Literature DB >> 19245259

Biohalogenation: nature's way to synthesize halogenated metabolites.

Claudia Wagner1, Mustafa El Omari, Gabriele M König.   

Abstract

Halogenated natural products are widely distributed in nature, some of them showing potent biological activities. Incorporation of halogen atoms in drug leads is a common strategy to modify molecules in order to vary their bioactivities and specificities. Chemical halogenation, however, often requires harsh reaction conditions and results in unwanted byproduct formation. It is thus of great interest to investigate the biosynthesis of halogenated natural products and the biotechnological potential of halogenating enzymes. This review aims to give a comprehensive overview on the current knowledge concerning biological halogenations.

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Year:  2009        PMID: 19245259     DOI: 10.1021/np800651m

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  46 in total

1.  Iodide accumulation by aerobic bacteria isolated from subsurface sediments of a 129I-contaminated aquifer at the Savannah River site, South Carolina.

Authors:  Hsiu-Ping Li; Robin Brinkmeyer; Whitney L Jones; Saijin Zhang; Chen Xu; Kathy A Schwehr; Peter H Santschi; Daniel I Kaplan; Chris M Yeager
Journal:  Appl Environ Microbiol       Date:  2011-01-28       Impact factor: 4.792

Review 2.  Enzymatic functionalization of carbon-hydrogen bonds.

Authors:  Jared C Lewis; Pedro S Coelho; Frances H Arnold
Journal:  Chem Soc Rev       Date:  2010-11-15       Impact factor: 54.564

3.  The Vanadium Iodoperoxidase from the marine flavobacteriaceae species Zobellia galactanivorans reveals novel molecular and evolutionary features of halide specificity in the vanadium haloperoxidase enzyme family.

Authors:  Jean-Baptiste Fournier; Etienne Rebuffet; Ludovic Delage; Romain Grijol; Laurence Meslet-Cladière; Justyna Rzonca; Philippe Potin; Gurvan Michel; Mirjam Czjzek; Catherine Leblanc
Journal:  Appl Environ Microbiol       Date:  2014-09-26       Impact factor: 4.792

4.  Evidence That Chlorinated Auxin Is Restricted to the Fabaceae But Not to the Fabeae.

Authors:  Hong Kiat Lam; Scott A M McAdam; Erin L McAdam; John J Ross
Journal:  Plant Physiol       Date:  2015-05-13       Impact factor: 8.340

5.  Suppression of nitric oxide synthase by thienodolin in lipopolysaccharide-stimulated RAW 264.7 murine macrophage cells.

Authors:  Eun-Jung Park; John M Pezzuto; Kyoung Hwa Jang; Sang-Jip Nam; Sergio A Bucarey; William Fenical
Journal:  Nat Prod Commun       Date:  2012-06       Impact factor: 0.986

6.  Substrate placement influences reactivity in non-heme Fe(II) halogenases and hydroxylases.

Authors:  Heather J Kulik; Catherine L Drennan
Journal:  J Biol Chem       Date:  2013-02-28       Impact factor: 5.157

7.  Natural products as inspiration for the development of new synthetic methods.

Authors:  Zhiqiang Ma; Chuo Chen
Journal:  J Chin Chem Soc       Date:  2017-08-09       Impact factor: 1.967

Review 8.  Halogenated indole alkaloids from marine invertebrates.

Authors:  Patrícia Mendonça Pauletti; Lucas Silva Cintra; Caio Guedes Braguine; Ademar Alves da Silva Filho; Márcio Luís Andrade E Silva; Wilson Roberto Cunha; Ana Helena Januário
Journal:  Mar Drugs       Date:  2010-04-28       Impact factor: 5.118

Review 9.  The halogenated metabolism of brown algae (Phaeophyta), its biological importance and its environmental significance.

Authors:  Stéphane La Barre; Philippe Potin; Catherine Leblanc; Ludovic Delage
Journal:  Mar Drugs       Date:  2010-03-31       Impact factor: 5.118

10.  Specific chlorination of isoquinolines by a fungal flavin-dependent halogenase.

Authors:  Jia Zeng; Anna K Lytle; David Gage; Sean J Johnson; Jixun Zhan
Journal:  Bioorg Med Chem Lett       Date:  2012-12-21       Impact factor: 2.823

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