Literature DB >> 27122598

Physiology, Biochemistry, and Applications of F420- and Fo-Dependent Redox Reactions.

Chris Greening1, F Hafna Ahmed2, A Elaaf Mohamed2, Brendon M Lee2, Gunjan Pandey3, Andrew C Warden3, Colin Scott3, John G Oakeshott3, Matthew C Taylor3, Colin J Jackson4.   

Abstract

5-Deazaflavin cofactors enhance the metabolic flexibility of microorganisms by catalyzing a wide range of challenging enzymatic redox reactions. While structurally similar to riboflavin, 5-deazaflavins have distinctive and biologically useful electrochemical and photochemical properties as a result of the substitution of N-5 of the isoalloxazine ring for a carbon. 8-Hydroxy-5-deazaflavin (Fo) appears to be used for a single function: as a light-harvesting chromophore for DNA photolyases across the three domains of life. In contrast, its oligoglutamyl derivative F420 is a taxonomically restricted but functionally versatile cofactor that facilitates many low-potential two-electron redox reactions. It serves as an essential catabolic cofactor in methanogenic, sulfate-reducing, and likely methanotrophic archaea. It also transforms a wide range of exogenous substrates and endogenous metabolites in aerobic actinobacteria, for example mycobacteria and streptomycetes. In this review, we discuss the physiological roles of F420 in microorganisms and the biochemistry of the various oxidoreductases that mediate these roles. Particular focus is placed on the central roles of F420 in methanogenic archaea in processes such as substrate oxidation, C1 pathways, respiration, and oxygen detoxification. We also describe how two F420-dependent oxidoreductase superfamilies mediate many environmentally and medically important reactions in bacteria, including biosynthesis of tetracycline and pyrrolobenzodiazepine antibiotics by streptomycetes, activation of the prodrugs pretomanid and delamanid by Mycobacterium tuberculosis, and degradation of environmental contaminants such as picrate, aflatoxin, and malachite green. The biosynthesis pathways of Fo and F420 are also detailed. We conclude by considering opportunities to exploit deazaflavin-dependent processes in tuberculosis treatment, methane mitigation, bioremediation, and industrial biocatalysis.
Copyright © 2016, American Society for Microbiology. All Rights Reserved.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 27122598      PMCID: PMC4867364          DOI: 10.1128/MMBR.00070-15

Source DB:  PubMed          Journal:  Microbiol Mol Biol Rev        ISSN: 1092-2172            Impact factor:   11.056


  428 in total

Review 1.  Oceanic methane biogeochemistry.

Authors:  William S Reeburgh
Journal:  Chem Rev       Date:  2007-01-30       Impact factor: 60.622

2.  Structural and evolutionary aspects of antenna chromophore usage by class II photolyases.

Authors:  Stephan Kiontke; Petra Gnau; Reinhard Haselsberger; Alfred Batschauer; Lars-Oliver Essen
Journal:  J Biol Chem       Date:  2014-05-21       Impact factor: 5.157

3.  Function of H2-forming methylenetetrahydromethanopterin dehydrogenase from methanobacterium thermoautotrophicum in coenzyme F420 reduction with H2

Authors: 
Journal:  Arch Microbiol       Date:  1998-03       Impact factor: 2.552

4.  Crystal structure of archaeal photolyase from Sulfolobus tokodaii with two FAD molecules: implication of a novel light-harvesting cofactor.

Authors:  Masahiro Fujihashi; Nobutaka Numoto; Yukiko Kobayashi; Akira Mizushima; Masanari Tsujimura; Akira Nakamura; Yutaka Kawarabayasi; Kunio Miki
Journal:  J Mol Biol       Date:  2006-10-07       Impact factor: 5.469

Review 5.  Structure and function of photolyase and in vivo enzymology: 50th anniversary.

Authors:  Aziz Sancar
Journal:  J Biol Chem       Date:  2008-08-04       Impact factor: 5.157

6.  F420H2: quinone oxidoreductase from Archaeoglobus fulgidus. Characterization of a membrane-bound multisubunit complex containing FAD and iron-sulfur clusters.

Authors:  J Kunow; D Linder; K O Stetter; R K Thauer
Journal:  Eur J Biochem       Date:  1994-07-15

7.  Cofactor contents of methanogenic bacteria reviewed.

Authors:  L G Gorris; C van der Drift
Journal:  Biofactors       Date:  1994-05       Impact factor: 6.113

8.  Purification and properties of N5, N10-methylenetetrahydromethanopterin reductase from Methanobacterium thermoautotrophicum (strain Marburg).

