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空肠弯曲菌和结肠弯曲菌中超氧化物歧化酶编码基因的克隆、核苷酸序列及特性分析

Cloning, nucleotide sequence and characterization of a gene encoding superoxide dismutase from Campylobacter jejuni and Campylobacter coli.

作者信息

Purdy D, Park S F

机构信息

Institute of Food Research, Reading Laboratory, UK.

出版信息

Microbiology (Reading). 1994 May;140 ( Pt 5):1203-8. doi: 10.1099/13500872-140-5-1203.

Abstract

Genes encoding superoxide dismutase (SOD: EC 1.15.1.1) were cloned from Campylobacter jejuni NCTC 11351 and Campylobacter coli UA585 by heterologous complementation of a SOD-deficient Escherichia coli mutant. Deletion analysis of the cloned C. jejuni DNA assigned the sod gene to a 1.2 kb insert and this contained an open reading frame of 660 bp. The deduced gene product of 220 amino acids was 71% identical to the E. coli iron-containing SOD and 60% identical to the E. coli manganese-containing SOD. The recombinant SOD was expressed at high levels in E. coli and protected a sodA sodB double mutant from the toxic effects of methyl viologen. Nucleotide sequence analysis of the corresponding gene from C. coli showed it to be 92% identical to that from C. jejuni.

摘要

通过超氧化物歧化酶(SOD:EC 1.15.1.1)缺陷型大肠杆菌突变体的异源互补,从空肠弯曲菌NCTC 11351和大肠弯曲菌UA585中克隆了编码超氧化物歧化酶的基因。对克隆的空肠弯曲菌DNA进行缺失分析,将sod基因定位到一个1.2 kb的插入片段上,该片段包含一个660 bp的开放阅读框。推导的由220个氨基酸组成的基因产物与大肠杆菌含铁超氧化物歧化酶的同一性为71%,与大肠杆菌含锰超氧化物歧化酶的同一性为60%。重组超氧化物歧化酶在大肠杆菌中高水平表达,并保护sodA sodB双突变体免受甲基紫精的毒性作用。对来自大肠弯曲菌的相应基因进行核苷酸序列分析,结果表明它与来自空肠弯曲菌的相应基因的同一性为92%。

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