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1
Cytochrome c-553 is not required for photosynthetic activity in the cyanobacterium Synechococcus.蓝藻聚球藻的光合活性并不需要细胞色素c-553。
Plant Cell. 1990 Sep;2(9):913-24. doi: 10.1105/tpc.2.9.913.
2
Functional characterization of Synechocystis sp. PCC 6803 delta psbU and delta psbV mutants reveals important roles of cytochrome c-550 in cyanobacterial oxygen evolution.集胞藻PCC 6803 ΔpsbU和ΔpsbV突变体的功能表征揭示了细胞色素c-550在蓝藻放氧过程中的重要作用。
Biochemistry. 1998 Feb 10;37(6):1551-8. doi: 10.1021/bi971676i.
3
Targeted inactivation of the gene psaI encoding a subunit of photosystem I of the cyanobacterium Synechocystis sp. PCC 6803.对编码集胞藻6803光合系统I一个亚基的psaI基因进行靶向失活。
Plant Cell Physiol. 1995 Dec;36(8):1579-87.
4
A novel nitrite reductase gene from the cyanobacterium Plectonema boryanum.来自蓝藻颤藻的一种新型亚硝酸还原酶基因。
J Bacteriol. 1995 Nov;177(21):6137-43. doi: 10.1128/jb.177.21.6137-6143.1995.
5
Molecular characterization of ferredoxin-NADP+ oxidoreductase in cyanobacteria: cloning and sequence of the petH gene of Synechococcus sp. PCC 7002 and studies on the gene product.蓝藻中ferredoxin-NADP⁺氧化还原酶的分子特征:聚球藻属PCC 7002的petH基因的克隆与序列分析及对基因产物的研究
Biochemistry. 1992 Mar 31;31(12):3092-102. doi: 10.1021/bi00127a009.
6
IdiA, a 34 kDa protein in the cyanobacteria Synechococcus sp. strains PCC 6301 and PCC 7942, is required for growth under iron and manganese limitations.IdiA是一种存在于蓝藻聚球藻属菌株PCC 6301和PCC 7942中的34 kDa蛋白质,在铁和锰限制条件下的生长过程中是必需的。
Microbiology (Reading). 1996 Sep;142 ( Pt 9):2635-45. doi: 10.1099/00221287-142-9-2635.
7
The role of cytochrome c-550 as studied through reverse genetics and mutant characterization in Synechocystis sp. PCC 6803.通过反向遗传学和聚球藻属PCC 6803中的突变体表征对细胞色素c-550作用的研究。
J Biol Chem. 1995 Mar 24;270(12):6901-7. doi: 10.1074/jbc.270.12.6901.
8
Functional analysis of psbV and a novel c-type cytochrome gene psbV2 of the thermophilic cyanobacterium Thermosynechococcus elongatus strain BP-1.嗜热蓝藻伸长聚球藻菌株BP-1的psbV和新型c型细胞色素基因psbV2的功能分析。
Plant Cell Physiol. 2001 Jun;42(6):599-607. doi: 10.1093/pcp/pce074.
9
Photoautotrophic growth of the cyanobacterium Synechocystis sp. PCC 6803 in the absence of cytochrome c553 and plastocyanin.集胞藻PCC 6803在缺乏细胞色素c553和质体蓝素的情况下进行光合自养生长。
J Biol Chem. 1994 Feb 18;269(7):5036-42.
10
Cloning of a sensory-kinase-encoding gene that belongs to the two-component regulatory family from the cyanobacterium Synechococcus sp. PCC7942.从蓝藻聚球藻属PCC7942中克隆出一个属于双组分调节家族的编码感官激酶的基因。
Gene. 1993 Sep 6;131(1):119-24. doi: 10.1016/0378-1119(93)90679-w.

