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吐温与植物乳杆菌的膜性质和耐压性的相互关系。

Interrelation between Tween and the membrane properties and high pressure tolerance of Lactobacillus plantarum.

机构信息

Technische Universität München, Freising, Germany.

出版信息

BMC Microbiol. 2018 Jul 13;18(1):72. doi: 10.1186/s12866-018-1203-y.

Abstract

Tween® 80 is a frequently used supplement of media for the cultivation of lactic acid bacteria. We investigated its effect on the cell physiology and stress tolerance of Lactobacillus (L.) plantarum. Data on the transcriptomic response to Tween 80 supplementation and its effects on cellular fatty acid profiles and growth characteristics are compared with data characterizing the effect of Tween 80, other Tween types and free fatty acids on the high hydrostatic pressure (HHP) tolerance of L. plantarum strain TMW 1.708. These include effects on cell viability, sub-lethal injury, metabolic activity, protein release and propidium iodide uptake. Tween 80 caused the downregulation of fatty acid biosynthesis and an increase in oleic acid and cyclopropane fatty acid levels in the cell membrane. Tween 20, Tween 80 and free oleic acid, but not Tween 40, Tween 60 and other free fatty acids, conferred resistance against HHP. Tween 80 diminished pressure-induced loss of metabolic activity, protein release and uptake of propidium iodide. However, loss of cell viability exceeded by far membrane permeabilization, suggesting that membrane permeabilization, which has frequently been postulated as a major factor in HHP inactivation of microbes, is not necessarily required for HHP-induced cell death of Lactobacillus plantarum.

摘要

吐温 80 是一种常用于培养乳酸菌的培养基添加剂。我们研究了它对植物乳杆菌细胞生理学和应激耐受性的影响。将转录组响应吐温 80 补充的数据分析与表征吐温 80、其他吐温类型和游离脂肪酸对植物乳杆菌菌株 TMW 1.708 耐高静压(HHP)的影响的数据进行了比较。这些影响包括对细胞活力、亚致死损伤、代谢活性、蛋白质释放和碘化丙啶摄取的影响。吐温 80 导致脂肪酸生物合成下调,细胞膜中油酸和环丙烷脂肪酸水平增加。吐温 20、吐温 80 和游离油酸,但不是吐温 40、吐温 60 和其他游离脂肪酸,赋予了对 HHP 的抗性。吐温 80 减少了压力诱导的代谢活性、蛋白质释放和碘化丙啶摄取损失。然而,细胞活力的损失远远超过了膜通透性,这表明膜通透性,它经常被推测为 HHP 使微生物失活的主要因素,对于 HHP 诱导的植物乳杆菌细胞死亡不一定是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b5ef/6044075/6ba200ff2bff/12866_2018_1203_Fig1_HTML.jpg

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