Taton M, Benveniste P, Rahier A
Institut de Botanique, Unité Associée 1182 du Centre National de la Recherche Scientifique, Strasbourg, France.
Eur J Biochem. 1989 Nov 20;185(3):605-14. doi: 10.1111/j.1432-1033.1989.tb15156.x.
An enzymatic assay for delta 8,14-sterol delta 14-reductase, an enzyme involved in sterol biosynthesis, has been developed for the first time in higher plants. The properties of the microsomal enzyme have been established with respect to cofactor requirements, kinetics and substrate specificity. This enzymatic double-bound reduction is thought to proceed through an electrophilic addition mechanism, involving a C14 putative carbonium ion high-energy intermediate. Using this in vitro assay, ammonium and iminium analogues of this cationic intermediate were shown to be potent inhibitors of the reduction reaction. Thus, compounds of the N-alkyl-8-aza-4 alpha,10-dimethyl-trans-decal-3 beta-ol series strongly inhibited sterol reductase (I50 = 0.07 - 4 microM) (I50/Km = 10(-4) - 10(-3), as did the antimycotic agent 15-azasterol (I50 = 0.03 microM); all of these compounds act as reaction-intermediate analogues of the proposed C14 carbonium ion intermediate. Moreover, the in vitro inhibition of the plant sterol reductase by a series of ammonium-ion-containing fungicides was demonstrated. The relative specificity of these different series of inhibitors toward cycloeucalenol-obtusifoliol isomerase, delta 8----delta 7-sterol isomerase and delta 8,14-sterol delta 14-reductase, was directly studied.
首次在高等植物中开发了一种用于检测δ8,14 - 甾醇δ14 - 还原酶的酶促测定法,该酶参与甾醇生物合成。已确定微粒体酶在辅因子需求、动力学和底物特异性方面的特性。这种酶促双键还原被认为是通过亲电加成机制进行的,涉及一个C14假定碳正离子高能中间体。使用这种体外测定法,该阳离子中间体的铵和亚胺类似物被证明是还原反应的有效抑制剂。因此,N - 烷基 - 8 - 氮杂 - 4α,10 - 二甲基 - 反式 - 十氢萘 - 3β - 醇系列化合物强烈抑制甾醇还原酶(I50 = 0.07 - 4 microM)(I50/Km = 10(-4) - 10(-3)),抗真菌剂15 - 氮杂甾醇也是如此(I50 = 0.03 microM);所有这些化合物都作为所提出的C14碳正离子中间体的反应中间体类似物。此外,还证明了一系列含铵离子的杀菌剂对植物甾醇还原酶的体外抑制作用。直接研究了这些不同系列抑制剂对环桉叶醇 - obtusifoliol异构酶、δ8----δ7 - 甾醇异构酶和δ8,14 - 甾醇δ14 - 还原酶的相对特异性。