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Taxonomic Description and Complete Genome Sequencing of Pseudomonas silvicola sp. nov. Isolated from Cunninghamia laceolata
The Pseudomonas strain T1-3-2T isolated from the cone of Cunninghamia laceolata exhibited growth-promoting and antifungal activity. Strain T1-3-2T was characterized by a polyphasic taxonomy and complete genome sequencing analysis to explore its taxonomic position and biocontrol potentials fully. The...
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Published in: | Forests 2023-06, Vol.14 (6), p.1089 |
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description | The Pseudomonas strain T1-3-2T isolated from the cone of Cunninghamia laceolata exhibited growth-promoting and antifungal activity. Strain T1-3-2T was characterized by a polyphasic taxonomy and complete genome sequencing analysis to explore its taxonomic position and biocontrol potentials fully. The results revealed that strain T1-3-2T shares a high degree of similarity with Pseudomonas eucalypticola and is distinct from any known Pseudomonas species. The G + C content was 61.65%, and the difference was greater than 1 compared to “P. eucalypticola”. Additionally, values of the average nucleotide identity blast (ANIb), average nucleotide identity MUMmer (ANIm), and DNA-DNA hybridization (DDH) between T1-3-2T and its closest known related species, “P. eucalypticola”, were below the thresholds necessary for species delineation. Furthermore, the T1-3-2T strain exhibited the distinctions with the multiple polar flagella and the specific quinone system with MK8 compared with that of “P. eucalypticola”. Collectively, these findings affirm the designation of strain T1-3-2T as a new Pseudomonas species, proposed to be named Pseudomonas silvicola, with T1-3-2T as the type strain. Genomic analyses revealed strain T1-3-2T contains three circular DNA contigs, including a 7,613,303 bp chromosome and two plasmids (952,764 bp and 84,880 bp). Bioinformatics analyses further offered potential insight into the molecular mechanisms whereby this strain can promote plant growth and control disease, revealing encoded genes related to antibiotic and secondary metabolite production, the uptake and biosynthesis of siderophores, and pyoverdine biosynthesis. These genomic data offer a valuable foundation for future efforts to apply the T1-3-2T strain in research contexts. |
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Isolated from Cunninghamia laceolata</title><source>Publicly Available Content Database</source><creator>Tian, Longyan ; Zhang, Yanfeng ; Yang, Hua ; Zhao, Qian ; Qiu, Hualong ; Xu, Jinzhu ; Qin, Changsheng</creator><creatorcontrib>Tian, Longyan ; Zhang, Yanfeng ; Yang, Hua ; Zhao, Qian ; Qiu, Hualong ; Xu, Jinzhu ; Qin, Changsheng</creatorcontrib><description>The Pseudomonas strain T1-3-2T isolated from the cone of Cunninghamia laceolata exhibited growth-promoting and antifungal activity. Strain T1-3-2T was characterized by a polyphasic taxonomy and complete genome sequencing analysis to explore its taxonomic position and biocontrol potentials fully. The results revealed that strain T1-3-2T shares a high degree of similarity with Pseudomonas eucalypticola and is distinct from any known Pseudomonas species. The G + C content was 61.65%, and the difference was greater than 1 compared to “P. eucalypticola”. Additionally, values of the average nucleotide identity blast (ANIb), average nucleotide identity MUMmer (ANIm), and DNA-DNA hybridization (DDH) between T1-3-2T and its closest known related species, “P. eucalypticola”, were below the thresholds necessary for species delineation. Furthermore, the T1-3-2T strain exhibited the distinctions with the multiple polar flagella and the specific quinone system with MK8 compared with that of “P. eucalypticola”. Collectively, these findings affirm the designation of strain T1-3-2T as a new Pseudomonas species, proposed to be named Pseudomonas silvicola, with T1-3-2T as the type strain. Genomic analyses revealed strain T1-3-2T contains three circular DNA contigs, including a 7,613,303 bp chromosome and two plasmids (952,764 bp and 84,880 bp). Bioinformatics analyses further offered potential insight into the molecular mechanisms whereby this strain can promote plant growth and control disease, revealing encoded genes related to antibiotic and secondary metabolite production, the uptake and biosynthesis of siderophores, and pyoverdine biosynthesis. These genomic data offer a valuable foundation for future efforts to apply the T1-3-2T strain in research contexts.