Your browser doesn't support javascript.
loading
Engineering Electron Transfer Pathway of Cytochrome P450s.
He, Jingting; Liu, Xin; Li, Chun.
Affiliation
  • He J; Key Laboratory for Green Processing of Chemical Engineering of Xinjiang Bingtuan, School of Chemistry and Chemical Engineering, Shihezi 832003, China.
  • Liu X; Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.
  • Li C; Key Lab for Industrial Biocatalysis, Ministry of Education, Tsinghua University, Beijing 100084, China.
Molecules ; 29(11)2024 May 24.
Article in En | MEDLINE | ID: mdl-38893355
ABSTRACT
Cytochrome P450s (P450s), a superfamily of heme-containing enzymes, existed in animals, plants, and microorganisms. P450s can catalyze various regional and stereoselective oxidation reactions, which are widely used in natural product biosynthesis, drug metabolism, and biotechnology. In a typical catalytic cycle, P450s use redox proteins or domains to mediate electron transfer from NAD(P)H to heme iron. Therefore, the main factors determining the catalytic efficiency of P450s include not only the P450s themselves but also their redox-partners and electron transfer pathways. In this review, the electron transfer pathway engineering strategies of the P450s catalytic system are reviewed from four aspects cofactor regeneration, selection of redox-partners, P450s and redox-partner engineering, and electrochemically or photochemically driven electron transfer.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxidation-Reduction / Protein Engineering / Cytochrome P-450 Enzyme System Limits: Animals / Humans Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxidation-Reduction / Protein Engineering / Cytochrome P-450 Enzyme System Limits: Animals / Humans Language: En Journal: Molecules Journal subject: BIOLOGIA Year: 2024 Document type: Article Affiliation country: China Country of publication: Switzerland