Gordonia jinhuaensis sp. nov., a novel actinobacterium, isolated from a VBNC (viable but non-culturable) state in pharmaceutical wastewater
A Gram-stain positive, aerobic, non-motile and rod-shaped actinobacterial strain, designated as ZYR 51ᵀ, was isolated from pharmaceutical wastewater in Jinhua city, Zhejiang province, Eastern China. Isolation was aided by using a resuscitation-promoting factor, suggesting the strain was recovered fr...
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creator | Li, Shan-Hui Jin, Yi Cheng, Juan Park, Dong-Jin Kim, Chang-Jin Hozzein, Wael N Wadaan, Mohammed A. M Shu, Wen-Sheng Ding, Lin-Xian Li, Wen-Jun |
description | A Gram-stain positive, aerobic, non-motile and rod-shaped actinobacterial strain, designated as ZYR 51ᵀ, was isolated from pharmaceutical wastewater in Jinhua city, Zhejiang province, Eastern China. Isolation was aided by using a resuscitation-promoting factor, suggesting the strain was recovered from a viable but non-culturable state. Strain ZYR 51ᵀ was characterized by a polyphasic taxonomic approach. Growth was found to occur at 10–45 °C, pH 6.0–10.0 and 0–9 % NaCl (w/v). Based on the 16S rRNA gene sequence, phylogenetic analysis clearly demonstrated that strain ZYR 51ᵀ belongs to the genus Gordonia and showed low level similarities (below 97 %) with all other members of this genus. The strain was found to possess meso-diaminopimelic acid (meso-DAP), along with MK-9(H₂) as the predominant menaquonine. Mycolic acids were found to be present. C₁₆:₀ (34.9 %), 10-methyl C₁₈:₀ (30.3 %), iso-C₁₈:₀(8.2 %), and summed feature 3 (C₁₆:₁ ω6c and/or C₁₆:₁ω7c as define by MIDI; 18.8 %) were identified as the major cellular fatty acids. The polar lipid profile of strain ZYR 51ᵀ was found to consist of diphosphatidylglycerol, phosphatidylinositol, phosphatidylinositol mannosides and some unknown lipids. The genomic DNA G+C content of strain ZYR 51ᵀ was determined to be 67.7 mol%. The combined genotypic and phenotypic data showed that the strain represents a novel species of the genus Gordonia, for which the name Gordonia jinhuaensis sp. nov. is proposed, with the type strain is ZYR 51ᵀ (=CGMCC 1.12827ᵀ = NBRL B-59111ᵀ = NBRC 110001ᵀ). |
doi_str_mv | 10.1007/s10482-014-0207-3 |
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M ; Shu, Wen-Sheng ; Ding, Lin-Xian ; Li, Wen-Jun</creator><creatorcontrib>Li, Shan-Hui ; Jin, Yi ; Cheng, Juan ; Park, Dong-Jin ; Kim, Chang-Jin ; Hozzein, Wael N ; Wadaan, Mohammed A. M ; Shu, Wen-Sheng ; Ding, Lin-Xian ; Li, Wen-Jun</creatorcontrib><description>A Gram-stain positive, aerobic, non-motile and rod-shaped actinobacterial strain, designated as ZYR 51ᵀ, was isolated from pharmaceutical wastewater in Jinhua city, Zhejiang province, Eastern China. Isolation was aided by using a resuscitation-promoting factor, suggesting the strain was recovered from a viable but non-culturable state. Strain ZYR 51ᵀ was characterized by a polyphasic taxonomic approach. Growth was found to occur at 10–45 °C, pH 6.0–10.0 and 0–9 % NaCl (w/v). Based on the 16S rRNA gene sequence, phylogenetic analysis clearly demonstrated that strain ZYR 51ᵀ belongs to the genus Gordonia and showed low level similarities (below 97 %) with all other members of this genus. The strain was found to possess meso-diaminopimelic acid (meso-DAP), along