Literature DB >> 23034231

The rare fluorinated natural products and biotechnological prospects for fluorine enzymology.

K K Jason Chan1, David O'Hagan.   

Abstract

Nature has hardly evolved a biochemistry of fluorine although there is a low-level occurrence of fluoroacetate found in selected tropical and subtropical plants. This compound, which is generally produced in low concentrations, has been identified in the plants due to its high toxicity, although to date the biosynthesis of fluoroacetate in plants remains unknown. After that, fluorinated entities in nature are extremely rare, and despite increasingly sophisticated screening and analytical methods applied to natural product extraction, it has been 25 years since the last bona fide fluorinated natural product was identified from an organism. This was the reported isolation of the antibiotic 4-fluorothreonine and the toxin fluoroacetate in 1986 from Streptomyces cattleya. This bacterium has proven amenable to biochemical investigation, the fluorination enzyme (fluorinase) has been isolated and characterized, and the biosynthetic pathway to these bacterial metabolites has been elucidated. Also the fluorinase gene has been cloned into a host bacterium (Salinispora tropica), and this has enabled the de novo production of a bioactive fluorinated metabolite from fluoride ion, by genetic engineering. Biotechnological manipulation of the fluorinase offers the prospects for the assembly of novel fluorinated metabolites by fermentation technology. This is particularly attractive, given the backdrop that about 15-20% of pharmaceuticals licensed each year (new chemical entities) contain a fluorine atom.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 23034231     DOI: 10.1016/B978-0-12-394291-3.00003-4

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  12 in total

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Review 2.  Mass Spectrometry-Based Protein Footprinting for Higher-Order Structure Analysis: Fundamentals and Applications.

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3.  Mutasynthesis of fluorinated pactamycin analogues and their antimalarial activity.

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4.  Preparation, Assay, and Application of Chlorinase SalL for the Chemoenzymatic Synthesis of S-Adenosyl-l-Methionine and Analogs.

Authors:  Tony D Davis; Sylvia Kunakom; Michael D Burkart; Alessandra S Eustaquio
Journal:  Methods Enzymol       Date:  2018-04-02       Impact factor: 1.600

5.  Catalytic Enantioselective Synthesis of Difluorinated Alkyl Bromides.

Authors:  Mark D Levin; John M Ovian; Jacquelyne A Read; Matthew S Sigman; Eric N Jacobsen
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6.  Precursor-Directed Combinatorial Biosynthesis of Cinnamoyl, Dihydrocinnamoyl, and Benzoyl Anthranilates in Saccharomyces cerevisiae.

Authors:  Aymerick Eudes; Veronica Teixeira Benites; George Wang; Edward E K Baidoo; Taek Soon Lee; Jay D Keasling; Dominique Loqué
Journal:  PLoS One       Date:  2015-10-02       Impact factor: 3.240

7.  The cycloaspeptides: uncovering a new model for methylated nonribosomal peptide biosynthesis.

Authors:  Kate M J de Mattos-Shipley; Claudio Greco; David M Heard; Gemma Hough; Nicholas P Mulholland; Jason L Vincent; Jason Micklefield; Thomas J Simpson; Christine L Willis; Russell J Cox; Andrew M Bailey
Journal:  Chem Sci       Date:  2018-04-10       Impact factor: 9.825

8.  A Chiron approach towards the stereoselective synthesis of polyfluorinated carbohydrates.

Authors:  Vincent Denavit; Danny Lainé; Jacob St-Gelais; Paul A Johnson; Denis Giguère
Journal:  Nat Commun       Date:  2018-11-09       Impact factor: 14.919

9.  Enhancing glycan stability via site-selective fluorination: modulating substrate orientation by molecular design.

Authors:  Alexander Axer; Ravindra P Jumde; Sebastian Adam; Andreas Faust; Michael Schäfers; Manfred Fobker; Jesko Koehnke; Anna K H Hirsch; Ryan Gilmour
Journal:  Chem Sci       Date:  2020-11-23       Impact factor: 9.825

10.  ATP-Dependent C-F Bond Cleavage Allows the Complete Degradation of 4-Fluoroaromatics without Oxygen.

Authors:  Oliver Tiedt; Mario Mergelsberg; Kerstin Boll; Michael Müller; Lorenz Adrian; Nico Jehmlich; Martin von Bergen; Matthias Boll
Journal:  mBio       Date:  2016-08-09       Impact factor: 7.867

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