Literature DB >> 11895118

Versatility and specificity in flavoenzymes: control mechanisms of flavin reactivity.

R Miura1.   

Abstract

Flavoenzymes are characterized by their remarkable versatility and strict specificity. The former can be grasped when flavoenzymes are treated as a whole, while the latter refers to each flavoenzyme in which the broad versatility of flavin is specifically controlled. The versatility stems from the variety of the redox, ionic, and electronic states that the flavin ring system can adopt. Versatility of flavoenzymes is reflected in their classification, which has generally been based on substrates and reactions catalyzed. A different classification is presented according to the number of electrons transferred in the reductive and oxidative half reactions. Specificity of each flavoenzyme is understood in terms of the regulatory mechanism of the broad reactive potentiality of flavin. The elements of this regulatory mechanism include hydrogen-bonding network, electrostatic effect, charge-transfer interaction, positioning between a substrate/ligand and flavin, and modulation of resonance hybridization, each of which is explained with relevant examples provided mainly by studies from the author's group.

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Year:  2001        PMID: 11895118     DOI: 10.1002/tcr.1007

Source DB:  PubMed          Journal:  Chem Rec        ISSN: 1528-0691            Impact factor:   6.771


  20 in total

1.  New role of flavin as a general acid-base catalyst with no redox function in type 2 isopentenyl-diphosphate isomerase.

Authors:  Hideaki Unno; Satoshi Yamashita; Yosuke Ikeda; Shin-Ya Sekiguchi; Norie Yoshida; Tohru Yoshimura; Masami Kusunoki; Toru Nakayama; Tokuzo Nishino; Hisashi Hemmi
Journal:  J Biol Chem       Date:  2009-01-21       Impact factor: 5.157

2.  Equilibrium and ultrafast kinetic studies manipulating electron transfer: A short-lived flavin semiquinone is not sufficient for electron bifurcation.

Authors:  John P Hoben; Carolyn E Lubner; Michael W Ratzloff; Gerrit J Schut; Diep M N Nguyen; Karl W Hempel; Michael W W Adams; Paul W King; Anne-Frances Miller
Journal:  J Biol Chem       Date:  2017-06-14       Impact factor: 5.157

3.  Redox modulation of flavin and tyrosine determines photoinduced proton-coupled electron transfer and photoactivation of BLUF photoreceptors.

Authors:  Tilo Mathes; Ivo H M van Stokkum; Manuela Stierl; John T M Kennis
Journal:  J Biol Chem       Date:  2012-07-25       Impact factor: 5.157

4.  Spectroscopic evidence for direct flavin-flavin contact in a bifurcating electron transfer flavoprotein.

Authors:  H Diessel Duan; Nishya Mohamed-Raseek; Anne-Frances Miller
Journal:  J Biol Chem       Date:  2020-07-13       Impact factor: 5.157

5.  Photochemical processes in flavo-enzymes as a probe for active site dynamics: TrmFO of Thermus thermophilus.

Authors:  Bo Zhuang; Lipsa Nag; Pierre Sournia; Anastasia Croitoru; Rivo Ramodiharilafy; Jean-Christophe Lambry; Hannu Myllykallio; Alexey Aleksandrov; Ursula Liebl; Marten H Vos
Journal:  Photochem Photobiol Sci       Date:  2021-05-11       Impact factor: 3.982

Review 6.  Genetic control of biosynthesis and transport of riboflavin and flavin nucleotides and construction of robust biotechnological producers.

Authors:  Charles A Abbas; Andriy A Sibirny
Journal:  Microbiol Mol Biol Rev       Date:  2011-06       Impact factor: 11.056

7.  Hydrogen-bond switching through a radical pair mechanism in a flavin-binding photoreceptor.

Authors:  Magdalena Gauden; Ivo H M van Stokkum; Jason M Key; Daniel Ch Lührs; Rienk van Grondelle; Peter Hegemann; John T M Kennis
Journal:  Proc Natl Acad Sci U S A       Date:  2006-07-07       Impact factor: 11.205

8.  Interplay of flavin's redox states and protein dynamics: an insight from QM/MM simulations of dihydronicotinamide riboside quinone oxidoreductase 2.

Authors:  Robyn M Mueller; Michael A North; Chee Yang; Sanchita Hati; Sudeep Bhattacharyya
Journal:  J Phys Chem B       Date:  2011-03-16       Impact factor: 2.991

9.  Robust in vitro activity of RebF and RebH, a two-component reductase/halogenase, generating 7-chlorotryptophan during rebeccamycin biosynthesis.

Authors:  Ellen Yeh; Sylvie Garneau; Christopher T Walsh
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-02       Impact factor: 11.205

10.  Mutants of Cytochrome P450 Reductase Lacking Either Gly-141 or Gly-143 Destabilize Its FMN Semiquinone.

Authors:  Freeborn Rwere; Chuanwu Xia; Sangchoul Im; Mohammad M Haque; Dennis J Stuehr; Lucy Waskell; Jung-Ja P Kim
Journal:  J Biol Chem       Date:  2016-05-09       Impact factor: 5.157

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