Polyketide and nonribosomal peptide retro-biosynthesis and global gene cluster matching

被引:99
作者
Dejong, Chris A. [1 ,2 ]
Chen, Gregory M. [1 ,2 ]
Li, Haoxin [1 ,2 ]
Johnston, Chad W. [1 ,2 ]
Edwards, Mclean R. [1 ,2 ]
Rees, Philip N. [1 ,2 ]
Skinnider, Michael A. [1 ,2 ]
Webster, Andrew L. H. [1 ,2 ]
Magarvey, Nathan A. [1 ,2 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON, Canada
[2] McMaster Univ, Dept Chem & Chem Biol, MG DeGroote Inst Infect Dis Res, Hamilton, ON, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
NATURAL-PRODUCT DISCOVERY; STRUCTURE ELUCIDATION; ANTIBIOTICS; PREDICTION; GENOMICS; SEQUENCE; MINIMUM; CULTURE; SEARCH; LOGIC;
D O I
10.1038/nchembio.2188
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polyketides (PKs) and nonribosomal peptides (NRPs) are profoundly important natural products, forming the foundations of many therapeutic regimes. Decades of research have revealed over 11,000 PK and NRP structures, and genome sequencing is uncovering new PK and NRP gene clusters at an unprecedented rate. However, only similar to 10% of PK and NRPs are currently associated with gene clusters, and it is unclear how many of these orphan gene clusters encode previously isolated molecules. Therefore, to efficiently guide the discovery of new molecules, we must first systematically de-orphan emergent gene clusters from genomes. Here we provide to our knowledge the first comprehensive retro-biosynthetic program, generalized retro-biosynthetic assembly prediction engine (GRAPE), for PK and NRP families and introduce a computational pipeline, global alignment for natural products cheminformatics (GARLIC), to uncover how observed biosynthetic gene clusters relate to known molecules, leading to the identification of gene clusters that encode new molecules.
引用
收藏
页码:1007 / +
页数:11
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