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The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification

Strain ATCC 31962 was formerly taxonomically classified as Empedobacter haloabium and reported to be the producer of the lipopeptide antibiotic empedopeptin. Here, we report the draft genome sequence of ATCC 31962, which encodes regions that suggest a distinct biosynthetic capacity and suggests its...

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Autores principales: Miess, Henrike, Arlt, Patricia, Apel, Alexander Kristian, Weber, Tilmann, Nieselt, Kay, Hanssen, Friederike, Czemmel, Stefan, Nahnsen, Sven, Gross, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838624/
https://www.ncbi.nlm.nih.gov/pubmed/31699766
http://dx.doi.org/10.1128/MRA.01120-19
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author Miess, Henrike
Arlt, Patricia
Apel, Alexander Kristian
Weber, Tilmann
Nieselt, Kay
Hanssen, Friederike
Czemmel, Stefan
Nahnsen, Sven
Gross, Harald
author_facet Miess, Henrike
Arlt, Patricia
Apel, Alexander Kristian
Weber, Tilmann
Nieselt, Kay
Hanssen, Friederike
Czemmel, Stefan
Nahnsen, Sven
Gross, Harald
author_sort Miess, Henrike
collection PubMed
description Strain ATCC 31962 was formerly taxonomically classified as Empedobacter haloabium and reported to be the producer of the lipopeptide antibiotic empedopeptin. Here, we report the draft genome sequence of ATCC 31962, which encodes regions that suggest a distinct biosynthetic capacity and suggests its taxonomic reclassification.
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spelling pubmed-68386242019-11-15 The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification Miess, Henrike Arlt, Patricia Apel, Alexander Kristian Weber, Tilmann Nieselt, Kay Hanssen, Friederike Czemmel, Stefan Nahnsen, Sven Gross, Harald Microbiol Resour Announc Genome Sequences Strain ATCC 31962 was formerly taxonomically classified as Empedobacter haloabium and reported to be the producer of the lipopeptide antibiotic empedopeptin. Here, we report the draft genome sequence of ATCC 31962, which encodes regions that suggest a distinct biosynthetic capacity and suggests its taxonomic reclassification. American Society for Microbiology 2019-11-07 /pmc/articles/PMC6838624/ /pubmed/31699766 http://dx.doi.org/10.1128/MRA.01120-19 Text en Copyright © 2019 Miess et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Genome Sequences
Miess, Henrike
Arlt, Patricia
Apel, Alexander Kristian
Weber, Tilmann
Nieselt, Kay
Hanssen, Friederike
Czemmel, Stefan
Nahnsen, Sven
Gross, Harald
The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification
title The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification
title_full The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification
title_fullStr The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification
title_full_unstemmed The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification
title_short The Draft Whole-Genome Sequence of the Antibiotic Producer Empedobacter haloabium ATCC 31962 Provides Indications for Its Taxonomic Reclassification
title_sort draft whole-genome sequence of the antibiotic producer empedobacter haloabium atcc 31962 provides indications for its taxonomic reclassification
topic Genome Sequences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6838624/
https://www.ncbi.nlm.nih.gov/pubmed/31699766
http://dx.doi.org/10.1128/MRA.01120-19
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