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大肠杆菌K12可见光敏感突变体的分离与鉴定

Isolation and characterization of visible light-sensitive mutants of Escherichia coli K12.

作者信息

Miyamoto K, Nakahigashi K, Nishimura K, Inokuchi H

机构信息

Department of Biophysics, Faculty of Science, Kyoto University, Japan.

出版信息

J Mol Biol. 1991 Jun 5;219(3):393-8. doi: 10.1016/0022-2836(91)90180-e.

DOI:10.1016/0022-2836(91)90180-e
PMID:2051480
Abstract

Six mutants of Escherichia coli K12 that are sensitive to visible light have been isolated. Five of them, including an amber mutant, are defective in a gene that maps near 11 minutes on the linkage map of the chromosome, and this gene has been designated visA. The sixth mutant, which was isolated from bacteria that carried the visA+/visA+ diploid allele, is defective in a gene that maps near 63 minutes on the linkage map, which has been designated visB. These mutant strains of bacteria are killed by illumination with visible light. The effective wavelength of the light is around 460 nm. The nucleotide sequence of the visA gene was determined. As a result of a search for homologous products, we found that visA may be identical to hemH, the structural gene for ferrochelatase which catalyzes a final step in the biosynthesis of heme. A possible mechanism for the killing of the visA mutant bacteria is discussed.

摘要

已分离出6株对可见光敏感的大肠杆菌K12突变体。其中5株,包括1株琥珀突变体,在染色体连锁图上位于约11分钟处的一个基因有缺陷,该基因被命名为visA。从携带visA+/visA+二倍体等位基因的细菌中分离出的第6个突变体,在连锁图上位于约63分钟处的一个基因有缺陷,该基因被命名为visB。这些细菌突变株经可见光照射后会死亡。光的有效波长约为460纳米。测定了visA基因的核苷酸序列。通过搜索同源产物,我们发现visA可能与hemH相同,hemH是催化血红素生物合成最后一步的铁螯合酶的结构基因。讨论了visA突变细菌致死的可能机制。

相似文献

1
Isolation and characterization of visible light-sensitive mutants of Escherichia coli K12.大肠杆菌K12可见光敏感突变体的分离与鉴定
J Mol Biol. 1991 Jun 5;219(3):393-8. doi: 10.1016/0022-2836(91)90180-e.
2
Isolation and characterization of a light-sensitive mutant of Escherichia coli K-12 with a mutation in a gene that is required for the biosynthesis of ubiquinone.分离和鉴定一株大肠杆菌K-12的光敏感突变体,该突变体中一个参与泛醌生物合成的基因发生了突变。
J Bacteriol. 1992 Nov;174(22):7352-9. doi: 10.1128/jb.174.22.7352-7359.1992.
3
The Escherichia coli visA gene encodes ferrochelatase, the final enzyme of the heme biosynthetic pathway.大肠杆菌visA基因编码亚铁螯合酶,这是血红素生物合成途径中的最后一种酶。
J Bacteriol. 1993 Apr;175(7):2154-6. doi: 10.1128/jb.175.7.2154-2156.1993.
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Cloning and sequencing of the hemE gene encoding uroporphyrinogen III decarboxylase (UPD) from Escherichia coli K-12.从大肠杆菌K-12中克隆和测序编码尿卟啉原III脱羧酶(UPD)的hemE基因。
Gene. 1993 Oct 29;133(1):109-13. doi: 10.1016/0378-1119(93)90233-s.
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Cloning and sequencing of a previously unidentified gene that is involved in the biosynthesis of heme in Escherichia coli.对大肠杆菌中一种先前未鉴定的、参与血红素生物合成的基因进行克隆和测序。
Gene. 1995 Feb 3;153(1):67-70. doi: 10.1016/0378-1119(94)00805-3.
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Cloning and sequencing of an Escherichia coli K12 gene which encodes a polypeptide having similarity to the human ferritin H subunit.编码与人类铁蛋白H亚基具有相似性的多肽的大肠杆菌K12基因的克隆与测序。
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Photosensitivity of a protoporphyrin-accumulating, light-sensitive mutant (visA) of Escherichia coli K-12.
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Isolation and characterization of a cDNA from soybean and its homolog from Escherichia coli, which both complement the light sensitivity of Escherichia coli hemH mutant strain VS101.
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The essential Escherichia coli msgB gene, a multicopy suppressor of a temperature-sensitive allele of the heat shock gene grpE, is identical to dapE.必需的大肠杆菌msgB基因,即热休克基因grpE的温度敏感等位基因的多拷贝抑制子,与dapE相同。
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Accumulation of protoporphyrin IX in light-sensitive mutants of Escherichia coli.
FEBS Lett. 1992 Oct 5;310(3):246-8. doi: 10.1016/0014-5793(92)81341-i.

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