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新型化合物1-甲基-1-哌啶基甲磺酸盐(MPMS)对大肠杆菌中甘氨酸甜菜碱、胆碱和L-脯氨酸渗透保护活性的影响

Effect of novel compound, 1-methyl-1-piperidino methane sulfonate (MPMS), on the osmoprotectant activity of glycine betaine, choline and L-proline in Escherichia coli.

作者信息

Kunin C M, Tong H H, Miller D D, Abdel-Ghany Y, Poggi M C, LeRudulier D

机构信息

Department of Internal Medicine, College of Medicine, Ohio State University, Columbus 43210.

出版信息

Arch Microbiol. 1993;160(2):81-6. doi: 10.1007/BF00288707.

Abstract

A novel compound, 1-methyl-1-piperidino methane sulfonate (MPMS), was found to block the osmoprotectant activity of choline and L-proline, but not glycine betaine in Escherichia coli. MPMS was more active against salt-sensitive than salt-resistant strains, but had no effect on the salt tolerance of a mutant which was unable to transport choline, glycine betaine and proline. Growth of E. coli in NaCl was inhibited by MPMS and restored by glycine betaine, but not by choline or L-proline. Uptake of radiolabeled glycine betaine, choline or L-proline by cells grown at high osmolarity was not inhibited when MPMS and the radioactive substrates were added simultaneously. Preincubation for 5 min with MPMS reduced the uptake of choline and L-proline, but not glycine betaine. Similar incubation with MPMS had no effect on the uptake of radiolabeled glucose or succinate. The toxicity of MPMS was much lower than that of the L-proline analogues L-azetidine-2-carboxylic acid and 3,4-dehydro-DL-proline. The exact mechanism by which MPMS exerts its effect is not entirely clear. MPMS or a metabolite may interfere with the activity of several independent permeases involved in the uptake of osmoprotective compounds, or the conversion of choline to glycine betaine, or effect the expression of some of the osmoregulatory genes.

摘要

一种新型化合物,1-甲基-1-哌啶基甲磺酸盐(MPMS),被发现可阻断大肠杆菌中胆碱和L-脯氨酸的渗透保护活性,但对甘氨酸甜菜碱没有影响。MPMS对盐敏感菌株的活性比对耐盐菌株更强,但对无法转运胆碱、甘氨酸甜菜碱和脯氨酸的突变体的耐盐性没有影响。MPMS可抑制大肠杆菌在氯化钠中的生长,甘氨酸甜菜碱可恢复其生长,但胆碱或L-脯氨酸则不能。当同时添加MPMS和放射性底物时,高渗透压下生长的细胞对放射性标记的甘氨酸甜菜碱、胆碱或L-脯氨酸的摄取不受抑制。用MPMS预孵育5分钟可减少胆碱和L-脯氨酸的摄取,但不影响甘氨酸甜菜碱的摄取。与MPMS进行类似孵育对放射性标记的葡萄糖或琥珀酸的摄取没有影响。MPMS的毒性远低于L-脯氨酸类似物L-氮杂环丁烷-2-羧酸和3,4-脱氢-DL-脯氨酸。MPMS发挥作用的确切机制尚不完全清楚。MPMS或其代谢产物可能会干扰参与渗透保护化合物摄取的几种独立通透酶的活性,或胆碱向甘氨酸甜菜碱的转化,或影响一些渗透调节基因的表达。

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