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LICRED:一种通用的插入载体,可快速生成氧化还原自足细胞色素 P450。

LICRED: a versatile drop-in vector for rapid generation of redox-self-sufficient cytochrome P450s.

机构信息

Centre for Novel Agricultural Products, Department of Biology, University of York, YO10 5YW York, UK.

出版信息

Chembiochem. 2010 May 3;11(7):987-94. doi: 10.1002/cbic.201000104.

Abstract

Cytochromes P450 (P450s) are a family of haem-containing oxidases with considerable potential as tools for industrial biocatalysis. Organismal genomes are revealing thousands of gene sequences that encode P450s of as yet unknown function, the exploitation of which will require high-throughput tools for their isolation and characterisation. In this report, a ligationindependent cloning vector "LICRED" is described that enables the high-throughput generation of libraries of redox-self-sufficient P450s by fusing a range of P450 haem domains to the reductase of P450RhF (RhF-Red) in a robust and generically applicable way. Cloning and expression of fusions of RhF-Red with the haem domains of P450cam and P450-XplA resulted in soluble, active, redox-self-sufficient, chimeric enzymes. In vitro studies also revealed that electron transfer from NADPH to haem was primarily intramolecular. The general applicability of the LICRED platform was then demonstrated through the creation of a library of RhF-Red fusion constructs by using the diverse complement of P450 haem domains identified in the genome of Nocardia farcinica. The resultant fusion-protein library was then screened against a panel of substrates; this revealed chimeric enzymes competent for the hydroxylation of testosterone and methyltestosterone, and the dealkylation of 7-ethoxycoumarin.

摘要

细胞色素 P450(P450s)是一类含有血红素的氧化酶,具有很大的工业生物催化工具潜力。生物基因组揭示了成千上万条编码 P450 的基因序列,这些 P450 的功能尚不清楚,需要高通量工具来分离和鉴定它们。本报告介绍了一种称为 LICRED 的无连接克隆载体,它可以通过将一系列 P450 血红素结构域与 P450RhF(RhF-Red)的还原酶融合,以稳健且通用的方式高通量生成氧化还原自给自足的 P450 文库。RhF-Red 与 P450cam 和 P450-XplA 的血红素结构域的融合克隆和表达产生了可溶性、活性、氧化还原自给自足的嵌合酶。体外研究还表明,电子从 NADPH 向血红素的转移主要是分子内的。然后,通过使用在诺卡氏菌基因组中鉴定出的多样化的 P450 血红素结构域,创建了 RhF-Red 融合构建体的文库,证明了 LICRED 平台的通用性。然后,用该融合蛋白文库筛选了一组底物;结果表明,这些嵌合酶能够对睾酮和甲基睾酮进行羟化,对 7-乙氧基香豆素进行脱烷基化。

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