(-1). We show that photoinhibition correlates with an increased redox potential of the reaction center quinone Q(A)(-) and a decreased redox potential of Q(B)(-). Analysis reveals that membrane integration of the D1 precursor protein is affected, leading to the accumulation of pD1 in the membrane phase. We show that Slr1471p interacts directly with the D1 protein and discuss why the accumulation of pD1 in two reaction center assembly intermediates is dependent on Slr1471p.

摘要

集胞藻PCC 6803的Slr1471p是一种Oxa1p/Alb3/YidC同源物，是细胞生存能力所必需的蛋白质，有人提出它在类囊体膜生物发生和细胞分裂中发挥作用。通过将绿色荧光蛋白融合到Slr1471p的C末端，我们发现当光强增加到80微摩尔·米-2·秒-1时，突变体slr1471-gfp受到光化学抑制。我们表明，光抑制与反应中心醌Q(A)(-)的氧化还原电位增加和Q(B)(-)的氧化还原电位降低相关。分析表明，D1前体蛋白的膜整合受到影响，导致pD1在膜相中积累。我们表明，Slr1471p与D1蛋白直接相互作用，并讨论了为什么pD1在两个反应中心组装中间体中的积累依赖于Slr1471p。