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大肠杆菌莽草酸激酶I编码基因(aroK)的鉴定。

Identification of the gene (aroK) encoding shikimic acid kinase I of Escherichia coli.

作者信息

Løbner-Olesen A, Marinus M G

机构信息

Department of Microbiology, Technical University of Denmark, Lyngby, Copenhagen.

出版信息

J Bacteriol. 1992 Jan;174(2):525-9. doi: 10.1128/jb.174.2.525-529.1992.

Abstract

DNA sequence analysis has revealed that an unidentified open reading frame (ufr1) is present immediately preceding the aroB gene of Escherichia coli. The predicted protein product of urf1 contains a consensus ATP-binding-site sequence and shows 34% amino acid homology to shikimate kinase II in a 97-amino-acid region. Inactivation of urf1 by insertion of an antibiotic resistance gene had a polar effect on aroB, indicating that these two genes constitute a transcriptional unit. The auxotrophic requirements of a strain mutant for both urf1 and aroL (encoding shikimate kinase II) are consistent with shikimate kinase deficiency. We propose that urf1 encodes shikimate kinase I and that it be designated aroK.

摘要

DNA序列分析显示,在大肠杆菌的aroB基因之前紧邻存在一个未鉴定的开放阅读框(urf1)。urf1的预测蛋白质产物含有一个共有ATP结合位点序列,并且在一个97个氨基酸的区域内与莽草酸激酶II有34%的氨基酸同源性。通过插入抗生素抗性基因使urf1失活对aroB产生了极性效应,表明这两个基因构成一个转录单元。urf1和aroL(编码莽草酸激酶II)双突变菌株的营养缺陷需求与莽草酸激酶缺陷一致。我们提出urf1编码莽草酸激酶I,并将其命名为aroK。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a88/205746/6f612c783e7a/jbacter00068-0195-a.jpg

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