Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid

Because of its small size, Gram-negative Sphingomonas paucimobilis can pose a risk of nosocomial infection. We report the complete circular genome sequence of S. paucimobilis strain Kira, which was isolated from retinoic acid-supplemented SH-SY5Y human cell cultures, to be 3,917,410 bp (G+C content,...

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Autores principales: Nishimura, Kohei, Ikarashi, Mirai, Yasuda, Yuji, Sato, Mayu, Cano Guerrero, Marta, Galipon, Josephine, Arakawa, Kazuharu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2021
Materias:
Genome Sequences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883840/
https://www.ncbi.nlm.nih.gov/pubmed/33574107
http://dx.doi.org/10.1128/MRA.01156-20
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author Nishimura, Kohei
Ikarashi, Mirai
Yasuda, Yuji
Sato, Mayu
Cano Guerrero, Marta
Galipon, Josephine
Arakawa, Kazuharu
author_facet Nishimura, Kohei
Ikarashi, Mirai
Yasuda, Yuji
Sato, Mayu
Cano Guerrero, Marta
Galipon, Josephine
Arakawa, Kazuharu
author_sort Nishimura, Kohei
collection PubMed
description Because of its small size, Gram-negative Sphingomonas paucimobilis can pose a risk of nosocomial infection. We report the complete circular genome sequence of S. paucimobilis strain Kira, which was isolated from retinoic acid-supplemented SH-SY5Y human cell cultures, to be 3,917,410 bp (G+C content, 65.7%; 3,672 protein-coding sequences), with two plasmids (79,575 bp and 44,333 bp).
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spelling pubmed-78838402021-02-19 Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid Nishimura, Kohei Ikarashi, Mirai Yasuda, Yuji Sato, Mayu Cano Guerrero, Marta Galipon, Josephine Arakawa, Kazuharu Microbiol Resour Announc Genome Sequences Because of its small size, Gram-negative Sphingomonas paucimobilis can pose a risk of nosocomial infection. We report the complete circular genome sequence of S. paucimobilis strain Kira, which was isolated from retinoic acid-supplemented SH-SY5Y human cell cultures, to be 3,917,410 bp (G+C content, 65.7%; 3,672 protein-coding sequences), with two plasmids (79,575 bp and 44,333 bp). American Society for Microbiology 2021-02-11 /pmc/articles/PMC7883840/ /pubmed/33574107 http://dx.doi.org/10.1128/MRA.01156-20 Text en Copyright © 2021 Nishimura 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
Nishimura, Kohei
Ikarashi, Mirai
Yasuda, Yuji
Sato, Mayu
Cano Guerrero, Marta
Galipon, Josephine
Arakawa, Kazuharu
Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid
title Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid
title_full Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid
title_fullStr Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid
title_full_unstemmed Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid
title_short Complete Genome Sequence of Sphingomonas paucimobilis Strain Kira, Isolated from Human Neuroblastoma SH-SY5Y Cell Cultures Supplemented with Retinoic Acid
title_sort complete genome sequence of sphingomonas paucimobilis strain kira, isolated from human neuroblastoma sh-sy5y cell cultures supplemented with retinoic acid
topic Genome Sequences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7883840/
https://www.ncbi.nlm.nih.gov/pubmed/33574107
http://dx.doi.org/10.1128/MRA.01156-20
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