Rokita S E, Srere P A, Walsh C T
Biochemistry. 1982 Aug 3;21(16):3765-74. doi: 10.1021/bi00259a007.
The interaction of a novel fluorinated analogue of citrate, 3-fluoro-3-deoxycitrate (3-fluorocitrate), with the four known citrate-processing enzymes is described in this report. Three of the citrate-processing enzymes, citrate synthase, ATP citrate lyase, and citrate lyase, catalyze reversible aldol-type condensations. The fate of 3-fluorocitrate with each enzyme is uniquely related to their mechanisms of action. For citrate synthase, 3-fluorocitrate is a competitive inhibitor. 3-Fluorocitrate is a substrate for the carboxylate activation half-reaction catalyzed by ATP citrate lyase and induces a net ATPase action during conversion to 3-fluorocitryl-S-coenzyme A. Because of the unusual mechanism of citrate cleavage catalyzed by bacterial citrate lyase, 3-fluorocitrate is a mechanism-based inhibitor, acting at two points during turnover of the acetyl enzyme. The fourth citrate-processing enzyme, aconitase, does turn over 3-fluorocitrate catalytically. This enzyme, catalyzing a dehydration and rehydration of citrate, also catalyzes the elimination of HF from 3-fluorocitrate, yielding cis-aconitate and fluoride.
本报告描述了一种新型柠檬酸氟化类似物3-氟-3-脱氧柠檬酸(3-氟柠檬酸)与四种已知柠檬酸加工酶的相互作用。三种柠檬酸加工酶,即柠檬酸合酶、ATP柠檬酸裂解酶和柠檬酸裂解酶,催化可逆的醛醇型缩合反应。3-氟柠檬酸与每种酶的作用结果与其作用机制独特相关。对于柠檬酸合酶,3-氟柠檬酸是一种竞争性抑制剂。3-氟柠檬酸是ATP柠檬酸裂解酶催化的羧酸盐活化半反应的底物,并在转化为3-氟柠檬酰-S-辅酶A的过程中诱导净ATP酶作用。由于细菌柠檬酸裂解酶催化的柠檬酸裂解机制不同寻常,3-氟柠檬酸是一种基于机制的抑制剂,在乙酰酶周转过程中的两个点起作用。第四种柠檬酸加工酶,即乌头酸酶,确实能催化3-氟柠檬酸的周转。这种酶催化柠檬酸的脱水和再水化,也催化从3-氟柠檬酸中消除HF,生成顺乌头酸和氟化物。