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血红素及其配体在CooA(一氧化碳感应转录激活因子)激活过程中的作用。

Roles of the heme and heme ligands in the activation of CooA, the CO-sensing transcriptional activator.

作者信息

Youn Hwan, Conrad Mary, Chung Soo-Yeol, Roberts Gary P

机构信息

Department of Bacteriology, University of Wisconsin-Madison, Madison, WI 53706, USA.

出版信息

Biochem Biophys Res Commun. 2006 Sep 22;348(2):345-50. doi: 10.1016/j.bbrc.2006.06.200. Epub 2006 Jul 28.

Abstract

CooA of Rhodospirillum rubrum is a CO-sensing, heme-containing transcriptional activator that regulates the expression of the genes responsible for CO oxidation. We randomized the codons for residues 75-77 of CooA which include two proximal heme ligands, screened for both CO-dependent and CO-independent variants, and characterized in vivo and in vitro properties of selected CooA variants. The analysis showed that small residues at position 75 are critical and that, as previously suspected, His77 is absolutely necessary for CO responsiveness of CooA. Many hemeless variants altered at those residues were found to be constitutively active. We propose that proximal heme pocket residues of wild-type CooA have important role in stabilizing both active and inactive heme positions for its CO-sensing function.

摘要

红螺菌的CooA是一种可感知一氧化碳、含血红素的转录激活因子,它调节负责一氧化碳氧化的基因的表达。我们对CooA中75-77位残基的密码子进行了随机化处理,这些残基包括两个近端血红素配体,筛选了依赖一氧化碳和不依赖一氧化碳的变体,并对所选CooA变体的体内和体外特性进行了表征。分析表明,75位的小残基至关重要,并且如先前所怀疑的,His77对于CooA的一氧化碳反应性绝对必要。在这些残基处发生改变的许多无血红素变体被发现具有组成型活性。我们提出,野生型CooA的近端血红素口袋残基在稳定其一氧化碳传感功能的活性和非活性血红素位置方面具有重要作用。

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