Small molecules from the human microbiota

被引:601
作者
Donia, Mohamed S.
Fischbach, Michael A.
机构
[1] Department of Molecular Biology, Princeton University, Princeton, 08544, NJ
[2] Department of Bioengineering and Therapeutic Sciences, California Institute for Quantitative Biosciences, University of California, San Francisco, 94158, CA
关键词
FRAGILIS CAPSULAR POLYSACCHARIDE; NONRIBOSOMAL PEPTIDE SYNTHETASE; LANTIBIOTIC SALIVARICIN-A; STAPHYLOCOCCUS-AUREUS; NATURAL-PRODUCTS; MYCOBACTERIUM-ULCERANS; GENE-CLUSTER; SIDEROPHORE BIOSYNTHESIS; STREPTOCOCCUS-MUTANS; SECONDARY METABOLISM;
D O I
10.1126/science.1254766
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
Developments in the use of genomics to guide natural product discovery and a recent emphasis on understanding the molecular mechanisms of microbiota-host interactions have converged on the discovery of small molecules from the human microbiome. Here, we review what is known about small molecules produced by the human microbiota. Numerous molecules representing each of the major metabolite classes have been found that have a variety of biological activities, including immune modulation and antibiosis. We discuss technologies that will affect how microbiota-derived molecules are discovered in the future and consider the challenges inherent in finding specific molecules that are critical for driving microbe-host and microbe-microbe interactions and understanding their biological relevance.
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页数:11
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