Talmann Lea, Wiesner Jochen, Vilcinskas Andreas
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Z Naturforsch C J Biosci. 2017 Sep 26;72(9-10):405-415. doi: 10.1515/znc-2017-0041.
Cytochrome P450 monooxygenases (P450s) are ubiquitous enzymes with a broad substrate spectrum. Insect P450s are known to catalyze reactions such as the detoxification of insecticides and the synthesis of hydrocarbons, which makes them useful for many industrial processes. Unfortunately, it is difficult to utilize P450s effectively because they must be paired with cytochrome P450 reductases (CPRs) to facilitate electron transfer from reduced nicotinamide adenine dinucleotide phosphate (NADPH). Furthermore, eukaryotic P450s and CPRs are membrane-anchored proteins, which means they are insoluble and therefore difficult to purify when expressed in their native state. Both challenges can be addressed by creating fusion proteins that combine the P450 and CPR functions while eliminating membrane anchors, allowing the production and purification of soluble multifunctional polypeptides suitable for industrial applications. Here we discuss several strategies for the construction of fusion enzymes combining insect P450 with CPRs.
细胞色素P450单加氧酶(P450s)是一类广泛存在且底物谱宽泛的酶。已知昆虫P450s能催化诸如杀虫剂解毒和碳氢化合物合成等反应,这使得它们在许多工业过程中具有应用价值。不幸的是,有效利用P450s存在困难,因为它们必须与细胞色素P450还原酶(CPRs)配对,以促进电子从还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)转移。此外,真核生物的P450s和CPRs是膜锚定蛋白,这意味着它们不溶于水,因此在以天然状态表达时难以纯化。通过创建融合蛋白可以解决这两个挑战,该融合蛋白结合了P450和CPR的功能,同时消除了膜锚定结构,从而能够生产和纯化适合工业应用的可溶性多功能多肽。在此,我们讨论几种将昆虫P450与CPRs结合构建融合酶的策略。