</description><identifier>ISSN: 1999-4907</identifier><identifier>EISSN: 1999-4907</identifier><identifier>DOI: 10.3390/f14061089</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Antifungal activity ; Bioinformatics ; Biological control ; Biosynthesis ; Chromosomes ; Circular DNA ; Cunninghamia ; Deoxyribonucleic acid ; DNA ; Fatty acids ; Flagella ; Fungicides ; Gene sequencing ; Genes ; genome ; Genomes ; Genomic analysis ; Hybridization ; Metabolites ; Molecular modelling ; New species ; Nucleotides ; Phylogenetics ; Plant growth ; Plasmids ; Pseudomonas ; Pyoverdines ; Quinones ; Sequence analysis ; Siderophores ; Strain analysis ; taxonomic description ; Taxonomy ; Trees</subject><ispartof>Forests, 2023-06, Vol.14 (6), p.1089</ispartof><rights>2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c318t-e08d4de53fda43893e2b96578730ceae983f5edd179c87e625b9ab9a751119ff3</cites><orcidid>0000-0002-7213-7204</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2829810485/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2829810485?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25752,27923,27924,37011,44589,74997</link.rule.ids></links><search><creatorcontrib>Tian, Longyan</creatorcontrib><creatorcontrib>Zhang, Yanfeng</creatorcontrib><creatorcontrib>Yang, Hua</creatorcontrib><creatorcontrib>Zhao, Qian</creatorcontrib><creatorcontrib>Qiu, Hualong</creatorcontrib><creatorcontrib>Xu, Jinzhu</creatorcontrib><creatorcontrib>Qin, Changsheng</creatorcontrib><title>Taxonomic Description and Complete Genome Sequencing of Pseudomonas silvicola sp. nov. Isolated from Cunninghamia laceolata</title><title>Forests</title><description>The Pseudomonas strain T1-3-2T isolated from the cone of Cunninghamia laceolata exhibited growth-promoting and antifungal activity. Strain T1-3-2T was characterized by a polyphasic taxonomy and complete genome sequencing analysis to explore its taxonomic position and biocontrol potentials fully. The results revealed that strain T1-3-2T shares a high degree of similarity with Pseudomonas eucalypticola and is distinct from any known Pseudomonas species. The G + C content was 61.65%, and the difference was greater than 1 compared to “P. eucalypticola”. Additionally, values of the average nucleotide identity blast (ANIb), average nucleotide identity MUMmer (ANIm), and DNA-DNA hybridization (DDH) between T1-3-2T and its closest known related species, “P. eucalypticola”, were below the thresholds necessary for species delineation. 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These genomic data offer a valuable foundation for future efforts to apply the T1-3-2T strain in research contexts.</description><subject>Antifungal activity</subject><subject>Bioinformatics</subject><subject>Biological control</subject><subject>Biosynthesis</subject><subject>Chromosomes</subject><subject>Circular DNA</subject><subject>Cunninghamia</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>Fatty acids</subject><subject>Flagella</subject><subject>Fungicides</subject><subject>Gene sequencing</subject><subject>Genes</subject><subject>genome</subject><subject>Genomes</subject><subject>Genomic analysis</subject><subject>Hybridization</subject><subject>Metabolites</subject><subject>Molecular modelling</subject><subject>New species</subject><subject>Nucleotides</subject><subject>Phylogenetics</subject><subject>Plant growth</subject><subject>Plasmids</subject><subject>Pseudomonas</subject><subject>Pyoverdines</subject><subject>Quinones</subject><subject>Sequence analysis</subject><subject>Siderophores</subject><subject>Strain analysis</subject><subject>taxonomic