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质粒NAH7基因nahR的核苷酸序列及nahR产物的DNA结合

Nucleotide sequence of plasmid NAH7 gene nahR and DNA binding of the nahR product.

作者信息

You I S, Ghosal D, Gunsalus I C

机构信息

Department of Biochemistry, University of Illinois, Urbana 61801.

出版信息

J Bacteriol. 1988 Dec;170(12):5409-15. doi: 10.1128/jb.170.12.5409-5415.1988.

Abstract

The nah and sal operons of the 80-kilobase-pair (kb) NAH7 plasmid specify catabolism of naphthalene and salicylate under positive regulation by gene nahR. A 1.75-kb fragment (PstI-HindIII) cloned into the pCP13 derivative of vector RK2 complemented in trans five nahR mutations. The fragment sequence contained a 1,122-base-pair open reading frame with a predicted sequence of 374 residues that was rich in basic amino acids with regions similar to known DNA-binding proteins. Clones from the nahR gene region were expressed in mexicells. Plasmid pY1923, carrying the 1.75-kb PstI-HindIII fragment, expressed a protein of Mr ca. 35,000 which bound to the upstream region of gene nahR in a gel electrophoresis DNA-binding assay. Other clones expressed proteins of currently unknown function; pY1311, with the 1.1-kb HindIII fragment, produced a polypeptide with an Mr of 23,000, and pY1812, with the 1.2-kb PstI-SphI fragment, produced a polypeptide (Mr 41,000) which appeared to be a fused nahR-lacZ product.

摘要

80千碱基对(kb)的NAH7质粒的nah和sal操纵子在基因nahR的正调控下指定萘和水杨酸盐的分解代谢。克隆到载体RK2的pCP13衍生物中的一个1.75 kb片段(PstI-HindIII)反式互补了五个nahR突变。该片段序列包含一个1122碱基对的开放阅读框,其预测序列为374个残基,富含碱性氨基酸,且具有与已知DNA结合蛋白相似的区域。来自nahR基因区域的克隆在mexicells中表达。携带1.75 kb PstI-HindIII片段的质粒pY1923表达了一种约35,000道尔顿的蛋白质,该蛋白质在凝胶电泳DNA结合试验中与nahR基因的上游区域结合。其他克隆表达目前功能未知的蛋白质;携带1.1 kb HindIII片段的pY1311产生了一种23,000道尔顿的多肽,携带1.2 kb PstI-SphI片段的pY1812产生了一种似乎是融合的nahR-lacZ产物的多肽(41,000道尔顿)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ae06/211631/2ee3bcbfd51a/jbacter00190-0019-a.jpg

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