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起始因子3及两种氨酰-tRNA合成酶基因的分子克隆与表达调控。

Molecular cloning and regulation of expression of the genes for initiation factor 3 and two aminoacyl-tRNA synthetases.

作者信息

Elseviers D, Gallagher P, Hoffman A, Weinberg B, Schwartz I

出版信息

J Bacteriol. 1982 Oct;152(1):357-62. doi: 10.1128/jb.152.1.357-362.1982.

Abstract

A 22-kilobase fragment of the Escherichia coli chromosome which contains the genes for translation initiation factor 3, phenylalanyl-tRNA synthetase, and threonyl-tRNA synthetase was cloned into plasmid pACYC184. The hybrid plasmid (designated pID1) complements a temperature-sensitive pheS lesion in E. coli NP37. pID1-transformed NP37 overproduce initiation factor 3 and phenylalanyl-tRNA synthetase. Gene expression from pID1 was studied in vitro in a coupled transcription-translation system and in minicells. The results suggest that the genes for initiation factor 3 and phenylalanyl- and threonyl-tRNA synthetase are regulated by different mechanisms.

摘要

一段包含翻译起始因子3、苯丙氨酰-tRNA合成酶和苏氨酰-tRNA合成酶基因的22千碱基大肠杆菌染色体片段被克隆到质粒pACYC184中。该杂种质粒(命名为pID1)可弥补大肠杆菌NP37中一个温度敏感型pheS损伤。用pID1转化的NP37过量产生起始因子3和苯丙氨酰-tRNA合成酶。在体外偶联转录-翻译系统和微细胞中研究了pID1的基因表达。结果表明,起始因子3以及苯丙氨酰-tRNA合成酶和苏氨酰-tRNA合成酶的基因受不同机制调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/034a/221418/3ad6920998d3/jbacter00251-0371-a.jpg

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