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深红红螺菌nifH基因的克隆与功能表征

The cloning and functional characterization of the nifH gene of Rhodospirillum rubrum.

作者信息

Lehman L J, Fitzmaurice W P, Roberts G P

机构信息

Department of Bacteriology, College of Agricultural and Life Sciences, University of Wisconsin-Madison 53706.

出版信息

Gene. 1990 Oct 30;95(1):143-7. doi: 10.1016/0378-1119(90)90426-r.

Abstract

Dinitrogenase reductase (the nifH product) from Rhodospirillum rubrum is regulated by a post-translational modification system encoded by draTG. As demonstrated in this report, the cloning, sequencing, and functional characterization of the nifH gene provides a basis for further analysis as well as revealing interesting features of gene organization. The coding regions of nifH and draT are separated by only 400 bp, though the genes are divergently transcribed and differentially regulated. The construction of a nifH insertion caused a Nif- phenotype and destroyed the mutant's ability to synthesize both dinitrogenase and dinitrogenase reductase, verifying functionality and transcriptional organization of the nifHDK genes.

摘要

来自红螺菌的固氮酶还原酶(nifH基因产物)受draTG编码的翻译后修饰系统调控。如本报告所示,nifH基因的克隆、测序和功能表征为进一步分析提供了基础,同时也揭示了基因组织的有趣特征。尽管nifH和draT基因是反向转录且调控方式不同,但其编码区仅相隔400 bp。构建nifH插入突变体导致了固氮缺陷型表型,并破坏了突变体合成固氮酶和固氮酶还原酶的能力,从而验证了nifHDK基因的功能和转录组织。

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