with MK-9(H₂) as the predominant menaquonine. Mycolic acids were found to be present. C₁₆:₀ (34.9 %), 10-methyl C₁₈:₀ (30.3 %), iso-C₁₈:₀(8.2 %), and summed feature 3 (C₁₆:₁ ω6c and/or C₁₆:₁ω7c as define by MIDI; 18.8 %) were identified as the major cellular fatty acids. The polar lipid profile of strain ZYR 51ᵀ was found to consist of diphosphatidylglycerol, phosphatidylinositol, phosphatidylinositol mannosides and some unknown lipids. The genomic DNA G+C content of strain ZYR 51ᵀ was determined to be 67.7 mol%. The combined genotypic and phenotypic data showed that the strain represents a novel species of the genus Gordonia, for which the name Gordonia jinhuaensis sp. nov. is proposed, with the type strain is ZYR 51ᵀ (=CGMCC 1.12827ᵀ = NBRL B-59111ᵀ = NBRC 110001ᵀ).</description><identifier>ISSN: 0003-6072</identifier><identifier>EISSN: 1572-9699</identifier><identifier>DOI: 10.1007/s10482-014-0207-3</identifier><identifier>PMID: 24912980</identifier><language>eng</language><publisher>Netherlands: Springer-Verlag</publisher><subject>Actinobacteria - classification ; Actinobacteria - genetics ; Actinobacteria - isolation & purification ; Actinobacteria - physiology ; Aerobiosis ; Bacterial Typing Techniques ; Base Composition ; Cell Wall - chemistry ; China ; Cluster Analysis ; Cytosol - chemistry ; Diaminopimelic Acid ; DNA ; DNA, Bacterial - chemistry ; DNA, Bacterial - genetics ; DNA, Ribosomal - chemistry ; DNA, Ribosomal - genetics ; fatty acids ; Fatty Acids - analysis ; Gordonia ; hydrogen ; Hydrogen-Ion Concentration ; Industrial Waste ; Microscopy, Electron, Scanning ; Molecular Sequence Data ; nucleotide sequences ; Phospholipids - analysis ; Phylogeny ; ribosomal RNA ; RNA, Ribosomal, 16S - genetics ; Sequence Analysis, DNA ; sodium chloride ; Sodium Chloride - metabolism ; Temperature ; Vitamin K 2 - analysis ; Waste Water - microbiology ; wastewater</subject><ispartof>Antonie van Leeuwenhoek, 2014-08, Vol.106 (2), p.347-356</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-1c1b2091c389b26cef090e03158c87d8f188da68bf84562e0b4766daf4b2fdc3</citedby><cites>FETCH-LOGICAL-c358t-1c1b2091c389b26cef090e03158c87d8f188da68bf84562e0b4766daf4b2fdc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24912980$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Shan-Hui</creatorcontrib><creatorcontrib>Jin, Yi</creatorcontrib><creatorcontrib>Cheng, Juan</creatorcontrib><creatorcontrib>Park, Dong-Jin</creatorcontrib><creatorcontrib>Kim, Chang-Jin</creatorcontrib><creatorcontrib>Hozzein, Wael N</creatorcontrib><creatorcontrib>Wadaan, Mohammed A. M</creatorcontrib><creatorcontrib>Shu, Wen-Sheng</creatorcontrib><creatorcontrib>Ding, Lin-Xian</creatorcontrib><creatorcontrib>Li, Wen-Jun</creatorcontrib><title>Gordonia jinhuaensis sp. nov., a novel actinobacterium, isolated from a VBNC (viable but non-culturable) state in pharmaceutical wastewater</title><title>Antonie van Leeuwenhoek</title><addtitle>Antonie Van Leeuwenhoek</addtitle><description>A Gram-stain positive, aerobic, non-motile and rod-shaped actinobacterial strain, designated as ZYR 51ᵀ, was isolated from pharmaceutical wastewater in Jinhua city, Zhejiang province, Eastern China. Isolation was aided by using a resuscitation-promoting factor, suggesting the strain was recovered from a viable but non-culturable state. Strain ZYR 51ᵀ was characterized by a polyphasic taxonomic approach. Growth was found to occur at 10–45 °C, pH 6.0–10.0 and 0–9 % NaCl (w/v). Based on the 16S rRNA gene sequence, phylogenetic analysis clearly demonstrated that strain ZYR 51ᵀ belongs to the genus Gordonia and showed low level similarities (below 97 %) with all other members of this genus. The strain was found to possess meso-diaminopimelic acid (meso-DAP), along with MK-9(H₂) as the predominant menaquonine. Mycolic acids were found to be present. C₁₆:₀ (34.9 %), 10-methyl C₁₈:₀ (30.3 %), iso-C₁₈:₀(8.2 %), and summed feature 3 (C₁₆:₁ ω6c and/or C₁₆:₁ω7c as define by MIDI; 18.8 %) were identified as the major cellular fatty acids. The polar lipid profile of strain ZYR 51ᵀ was found to consist of diphosphatidylglycerol, phosphatidylinositol, phosphatidylinositol mannosides and some unknown lipids. The genomic DNA G+C content of strain ZYR 51ᵀ was determined to be 67.7 mol%. The combined genotypic and phenotypic data showed that the strain represents a novel species of the genus Gordonia, for which the name Gordonia jinhuaensis sp. nov. is proposed, with the type strain is ZYR 51ᵀ (=CGMCC 1.12827ᵀ = NBRL B-59111ᵀ = NBRC 110001ᵀ).</description><subject>Actinobacteria - classification</subject><subject>Actinobacteria - genetics</subject><subject>Actinobacteria - isolation & purification</subject><subject>Actinobacteria - physiology</subject><subject>Aerobiosis</subject><subject>Bacterial Typing Techniques</subject><subject>Base Composition</subject><subject>Cell Wall - chemistry</subject><subject>China</subject><subject>Cluster Analysis</subject><subject>Cytosol - chemistry</subject><subject>Diaminopimelic Acid</subject><subject>DNA</subject><subject>DNA, Bacterial - chemistry</subject><subject>DNA, Bacterial - genetics</subject><subject>DNA, Ribosomal - chemistry</subject><subject>DNA, Ribosomal - genetics</subject><subject>fatty acids</subject><subject>Fatty Acids - analysis</subject><subject>Gordonia</subject><subject>hydrogen</subject><subject>Hydrogen-Ion Concentration</subject><subject>Industrial Waste</subject><subject>Microscopy, Electron, Scanning</subject><subject>Molecular Sequence Data</subject><subject>nucleotide sequences</subject><subject>Phospholipids - analysis</subject><subject>Phylogeny</subject><subject>ribosomal RNA</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>Sequence Analysis, DNA</subject><subject>sodium chloride</subject><subject>Sodium Chloride - metabolism</subject><subject>Temperature</subject><subject>Vitamin K 2 - analysis</subject><subject>Waste Water - microbiology</subject><subject>wastewater</subject><issn>0003-6072</issn><issn>1572-9699</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkc1uFSEYhonR2GP1Atwoy5qU48fPMLCsJ1pNGl1Y3RJgwNLMDEeYaeM1eNNycqprV2_ge9538yD0ksKWAvRvKwWhGAEqCDDoCX-ENrTrGdFS68doAwCcSOjZCXpW6217aqn6p-iECU2ZVrBBvy9zGfKcLL5N881qw1xTxXW_xXO-255je8gwYuuXNGfXIpS0Tuc41TzaJQw4ljw17Pu7zzt8dpesGwN269J6M_HruKzl8PUG16XhOM14f2PLZH1Yl-TtiO9tXcJ9u5Xn6Em0Yw0vHvIUXX94f737SK6-XH7aXVwRzzu1EOqpY6Cp50o7Jn2IoCEAp53yqh9UpEoNVioXlegkC-BEL-Vgo3AsDp6forPj7L7kn2uoi5lS9WEc7RzyWg3tJFAmZK__AxWdoEpS0VB6RH3JtZYQzb6kyZZfhoI52DJHW6bZMgdbhrfOq4f51U1h-Nf4q6cBr49AtNnYHyVV8-0rawsAlIu-0_wPq1OZ7w</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Li, Shan-Hui</creator><creator>Jin, Yi</creator><creator>Cheng, Juan</creator><creator>Park, Dong-Jin</creator><creator>Kim, Chang-Jin</creator><creator>Hozzein, Wael