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首页> 外文期刊>Journal of Applied Bacteriology >METHYLCHLOROISOTHIAZOLONE-INDUCED GROWTH INHIBITION AND LETHALITY IN ESCHERICHIA COLI
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METHYLCHLOROISOTHIAZOLONE-INDUCED GROWTH INHIBITION AND LETHALITY IN ESCHERICHIA COLI

机译:甲基氯异噻唑酮对大肠杆菌的生长抑制和致死性

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摘要

Exposure of log phase Escherichia roil cells to inhibitory levels of 5-chloro-2-methyl-isothiazolin-3-one (MCI) results in rapid bacteriostasis and a delayed onset of bactericidal activity. Inhibition of respiration occurs within the same time frame as bacteriostasis, and is followed by a decline in intracellular ATP levels. In vitro and in vivo experiments suggest that growth inhibition is the result of selective inhibition of particular targets, with succinate dehydrogenase being identified as a possible target. Such selectivity was not anticipated from this highly reactive molecule. MCI-induced lethality is positively correlated with a loss of reduced protein sulphydryls (r(2) = 0.79). A greater than equimolar loss of reduced protein sulphydryls, compared with the number of MCI molecules added, and a reduction in killing by MCI after induction of the OxyR regulon suggest that free radical generation may have a role in the antibacterial activity of MCI. We present an examination of the in vivo effects of MCI exposure on bacterial cells, and evidence that the isothiazolones exhibit selectivity in their cellular targets and antimicrobial effects.
机译:对数期大肠埃希氏杆菌细胞暴露于抑制水平的5-氯-2-甲基-异噻唑啉-3-酮(MCI)会导致快速的抑菌作用和延迟的杀菌活性。抑制呼吸作用与抑菌作用发生在同一时间范围内,随后细胞内ATP水平下降。体外和体内实验表明,生长抑制是选择性抑制特定靶标的结果,琥珀酸脱氢酶被确定为可能的靶标。从这种高反应性分子没有预料到这样的选择性。 MCI诱导的致死率与蛋白质硫减少的损失呈正相关(r(2)= 0.79)。与添加的MCI分子数量相比,还原的蛋白质巯基的损失大于等摩尔,并且在OxyR regulon诱导后MCI的杀伤力降低,表明自由基的产生可能在MCI的抗菌活性中起作用。我们提出了对细菌细胞MCI暴露的体内影响的检查,并证明异噻唑酮在其细胞靶标和抗菌作用中表现出选择性。

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