Bioengineering natural product biosynthetic pathways for therapeutic applications

被引:25
|
作者
Wu, Ming-Cheng [1 ,2 ]
Law, Brian [1 ,2 ]
Wilkinson, Barrie [3 ]
Micklefield, Jason [1 ,2 ]
机构
[1] Univ Manchester, Sch Chem, Manchester M1 7DN, Lancs, England
[2] Univ Manchester, Manchester Interdisciplinary Bioctr, Manchester M1 7DN, Lancs, England
[3] Biot Technol Ltd, Cambridge CB21 6AD, England
基金
英国生物技术与生命科学研究理事会;
关键词
NONRIBOSOMAL PEPTIDE SYNTHETASE; STREPTOMYCES-COELICOLOR; ANTIBIOTIC PRODUCTION; HETEROLOGOUS EXPRESSION; SECONDARY METABOLITES; DIRECTED EVOLUTION; DRUG DISCOVERY; CHEMICAL SPACE; GENE CLUSTERS; DERIVATIVES;
D O I
10.1016/j.copbio.2012.03.008
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With the advent of next-generation DNA sequencing technologies, the number of microbial genome sequences has increased dramatically, revealing a vast array of new biosynthetic gene clusters. Genomics data provide a tremendous opportunity to discover new natural products, and also to guide the bioengineering of new and existing natural product scaffolds for therapeutic applications. Notably, it is apparent that the vast majority of biosynthetic gene clusters are either silent or produce very low quantities of the corresponding natural products. It is imperative therefore to devise methods for activating unproductive biosynthetic pathways to provide the quantities of natural products needed for further development. Moreover, on the basis of our expanding mechanistic and structural knowledge of biosynthetic assembly-line enzymes, new strategies for re-programming biosynthetic pathways have emerged, resulting in focused libraries of modified products with potentially improved biological properties. In this review we will focus on the latest bioengineering approaches that have been utilised to optimise yields and increase the structural diversity of natural product scaffolds for future clinical applications.
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页码:931 / 940
页数:10
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