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肺炎克雷伯菌氮调节的谷氨酰胺合成酶基因(glnA)和固氮调节基因(nifLA)启动子体外转录激活的要求:对激活剂浓度的依赖性

Requirements for transcriptional activation in vitro of the nitrogen-regulated glnA and nifLA promoters from Klebsiella pneumoniae: dependence on activator concentration.

作者信息

Austin S, Henderson N, Dixon R

机构信息

AFRC Unit of Nitrogen Fixation, University of Sussex, Brighton, UK.

出版信息

Mol Microbiol. 1987 Jul;1(1):92-100. doi: 10.1111/j.1365-2958.1987.tb00532.x.

Abstract

Three proteins involved in nitrogen regulation in Klebsiella pneumoniae, NTRA, NTRB and NTRC, have been purified. In a defined in vitro system all three NTR proteins are required for initiation of transcription at the ntr activatable glnA and nifLA promoters. However, in crude S-30 extracts, transcription from the glnA promoter, but not the nifLA promoter, can be activated in the absence of NTRB. A higher concentration of NTRC is required for activation of nifLA transcription than for glnA transcription. Sequences located between -227 and -158 with respect to the nifL transcription start site are required for efficient activation of the nifLA promoter in vitro.

摘要

肺炎克雷伯菌中参与氮调节的三种蛋白质NTRA、NTRB和NTRC已被纯化。在一个特定的体外系统中,所有这三种NTR蛋白都是ntr可激活的glnA和nifLA启动子转录起始所必需的。然而,在粗制的S-30提取物中,在没有NTRB的情况下,glnA启动子的转录可以被激活,但nifLA启动子的转录不能被激活。与glnA转录相比,激活nifLA转录需要更高浓度的NTRC。相对于nifL转录起始位点,位于-227至-158之间的序列是体外高效激活nifLA启动子所必需的。

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