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大肠杆菌purG和purI基因所编码的酶促反应的鉴定

Identification of the enzymatic reactions encoded by the purG and purI genes of Escherichia coli.

作者信息

Houlberg U, Hove-Jensen B, Jochimsen B, Nygaard P

出版信息

J Bacteriol. 1983 Jun;154(3):1485-8. doi: 10.1128/jb.154.3.1485-1488.1983.

Abstract

The chromosomal locations of the genes purG and purI on the Escherichia coli linkage map are the opposites of those of Salmonella typhimurium. By methods which permit the identification of lesions in any of the five early enzymes of the purine de novo pathway, the gene-enzyme relationships of the purG and purI loci have been reevaluated in these two organisms. The results demonstrate that the relative locations of the genes encoding the two enzymes (phosphoribosylformylglycinamidine synthetase and phosphoribosylaminoimidazole synthetase) are similar in the two organisms. The gene products have been correctly determined in S. typhimurium. The gene products currently listed for the loci in E. coli are incorrect. The E. coli purG locus is equivalent to the S. typhimurium purI locus, and the E. coli purI locus is equivalent to the S. typhimurium purG locus.

摘要

在大肠杆菌连锁图谱上,基因purG和purI的染色体位置与鼠伤寒沙门氏菌的相反。通过能够鉴定嘌呤从头合成途径中五种早期酶中任何一种损伤的方法,对这两种生物中purG和purI基因座的基因-酶关系进行了重新评估。结果表明,编码这两种酶(磷酸核糖甲酰甘氨脒合成酶和磷酸核糖氨基咪唑合成酶)的基因在这两种生物中的相对位置相似。在鼠伤寒沙门氏菌中已正确确定了基因产物。目前列出的大肠杆菌中这些基因座的基因产物是错误的。大肠杆菌的purG基因座等同于鼠伤寒沙门氏菌的purI基因座,而大肠杆菌的purI基因座等同于鼠伤寒沙门氏菌的purG基因座。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/220a/217631/6d459d86335f/jbacter00247-0464-a.jpg

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