Literature DB >> 22819837

The enigmatic reaction of flavins with oxygen.

Pimchai Chaiyen1, Marco W Fraaije, Andrea Mattevi.   

Abstract

The reaction of flavoenzymes with oxygen remains a fascinating area of research because of its relevance for reactive oxygen species (ROS) generation. Several exciting recent studies provide consistent mechanistic clues about the specific functional and structural properties of the oxidase and monooxygenase flavoenzymatic systems. Specifically, the spatial arrangement of the reacting oxygen that is in direct contact with the flavin group is emerging as a crucial factor that differentiates between oxidase and monooxygenase enzymes. A challenge for the future will be to use these emerging concepts to rationally engineer flavoenzymes, paving the way to new research avenues with far-reaching implications for oxidative biocatalysis and metabolic engineering.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22819837     DOI: 10.1016/j.tibs.2012.06.005

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  66 in total

1.  Mechanistic insights into the dual activities of the single active site of l-lysine oxidase/monooxygenase from Pseudomonas sp. AIU 813.

Authors:  Duangthip Trisrivirat; Narin Lawan; Pirom Chenprakhon; Daisuke Matsui; Yasuhisa Asano; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2020-06-11       Impact factor: 5.157

Review 2.  Heteroatom-Heteroatom Bond Formation in Natural Product Biosynthesis.

Authors:  Abraham J Waldman; Tai L Ng; Peng Wang; Emily P Balskus
Journal:  Chem Rev       Date:  2017-04-04       Impact factor: 60.622

Review 3.  Monooxygenation of aromatic compounds by flavin-dependent monooxygenases.

Authors:  Pirom Chenprakhon; Thanyaporn Wongnate; Pimchai Chaiyen
Journal:  Protein Sci       Date:  2019-01       Impact factor: 6.725

4.  A complete bioconversion cascade for dehalogenation and denitration by bacterial flavin-dependent enzymes.

Authors:  Panu Pimviriyakul; Pimchai Chaiyen
Journal:  J Biol Chem       Date:  2018-10-03       Impact factor: 5.157

5.  Biochemical Establishment and Characterization of EncM's Flavin-N5-oxide Cofactor.

Authors:  Robin Teufel; Frederick Stull; Michael J Meehan; Quentin Michaudel; Pieter C Dorrestein; Bruce Palfey; Bradley S Moore
Journal:  J Am Chem Soc       Date:  2015-06-19       Impact factor: 15.419

6.  Beyond the Protein Matrix: Probing Cofactor Variants in a Baeyer-Villiger Oxygenation Reaction.

Authors:  Christian Martinoli; Hanna M Dudek; Roberto Orru; Dale E Edmondson; Marco W Fraaije; Andrea Mattevi
Journal:  ACS Catal       Date:  2013       Impact factor: 13.084

7.  How a cofactor-free protein environment lowers the barrier to O2 reactivity.

Authors:  Melodie M Machovina; Emerald S Ellis; Thomas J Carney; Fikile R Brushett; Jennifer L DuBois
Journal:  J Biol Chem       Date:  2019-01-02       Impact factor: 5.157

8.  Aminoperoxide adducts expand the catalytic repertoire of flavin monooxygenases.

Authors:  Arne Matthews; Raspudin Saleem-Batcha; Jacob N Sanders; Frederick Stull; K N Houk; Robin Teufel
Journal:  Nat Chem Biol       Date:  2020-02-17       Impact factor: 15.040

9.  Camphor pathway redux: functional recombinant expression of 2,5- and 3,6-diketocamphane monooxygenases of Pseudomonas putida ATCC 17453 with their cognate flavin reductase catalyzing Baeyer-Villiger reactions.

Authors:  Hiroaki Iwaki; Stephan Grosse; Hélène Bergeron; Hannes Leisch; Krista Morley; Yoshie Hasegawa; Peter C K Lau
Journal:  Appl Environ Microbiol       Date:  2013-03-22       Impact factor: 4.792

10.  Oxidation mode of pyranose 2-oxidase is controlled by pH.

Authors:  Methinee Prongjit; Jeerus Sucharitakul; Bruce A Palfey; Pimchai Chaiyen
Journal:  Biochemistry       Date:  2013-02-12       Impact factor: 3.162

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