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费氏丙酸杆菌hemYHBXRL基因簇,其编码参与从谷氨酸到原血红素生物合成途径的酶和一种调节因子。

The Propionibacterium freudenreichii hemYHBXRL gene cluster, which encodes enzymes and a regulator involved in the biosynthetic pathway from glutamate to protoheme.

作者信息

Hashimoto Y, Yamashita M, Murooka Y

机构信息

Department of Biotechnology, Graduate School of Engineering, Osaka University, Osaka, Japan.

出版信息

Appl Microbiol Biotechnol. 1997 Apr;47(4):385-92. doi: 10.1007/s002530050945.

Abstract

A clone that can complement both Escherichia coli hemB and hemL mutations was found among plasmids containing the Propionibacterium freudenreichii hemB gene, which encodes delta-aminolevulinic acid dehydratase. The regions upstream and downstream of the hemB gene were sequenced. Two open-reading frames (ORF1 and -2), which were similar to the hemY gene encoding protoporphyrinogen oxidase and the hemH gene encoding ferrochelatase from Bacillus subtilis, were found upstream of the hemB gene. ORF1 and -2 complemented the E. coli hemG mutation, defective in protoporphyrinogen oxidase, and the hemH gene respectively. Since ORF1 had no homology to hemG, the gene was designated hemY. The hemYHB genes appeared to be within the same transcription unit. Downstream from the hemB gene, three open-reading frames were found. One of these, transcribed in the same direction as the hemB gene, was identical to be the hemL gene, which encodes glutamate-1-semialdehyde 2,1-aminomutase. The other two open-reading frames, located between the hemYHB and hemL genes, were transcribed divergently, and their deduced amino acid sequences showed similarities to a membrane-bound transport protein and a transcriptional regulatory protein respectively. The two genes may thus be involved in hem transport and the regulation of hem gene expression respectively, and were tentatively named hemX and hemR. Although hemX and hemL are unlikely to be part of the same operon, hemYHBXRL are clustered on the P. freudenreichii chromosome.

摘要

在含有费氏丙酸杆菌hemB基因(编码δ-氨基乙酰丙酸脱水酶)的质粒中,发现了一个能够互补大肠杆菌hemB和hemL突变的克隆。对hemB基因的上下游区域进行了测序。在hemB基因上游发现了两个开放阅读框(ORF1和-2),它们分别与枯草芽孢杆菌中编码原卟啉原氧化酶的hemY基因和编码亚铁螯合酶的hemH基因相似。ORF1和-2分别互补了大肠杆菌中在原卟啉原氧化酶方面有缺陷的hemG突变和hemH基因。由于ORF1与hemG没有同源性,该基因被命名为hemY。hemYHB基因似乎位于同一个转录单元内。在hemB基因下游,发现了三个开放阅读框。其中一个与hemB基因同向转录,与编码谷氨酸-1-半醛2,1-氨基变位酶的hemL基因相同。另外两个开放阅读框位于hemYHB和hemL基因之间,呈发散转录,其推导的氨基酸序列分别与一种膜结合转运蛋白和一种转录调节蛋白相似。因此,这两个基因可能分别参与血红素的转运和血红素基因表达的调控,暂被命名为hemX和hemR。虽然hemX和hemL不太可能是同一个操纵子的一部分,但hemYHBXRL在费氏丙酸杆菌染色体上是成簇的。

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