Isolation and characterization of Bacillus subtilis strain 1-L-29, an endophytic bacteria from Camellia oleifera with antimicrobial activity and efficient plant-root colonization
Endophytic bacteria, which are common in plant tissues, may help to control plant pathogens and enhance plant growth. Camellia oleifera, an oil-producing plant, is widely grown in warm, subtropical, hilly regions in China. However, C. oleifera is strongly negatively affected by C. oleifera anthracno...
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description | Endophytic bacteria, which are common in plant tissues, may help to control plant pathogens and enhance plant growth. Camellia oleifera, an oil-producing plant, is widely grown in warm, subtropical, hilly regions in China. However, C. oleifera is strongly negatively affected by C. oleifera anthracnose, which is caused by Colletetrichum fructicola. To find a suitable biocontrol agent for C. oleifera anthracnose, 41 endophytes were isolated from the stems, leaves, and roots of C. oleifera. Bacterial cultures were identified based on analyses of 16S rDNA sequences; most strains belonged to the genus Bacillus. The antagonistic effects of these strains on C. fructicola were tested in vitro. In total, 16 strains inhibited C. fructicola growth, with B. subtilis strain 1-L-29 being the most efficient. Strain 1-L-29 demonstrated antagonistic activity against C. siamense, C. asianum, Fusarium proliferatum, Agaricodochium camellia, and Pseudomonas syringae. In addition, this strain produced indole acetic acid, solubilized phosphate, grew on N-free media, and produced siderophores. To facilitate further microecological studies of this strain, a rifampicin-resistant, green fluorescent protein (GFP)-labeled strain, 1-L-29gfpr, was created using protoplast transformation. This plasmid had good segregational stability. Strain 1-L-29gfpr was re-introduced into C. oleifera and successfully colonized root, stem, and leaf tissues. This strain remained at a stable concentration in the root more than 20 d after inoculation. Fluorescence microscopic analysis showed that strain 1-L-29gfpr thoroughly colonized the root surfaces of C. fructicola as well as the root vascular tissues of Arabidopsis thaliana. |
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Camellia oleifera, an oil-producing plant, is widely grown in warm, subtropical, hilly regions in China. However, C. oleifera is strongly negatively affected by C. oleifera anthracnose, which is caused by Colletetrichum fructicola. To find a suitable biocontrol agent for C. oleifera anthracnose, 41 endophytes were isolated from the stems, leaves, and roots of C. oleifera. Bacterial cultures were identified based on analyses of 16S rDNA sequences; most strains belonged to the genus Bacillus. The antagonistic effects of these strains on C. fructicola were tested in vitro. In total, 16 strains inhibited C. fructicola growth, with B. subtilis strain 1-L-29 being the most efficient. Strain 1-L-29 demonstrated antagonistic activity against C. siamense, C. asianum, Fusarium proliferatum, Agaricodochium camellia, and Pseudomonas syringae. In addition, this strain produced indole acetic acid, solubilized phosphate, grew on N-free media, and produced siderophores. To facilitate further microecological studies of this strain, a rifampicin-resistant, green fluorescent protein (GFP)-labeled strain, 1-L-29gfpr, was created using protoplast transformation. This plasmid had good segregational stability. Strain 1-L-29gfpr was re-introduced into C. oleifera and successfully colonized root, stem, and leaf tissues. This strain remained at a stable concentration in the root more than 20 d after inoculation. Fluorescence microscopic analysis showed that strain 1-L-29gfpr thoroughly colonized the root surfaces of C. fructicola as well as the root vascular tissues of Arabidopsis thaliana.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0232096</identifier><identifier>PMID: 32339210</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Acetic acid ; Analysis ; Anthracnose ; Antimicrobial activity ; Arabidopsis ; Arabidopsis thaliana ; Bacteria ; Biological control ; Biological pest control ; Biology and Life Sciences ; Camellia oleifera ; Characterization ; Colonization ; Deoxyribonucleic acid ; DNA ; Education ; Endophytes ; Fluorescence ; Fluorescence microscopy ; Forestry ; Genetic transformation ; Glycerol ; Grasslands ; Green fluorescent protein ; Indoleacetic acid ; Inoculation ; Isolation ; Laboratories ; Leaves ; Li, Yang ; Medicine and Health Sciences ; Methods ; Microorganisms ; Microscopic