Cloning and analysis of the rnc-era-recO operon from Pseudomonas aeruginosa

被引:11
作者
Powell, B
Peters, HK
Nakamura, Y
Court, D
机构
[1] NCI, Frederick Canc Res & Dev Ctr, ABL Basic Res Program, Gene Regulat & Chromosome Biol Lab, Frederick, MD 21702 USA
[2] Univ Tokyo, Inst Med Sci, Dept Tumor Biol, Tokyo 108, Japan
关键词
D O I
10.1128/JB.181.16.5111-5113.1999
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The me operon from Pseudomonas aeruginosa has been cloned and characterized. The three genes comprising this operon, me, era, and recO, are arranged similarly to those in some other gram-negative bacteria. Multicopy plasmids carrying the me operon of P. aeruginosa functionally complement mutations of the me, era, and recO genes in Escherichia coli. In particular, the P, aeruginosa era homolog rescues the conditional lethality of era mutants in E, coli, and the presumptive protein has 60% identity with the Era of E. coli. We discuss these data and evidence suggesting that a GTPase previously purified from P. aeruginosa and designated Pra is not an Era homolog.
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收藏
页码:5111 / 5113
页数:3
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