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[杀菌剂及其他化合物对鲁氏毛霉几丁质合成酶的体外抑制作用]

[Inhibition of chitin synthetase of Mucor rouxii in vitro by fungicides and other compounds].

作者信息

Lyr H, Seyd W

出版信息

Z Allg Mikrobiol. 1978;18(10):721-9. doi: 10.1002/jobm.3630181004.

Abstract

Comparative investigations on the inhibition of chitin synthetase of Mucor rouxii revealed that in contrast to results obtained in vivo, only few fungicides and other compounds inhibit the enzyme in vitro. Besides the well-known effect of polyoxin D, an inhibition was demonstrated for terrazol, tridemorph, hinosan, and formulated preparations of dimilin (PH 60--40, 60--38). The latter preparations, however, showed growth inhibition also with fungal species which do not synthesize chitin and the pure compounds are ineffective. Inhibition by phospholipase C, unsaturated fatty acids, and the reversibility of the inhibition caused by terrazol after addition of procain-hydrochloride demonstrates that phospholipids are essential for the activity of the enzyme, whereas sterols seem to be ineffective. Action of trypsin, PCNB, pentachlorophenol, and some similar compounds results in significantly increased activity, which in the case of trypsin could be due to the hydrolysis of a protein inhibitor. Hinosan inhibits the enzyme indirectly in a still unexplored manner.

摘要

对鲁氏毛霉几丁质合成酶抑制作用的比较研究表明,与体内实验结果相反,体外只有少数杀菌剂和其他化合物能抑制该酶。除了多氧霉素D的已知作用外,还证明了福美双、十三吗啉、氯硝柳胺和灭幼脲制剂(PH 60 - 40、60 - 38)有抑制作用。然而,后一种制剂对不合成几丁质的真菌种类也有生长抑制作用,而纯化合物则无效。磷脂酶C、不饱和脂肪酸的抑制作用以及加入盐酸普鲁卡因后福美双引起的抑制作用的可逆性表明,磷脂对该酶的活性至关重要,而固醇似乎无效。胰蛋白酶、五氯硝基苯、五氯苯酚和一些类似化合物的作用导致活性显著增加,就胰蛋白酶而言,这可能是由于一种蛋白质抑制剂的水解。氯硝柳胺以一种尚未明确的方式间接抑制该酶。

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