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渗透保护剂甘氨酸甜菜碱抑制粪肠球菌中盐诱导的对致死处理的交叉耐受性。

The osmoprotectant glycine betaine inhibits salt-induced cross-tolerance towards lethal treatment in Enterococcus faecalis.

作者信息

Pichereau Vianney, Bourot Stéphane, Flahaut Sigrid, Blanco Carlos, Auffray Yanick, Bernard Théophile

机构信息

UPRES-A CNRS 6026, Départment Membranes & Osmorégulation, Université de Rennes l, Campus de Beaulieu, 35042 Renes, France.

Laboratoire de Microbiologie de l'Environnement, Université de Caen, 14032 Caen, France.

出版信息

Microbiology (Reading). 1999 Feb;145 ( Pt 2):427-435. doi: 10.1099/13500872-145-2-427.

Abstract

The response of Enterococcus faecalis ATCC 19433 to salt stress has been characterized previously in complex media. In this report, it has been demonstrated that this bacterium actively accumulates the osmoprotectant glycine betaine (GB) from salt-enriched complex medium BHI. To further understand the specific effects of GB and other osmoprotective compounds in salt adaptation and salt-induced cross-tolerance to lethal challenges, a chemically defined medium lacking putative osmoprotectants was used. In this medium, bacterial growth was significantly reduced by increasing concentrations of NaCl. At 0.75 M NaCl, 90% inhibition of the growth rate was observed; GB and its structural analogues restored growth to the non-salt-stressed level. In contrast, proline, pipecolate and ectoine did not allow growth recovery of stressed cells. Kinetic studies showed that the uptake of betaines shows strong structural specificity and occurs through a salt-stress-inducible high-affinity porter [Km = 3.3 microM; Vmax = 130 nmol min(-1) (mg protein)(-1); the uptake activity increased 400-fold in the presence of 0.5 M NaCl]. Moreover, GB and its analogues were accumulated as non-metabolizable cytosolic osmolytes and reached intracellular levels ranging from 1-3 to 1.5 micromol (mg protein)(-1). In contrast to the beneficial effect of GB on the growth of salt-stressed cultures of E. faecalis, its accumulation inhibits the salt-induced cross-tolerance to a heterologous lethal challenge. Indeed, pretreatment of bacterial cells with 0.5 M NaCl induced resistance to 0.3% bile salts (survival of adapted cells increased by a factor of 6800). The presence of GB in the adaptation medium reduced the acquisition of bile salts resistance 680-fold. The synthesis of 11 of the 13 proteins induced during salt adaptation was significantly reduced in the presence of GB. These results raise questions about the actual beneficial effect of GB in natural environments where bacteria are often subjected to various stresses.

摘要

粪肠球菌ATCC 19433对盐胁迫的反应先前已在复杂培养基中进行了表征。在本报告中,已证明该细菌能从富含盐的复杂培养基脑心浸液(BHI)中主动积累渗透保护剂甘氨酸甜菜碱(GB)。为了进一步了解GB和其他渗透保护化合物在盐适应及盐诱导的对致死性挑战的交叉耐受性中的具体作用,使用了一种缺乏假定渗透保护剂的化学成分确定的培养基。在这种培养基中,随着NaCl浓度的增加,细菌生长显著降低。在0.75 M NaCl时,观察到生长速率受到90%的抑制;GB及其结构类似物可将生长恢复到无盐胁迫水平。相比之下,脯氨酸、哌可酸和四氢嘧啶不能使受胁迫细胞的生长恢复。动力学研究表明,甜菜碱的摄取表现出很强的结构特异性,并且通过盐胁迫诱导的高亲和力转运体发生[Km = 3.3 microM;Vmax = 130 nmol min(-1)(mg蛋白质)(-1);在0.5 M NaCl存在下,摄取活性增加400倍]。此外,GB及其类似物作为不可代谢的胞质渗透剂积累,细胞内水平范围为1 - 3至1.5微摩尔(mg蛋白质)(-1)。与GB对盐胁迫的粪肠球菌培养物生长的有益作用相反,其积累抑制了盐诱导的对异源致死性挑战的交叉耐受性。事实上,用0.5 M NaCl预处理细菌细胞可诱导对0.3%胆盐的抗性(适应细胞的存活率提高了6800倍)。适应培养基中GB的存在使胆盐抗性的获得降低了680倍。在盐适应过程中诱导的13种蛋白质中的11种蛋白质的合成在GB存在下显著减少。这些结果引发了关于GB在细菌经常受到各种胁迫的自然环境中的实际有益作用的疑问。

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