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变形链球菌GS-5对糖酵解的不可逆对羟基苯甲酸酯抑制作用。

Irreversible paraben inhibition of glycolysis by Streptococcus mutans GS-5.

作者信息

Ma Y, Marquis R E

机构信息

Department of Microbiology and Immunology, University of Rochester, School of Medicine and Dentistry, NY, USA.

出版信息

Lett Appl Microbiol. 1996 Nov;23(5):329-33. doi: 10.1111/j.1472-765x.1996.tb00201.x.

Abstract

Parabens were found to inhibit irreversibly glycolysis by the cariogenic dental plaque bacterium Streptococcus mutans GS-5 and to decrease the capacity of the bacterium to lower the pH in dense cell suspensions containing excess glucose. The hierarchy of effectiveness was butyl > propyl > ethyl > methyl paraben. Results of studies of the nature of glycolytic inhibition by butyl paraben indicated that it could act at millimolar concentrations as an irreversible inhibitor of the phosphotransferase system for sugar uptake and was lethal for the bacterium at these same levels. Butyl paraben acted also as a reversible inhibitor of the F-ATPase of the organism. Overall, it appeared that the lethal actions of parabens can be interpreted at least in part as due to irreversible damage to key enzymes, such as those of the phosphotransferase system.

摘要

对羟基苯甲酸酯被发现可不可逆地抑制致龋牙菌斑细菌变形链球菌GS-5的糖酵解,并降低该细菌在含有过量葡萄糖的高密度细胞悬液中降低pH值的能力。其有效性顺序为:对羟基苯甲酸丁酯>对羟基苯甲酸丙酯>对羟基苯甲酸乙酯>对羟基苯甲酸甲酯。对对羟基苯甲酸丁酯糖酵解抑制性质的研究结果表明,它在毫摩尔浓度下可作为糖摄取磷酸转移酶系统的不可逆抑制剂起作用,并且在这些相同水平下对该细菌具有致死性。对羟基苯甲酸丁酯还作为该生物体F-ATP酶的可逆抑制剂起作用。总体而言,对羟基苯甲酸酯的致死作用似乎至少部分可以解释为是由于对关键酶(如磷酸转移酶系统的酶)的不可逆损伤。

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