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1.
Nucleic Acids Res ; 43(W1): W237-43, 2015 Jul 01.
Artículo en Inglés | MEDLINE | ID: mdl-25948579

RESUMEN

Microbial secondary metabolism constitutes a rich source of antibiotics, chemotherapeutics, insecticides and other high-value chemicals. Genome mining of gene clusters that encode the biosynthetic pathways for these metabolites has become a key methodology for novel compound discovery. In 2011, we introduced antiSMASH, a web server and stand-alone tool for the automatic genomic identification and analysis of biosynthetic gene clusters, available at http://antismash.secondarymetabolites.org. Here, we present version 3.0 of antiSMASH, which has undergone major improvements. A full integration of the recently published ClusterFinder algorithm now allows using this probabilistic algorithm to detect putative gene clusters of unknown types. Also, a new dereplication variant of the ClusterBlast module now identifies similarities of identified clusters to any of 1172 clusters with known end products. At the enzyme level, active sites of key biosynthetic enzymes are now pinpointed through a curated pattern-matching procedure and Enzyme Commission numbers are assigned to functionally classify all enzyme-coding genes. Additionally, chemical structure prediction has been improved by incorporating polyketide reduction states. Finally, in order for users to be able to organize and analyze multiple antiSMASH outputs in a private setting, a new XML output module allows offline editing of antiSMASH annotations within the Geneious software.


Asunto(s)
Bacterias/genética , Hongos/genética , Metabolismo Secundario/genética , Programas Informáticos , Algoritmos , Bacterias/metabolismo , Vías Biosintéticas/genética , Dominio Catalítico , Minería de Datos , Enzimas/química , Hongos/metabolismo , Genómica/métodos , Internet , Policétidos
2.
Nat Chem Biol ; 11(9): 625-31, 2015 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-26284661
3.
Nat Commun ; 9(1): 803, 2018 02 23.
Artículo en Inglés | MEDLINE | ID: mdl-29476047

RESUMEN

Some bacterial clades are important sources of novel bioactive natural products. Estimating the magnitude of chemical diversity available from such a resource is complicated by issues including cultivability, isolation bias and limited analytical data sets. Here we perform a systematic metabolite survey of ~2300 bacterial strains of the order Myxococcales, a well-established source of natural products, using mass spectrometry. Our analysis encompasses both known and previously unidentified metabolites detected under laboratory cultivation conditions, thereby enabling large-scale comparison of production profiles in relation to myxobacterial taxonomy. We find a correlation between taxonomic distance and the production of distinct secondary metabolite families, further supporting the idea that the chances of discovering novel metabolites are greater by examining strains from new genera rather than additional representatives within the same genus. In addition, we report the discovery and structure elucidation of rowithocin, a myxobacterial secondary metabolite featuring an uncommon phosphorylated polyketide scaffold.


Asunto(s)
Productos Biológicos/química , Myxococcales/química , Productos Biológicos/metabolismo , Evaluación Preclínica de Medicamentos , Espectrometría de Masas , Myxococcales/clasificación , Myxococcales/metabolismo , Filogenia
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