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本文引用的文献

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Construction of an Obligate Photoheterotrophic Mutant of the Cyanobacterium Synechocystis 6803 : Inactivation of the psbA Gene Family.构建一株蓝藻集胞藻 6803 的严格依赖光照的营养缺陷型突变体:psbA 基因家族的失活。
Plant Physiol. 1987 Dec;85(4):1021-5. doi: 10.1104/pp.85.4.1021.
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A model for the photosystem II reaction center core including the structure of the primary donor P680.一种包含初级供体P680结构的光系统II反应中心核心模型。
Biochemistry. 1996 Nov 19;35(46):14486-502. doi: 10.1021/bi960764k.
3
Degradation pattern of photosystem II reaction center protein D1 in intact leaves. The major photoinhibition-induced cleavage site in D1 polypeptide is located amino terminally of the DE loop.完整叶片中光系统II反应中心蛋白D1的降解模式。D1多肽中主要的光抑制诱导切割位点位于DE环的氨基末端。
Plant Physiol. 1996 Aug;111(4):1183-90. doi: 10.1104/pp.111.4.1183.
4
Differential expression of the psbA genes in the cyanobacterium Synechocystis 6803.集胞藻6803中psbA基因的差异表达
Mol Gen Genet. 1993 Apr;238(1-2):161-8. doi: 10.1007/BF00279543.
5
Rapid interchange between two distinct forms of cyanobacterial photosystem II reaction-center protein D1 in response to photoinhibition.两种不同形式的蓝藻光合系统II反应中心蛋白D1响应光抑制而快速互换。
Proc Natl Acad Sci U S A. 1993 Nov 1;90(21):9973-7. doi: 10.1073/pnas.90.21.9973.
6
Site-specific mutations in the D1 polypeptide affect the susceptibility of Synechocystis 6803 cells to photoinhibition.D1多肽中的位点特异性突变会影响集胞藻6803细胞对光抑制的敏感性。
Plant Mol Biol. 1993 Apr;22(1):1-12. doi: 10.1007/BF00038991.
7
Changes of amino acid sequence in PEST-like area and QEEET motif affect degradation rate of D1 polypeptide in photosystem II.光系统II中类PEST区域和QEEET基序的氨基酸序列变化会影响D1多肽的降解速率。
Plant Mol Biol. 1994 Jun;25(3):517-26. doi: 10.1007/BF00043879.
8
Specific binding of Synechococcus sp. strain PCC 7942 proteins to the enhancer element of psbAII required for high-light-induced expression.聚球藻属菌株PCC 7942的蛋白质与高光诱导表达所需的psbAII增强子元件的特异性结合。
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9
Deletion of the PEST-like region of photosystem two modifies the QB-binding pocket but does not prevent rapid turnover of D1.删除光系统II的类PEST区域会改变QB结合口袋,但不会阻止D1的快速周转。
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10
Amino acid residues that influence the binding of manganese or calcium to photosystem II. 2. The carboxy-terminal domain of the D1 polypeptide.影响锰或钙与光系统II结合的氨基酸残基。2. D1多肽的羧基末端结构域。
Biochemistry. 1995 May 2;34(17):5859-82. doi: 10.1021/bi00017a017.

集胞藻6803株蓝细菌中沉默的psbA1基因的激活产生了一种新型功能性D1蛋白。

Activation of the silent psbA1 gene in the cyanobacterium Synechocystis sp strain 6803 produces a novel and functional D1 protein.

作者信息

Salih G F, Jansson C

机构信息

Department of Biochemistry, Arrhenius Laboratories, Stockholm University, Sweden.

出版信息

Plant Cell. 1997 Jun;9(6):869-78. doi: 10.1105/tpc.9.6.869.

DOI:10.1105/tpc.9.6.869
PMID:9212463
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC156964/
Abstract

The photosystem II reaction center protein D1 in Synechocystis sp strain 6803 is encoded by the psbA2 and psbA3 genes of the three-membered psbA gene family. The silent and divergent psbA1 copy of the psbA gene family was activated by exchanging part of its upstream region with a corresponding fragment of the psbA2 copy. The light-regulated expression of the activated psbA1 gene showed that the inserted psbA2 segment contains the information necessary for light-dependent as well as high-light-stimulated transcription. The activated psbA1 gene expressed a novel D1 protein, D1'. A mutant strain containing psbA1 as the only active psbA gene grew photoautotrophically at a rate comparable to that of the wild type. This finding demonstrates that despite its unusual amino acid sequence, D1 is exchangeable for D1 in the photosystem II complex, at least under normal laboratory conditions. The D1' protein was found to have a degradation rate similar to that of the D1 protein under low- or high-light conditions. Another mutant containing the activated psbA1 gene together with the psbA2 and psbA3 genes produced both the D1 and D1' proteins.

摘要

集胞藻6803菌株中的光系统II反应中心蛋白D1由psbA基因家族中三个成员的psbA2和psbA3基因编码。通过将psbA基因家族中沉默且有差异的psbA1拷贝的部分上游区域与psbA2拷贝的相应片段进行交换,激活了该拷贝。激活的psbA1基因的光调节表达表明,插入的psbA2片段包含光依赖性以及高光刺激转录所需的信息。激活的psbA1基因表达了一种新的D1蛋白,即D1'。一个以psbA1作为唯一活性psbA基因的突变菌株能够以与野生型相当的速率进行光合自养生长。这一发现表明,尽管D1'的氨基酸序列不同寻常,但至少在正常实验室条件下,它在光系统II复合物中可替代D1。研究发现,在低光或高光条件下,D1'蛋白的降解速率与D1蛋白相似。另一个含有激活的psbA1基因以及psbA2和psbA3基因的突变体同时产生了D1和D1'蛋白。