PIPECOLIC ACID IS AN OSMOPROTECTANT FOR ESCHERICHIA-COLI TAKEN UP BY THE GENERAL OSMOPORTERS PROU AND PROP

被引:61
作者
GOUESBET, G [1 ]
JEBBAR, M [1 ]
TALIBART, R [1 ]
BERNARD, T [1 ]
BLANCO, C [1 ]
机构
[1] UNIV RENNES 1, DEPT MEMBRANES & OSMOREGULAT, CNRS, URA 256, F-35042 RENNES, FRANCE
来源
MICROBIOLOGY-SGM | 1994年 / 140卷
关键词
ESCHERICHIA COLI; OSMOPROTECTION; PIPECOLIC ACID; PROP AND PROU SYSTEMS; PERIPLASMIC BINDING PROTEIN;
D O I
10.1099/13500872-140-9-2415
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Exogenously supplied L-pipecolic acid was accumulated by Escherichia coli cells and protected them while growing at inhibitory osmolarity. Using specific uptake mutants and competitive assays, we established that the imino acid enters the cells through the ProP and ProU systems with K-m values of 225 and 53 mu M. respectively. Surprisingly, in spite of the requirement for tire wild-type proX gene for osmoprotective ability, no binding activity of labelled pipecolate with the periplasmic protein encoded by proX could be detected. In an attempt to demonstrate whether the two porters (Prop and ProU) are the only carriers involved in osmoregulation, a variety of molecules known for their intracellular osmolarity-dependent accumulation in various organisms were investigated. N-Dimethylproline (proline betaine), N-dimethylglycine, homobetaine (beta-aranine betaine), gamma-butyrobetaine and dimethylsulfoniopropionate were found to be capable of promoting the growth of osmotically stressed E. coli. All of these molecules enter bacterial cells via prop and ProU porters. None of the osmoprotectants except N-dimethylproline was able to bind the periplasmic protein encoded by ProX, while this protein was necessary for their uptake. Apparently, prop and ProU are the sole osmoporters involved in osmolyte influx into E. coli cells.
引用
收藏
页码:2415 / 2422
页数:8
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