MbtH homology codes to identify gifted microbes for genome mining

被引:24
作者
Baltz, Richard H. [1 ]
机构
[1] CognoGen Biotechnol Consulting, Sarasota, FL 34238 USA
关键词
Actinomycetes; Genome mining; Gifted microbes; Glycopeptide; Lipopeptide; MbtH; Mixed PKS-NRPS; NRPS; Streptomyces; BIOSYNTHETIC GENE-CLUSTER; NONRIBOSOMAL PEPTIDE SYNTHETASES; MOLECULAR-CLONING; HETEROLOGOUS EXPRESSION; SECONDARY METABOLITES; ADENYLATION DOMAIN; MASS-SPECTROMETRY; SEQUENCE-ANALYSIS; BLEOMYCIN FAMILY; NATURAL-PRODUCTS;
D O I
10.1007/s10295-013-1360-9
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Advances in DNA sequencing technologies have made it possible to sequence large numbers of microbial genomes rapidly and inexpensively. In recent years, genome sequencing initiatives have demonstrated that actinomycetes with large genomes generally have the genetic potential to produce many secondary metabolites, most of which remain cryptic. Since the numbers of new and novel pathways vary considerably among actinomycetes, and the correct assembly of secondary metabolite pathways containing type I polyketide synthase or nonribosomal peptide synthetase (NRPS) genes is costly and time consuming, it would be advantageous to have simple genetic predictors for the number and potential novelty of secondary metabolite pathways in targeted microorganisms. For secondary metabolite pathways that utilize NRPS mechanisms, the small chaperone-like proteins related to MbtH encoded by Mycobacterium tuberculosis offer unique probes or beacons to identify gifted microbes encoding large numbers of diverse NRPS pathways because of their unique function(s) and small size. The small size of the mbtH-homolog genes makes surveying large numbers of genomes straight-forward with less than ten-fold sequencing coverage. Multiple MbtH orthologs and paralogs have been coupled to generate a 24-mer multiprobe to assign numerical codes to individual MbtH homologs by BLASTp analysis. This multiprobe can be used to identify gifted microbes encoding new and novel secondary metabolites for further focused exploration by extensive DNA sequencing, pathway assembly and annotation, and expression studies in homologous or heterologous hosts.
引用
收藏
页码:357 / 369
页数:13
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