大肠杆菌
生物合成
酶
脯氨酸
基因
生物化学
化学
生物
微生物学
氨基酸
作者
David J. Hayzer,T Leisinger
出处
期刊:Microbiology
[Microbiology Society]
日期:1980-06-01
卷期号:118 (2): 287-293
被引量:161
标识
DOI:10.1099/00221287-118-2-287
摘要
A simple chromatographic procedure has been devised to separate γ-glutamyl phosphate reductase and 1-pyrroline-5-carboxylate reductase, allowing the measurement of the former in crude Escherichia coli extracts. Analysis of a number of strains of E. coli has demonstrated that gene pro A codes for γ-glutamyl phosphate reductase and proB for γ-glutamyl kinase. Introduction of a ColEl hybrid plasmid containing the proA,B region into a strain with a chromosomal deletion of proA,B led to 3- and 17-fold increases in the specific activities of γ-glutamyl kinase and γ-glutamyl phosphate reductase, respectively.
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