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小孢子菌属和毛癣菌属菌种对多胺生物合成自杀性抑制剂的敏感性。

Susceptibility of Microsporum and Trichophyton species to suicide inhibitors of polyamine biosynthesis.

作者信息

Boyle S M, Sriranganathan N, Cordes D

机构信息

Department of Pathobiology, Virginia-Maryland Regional College of Veterinary Medicine, Virginia Polytechnic Institute and State University, Blacksburg 24061.

出版信息

J Med Vet Mycol. 1988;26(4):227-35.

PMID:3145970
Abstract

DFMO (difluoromethylornithine) and DFMA (difluoromethylarginine), irreversible suicide inhibitors of ornithine and arginine decarboxylase activities (ODC and ADC) respectively, inhibit the growth of six species of Microsporum and six species of Trichophyton. Trichophyton species in general, are more sensitive than Microsporum species. DFMA inhibits growth as effectively as DFMO but at a 10-fold lower concentration. Inhibition is specific, as a number of substrates and end products of ODC and ADC activities antagonize DFMA and DFMO (i.e. ornithine greater than putrescine = spermidine greater than agmatine). The methylester analogue of ornithine, MFMOme (monofluormethyldehydroornithine methylester) is at least a 25-fold more effective inhibitor than DFMO; the inhibition is specific as it is reversed by ornithine.

摘要

二氟甲基鸟氨酸(DFMO)和二氟甲基精氨酸(DFMA)分别是鸟氨酸脱羧酶(ODC)和精氨酸脱羧酶(ADC)活性的不可逆自杀性抑制剂,它们能抑制六种小孢子菌属和六种毛癣菌属真菌的生长。一般来说,毛癣菌属比小孢子菌属更敏感。DFMA抑制生长的效果与DFMO相当,但浓度低10倍。这种抑制具有特异性,因为ODC和ADC活性的一些底物和终产物可拮抗DFMA和DFMO(即鸟氨酸>腐胺 = 亚精胺>胍丁胺)。鸟氨酸的甲酯类似物MFMOme(单氟甲基脱氢鸟氨酸甲酯)的抑制效果至少比DFMO强25倍;这种抑制具有特异性,因为它可被鸟氨酸逆转。

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