Literature DB >> 24197465

MbtH homology codes to identify gifted microbes for genome mining.

Richard H Baltz1.   

Abstract

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.

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Year:  2013        PMID: 24197465     DOI: 10.1007/s10295-013-1360-9

Source DB:  PubMed          Journal:  J Ind Microbiol Biotechnol        ISSN: 1367-5435            Impact factor:   3.346


  87 in total

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Review 4.  Genomic basis for natural product biosynthetic diversity in the actinomycetes.

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Authors:  Elizabeth A Felnagle; Angela M Podevels; John J Barkei; Michael G Thomas
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7.  Activation of the pacidamycin PacL adenylation domain by MbtH-like proteins.

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10.  Deciphering tuberactinomycin biosynthesis: isolation, sequencing, and annotation of the viomycin biosynthetic gene cluster.

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  9 in total

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Review 4.  Non-ribosomal peptide synthetases: Identifying the cryptic gene clusters and decoding the natural product.

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5.  An Activator of an Adenylation Domain Revealed by Activity but Not Sequence Homology.

Authors:  Shalini Saha; Steven E Rokita
Journal:  Chembiochem       Date:  2016-08-25       Impact factor: 3.164

Review 6.  Structural insight into the necessary conformational changes of modular nonribosomal peptide synthetases.

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Journal:  Curr Opin Chem Biol       Date:  2016-09-25       Impact factor: 8.822

7.  Genome Analysis of the Fruiting Body-Forming Myxobacterium Chondromyces crocatus Reveals High Potential for Natural Product Biosynthesis.

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Review 8.  Microbial genome mining for accelerated natural products discovery: is a renaissance in the making?

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9.  Genome mining for drug discovery: cyclic lipopeptides related to daptomycin.

Authors:  Richard H Baltz
Journal:  J Ind Microbiol Biotechnol       Date:  2021-06-04       Impact factor: 4.258

  9 in total

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