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从厌氧细菌若穗梭菌中克隆和测序一些负责卟啉生物合成的基因。

Cloning and sequencing of some genes responsible for porphyrin biosynthesis from the anaerobic bacterium Clostridium josui.

作者信息

Fujino E, Fujino T, Karita S, Sakka K, Ohmiya K

机构信息

School of Bioresources, Mie University, Tsu, Japan.

出版信息

J Bacteriol. 1995 Sep;177(17):5169-75. doi: 10.1128/jb.177.17.5169-5175.1995.

Abstract

The 6.2-kbp DNA fragment encoding the enzymes in the porphyrin synthesis pathway of a cellulolytic anaerobe, Clostridium josui, was cloned into Escherichia coli and sequenced. This fragment contained four hem genes, hemA, hemC, hemD, and hemB, in order, which were homologous to the corresponding genes from E. coli and Bacillus subtilis. A typical promoter sequence was found only upstream of hemA, suggesting that these four genes were under the control of this promoter as an operon. The hemA and hemD genes cloned from C. josui were able to complement the hemA and hemD mutations, respectively, of E. coli. The COOH-terminal region of C. josui HemA and the NH2-terminal region of C. josui HemD were homologous to E. coli CysG (Met-1 to Leu-151) and to E. coli CysG (Asp-213 to Phe-454) and Pseudomonas denitrificans CobA, respectively. Furthermore, the cloned 6.2-kbp DNA fragment complemented E. coli cysG mutants. These results suggested that both C. josui hemA and hemD encode bifunctional enzymes.

摘要

将纤维素分解厌氧菌若松梭菌卟啉合成途径中编码酶的6.2-kbp DNA片段克隆到大肠杆菌中并进行测序。该片段依次包含四个血红素基因hemA、hemC、hemD和hemB,它们与来自大肠杆菌和枯草芽孢杆菌的相应基因同源。仅在hemA上游发现了典型的启动子序列,这表明这四个基因作为一个操纵子受该启动子的控制。从若松梭菌克隆的hemA和hemD基因分别能够互补大肠杆菌的hemA和hemD突变。若松梭菌HemA的COOH末端区域和若松梭菌HemD的NH2末端区域分别与大肠杆菌CysG(Met-1至Leu-151)、大肠杆菌CysG(Asp-213至Phe-454)以及反硝化假单胞菌CobA同源。此外,克隆的6.2-kbp DNA片段互补了大肠杆菌cysG突变体。这些结果表明若松梭菌的hemA和hemD均编码双功能酶。

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