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A Promiscuous Cytochrome P450 Hydroxylates Aliphatic and Aromatic C−H Bonds of Aromatic 2,5‐Diketopiperazines

Title: A Promiscuous Cytochrome P450 Hydroxylates Aliphatic and Aromatic C−H Bonds of Aromatic 2,5‐Diketopiperazines
Authors: Jiang, Guangde; Zhang, Yi; Powell, Magan M.; Hylton, Sarah M.; Hiller, Nicholas W.; Loria, Rosemary; Ding, Yousong
Contributors: U.S. Air Force
Source: ChemBioChem ; volume 20, issue 8, page 1068-1077 ; ISSN 1439-4227 1439-7633
Publisher Information: Wiley
Publication Year: 2019
Collection: Wiley Online Library (Open Access Articles via Crossref)
Description: Cytochrome P450 enzymes generally functionalize inert C−H bonds, and thus, they are important biocatalysts for chemical synthesis. However, enzymes that catalyze both aliphatic and aromatic hydroxylation in the same biotransformation process have rarely been reported. A recent biochemical study demonstrated the P450 TxtC for the biosynthesis of herbicidal thaxtomins as the first example of this unique type of enzyme. Herein, the detailed characterization of substrate requirements and biocatalytic applications of TxtC are reported. The results reveal the importance of N‐methylation of the thaxtomin diketopiperazine (DKP) core on enzyme reactions and demonstrate the tolerance of the enzyme to modifications on the indole and phenyl moieties of its substrates. Furthermore, hydroxylated, methylated, aromatic DKPs are synthesized through a biocatalytic route comprising TxtC and the promiscuous N ‐methyltransferase Amir_4628; thus providing a basis for the broad application of this unique P450.
Document Type: article in journal/newspaper
Language: English
DOI: 10.1002/cbic.201800736
Availability: https://doi.org/10.1002/cbic.201800736; https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fcbic.201800736; https://onlinelibrary.wiley.com/doi/pdf/10.1002/cbic.201800736; https://onlinelibrary.wiley.com/doi/full-xml/10.1002/cbic.201800736; https://chemistry-europe.onlinelibrary.wiley.com/doi/am-pdf/10.1002/cbic.201800736
Rights: http://onlinelibrary.wiley.com/termsAndConditions#am ; http://onlinelibrary.wiley.com/termsAndConditions#vor
Accession Number: edsbas.A0A229B6
Database: BASE