Institute of Molecular Enzyme Technology, Heinrich-Heine-University of Düsseldorf, Research Centre Jülich, Stetternicher Forst, 52426, Jülich, Germany.
Adv Biochem Eng Biotechnol. 2010;120:195-242. doi: 10.1007/10_2009_55.
Dehydrogenases which depend on nicotinamide coenzymes are of increasing interest for the preparation of chiral compounds, either by reduction of a prochiral precursor or by oxidative resolution of their racemate. The regeneration of oxidized and reduced nicotinamide cofactors is a very crucial step because the use of these cofactors in stoichiometric amounts is too expensive for application. There are several possibilities to regenerate nicotinamide cofactors: established methods such as formate/formate dehydrogenase (FDH) for the regeneration of NADH, recently developed electrochemical methods based on new mediator structures, or the application of gene cloning methods for the construction of "designed" cells by heterologous expression of appropriate genes.A very promising approach is enzymatic cofactor regeneration. Only a few enzymes are suitable for the regeneration of oxidized nicotinamide cofactors. Glutamate dehydrogenase can be used for the oxidation of NADH as well as NADPH while L: -lactate dehydrogenase is able to oxidize NADH only. The reduction of NAD(+) is carried out by formate and FDH. Glucose-6-phosphate dehydrogenase and glucose dehydrogenase are able to reduce both NAD(+) and NADP(+). Alcohol dehydrogenases (ADHs) are either NAD(+)- or NADP(+)-specific. ADH from horse liver, for example, reduces NAD(+) while ADHs from Lactobacillus strains catalyze the reduction of NADP(+). These enzymes can be applied by their inclusion in whole cell biotransformations with an NAD(P)(+)-dependent primary reaction to achieve in situ the regeneration of the consumed cofactor.Another efficient method for the regeneration of nicotinamide cofactors is the electrochemical approach. Cofactors can be regenerated directly, for example at a carbon anode, or indirectly involving mediators such as redox catalysts based on transition-metal complexes.An increasing number of examples in technical scale applications are known where nicotinamide dependent enzymes were used together with cofactor regenerating enzymes.
依赖烟酰胺辅酶的脱氢酶在制备手性化合物方面越来越受到关注,无论是通过前手性前体的还原还是通过其外消旋体的氧化拆分。氧化和还原烟酰胺辅酶的再生是一个非常关键的步骤,因为这些辅酶以化学计量的量使用对于应用来说太贵了。有几种可能的方法来再生烟酰胺辅酶:已建立的方法,如甲酸盐/甲酸脱氢酶(FDH)用于 NADH 的再生,最近开发的基于新介体结构的电化学方法,或应用基因克隆方法通过异源表达适当的基因构建“设计”细胞。一种很有前途的方法是酶辅助因子再生。只有少数几种酶适合氧化烟酰胺辅酶的再生。谷氨酸脱氢酶可用于 NADH 和 NADPH 的氧化,而 L:-乳酸脱氢酶只能氧化 NADH。NAD(+)的还原由甲酸盐和 FDH 进行。葡萄糖-6-磷酸脱氢酶和葡萄糖脱氢酶能够还原 NAD(+)和 NADP(+)。醇脱氢酶(ADHs)要么是 NAD(+) - 特异性的,要么是 NADP(+) - 特异性的。例如,来自马肝的 ADH 还原 NAD(+),而来自乳杆菌属菌株的 ADHs催化 NADP(+)的还原。这些酶可以通过将其包含在全细胞生物转化中,与 NAD(P)(+) 依赖性的初级反应一起应用,以在原位实现消耗的辅因子的再生。另一种有效的烟酰胺辅酶再生方法是电化学方法。辅因子可以直接再生,例如在碳阳极上,或者间接涉及介体,如基于过渡金属配合物的氧化还原催化剂。在技术规模应用中,越来越多的例子已知使用依赖烟酰胺的酶与辅因子再生酶一起使用。