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口腔链球菌的磷酸烯醇丙酮酸:糖磷酸转移酶系统及其在糖代谢控制中的作用。

The phosphoenolpyruvate:sugar phosphotransferase system of oral streptococci and its role in the control of sugar metabolism.

作者信息

Vadeboncoeur C, Pelletier M

机构信息

Département de Biochimie (Sciences), Université Laval, Québec, Canada.

出版信息

FEMS Microbiol Rev. 1997 Feb;19(3):187-207. doi: 10.1111/j.1574-6976.1997.tb00297.x.

Abstract

Oral streptococci are sugar-fermentative bacteria comprising at least 19 distinct species and are a significant proportion of the normal microbial population of the mouth and upper respiratory tract of humans. These streptococci transport several sugars by the phosphoenolpyruvate:sugar phosphotransferase system (PTS) which concomitantly catalyzes the phosphorylation and translocation of mono- and disaccharides via a chain of enzymic reactions that transfer a phosphate group from phosphoenolpyruvate to the incoming sugar. A number of PTS components, including HPr, Enzyme I and some Enzymes II, have been studied at the biochemical and/or genetical level in Streptococcus salivarius, Streptococcus mutans and Streptococcus sobrinus. Moreover, compelling evidence indicates that the oral streptococcal PTS is involved in the regulation of sugar metabolism. Results are accumulating suggesting that a protein called IIABMan, as well as the phosphocarrier protein HPr, are key regulatory components that allow these bacteria to select rapidly metabolizable sugars, such as glucose or fructose, over less readily utilizable carbohydrates. Circumstantial evidence suggests that the molecular mechanisms by which oral streptococcal PTS exert their regulatory functions differ from mechanisms in other Gram-negative or Gram-positive bacteria.

摘要

口腔链球菌是一类可发酵糖类的细菌,至少包含19个不同的种,在人类口腔和上呼吸道的正常微生物群落中占很大比例。这些链球菌通过磷酸烯醇丙酮酸:糖磷酸转移酶系统(PTS)转运多种糖类,该系统通过一系列酶促反应同时催化单糖和双糖的磷酸化和转运,这些反应将磷酸基团从磷酸烯醇丙酮酸转移到进入的糖类上。在唾液链球菌、变形链球菌和远缘链球菌中,已经在生化和/或遗传水平上研究了许多PTS组分,包括HPr、酶I和一些酶II。此外,有力的证据表明口腔链球菌PTS参与糖代谢的调节。越来越多的结果表明,一种名为IIABMan的蛋白质以及磷酸载体蛋白HPr是关键的调节成分,使这些细菌能够优先选择易于快速代谢的糖类,如葡萄糖或果糖,而不是较难利用的碳水化合物。间接证据表明,口腔链球菌PTS发挥其调节功能的分子机制不同于其他革兰氏阴性或革兰氏阳性细菌中的机制。

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