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Structure and Biosynthesis of the Antibiotic Bottromycin D

[Image: see text] Drug resistant infectious diseases are quickly becoming a global health crisis. While Streptomyces spp. have been a major source of antibiotics over the past 50 years, efficient methods are needed to identify new antibiotics and greatly improve the rate of discovery. LCMS-based met...

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Autores principales: Hou, Yanpeng, Tianero, Ma. Diarey B., Kwan, Jason C., Wyche, Thomas P., Michel, Cole R., Ellis, Gregory A., Vazquez-Rivera, Emmanuel, Braun, Doug R., Rose, Warren E., Schmidt, Eric W., Bugni, Tim S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2012
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466018/
https://www.ncbi.nlm.nih.gov/pubmed/22984777
http://dx.doi.org/10.1021/ol3022758
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author Hou, Yanpeng
Tianero, Ma. Diarey B.
Kwan, Jason C.
Wyche, Thomas P.
Michel, Cole R.
Ellis, Gregory A.
Vazquez-Rivera, Emmanuel
Braun, Doug R.
Rose, Warren E.
Schmidt, Eric W.
Bugni, Tim S.
author_facet Hou, Yanpeng
Tianero, Ma. Diarey B.
Kwan, Jason C.
Wyche, Thomas P.
Michel, Cole R.
Ellis, Gregory A.
Vazquez-Rivera, Emmanuel
Braun, Doug R.
Rose, Warren E.
Schmidt, Eric W.
Bugni, Tim S.
author_sort Hou, Yanpeng
collection PubMed
description [Image: see text] Drug resistant infectious diseases are quickly becoming a global health crisis. While Streptomyces spp. have been a major source of antibiotics over the past 50 years, efficient methods are needed to identify new antibiotics and greatly improve the rate of discovery. LCMS-based metabolomics were applied to analyze extracts of 50 Streptomyes spp. Using this methodology, we discovered bottromycin D and used whole genome sequencing to determine its biosynthesis by a ribosomal pathway.
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spelling pubmed-34660182012-10-08 Structure and Biosynthesis of the Antibiotic Bottromycin D Hou, Yanpeng Tianero, Ma. Diarey B. Kwan, Jason C. Wyche, Thomas P. Michel, Cole R. Ellis, Gregory A. Vazquez-Rivera, Emmanuel Braun, Doug R. Rose, Warren E. Schmidt, Eric W. Bugni, Tim S. Org Lett [Image: see text] Drug resistant infectious diseases are quickly becoming a global health crisis. While Streptomyces spp. have been a major source of antibiotics over the past 50 years, efficient methods are needed to identify new antibiotics and greatly improve the rate of discovery. LCMS-based metabolomics were applied to analyze extracts of 50 Streptomyes spp. Using this methodology, we discovered bottromycin D and used whole genome sequencing to determine its biosynthesis by a ribosomal pathway. American Chemical Society 2012-09-17 2012-10-05 /pmc/articles/PMC3466018/ /pubmed/22984777 http://dx.doi.org/10.1021/ol3022758 Text en Copyright © 2012 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Hou, Yanpeng
Tianero, Ma. Diarey B.
Kwan, Jason C.
Wyche, Thomas P.
Michel, Cole R.
Ellis, Gregory A.
Vazquez-Rivera, Emmanuel
Braun, Doug R.
Rose, Warren E.
Schmidt, Eric W.
Bugni, Tim S.
Structure and Biosynthesis of the Antibiotic Bottromycin D
title Structure and Biosynthesis of the Antibiotic Bottromycin D
title_full Structure and Biosynthesis of the Antibiotic Bottromycin D
title_fullStr Structure and Biosynthesis of the Antibiotic Bottromycin D
title_full_unstemmed Structure and Biosynthesis of the Antibiotic Bottromycin D
title_short Structure and Biosynthesis of the Antibiotic Bottromycin D
title_sort structure and biosynthesis of the antibiotic bottromycin d
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3466018/
https://www.ncbi.nlm.nih.gov/pubmed/22984777
http://dx.doi.org/10.1021/ol3022758
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