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Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1

Bacteria have developed various motility mechanisms to adapt to a variety of solid surfaces. A rhizosphere isolate, Paenibacillus sp. NAIST15-1, exhibited unusual motility behavior. When spotted onto 1.5% agar media, Paenibacillus sp. formed many colonies, each of which moved around actively at a sp...

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Detalles Bibliográficos
Autores principales: Kobayashi, Kazuo, Kanesaki, Yu, Yoshikawa, Hirofumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072692/
https://www.ncbi.nlm.nih.gov/pubmed/27764113
http://dx.doi.org/10.1371/journal.pgen.1006387
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author Kobayashi, Kazuo
Kanesaki, Yu
Yoshikawa, Hirofumi
author_facet Kobayashi, Kazuo
Kanesaki, Yu
Yoshikawa, Hirofumi
author_sort Kobayashi, Kazuo
collection PubMed
description Bacteria have developed various motility mechanisms to adapt to a variety of solid surfaces. A rhizosphere isolate, Paenibacillus sp. NAIST15-1, exhibited unusual motility behavior. When spotted onto 1.5% agar media, Paenibacillus sp. formed many colonies, each of which moved around actively at a speed of 3.6 μm/sec. As their density increased, each moving colony began to spiral, finally forming a static round colony. Despite its unusual motility behavior, draft genome sequencing revealed that both the composition and organization of flagellar genes in Paenibacillus sp. were very similar to those in Bacillus subtilis. Disruption of flagellar genes and flagellar stator operons resulted in loss of motility. Paenibacillus sp. showed increased transcription of flagellar genes and hyperflagellation on hard agar media. Thus, increased flagella and their rotation drive Paenibacillus sp. motility. We also identified a large extracellular protein, CmoA, which is conserved only in several Paenibacillus and related species. A cmoA mutant could neither form moving colonies nor move on hard agar media; however, motility was restored by exogenous CmoA. CmoA was located around cells and enveloped cell clusters. Comparison of cellular behavior between the wild type and cmoA mutant indicated that extracellular CmoA is involved in drawing water out of agar media and/or smoothing the cell surface interface. This function of CmoA probably enables Paenibacillus sp. to move on hard agar media.
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spelling pubmed-50726922016-10-27 Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1 Kobayashi, Kazuo Kanesaki, Yu Yoshikawa, Hirofumi PLoS Genet Research Article Bacteria have developed various motility mechanisms to adapt to a variety of solid surfaces. A rhizosphere isolate, Paenibacillus sp. NAIST15-1, exhibited unusual motility behavior. When spotted onto 1.5% agar media, Paenibacillus sp. formed many colonies, each of which moved around actively at a speed of 3.6 μm/sec. As their density increased, each moving colony began to spiral, finally forming a static round colony. Despite its unusual motility behavior, draft genome sequencing revealed that both the composition and organization of flagellar genes in Paenibacillus sp. were very similar to those in Bacillus subtilis. Disruption of flagellar genes and flagellar stator operons resulted in loss of motility. Paenibacillus sp. showed increased transcription of flagellar genes and hyperflagellation on hard agar media. Thus, increased flagella and their rotation drive Paenibacillus sp. motility. We also identified a large extracellular protein, CmoA, which is conserved only in several Paenibacillus and related species. A cmoA mutant could neither form moving colonies nor move on hard agar media; however, motility was restored by exogenous CmoA. CmoA was located around cells and enveloped cell clusters. Comparison of cellular behavior between the wild type and cmoA mutant indicated that extracellular CmoA is involved in drawing water out of agar media and/or smoothing the cell surface interface. This function of CmoA probably enables Paenibacillus sp. to move on hard agar media. Public Library of Science 2016-10-20 /pmc/articles/PMC5072692/ /pubmed/27764113 http://dx.doi.org/10.1371/journal.pgen.1006387 Text en © 2016 Kobayashi et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Kobayashi, Kazuo
Kanesaki, Yu
Yoshikawa, Hirofumi
Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1
title Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1
title_full Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1
title_fullStr Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1
title_full_unstemmed Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1
title_short Genetic Analysis of Collective Motility of Paenibacillus sp. NAIST15-1
title_sort genetic analysis of collective motility of paenibacillus sp. naist15-1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5072692/
https://www.ncbi.nlm.nih.gov/pubmed/27764113
http://dx.doi.org/10.1371/journal.pgen.1006387
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