Recent advances in combinatorial biosynthesis for drug discovery

Huihua Sun,1,* Zihe Liu,1,* Huimin Zhao,1,2 Ee Lui Ang1 1Metabolic Engineering Research Laboratory, Institute of Chemical and Engineering Sciences, Agency for Science, Technology and Research, Singapore; 2Department of Chemical and Biomolecular Engineering, University of Illinois at Urban...

Full description

Bibliographic Details
Main Authors: Sun H, Liu Z, Zhao H, Ang EL
Format: Article
Language:English
Published: Dove Medical Press 2015-02-01
Series:Drug Design, Development and Therapy
Online Access:http://www.dovepress.com/recent-advances-in-combinatorial-biosynthesis-fornbspdrug-discovery-peer-reviewed-article-DDDT
id doaj-0f6300f0e3464b448eea27a75e2ce323
record_format Article
spelling doaj-0f6300f0e3464b448eea27a75e2ce3232020-11-24T23:09:36ZengDove Medical PressDrug Design, Development and Therapy1177-88812015-02-012015default82383320412Recent advances in combinatorial biosynthesis for drug discoverySun HLiu ZZhao HAng EL Huihua Sun,1,* Zihe Liu,1,* Huimin Zhao,1,2 Ee Lui Ang1 1Metabolic Engineering Research Laboratory, Institute of Chemical and Engineering Sciences, Agency for Science, Technology and Research, Singapore; 2Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA *These authors contributed equally to this work Abstract: Because of extraordinary structural diversity and broad biological activities, natural products have played a significant role in drug discovery. These therapeutically important secondary metabolites are assembled and modified by dedicated biosynthetic pathways in their host living organisms. Traditionally, chemists have attempted to synthesize natural product analogs that are important sources of new drugs. However, the extraordinary structural complexity of natural products sometimes makes it challenging for traditional chemical synthesis, which usually involves multiple steps, harsh conditions, toxic organic solvents, and byproduct wastes. In contrast, combinatorial biosynthesis exploits substrate promiscuity and employs engineered enzymes and pathways to produce novel “unnatural” natural products, substantially expanding the structural diversity of natural products with potential pharmaceutical value. Thus, combinatorial biosynthesis provides an environmentally friendly way to produce natural product analogs. Efficient expression of the combinatorial biosynthetic pathway in genetically tractable heterologous hosts can increase the titer of the compound, eventually resulting in less expensive drugs. In this review, we will discuss three major strategies for combinatorial biosynthesis: 1) precursor-directed biosynthesis; 2) enzyme-level modification, which includes swapping of the entire domains, modules and subunits, site-specific mutagenesis, and directed evolution; 3) pathway-level recombination. Recent examples of combinatorial biosynthesis employing these strategies will also be highlighted in this review. Keywords: combinatorial biosynthesis, drug discovery, natural products, polyketide synthases, nonribosomal peptide synthetases, biosynthetic pathwayshttp://www.dovepress.com/recent-advances-in-combinatorial-biosynthesis-fornbspdrug-discovery-peer-reviewed-article-DDDT
collection DOAJ
language English
format Article
sources DOAJ
author Sun H
Liu Z
Zhao H
Ang EL
spellingShingle Sun H
Liu Z
Zhao H
Ang EL
Recent advances in combinatorial biosynthesis for drug discovery
Drug Design, Development and Therapy
author_facet Sun H
Liu Z
Zhao H
Ang EL
author_sort Sun H
title Recent advances in combinatorial biosynthesis for drug discovery
title_short Recent advances in combinatorial biosynthesis for drug discovery
title_full Recent advances in combinatorial biosynthesis for drug discovery
title_fullStr Recent advances in combinatorial biosynthesis for drug discovery
title_full_unstemmed Recent advances in combinatorial biosynthesis for drug discovery
title_sort recent advances in combinatorial biosynthesis for drug discovery
publisher Dove Medical Press
series Drug Design, Development and Therapy
issn 1177-8881
publishDate 2015-02-01
description Huihua Sun,1,* Zihe Liu,1,* Huimin Zhao,1,2 Ee Lui Ang1 1Metabolic Engineering Research Laboratory, Institute of Chemical and Engineering Sciences, Agency for Science, Technology and Research, Singapore; 2Department of Chemical and Biomolecular Engineering, University of Illinois at Urbana-Champaign, Urbana, IL, USA *These authors contributed equally to this work Abstract: Because of extraordinary structural diversity and broad biological activities, natural products have played a significant role in drug discovery. These therapeutically important secondary metabolites are assembled and modified by dedicated biosynthetic pathways in their host living organisms. Traditionally, chemists have attempted to synthesize natural product analogs that are important sources of new drugs. However, the extraordinary structural complexity of natural products sometimes makes it challenging for traditional chemical synthesis, which usually involves multiple steps, harsh conditions, toxic organic solvents, and byproduct wastes. In contrast, combinatorial biosynthesis exploits substrate promiscuity and employs engineered enzymes and pathways to produce novel “unnatural” natural products, substantially expanding the structural diversity of natural products with potential pharmaceutical value. Thus, combinatorial biosynthesis provides an environmentally friendly way to produce natural product analogs. Efficient expression of the combinatorial biosynthetic pathway in genetically tractable heterologous hosts can increase the titer of the compound, eventually resulting in less expensive drugs. In this review, we will discuss three major strategies for combinatorial biosynthesis: 1) precursor-directed biosynthesis; 2) enzyme-level modification, which includes swapping of the entire domains, modules and subunits, site-specific mutagenesis, and directed evolution; 3) pathway-level recombination. Recent examples of combinatorial biosynthesis employing these strategies will also be highlighted in this review. Keywords: combinatorial biosynthesis, drug discovery, natural products, polyketide synthases, nonribosomal peptide synthetases, biosynthetic pathways
url http://www.dovepress.com/recent-advances-in-combinatorial-biosynthesis-fornbspdrug-discovery-peer-reviewed-article-DDDT
work_keys_str_mv AT sunh recentadvancesincombinatorialbiosynthesisfornbspdrugdiscovery
AT liuz recentadvancesincombinatorialbiosynthesisfornbspdrugdiscovery
AT zhaoh recentadvancesincombinatorialbiosynthesisfornbspdrugdiscovery
AT angel recentadvancesincombinatorialbiosynthesisfornbspdrugdiscovery
_version_ 1725610242204499968