Authors:  K Ma; R K Thauer
Journal:  Eur J Biochem       Date:  1990-07-20

9.  F420H2-dependent degradation of aflatoxin and other furanocoumarins is widespread throughout the actinomycetales.

Authors:  Gauri V Lapalikar; Matthew C Taylor; Andrew C Warden; Colin Scott; Robyn J Russell; John G Oakeshott
Journal:  PLoS One       Date:  2012-02-27       Impact factor: 3.240

10.  De novo modeling of the F(420)-reducing [NiFe]-hydrogenase from a methanogenic archaeon by cryo-electron microscopy.

Authors:  Deryck J Mills; Stella Vitt; Mike Strauss; Seigo Shima; Janet Vonck
Journal:  Elife       Date:  2013-03-05       Impact factor: 8.140

View more
  42 in total

1.  The Redox Cofactor F420 Protects Mycobacteria from Diverse Antimicrobial Compounds and Mediates a Reductive Detoxification System.

Authors:  Thanavit Jirapanjawat; Blair Ney; Matthew C Taylor; Andrew C Warden; Shahana Afroze; Robyn J Russell; Brendon M Lee; Colin J Jackson; John G Oakeshott; Gunjan Pandey; Chris Greening
Journal:  Appl Environ Microbiol       Date:  2016-09-16       Impact factor: 4.792

Review 2.  Energy Conservation and Hydrogenase Function in Methanogenic Archaea, in Particular the Genus Methanosarcina.

Authors:  Thomas D Mand; William W Metcalf
Journal:  Microbiol Mol Biol Rev       Date:  2019-09-18       Impact factor: 11.056

3.  The methanogenic redox cofactor F420 is widely synthesized by aerobic soil bacteria.

Authors:  Blair Ney; F Hafna Ahmed; Carlo R Carere; Ambarish Biswas; Andrew C Warden; Sergio E Morales; Gunjan Pandey; Stephen J Watt; John G Oakeshott; Matthew C Taylor; Matthew B Stott; Colin J Jackson; Chris Greening
Journal:  ISME J       Date:  2016-08-09       Impact factor: 10.302

4.  Mutations in fbiD (Rv2983) as a Novel Determinant of Resistance to Pretomanid and Delamanid in Mycobacterium tuberculosis.

Authors:  Dalin Rifat; Si-Yang Li; Thomas Ioerger; Keshav Shah; Jean-Philippe Lanoix; Jin Lee; Ghader Bashiri; James Sacchettini; Eric Nuermberger
Journal:  Antimicrob Agents Chemother       Date:  2020-12-16       Impact factor: 5.191

5.  Biosynthetic Pathway Connects Cryptic Ribosomally Synthesized Posttranslationally Modified Peptide Genes with Pyrroloquinoline Alkaloids.

Authors:  Peter A Jordan; Bradley S Moore
Journal:  Cell Chem Biol       Date:  2016-11-17       Impact factor: 8.116

6.  Isolation and characterization of a thermostable F420:NADPH oxidoreductase from Thermobifida fusca.

Authors:  Hemant Kumar; Quoc-Thai Nguyen; Claudia Binda; Andrea Mattevi; Marco W Fraaije
Journal:  J Biol Chem       Date:  2017-04-14       Impact factor: 5.157

7.  Rv2074 is a novel F420 H2 -dependent biliverdin reductase in Mycobacterium tuberculosis.

Authors:  F Hafna Ahmed; A Elaaf Mohamed; Paul D Carr; Brendon M Lee; Karmen Condic-Jurkic; Megan L O'Mara; Colin J Jackson
Journal:  Protein Sci       Date:  2016-07-17       Impact factor: 6.725

8.  Coenzyme F420-Dependent Glucose-6-Phosphate Dehydrogenase-Coupled Polyglutamylation of Coenzyme F420 in Mycobacteria.

Authors:  Endang Purwantini; Usha Loganathan; Biswarup Mukhopadhyay
Journal:  J Bacteriol       Date:  2018-11-06       Impact factor: 3.490

9.  Cofactor F420: an expanded view of its distribution, biosynthesis and roles in bacteria and archaea.

Authors:  Rhys Grinter; Chris Greening
Journal:  FEMS Microbiol Rev       Date:  2021-09-08       Impact factor: 16.408

10.  Heterologous Catalysis of the Final Steps of Tetracycline Biosynthesis by Saccharomyces cerevisiae.

Authors:  Ehud Herbst; Arden Lee; Yi Tang; Scott A Snyder; Virginia W Cornish
Journal:  ACS Chem Biol       Date:  2021-07-16       Impact factor: 5.100

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.