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利用P22攻击噬菌体对产气克雷伯菌put操纵子中氮激活蛋白DNA结合位点进行遗传分析。

Genetic analysis, using P22 challenge phage, of the nitrogen activator protein DNA-binding site in the Klebsiella aerogenes put operon.

作者信息

Chen L M, Goss T J, Bender R A, Swift S, Maloy S

机构信息

Department of Microbiology, University of Illinois, Urbana 61801, USA.

出版信息

J Bacteriol. 1998 Feb;180(3):571-7. doi: 10.1128/JB.180.3.571-577.1998.

Abstract

The nac gene product is a LysR regulatory protein required for nitrogen regulation of several operons from Klebsiella aerogenes and Escherichia coli. We used P22 challenge phage carrying the put control region from K. aerogenes to identify the nucleotide residues important for nitrogen assimilation control protein (NAC) binding in vivo. Mutations in an asymmetric 30-bp region prevented DNA binding by NAC. Gel retardation experiments confirmed that NAC specifically binds to this sequence in vitro, but NAC does not bind to the corresponding region from the put operon of Salmonella typhimurium, which is not regulated by NAC.

摘要

Nac基因产物是一种LysR调节蛋白,是产气克雷伯菌和大肠杆菌中几个操纵子氮调节所必需的。我们使用携带产气克雷伯菌put控制区的P22攻击噬菌体来鉴定体内对氮同化控制蛋白(NAC)结合至关重要的核苷酸残基。一个不对称的30bp区域中的突变阻止了NAC与DNA的结合。凝胶阻滞实验证实,NAC在体外特异性结合该序列,但NAC不与鼠伤寒沙门氏菌put操纵子的相应区域结合,该区域不受NAC调节。

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