analysis ; Microscopy ; Organic acids ; Pathogenic microorganisms ; Pathogens ; Pesticides ; Phosphates ; Plant growth ; Plant roots ; Plant tissues ; Research and Analysis Methods ; Rifampin ; rRNA 16S ; Siderophores ; Stems ; Strain analysis ; Strains (organisms) ; Vascular tissue</subject><ispartof>PloS one, 2020-04, Vol.15 (4), p.e0232096-e0232096</ispartof><rights>COPYRIGHT 2020 Public Library of Science</rights><rights>2020 Xu et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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Camellia oleifera, an oil-producing plant, is widely grown in warm, subtropical, hilly regions in China. However, C. oleifera is strongly negatively affected by C. oleifera anthracnose, which is caused by Colletetrichum fructicola. To find a suitable biocontrol agent for C. oleifera anthracnose, 41 endophytes were isolated from the stems, leaves, and roots of C. oleifera. Bacterial cultures were identified based on analyses of 16S rDNA sequences; most strains belonged to the genus Bacillus. The antagonistic effects of these strains on C. fructicola were tested in vitro. In total, 16 strains inhibited C. fructicola growth, with B. subtilis strain 1-L-29 being the most efficient. Strain 1-L-29 demonstrated antagonistic activity against C. siamense, C. asianum, Fusarium proliferatum, Agaricodochium camellia, and Pseudomonas syringae. In addition, this strain produced indole acetic acid, solubilized phosphate, grew on N-free media, and produced siderophores. To facilitate further microecological studies of this strain, a rifampicin-resistant, green fluorescent protein (GFP)-labeled strain, 1-L-29gfpr, was created using protoplast transformation. This plasmid had good segregational stability. Strain 1-L-29gfpr was re-introduced into C. oleifera and successfully colonized root, stem, and leaf tissues. This strain remained at a stable concentration in the root more than 20 d after inoculation. Fluorescence microscopic analysis showed that strain 1-L-29gfpr thoroughly colonized the root surfaces of C. fructicola as well as the root vascular tissues of Arabidopsis thaliana.</description><subject>Acetic acid</subject><subject>Analysis</subject><subject>Anthracnose</subject><subject>Antimicrobial activity</subject><subject>Arabidopsis</subject><subject>Arabidopsis thaliana</subject><subject>Bacteria</subject><subject>Biological control</subject><subject>Biological pest control</subject><subject>Biology and Life Sciences</subject><subject>Camellia oleifera</subject><subject>Characterization</subject><subject>Colonization</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Education</subject><subject>Endophytes</subject><subject>Fluorescence</subject><subject>Fluorescence microscopy</subject><subject>Forestry</subject><subject>Genetic transformation</subject><subject>Glycerol</subject><subject>Grasslands</subject><subject>Green fluorescent protein</subject><subject>Indoleacetic acid</subject><subject>Inoculation</subject><subject>Isolation</subject><subject>Laboratories</subject><subject>Leaves</subject><subject>Li, Yang</subject><subject>Medicine and Health Sciences</subject><subject>Methods</subject><subject>Microorganisms</subject><subject>Microscopic analysis</subject><subject>Microscopy</subject><subject>Organic acids</subject><subject>Pathogenic microorganisms</subject><subject>Pathogens</subject><subject>Pesticides</subject><subject>Phosphates</subject><subject>Plant growth</subject><subject>Plant roots</subject><subject>Plant tissues</subject><subject>Research and Analysis Methods</subject><subject>Rifampin</subject><subject>rRNA 16S</subject><subject>Siderophores</subject><subject>Stems</subject><subject>Strain analysis</subject><subject>Strains (organisms)</subject><subject>Vascular 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and characterization of Bacillus subtilis strain 1-L-29, an endophytic bacteria from Camellia oleifera with antimicrobial activity and efficient plant-root colonization</title><author>Xu, Jin-Xin ; Li, Zi-Yang ; Lv, Xing ; Yan, Hua ; Zhou, Guo-Ying ; Cao, Ling-Xue ; Yang, Qin ; He, Yuan-Hao</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c743t-25f5d4701e78d8cefd9d6345f3c8cf2d7b2204c6f93ccd6e0613fb273c9fd353</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acetic acid</topic><topic>Analysis</topic><topic>Anthracnose</topic><topic>Antimicrobial activity</topic><topic>Arabidopsis</topic><topic>Arabidopsis thaliana</topic><topic>Bacteria</topic><topic>Biological control</topic><topic>Biological pest control</topic><topic>Biology and Life Sciences</topic><topic>Camellia