Targeted metagenomics as a tool to tap into marine natural product diversity for the discovery and production of drug candidates

被引:71
|
作者
Trindade, Marla [1 ]
van Zyl, Leonardo Joaquim [1 ]
Navarro-Fernandez, Jose [1 ,2 ]
Elrazak, Ahmed Abd [1 ,3 ]
机构
[1] Univ Western Cape, Inst Microbial Biotechnol & Metagen, ZA-7535 Bellville, South Africa
[2] Univ Murcia, IMIB Arrixaca, Serv Hematol & Oncol Med, Ctr Reg Hemodonac, Murcia, Spain
[3] Mansoura Univ, Fac Sci, Dept Bot, Mansoura, Egypt
基金
新加坡国家研究基金会;
关键词
uncultured microbes; metagenomics; symbionts; marine natural products; drug discovery; functional screening; POLYKETIDE SYNTHASE GENE; UNCULTIVATED BACTERIAL SYMBIONT; HETEROLOGOUS EXPRESSION; SECONDARY METABOLITES; NONRIBOSOMAL PEPTIDES; MICROBIAL DIVERSITY; ANTITUMOR COMPOUNDS; ENDOBUGULA SERTULA; MASS-SPECTROMETRY; ESCHERICHIA-COLI;
D O I
10.3389/fmicb.2015.00890
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Microbial natural products exhibit immense structural diversity and complexity and have captured the attention of researchers for several decades. They have been explored for a wide spectrum of applications, most noteworthy being their prominent role in medicine, and their versatility expands to application as drugs for many diseases. Accessing unexplored environments harboring unique microorganisms is expected to yield novel bioactive metabolites with distinguishing functionalities, which can be supplied to the starved pharmaceutical market. For this purpose the oceans have turned out to be an attractive and productive field. Owing to the enormous biodiversity of marine microorganisms, as well as the growing evidence that many metabolites previously isolated from marine invertebrates and algae are actually produced by their associated bacteria, the interest in marine microorganisms has intensified. Since the majority of the microorganisms are uncultured, metagenomic tools are required to exploit the untapped biochemistry. However, after years of employing metagenomics for marine drug discovery, new drugs are vastly under-represented. While a plethora of natural product biosynthetic genes and clusters are reported, only a minor number of potential therapeutic compounds have resulted through functional metagenomic screening. This review explores specific obstacles that have led to the low success rate. In addition to the typical problems encountered with traditional functional metagenomic-based screens for novel biocatalysts, there are enormous limitations which are particular to drug-like metabolites. We also present how targeted and function-guided strategies, employing modern, and multi-disciplinary approaches have yielded some of the most exciting discoveries attributed to uncultured marine bacteria. These discoveries set the stage for progressing the production of drug candidates from uncultured bacteria for pre-clinical and clinical development.
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页数:14
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