N</creator><creator>Wadaan, Mohammed A. M</creator><creator>Shu, Wen-Sheng</creator><creator>Ding, Lin-Xian</creator><creator>Li, Wen-Jun</creator><general>Springer-Verlag</general><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7QH</scope><scope>7QL</scope><scope>7UA</scope><scope>C1K</scope><scope>F1W</scope><scope>H97</scope><scope>L.G</scope></search><sort><creationdate>20140801</creationdate><title>Gordonia jinhuaensis sp. nov., a novel actinobacterium, isolated from a VBNC (viable but non-culturable) state in pharmaceutical wastewater</title><author>Li, Shan-Hui ; Jin, Yi ; Cheng, Juan ; Park, Dong-Jin ; Kim, Chang-Jin ; Hozzein, Wael N ; Wadaan, Mohammed A. M ; Shu, Wen-Sheng ; Ding, Lin-Xian ; Li, Wen-Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-1c1b2091c389b26cef090e03158c87d8f188da68bf84562e0b4766daf4b2fdc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Actinobacteria - classification</topic><topic>Actinobacteria - genetics</topic><topic>Actinobacteria - isolation & purification</topic><topic>Actinobacteria - physiology</topic><topic>Aerobiosis</topic><topic>Bacterial Typing Techniques</topic><topic>Base Composition</topic><topic>Cell Wall - chemistry</topic><topic>China</topic><topic>Cluster Analysis</topic><topic>Cytosol - chemistry</topic><topic>Diaminopimelic Acid</topic><topic>DNA</topic><topic>DNA, Bacterial - chemistry</topic><topic>DNA, Bacterial - genetics</topic><topic>DNA, Ribosomal - chemistry</topic><topic>DNA, Ribosomal - genetics</topic><topic>fatty acids</topic><topic>Fatty Acids - analysis</topic><topic>Gordonia</topic><topic>hydrogen</topic><topic>Hydrogen-Ion Concentration</topic><topic>Industrial Waste</topic><topic>Microscopy, Electron, Scanning</topic><topic>Molecular Sequence Data</topic><topic>nucleotide sequences</topic><topic>Phospholipids - analysis</topic><topic>Phylogeny</topic><topic>ribosomal RNA</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>Sequence Analysis, DNA</topic><topic>sodium chloride</topic><topic>Sodium Chloride - metabolism</topic><topic>Temperature</topic><topic>Vitamin K 2 - analysis</topic><topic>Waste Water - microbiology</topic><topic>wastewater</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Shan-Hui</creatorcontrib><creatorcontrib>Jin, Yi</creatorcontrib><creatorcontrib>Cheng, Juan</creatorcontrib><creatorcontrib>Park, Dong-Jin</creatorcontrib><creatorcontrib>Kim, Chang-Jin</creatorcontrib><creatorcontrib>Hozzein, Wael N</creatorcontrib><creatorcontrib>Wadaan, Mohammed A. M</creatorcontrib><creatorcontrib>Shu, Wen-Sheng</creatorcontrib><creatorcontrib>Ding, Lin-Xian</creatorcontrib><creatorcontrib>Li, Wen-Jun</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Aqualine</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Water Resources Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ASFA: Aquatic Sciences and Fisheries Abstracts</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) 3: Aquatic Pollution & Environmental Quality</collection><collection>Aquatic Science & Fisheries Abstracts (ASFA) Professional</collection><jtitle>Antonie van Leeuwenhoek</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Shan-Hui</au><au>Jin, Yi</au><au>Cheng, Juan</au><au>Park, Dong-Jin</au><au>Kim, Chang-Jin</au><au>Hozzein, Wael