Literature DB >> 28466644

Development of Halogenase Enzymes for Use in Synthesis.

Jonathan Latham1, Eileen Brandenburger1, Sarah A Shepherd1, Binuraj R K Menon1, Jason Micklefield1.   

Abstract

Nature has evolved halogenase enzymes to regioselectively halogenate a diverse range of biosynthetic precursors, with the halogens introduced often having a profound effect on the biological activity of the resulting natural products. Synthetic endeavors to create non-natural bioactive small molecules for pharmaceutical and agrochemical applications have also arrived at a similar conclusion: halogens can dramatically improve the properties of organic molecules for selective modulation of biological targets in vivo. Consequently, a high proportion of pharmaceuticals and agrochemicals on the market today possess halogens. Halogenated organic compounds are also common intermediates in synthesis and are particularly valuable in metal-catalyzed cross-coupling reactions. Despite the potential utility of organohalogens, traditional nonenzymatic halogenation chemistry utilizes deleterious reagents and often lacks regiocontrol. Reliable, facile, and cleaner methods for the regioselective halogenation of organic compounds are therefore essential in the development of economical and environmentally friendly industrial processes. A potential avenue toward such methods is the use of halogenase enzymes, responsible for the biosynthesis of halogenated natural products, as biocatalysts. This Review will discuss advances in developing halogenases for biocatalysis, potential untapped sources of such biocatalysts and how further optimization of these enzymes is required to achieve the goal of industrial scale biohalogenation.

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Year:  2017        PMID: 28466644     DOI: 10.1021/acs.chemrev.7b00032

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  51 in total

Review 1.  Halogenase engineering and its utility in medicinal chemistry.

Authors:  Amy E Fraley; David H Sherman
Journal:  Bioorg Med Chem Lett       Date:  2018-04-30       Impact factor: 2.823

Review 2.  Enzymatic CH functionalizations for natural product synthesis.

Authors:  Fuzhuo Li; Xiao Zhang; Hans Renata
Journal:  Curr Opin Chem Biol       Date:  2018-09-27       Impact factor: 8.822

3.  Discovery of the Tyrobetaine Natural Products and Their Biosynthetic Gene Cluster via Metabologenomics.

Authors:  Elizabeth I Parkinson; James H Tryon; Anthony W Goering; Kou-San Ju; Ryan A McClure; Jeremy D Kemball; Sara Zhukovsky; David P Labeda; Regan J Thomson; Neil L Kelleher; William W Metcalf
Journal:  ACS Chem Biol       Date:  2018-03-13       Impact factor: 5.100

4.  Bioinspired chemical synthesis of monomeric and dimeric stephacidin A congeners.

Authors:  Ken Mukai; Danilo Pereira de Sant'Ana; Yasuo Hirooka; Eduardo V Mercado-Marin; David E Stephens; Kevin G M Kou; Sven C Richter; Naomi Kelley; Richmond Sarpong
Journal:  Nat Chem       Date:  2017-09-18       Impact factor: 24.427

5.  Structure-based switch of regioselectivity in the flavin-dependent tryptophan 6-halogenase Thal.

Authors:  Ann-Christin Moritzer; Hannah Minges; Tina Prior; Marcel Frese; Norbert Sewald; Hartmut H Niemann
Journal:  J Biol Chem       Date:  2018-12-17       Impact factor: 5.157

6.  Perfect merohedral twinning combined with noncrystallographic symmetry potentially causes the failure of molecular replacement with low-homology search models for the flavin-dependent halogenase HalX from Xanthomonas campestris.

Authors:  Maren Buss; Christina Geerds; Thomas Patschkowski; Karsten Niehaus; Hartmut H Niemann
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2018-05-18       Impact factor: 1.056

7.  Total Enzyme Syntheses of Napyradiomycins A1 and B1.

Authors:  Shaun M K McKinnie; Zachary D Miles; Peter A Jordan; Takayoshi Awakawa; Henry P Pepper; Lauren A M Murray; Jonathan H George; Bradley S Moore
Journal:  J Am Chem Soc       Date:  2018-12-14       Impact factor: 15.419

8.  Determining the Inherent Selectivity for Carbon Radical Hydroxylation versus Halogenation with FeIII(OH)(X) Complexes: Relevance to the Rebound Step in Non-heme Iron Halogenases.

Authors:  Vishal Yadav; Rodolfo J Rodriguez; Maxime A Siegler; David P Goldberg
Journal:  J Am Chem Soc       Date:  2020-04-13       Impact factor: 15.419

Review 9.  Synthetic biology enabling access to designer polyketides.

Authors:  Alexandra A Malico; Lindsay Nichols; Gavin J Williams
Journal:  Curr Opin Chem Biol       Date:  2020-08-04       Impact factor: 8.822

Review 10.  Understanding and Improving the Activity of Flavin-Dependent Halogenases via Random and Targeted Mutagenesis.

Authors:  Mary C Andorfer; Jared C Lewis
Journal:  Annu Rev Biochem       Date:  2018-03-28       Impact factor: 23.643

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