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Application of engineered cytochrome P450 mutants as biocatalysts for the synthesis of benzylic and aromatic metabolites of fenamic acid NSAIDs

机译:工程细胞色素P450突变体作为生物催化剂用于合成芬那酸非甾体抗炎药的苄​​基和芳香族代谢产物的应用

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Cytochrome P450 BM3 mutants are promising biocatalysts for the production of drug metabolites. In the present study, the ability of cytochrome P450 BM3 mutants to produce oxidative metabolites of structurally related NSAIDs meclofenamic acid, mefenamic acid and tolfenamic acid was investigated. A library of engineered P450 BM3 mutants was screened with meclofenamic acid (1) to identify catalytically active and selective mutants. Three mono-hydroxylated metabolites were identified for 1. The hydroxylated products were confirmed by NMR analysis to be 3'-OH-methyl-meclofenamic acid (la), 5-OH-meclofenamic acid (1b) and 4'-OH-meclofenamic acid (1c) which are human relevant metabolites. P450 BM3 variants containing V87I and V87F mutation showed high selectivity for benzylic and aromatic hydroxylation of 1 respectively. The applicability of these mutants to selectively hydroxylate structurally similar drugs such as mefenamic acid (2) and tolfenamic acid (3) was also investigated. The tested variants showed high total turnover numbers in the order of 4000-6000 and can be used as biocatalysts for preparative scale synthesis. Both 1 and 2 could undergo benzylic and aromatic hydroxylation by the P450 BM3 mutants, whereas 3 was hydroxylated only on aromatic rings. The P450 BM3 variant M11 V87F hydroxylated the aromatic ring at 4' position of all three drugs tested with high regioselectivity. Reference metabolites produced by P450 BM3 mutants allowed the characterisation of activity and regioselectivity of metabolism of all three NSAIDs by thirteen recombinant human P450s. In conclusion, engineered P450 BM3 mutants that are capable of benzylic or aromatic hydroxylation of fenamic acid containing NSAIDs, with high selectivity and turnover numbers have been identified. This shows their potential use as a greener alternative for the generation of drug metabolites. (C) 2014 Elsevier Ltd. All rights reserved.
机译:细胞色素P450 BM3突变体是用于生产药物代谢产物的有前途的生物催化剂。在本研究中,研究了细胞色素P450 BM3突变体产生与结构相关的NSAIDs甲氧芬那酸,甲芬那酸和甲苯磺酸的氧化代谢产物的能力。用甲氯芬那酸(1)筛选了工程化的P450 BM3突变体文库,以鉴定具有催化活性和选择性的突变体。鉴定出1的三种单羟基化代谢物。通过NMR分析确认羟基化产物为3'-OH-甲基-氯芬那酸(1a),5-OH-甲基氯芬那酸(1b)和4'-OH-甲基氯芬那酸(1c)与人类有关的代谢产物。包含V87I和V87F突变的P450 BM3变体分别显示出对1的苄基和芳族羟基化的高选择性。还研究了这些突变体在选择性羟化结构上相似的药物(如甲芬那酸(2)和甲苯磺酸(3))上的适用性。经测试的变体显示出高的总周转数,大约为4000-6000,可以用作制备规模合成的生物催化剂。 1和2均可通过P450 BM3突变体进行苄基和芳族羟基化,而3仅在芳环上被羟基化。 P450 BM3变体M11 V87F以高区域选择性对所有三种药物的4'位置的芳环进行了羟基化处理。由P450 BM3突变体产生的参考代谢物可以表征13种重组人P450的所有三种NSAID的活性和代谢的区域选择性。总之,已鉴定出能够对含有NSAID的芬那酸进行苄基或芳族羟基化的工程化P450 BM3突变体,具有很高的选择性和周转率。这表明了它们潜在的用途,可以更绿色地替代药物代谢物的产生。 (C)2014 Elsevier Ltd.保留所有权利。

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