Using natural products for drug discovery: the impact of the genomics era

被引:68
作者
Zhang, Mingzi M. [1 ]
Qiao, Yuan [1 ]
Ang, Ee Lui [1 ]
Zhao, Huimin [1 ,2 ]
机构
[1] ASTAR, Sci & Engn Inst, Metab Engn Res Lab, Singapore, Singapore
[2] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
Genome mining; biosynthetic gene clusters; secondary metabolites; metagenomics; bioinformatics; BIOSYNTHETIC GENE CLUSTERS; STREPTOMYCES-COELICOLOR A3(2); MODULAR POLYKETIDE SYNTHASES; ENVIRONMENTAL DNA LIBRARIES; MASS-SPECTROMETRY; HETEROLOGOUS EXPRESSION; FUNCTIONAL METAGENOMICS; SECONDARY METABOLOME; ASPERGILLUS-NIDULANS; NONRIBOSOMAL PEPTIDES;
D O I
10.1080/17460441.2017.1303478
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Evolutionarily selected over billions of years for their interactions with biomolecules, natural products have been and continue to be a major source of pharmaceuticals. In the 1990s, pharmaceutical companies scaled down their natural product discovery programs in favor of synthetic chemical libraries due to major challenges such as high rediscovery rates, challenging isolation, and low production titers. Propelled by advances in DNA sequencing and synthetic biology technologies, insights into microbial secondary metabolism provided have inspired a number of strategies to address these challenges. Areas covered: This review highlights the importance of genomics and metagenomics in natural product discovery, and provides an overview of the technical and conceptual advances that offer unprecedented access to molecules encoded by biosynthetic gene clusters. Expert opinion: Genomics and metagenomics revealed nature's remarkable biosynthetic potential and her vast chemical inventory that we can now prioritize and systematically mine for novel chemical scaffolds with desirable bioactivities. Coupled with synthetic biology and genome engineering technologies, significant progress has been made in identifying and predicting the chemical output of biosynthetic gene clusters, as well as in optimizing cluster expression in native and heterologous host systems for the production of pharmaceutically relevant metabolites and their derivatives.
引用
收藏
页码:475 / 487
页数:13
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