oleifera</topic><topic>Characterization</topic><topic>Colonization</topic><topic>Deoxyribonucleic 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Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Jin-Xin</au><au>Li, Zi-Yang</au><au>Lv, Xing</au><au>Yan, Hua</au><au>Zhou, Guo-Ying</au><au>Cao, Ling-Xue</au><au>Yang, Qin</au><au>He, Yuan-Hao</au><au>Morais, Paula V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Isolation and characterization of Bacillus subtilis strain 1-L-29, an endophytic bacteria from Camellia oleifera with antimicrobial activity and efficient plant-root colonization</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2020-04-27</date><risdate>2020</risdate><volume>15</volume><issue>4</issue><spage>e0232096</spage><epage>e0232096</epage><pages>e0232096-e0232096</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Endophytic bacteria, which are common in plant tissues, may help to control plant pathogens and enhance plant growth. Camellia oleifera, an oil-producing plant, is widely grown in warm, subtropical, hilly regions in China. However, C. oleifera is strongly negatively affected by C. oleifera anthracnose, which is caused by Colletetrichum fructicola. To find a suitable biocontrol agent for C. oleifera anthracnose, 41 endophytes were isolated from the stems, leaves, and roots of C. oleifera. Bacterial cultures were identified based on analyses of 16S rDNA sequences; most strains belonged to the genus Bacillus. The antagonistic effects of these strains on C. fructicola were tested in vitro. In total, 16 strains inhibited C. fructicola growth, with B. subtilis strain 1-L-29 being the most efficient. Strain 1-L-29 demonstrated antagonistic activity against C. siamense, C. asianum, Fusarium proliferatum, Agaricodochium camellia, and Pseudomonas syringae. In addition, this strain produced indole acetic acid, solubilized phosphate, grew on N-free media, and produced siderophores. To facilitate further microecological studies of this strain, a rifampicin-resistant, green fluorescent protein (GFP)-labeled strain, 1-L-29gfpr, was created using protoplast transformation. This plasmid had good segregational stability. Strain 1-L-29gfpr was re-introduced into C. oleifera and successfully colonized root, stem, and leaf tissues. This strain remained at a stable concentration in the root more than 20 d after inoculation. Fluorescence microscopic analysis showed that strain 1-L-29gfpr thoroughly colonized the root surfaces of C. fructicola as well as the root vascular tissues of Arabidopsis thaliana.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>32339210</pmid><doi>10.1371/journal.pone.0232096</doi><tpages>e0232096</tpages><orcidid>https://orcid.org/0000-0001-9055-1794</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acetic acid Analysis Anthracnose Antimicrobial activity Arabidopsis Arabidopsis thaliana Bacteria Biological control Biological pest control Biology and Life Sciences Camellia oleifera Characterization Colonization Deoxyribonucleic acid DNA Education Endophytes Fluorescence Fluorescence microscopy Forestry Genetic transformation Glycerol Grasslands Green fluorescent protein Indoleacetic acid Inoculation Isolation Laboratories Leaves Li, Yang Medicine and Health Sciences Methods Microorganisms Microscopic analysis Microscopy Organic acids Pathogenic microorganisms Pathogens Pesticides Phosphates Plant growth Plant roots Plant tissues Research and Analysis Methods Rifampin rRNA 16S Siderophores Stems Strain analysis Strains (organisms) Vascular tissue |
title | Isolation and characterization of Bacillus subtilis strain 1-L-29, an endophytic bacteria from Camellia oleifera with antimicrobial activity and efficient plant-root colonization |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T15%3A02%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_plos_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Isolation%20and%20characterization%20of%20Bacillus%20subtilis%20strain%201-L-29,%20an%20endophytic%20bacteria%20from%20Camellia%20oleifera%20with%20antimicrobial%20activity%20and%20efficient%20plant-root%20colonization&rft.jtitle=PloS%20one&rft.au=Xu,%20Jin-Xin&rft.date=2020-04-27&rft.volume=15&rft.issue=4&rft.spage=e0232096&rft.epage=e0232096&rft.pages=e0232096-e0232096&rft.issn=1932-6203&rft.eissn=1932-6203&rft_id=info:doi/10.1371/journal.pone.0232096&rft_dat=%3Cgale_plos_%3EA622117160%3C/gale_plos_%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2395249127&rft_id=info:pmid/32339210&rft_galeid=A622117160&rft_doaj_id=oai_doaj_org_article_5f517ea270c74888bedd82de0fb9433e&rfr_iscdi=true |