引用本文的文献

1
Genetic, Genomics, and Responses to Stresses in Cyanobacteria: Biotechnological Implications.蓝藻中的遗传、基因组学和应激反应:生物技术的影响。
Genes (Basel). 2021 Mar 29;12(4):500. doi: 10.3390/genes12040500.
2
Light adaptation of cyclic electron transport through Photosystem I in the cyanobacterium Synechococcus sp. PCC 7942.在蓝细菌集胞藻 PCC 7942 中通过光系统 I 的循环电子传递的光适应。
Photosynth Res. 1995 Nov;46(1-2):277-85. doi: 10.1007/BF00020441.
3
Membrane-anchored cytochrome c as an electron carrier in photosynthesis and respiration: past, present and future of an unexpected discovery.膜锚定细胞色素c作为光合作用和呼吸作用中的电子载体:一项意外发现的过去、现在与未来
Photosynth Res. 2003;76(1-3):127-34. doi: 10.1023/A:1024999101226.
4
Chlorophyll fluorescence analysis of cyanobacterial photosynthesis and acclimation.蓝藻光合作用与适应性的叶绿素荧光分析
Microbiol Mol Biol Rev. 1998 Sep;62(3):667-83. doi: 10.1128/MMBR.62.3.667-683.1998.
5
Lumenal proteins involved in respiratory electron transport in the cyanobacterium Synechocystis sp. PCC6803.参与集胞藻PCC6803呼吸电子传递的腔内蛋白。
Plant Mol Biol. 1997 Nov;35(4):407-16. doi: 10.1023/a:1005875124387.
6
Inactivation of the petE gene for plastocyanin lowers photosynthetic capacity and exacerbates chilling-induced photoinhibition in the cyanobacterium Synechococcus.质体蓝素的petE基因失活会降低蓝藻聚球藻的光合能力,并加剧冷胁迫诱导的光抑制。
Plant Physiol. 1996 Dec;112(4):1551-61. doi: 10.1104/pp.112.4.1551.
7
Insertional inactivation of genes to isolate mutants of Synechococcus sp. strain PCC 7942: isolation of filamentous strains.通过基因插入失活分离聚球藻属PCC 7942菌株的突变体:丝状菌株的分离
J Bacteriol. 1993 Dec;175(23):7644-51. doi: 10.1128/jb.175.23.7644-7651.1993.
8
Role of signal peptides in targeting of proteins in cyanobacteria.信号肽在蓝细菌中蛋白质靶向定位中的作用。
J Bacteriol. 1994 Apr;176(7):1857-64. doi: 10.1128/jb.176.7.1857-1864.1994.
9
A new type of signal peptide: central role of a twin-arginine motif in transfer signals for the delta pH-dependent thylakoidal protein translocase.一种新型信号肽:双精氨酸基序在依赖ΔpH的类囊体蛋白转运酶转运信号中的核心作用。
EMBO J. 1995 Jun 15;14(12):2715-22. doi: 10.1002/j.1460-2075.1995.tb07272.x.
10
Two enzymes together capable of cysteine biosynthesis are encoded on a cyanobacterial plasmid.两种共同具备半胱氨酸生物合成能力的酶由一种蓝细菌质粒编码。
Mol Gen Genet. 1995 Jun 10;247(5):623-32. doi: 10.1007/BF00290354.

