Literature DB >> 29949340

Peroxidase versus Peroxygenase Activity: Substrate Substituent Effects as Modulators of Enzyme Function in the Multifunctional Catalytic Globin Dehaloperoxidase.

Ashlyn H McGuire1, Leiah M Carey1, Vesna de Serrano1, Safaa Dali1, Reza A Ghiladi1.   

Abstract

The dehaloperoxidase-hemoglobin (DHP) from the terebellid polychaete Amphitrite ornata is a multifunctional hemoprotein that catalyzes the oxidation of a wide variety of substrates, including halo/nitrophenols, haloindoles, and pyrroles, via peroxidase and/or peroxygenase mechanisms. To probe whether substrate substituent effects can modulate enzyme activity in DHP, we investigated its reactiviy against a panel of o-guaiacol substrates given their presence (from native/halogenated and non-native/anthropogenic sources) in the benthic environment that A. ornata inhabits. Using biochemical assays supported by spectroscopic, spectrometric, and structural studies, DHP was found to catalyze the H2O2-dependent oxidative dehalogenation of 4-haloguaiacols (F, Cl, and Br) to 2-methoxybenzoquinone (2-MeOBQ). 18O labeling studies confirmed that O atom incorporation was derived exclusively from water, consistent with substrate oxidation via a peroxidase-based mechanism. The 2-MeOBQ product further reduced DHP to its oxyferrous state, providing a link between the substrate oxidation and O2 carrier functions of DHP. Nonnative substrates resulted in polymerization of the initial substrate with varying degrees of oxidation, with 2-MeOBQ identified as a minor product. When viewed alongside the reactivity of previously studied phenolic substrates, the results presented here show that simple substituent effects can serve as functional switches between peroxidase and peroxygenase activities in this multifunctional catalytic globin. More broadly, when recent findings on DHP activity with nitrophenols and azoles are included, the results presented here further demonstrate the breadth of heterocyclic compounds of anthropogenic origin that can potentially disrupt marine hemoglobins or function as environmental stressors, findings that may be important when assessing the environmental impact of these pollutants (and their metabolites) on aquatic systems.

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Year:  2018        PMID: 29949340     DOI: 10.1021/acs.biochem.8b00540

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  4 in total

Review 1.  Carbon-fluorine bond cleavage mediated by metalloenzymes.

Authors:  Yifan Wang; Aimin Liu
Journal:  Chem Soc Rev       Date:  2020-06-08       Impact factor: 54.564

2.  Exploiting Designed Oxidase-Peroxygenase Mutual Benefit System for Asymmetric Cascade Reactions.

Authors:  Da Yu; Jian-Bo Wang; Manfred T Reetz
Journal:  J Am Chem Soc       Date:  2019-04-01       Impact factor: 15.419

3.  High-throughput structures of protein-ligand complexes at room temperature using serial femtosecond crystallography.

Authors:  Tadeo Moreno-Chicano; Ali Ebrahim; Danny Axford; Martin V Appleby; John H Beale; Amanda K Chaplin; Helen M E Duyvesteyn; Reza A Ghiladi; Shigeki Owada; Darren A Sherrell; Richard W Strange; Hiroshi Sugimoto; Kensuke Tono; Jonathan A R Worrall; Robin L Owen; Michael A Hough
Journal:  IUCrJ       Date:  2019-10-10       Impact factor: 4.769

4.  Complementarity of neutron, XFEL and synchrotron crystallography for defining the structures of metalloenzymes at room temperature.

Authors:  Tadeo Moreno-Chicano; Leiah M Carey; Danny Axford; John H Beale; R Bruce Doak; Helen M E Duyvesteyn; Ali Ebrahim; Robert W Henning; Diana C F Monteiro; Dean A Myles; Shigeki Owada; Darren A Sherrell; Megan L Straw; Vukica Šrajer; Hiroshi Sugimoto; Kensuke Tono; Takehiko Tosha; Ivo Tews; Martin Trebbin; Richard W Strange; Kevin L Weiss; Jonathan A R Worrall; Flora Meilleur; Robin L Owen; Reza A Ghiladi; Michael A Hough
Journal:  IUCrJ       Date:  2022-07-25       Impact factor: 5.588

  4 in total

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