首页> 美国卫生研究院文献>Journal of Bacteriology >Glycerol monolaurate inhibits the production of beta-lactamase toxic shock toxin-1 and other staphylococcal exoproteins by interfering with signal transduction.
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Glycerol monolaurate inhibits the production of beta-lactamase toxic shock toxin-1 and other staphylococcal exoproteins by interfering with signal transduction.

机译:甘油单月桂酸酯通过干扰信号转导来抑制β-内酰胺酶中毒性休克毒素1和其他葡萄球菌外蛋白的产生。

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摘要

Glycerol monolaurate (GML) is a naturally occurring surfactant that is used widely as an emulsifier in the food and cosmetics industries and is generally regarded as lacking in important biological activities. The recent observation that it inhibits the production of staphylococcal toxic shock toxin-1 (P. M. Schlievert, J. R. Deringer, M. H. Kim, S. J. Projan, and R. P. Novick, Antimicrob. Agents Chemother. 36:626-631, 1992) is therefore rather surprising and raises the interesting question of how such a compound might interact with cells. In this report, we show that GML inhibits the synthesis of most staphylococcal toxins and other exoproteins and that it does so at the level of transcription. We find that GML blocks the induction but not the constitutive synthesis of beta-lactamase, suggesting that it acts by interfering with signal transduction.
机译:甘油单月桂酸酯(GML)是一种天然存在的表面活性剂,在食品和化妆品工业中被广泛用作乳化剂,通常被认为缺乏重要的生物活性。因此,最近发现它抑制葡萄球菌毒性休克毒素-1的产生(PM Schlievert,JR Deringer,MH Kim,SJ Projan,和RP Novick,Antimicrob.Agents Chemother.36:626-631,1992)。提出了一个有趣的问题,即这种化合物如何与细胞相互作用。在此报告中,我们表明GML抑制大多数葡萄球菌毒素和其他外蛋白的合成,并且在转录水平上如此。我们发现GML阻止了β-内酰胺酶的诱导,但没有阻断其组成性合成,表明GML通过干扰信号转导起作用。

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