N</au><au>Wadaan, Mohammed A. M</au><au>Shu, Wen-Sheng</au><au>Ding, Lin-Xian</au><au>Li, Wen-Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gordonia jinhuaensis sp. nov., a novel actinobacterium, isolated from a VBNC (viable but non-culturable) state in pharmaceutical wastewater</atitle><jtitle>Antonie van Leeuwenhoek</jtitle><addtitle>Antonie Van Leeuwenhoek</addtitle><date>2014-08-01</date><risdate>2014</risdate><volume>106</volume><issue>2</issue><spage>347</spage><epage>356</epage><pages>347-356</pages><issn>0003-6072</issn><eissn>1572-9699</eissn><abstract>A Gram-stain positive, aerobic, non-motile and rod-shaped actinobacterial strain, designated as ZYR 51ᵀ, was isolated from pharmaceutical wastewater in Jinhua city, Zhejiang province, Eastern China. Isolation was aided by using a resuscitation-promoting factor, suggesting the strain was recovered from a viable but non-culturable state. Strain ZYR 51ᵀ was characterized by a polyphasic taxonomic approach. Growth was found to occur at 10–45 °C, pH 6.0–10.0 and 0–9 % NaCl (w/v). Based on the 16S rRNA gene sequence, phylogenetic analysis clearly demonstrated that strain ZYR 51ᵀ belongs to the genus Gordonia and showed low level similarities (below 97 %) with all other members of this genus. The strain was found to possess meso-diaminopimelic acid (meso-DAP), along with MK-9(H₂) as the predominant menaquonine. Mycolic acids were found to be present. C₁₆:₀ (34.9 %), 10-methyl C₁₈:₀ (30.3 %), iso-C₁₈:₀(8.2 %), and summed feature 3 (C₁₆:₁ ω6c and/or C₁₆:₁ω7c as define by MIDI; 18.8 %) were identified as the major cellular fatty acids. The polar lipid profile of strain ZYR 51ᵀ was found to consist of diphosphatidylglycerol, phosphatidylinositol, phosphatidylinositol mannosides and some unknown lipids. The genomic DNA G+C content of strain ZYR 51ᵀ was determined to be 67.7 mol%. The combined genotypic and phenotypic data showed that the strain represents a novel species of the genus Gordonia, for which the name Gordonia jinhuaensis sp. nov. is proposed, with the type strain is ZYR 51ᵀ (=CGMCC 1.12827ᵀ = NBRL B-59111ᵀ = NBRC 110001ᵀ).</abstract><cop>Netherlands</cop><pub>Springer-Verlag</pub><pmid>24912980</pmid><doi>10.1007/s10482-014-0207-3</doi><tpages>10</tpages></addata></record> |
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subjects | Actinobacteria - classification Actinobacteria - genetics Actinobacteria - isolation & purification Actinobacteria - physiology Aerobiosis Bacterial Typing Techniques Base Composition Cell Wall - chemistry China Cluster Analysis Cytosol - chemistry Diaminopimelic Acid DNA DNA, Bacterial - chemistry DNA, Bacterial - genetics DNA, Ribosomal - chemistry DNA, Ribosomal - genetics fatty acids Fatty Acids - analysis Gordonia hydrogen Hydrogen-Ion Concentration Industrial Waste Microscopy, Electron, Scanning Molecular Sequence Data nucleotide sequences Phospholipids - analysis Phylogeny ribosomal RNA RNA, Ribosomal, 16S - genetics Sequence Analysis, DNA sodium chloride Sodium Chloride - metabolism Temperature Vitamin K 2 - analysis Waste Water - microbiology wastewater |
title | Gordonia jinhuaensis sp. nov., a novel actinobacterium, isolated from a VBNC (viable but non-culturable) state in pharmaceutical wastewater |
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