description</subject><subject>Taxonomy</subject><subject>Trees</subject><issn>1999-4907</issn><issn>1999-4907</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpNUU1LJDEQbRaFFfWw_yCwJw8zm3TS3clxGT92QFDQPYfqpOJm6E7apGdQ_PMbHRksCiqpvHqvKlVVPxhdcq7oL8cEbRmV6lt1wpRSC6Fod_Tl_L06z3lDizWdVLU4qd4e4SWGOHpDLjGb5KfZx0AgWLKK4zTgjOQGCwDJAz5vMRgfnkh05D7j1sYxBsgk-2HnTRyA5GlJQtwtyTqX64yWuBRHstqGUOr-weiBDGDw_RHOqmMHQ8bzz3ha_b2-elz9Wdze3axXv28XhjM5L5BKKyw23FkQXCqOda_aMkDHqUFAJblr0FrWKSM7bOumV1C8axhjyjl-Wq33vDbCRk_Jj5BedQSvPxIxPWlIszcD6o7RvhVM9YitEJaDMbTItxSclHWjCtfPPdeUYvmOPOtN3KZQ2te1rJVkVMimoC72KJNizgndQZVR_b4qfVgV_w9cR4at</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Tian, Longyan</creator><creator>Zhang, Yanfeng</creator><creator>Yang, Hua</creator><creator>Zhao, Qian</creator><creator>Qiu, Hualong</creator><creator>Xu, Jinzhu</creator><creator>Qin, Changsheng</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7SN</scope><scope>7SS</scope><scope>7X2</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>M0K</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-7213-7204</orcidid></search><sort><creationdate>20230601</creationdate><title>Taxonomic Description and Complete Genome Sequencing of Pseudomonas silvicola sp. nov. 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Isolated from Cunninghamia laceolata</atitle><jtitle>Forests</jtitle><date>2023-06-01</date><risdate>2023</risdate><volume>14</volume><issue>6</issue><spage>1089</spage><pages>1089-</pages><issn>1999-4907</issn><eissn>1999-4907</eissn><abstract>The Pseudomonas strain T1-3-2T isolated from the cone of Cunninghamia laceolata exhibited growth-promoting and antifungal activity. Strain T1-3-2T was characterized by a polyphasic taxonomy and complete genome sequencing analysis to explore its taxonomic position and biocontrol potentials fully. The results revealed that strain T1-3-2T shares a high degree of similarity with Pseudomonas eucalypticola and is distinct from any known Pseudomonas species. The G + C content was 61.65%, and the difference was greater than 1 compared to “P. eucalypticola”. Additionally, values of the average nucleotide identity blast (ANIb), average nucleotide identity MUMmer (ANIm), and DNA-DNA hybridization (DDH) between T1-3-2T and its closest known related species, “P. eucalypticola”, were below the thresholds necessary for species delineation. Furthermore, the T1-3-2T strain exhibited the distinctions with the multiple polar flagella and the specific quinone system with MK8 compared with that of “P. eucalypticola”. Collectively, these findings affirm the designation of strain T1-3-2T as a new Pseudomonas species, proposed to be named Pseudomonas silvicola, with T1-3-2T as the type strain. Genomic analyses revealed strain T1-3-2T contains three circular DNA contigs, including a 7,613,303 bp chromosome and two plasmids (952,764 bp and 84,880 bp). Bioinformatics analyses further offered potential insight into the molecular mechanisms whereby this strain can promote plant growth and control disease, revealing encoded genes related to antibiotic and secondary metabolite production, the uptake and biosynthesis of siderophores, and pyoverdine biosynthesis. These genomic data offer a valuable foundation for future efforts to apply the T1-3-2T strain in research contexts.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/f14061089</doi><orcidid>https://orcid.org/0000-0002-7213-7204</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antifungal activity Bioinformatics Biological control Biosynthesis Chromosomes Circular DNA Cunninghamia Deoxyribonucleic acid DNA Fatty acids Flagella Fungicides Gene sequencing Genes genome Genomes Genomic analysis Hybridization Metabolites Molecular modelling New species Nucleotides Phylogenetics Plant growth Plasmids Pseudomonas Pyoverdines Quinones Sequence analysis Siderophores Strain analysis taxonomic description Taxonomy Trees |
title | Taxonomic Description and Complete Genome Sequencing of Pseudomonas silvicola sp. nov. Isolated from Cunninghamia laceolata |
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