本文引用的文献

1
Identification and Purification of a Derepressible Alkaline Phosphatase from Anacystis nidulans R2.从鱼腥蓝细菌 R2 中鉴定和纯化一种可去阻遏的碱性磷酸酶。
Plant Physiol. 1988 Apr;86(4):1179-84. doi: 10.1104/pp.86.4.1179.
2
Electron donation to photosystem I.电子传递给光系统 I。
Plant Physiol. 1980 Apr;65(4):697-702. doi: 10.1104/pp.65.4.697.
3
The complete nucleotide sequence of a 16S ribosomal RNA gene from a blue-green alga, Anacystis nidulans.来自蓝藻(集胞藻)的16S核糖体RNA基因的完整核苷酸序列。
Mol Gen Genet. 1983;191(1):46-50. doi: 10.1007/BF00330888.
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Three-dimensional ultrastructure of a unicellular cyanobacterium.一种单细胞蓝细菌的三维超微结构
J Cell Biol. 1983 Sep;97(3):713-22. doi: 10.1083/jcb.97.3.713.
5
"A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum.一种将DNA限制性内切酶片段放射性标记至高比活度的技术。附录
Anal Biochem. 1984 Feb;137(1):266-7. doi: 10.1016/0003-2697(84)90381-6.
6
A new approach for molecular cloning in cyanobacteria: cloning of an Anacystis nidulans met gene using a Tn901-induced mutant.蓝细菌分子克隆的一种新方法:利用Tn901诱导突变体克隆集胞藻6803的met基因。
Gene. 1982 Nov;20(1):111-9. doi: 10.1016/0378-1119(82)90092-0.
7
Evidence for plastoquinol-cytochrome f/b-563 reductase as a common electron donor to P700 and cytochrome oxidase in cyanobacteria.质体醌醇-细胞色素f/b-563还原酶作为蓝细菌中P700和细胞色素氧化酶的共同电子供体的证据。
Biochem Biophys Res Commun. 1982 Oct 15;108(3):1188-95. doi: 10.1016/0006-291x(82)92126-x.
8
Structure and heme environment of ferrocytochrome c553 from 1H NMR studies.通过1H核磁共振研究亚铁细胞色素c553的结构与血红素环境
J Biol Chem. 1982 Aug 25;257(16):9356-64.
9
In vitro insertional mutagenesis with a selectable DNA fragment.利用可选择的DNA片段进行体外插入诱变。
Gene. 1984 Sep;29(3):303-13. doi: 10.1016/0378-1119(84)90059-3.
10
A new method for predicting signal sequence cleavage sites.一种预测信号序列切割位点的新方法。
Nucleic Acids Res. 1986 Jun 11;14(11):4683-90. doi: 10.1093/nar/14.11.4683.

蓝藻聚球藻的光合活性并不需要细胞色素c-553。

Cytochrome c-553 is not required for photosynthetic activity in the cyanobacterium Synechococcus.

作者信息

Laudenbach D E, Herbert S K, McDowell C, Fork D C, Grossman A R, Straus N A

机构信息

Carnegie Institution of Washington, Department of Plant Biology, Stanford, California 94305.

出版信息

Plant Cell. 1990 Sep;2(9):913-24. doi: 10.1105/tpc.2.9.913.

DOI:10.1105/tpc.2.9.913
PMID:1967057
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC159941/
Abstract

In cyanobacteria, the water-soluble cytochrome c-553 functions as a mobile carrier of electrons between the membrane-bound cytochrome b6-f complex and P-700 reaction centers of Photosystem I. The structural gene for cytochrome c-553 (designated cytA) of the cyanobacterium Synechococcus sp. PCC 7942 was cloned, and the deduced amino acid sequence was shown to be similar to known cyanobacterial cytochrome c-553 proteins. A deletion mutant was constructed that had no detectable cytochrome c-553 based on spectral analyses and tetramethylbenzidine-hydrogen peroxide staining of proteins resolved by polyacrylamide gel electrophoresis. The mutant strain was not impaired in overall photosynthetic activity. However, this mutant exhibited a decreased efficiency of cytochrome f oxidation. These results indicate that cytochrome c-553 is not an absolute requirement for reducing Photosystem I reaction centers in Synechococcus sp. PCC 7942.

摘要

在蓝细菌中,水溶性细胞色素c-553作为电子在膜结合的细胞色素b6-f复合物与光系统I的P-700反应中心之间的移动载体。蓝细菌聚球藻属PCC 7942的细胞色素c-553(命名为cytA)的结构基因被克隆,推导的氨基酸序列显示与已知的蓝细菌细胞色素c-553蛋白相似。构建了一个缺失突变体,基于光谱分析和通过聚丙烯酰胺凝胶电泳分离的蛋白质的四甲基联苯胺-过氧化氢染色,该突变体没有可检测到的细胞色素c-553。突变菌株的总体光合活性没有受损。然而,该突变体表现出细胞色素f氧化效率降低。这些结果表明,细胞色素c-553不是聚球藻属PCC 7942中还原光系统I反应中心的绝对必需物质。