Urban P, Lederer F
Eur J Biochem. 1984 Oct 15;144(2):345-51. doi: 10.1111/j.1432-1033.1984.tb08470.x.
It has been shown that reduced flavocytochrome b2 not only catalyzes reduction of bromopyruvate [P. Urban, P.M. Alliel and F. Lederer (1983) Eur. J. Biochem. 134, 275-281] but also transforms it into pyruvate in a reductive elimination process. The dehydrohalogenation reaction also takes place when oxidized enzyme acts on bromolactate, but the reaction is more difficult to observe under these conditions because of its low efficiency compared to the normal oxidative process. The maximal rates of pyruvate production from bromopyruvate and chloropyruvate differ by a factor of less than 10, whereas elimination from fluoropyruvate cannot be detected. These results support a mechanism in which the dehydrohalogenation reaction takes place from a carbanion intermediate of the normal reductive-oxidative pathway.
已表明,还原型黄素细胞色素b2不仅能催化溴丙酮酸的还原反应[P. 厄本、P.M. 阿利尔和F. 莱德勒(1983年)《欧洲生物化学杂志》134卷,275 - 281页],还能在还原消除过程中将其转化为丙酮酸。当氧化型酶作用于溴乳酸时,脱卤化氢反应也会发生,但由于与正常氧化过程相比效率较低,在这些条件下该反应更难观察到。由溴丙酮酸和氯丙酮酸生成丙酮酸的最大速率相差不到10倍,而氟丙酮酸的消除反应则无法检测到。这些结果支持了一种机制,即脱卤化氢反应发生在正常还原 - 氧化途径的碳负离子中间体上。