Amycolatopsis eburnea sp. nov., an actinomycete associated with arbuscular mycorrhizal fungal spores.
Identifieur interne : 000342 ( Main/Corpus ); précédent : 000341; suivant : 000343Amycolatopsis eburnea sp. nov., an actinomycete associated with arbuscular mycorrhizal fungal spores.
Auteurs : Leardwiriyakool Chaiya ; Atsuko Matsumoto ; Joachim Wink ; Yuki Inahashi ; Chandra Risdian ; Wasu Pathom-Aree ; Saisamorn LumyongSource :
- International journal of systematic and evolutionary microbiology [ 1466-5034 ] ; 2019.
English descriptors
- KwdEn :
- Actinobacteria (classification), Actinobacteria (isolation & purification), Bacterial Typing Techniques (MeSH), Base Composition (MeSH), Cell Wall (chemistry), DNA, Bacterial (genetics), Diaminopimelic Acid (chemistry), Fatty Acids (chemistry), Mycorrhizae (MeSH), Nucleic Acid Hybridization (MeSH), Phosphatidylethanolamines (chemistry), Phylogeny (MeSH), RNA, Ribosomal, 16S (genetics), Rhizosphere (MeSH), Sequence Analysis, DNA (MeSH), Soil Microbiology (MeSH), Spores, Fungal (MeSH), Thailand (MeSH), Vitamin K 2 (analogs & derivatives), Vitamin K 2 (chemistry).
- MESH :
- chemical , analogs & derivatives : Vitamin K 2.
- chemical , chemistry : Diaminopimelic Acid, Fatty Acids, Phosphatidylethanolamines, Vitamin K 2.
- chemical , genetics : DNA, Bacterial, RNA, Ribosomal, 16S.
- geographic : Thailand.
- chemistry : Cell Wall.
- classification : Actinobacteria.
- isolation & purification : Actinobacteria.
- Bacterial Typing Techniques, Base Composition, Mycorrhizae, Nucleic Acid Hybridization, Phylogeny, Rhizosphere, Sequence Analysis, DNA, Soil Microbiology, Spores, Fungal.
Abstract
A novel actinomycete, designated strain GLM-1T, was isolated from arbuscular mycorrhizal fungal spores from Funneliformis mosseae RYA08, collected from Aquilaria crassna Pierre ex Lec. rhizosphere soil in Klaeng, Rayong Province, Thailand. Morphological characteristics of this strain included long chains of rod-like cells and squarish elements. The cell-wall composition of this novel isolate contained meso-diaminopimelic acid. The whole-cell diagnostic sugars were arabinose and galactose. The predominant menaquinone was MK-9(H4). The major fatty acids were iso-C16 : 0 and iso-C15 : 0. Only phosphatidylethanolamine was detected as a polar lipid. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain GLM-1T was closely related to Amycolatopsis rhabdoformis SB026T (99.11 %) with a low DNA-DNA hybridization value of 22.6-34.7 %. Genome sequencing revealed a genome size of 10 Mbp. There were obvious distinctions in the average nucleotide identity values between stain GLM-1T and its closely related strains at around 86-93 % (ANIb) and 89-94 % (ANIm). The digital DNA-DNA hybridization values between strain GLM-1T and type strains of phylogenetically related species were 34-55 %. The G+C content of the genomic DNA was 71.8 mol%. Based on these data, strain GLM-1T is considered to represent a novel species of the genus Amycolatopsis, for which the name Amycolatopsiseburnea sp. nov. is proposed. The type strain is GLM-1T (=TBRC 9315T=NBRC 113658T).
DOI: 10.1099/ijsem.0.003669
PubMed: 31433288
Links to Exploration step
pubmed:31433288Le document en format XML
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sp. nov., an actinomycete associated with arbuscular mycorrhizal fungal spores.</title>
<author><name sortKey="Chaiya, Leardwiriyakool" sort="Chaiya, Leardwiriyakool" uniqKey="Chaiya L" first="Leardwiriyakool" last="Chaiya">Leardwiriyakool Chaiya</name>
<affiliation><nlm:affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</nlm:affiliation>
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<author><name sortKey="Matsumoto, Atsuko" sort="Matsumoto, Atsuko" uniqKey="Matsumoto A" first="Atsuko" last="Matsumoto">Atsuko Matsumoto</name>
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<affiliation><nlm:affiliation>Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</nlm:affiliation>
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<author><name sortKey="Risdian, Chandra" sort="Risdian, Chandra" uniqKey="Risdian C" first="Chandra" last="Risdian">Chandra Risdian</name>
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<author><name sortKey="Pathom Aree, Wasu" sort="Pathom Aree, Wasu" uniqKey="Pathom Aree W" first="Wasu" last="Pathom-Aree">Wasu Pathom-Aree</name>
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<author><name sortKey="Lumyong, Saisamorn" sort="Lumyong, Saisamorn" uniqKey="Lumyong S" first="Saisamorn" last="Lumyong">Saisamorn Lumyong</name>
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<sourceDesc><biblStruct><analytic><title xml:lang="en"><i>Amycolatopsis eburnea</i>
sp. nov., an actinomycete associated with arbuscular mycorrhizal fungal spores.</title>
<author><name sortKey="Chaiya, Leardwiriyakool" sort="Chaiya, Leardwiriyakool" uniqKey="Chaiya L" first="Leardwiriyakool" last="Chaiya">Leardwiriyakool Chaiya</name>
<affiliation><nlm:affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</nlm:affiliation>
</affiliation>
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<author><name sortKey="Matsumoto, Atsuko" sort="Matsumoto, Atsuko" uniqKey="Matsumoto A" first="Atsuko" last="Matsumoto">Atsuko Matsumoto</name>
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<affiliation><nlm:affiliation>Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</nlm:affiliation>
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<author><name sortKey="Wink, Joachim" sort="Wink, Joachim" uniqKey="Wink J" first="Joachim" last="Wink">Joachim Wink</name>
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</affiliation>
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<author><name sortKey="Inahashi, Yuki" sort="Inahashi, Yuki" uniqKey="Inahashi Y" first="Yuki" last="Inahashi">Yuki Inahashi</name>
<affiliation><nlm:affiliation>Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</nlm:affiliation>
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<affiliation><nlm:affiliation>Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</nlm:affiliation>
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<author><name sortKey="Risdian, Chandra" sort="Risdian, Chandra" uniqKey="Risdian C" first="Chandra" last="Risdian">Chandra Risdian</name>
<affiliation><nlm:affiliation>Research Unit for Clean Technology, Indonesian Institute of Sciences (LIPI), Bandung 40135, Indonesia.</nlm:affiliation>
</affiliation>
<affiliation><nlm:affiliation>Microbial Strain Collection, Helmholtz Centre for Infection Research (HZI), 38124, Braunschweig, Germany.</nlm:affiliation>
</affiliation>
</author>
<author><name sortKey="Pathom Aree, Wasu" sort="Pathom Aree, Wasu" uniqKey="Pathom Aree W" first="Wasu" last="Pathom-Aree">Wasu Pathom-Aree</name>
<affiliation><nlm:affiliation>Center of Excellence in Microbial Diversity and Sustainable Utilization, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand.</nlm:affiliation>
</affiliation>
<affiliation><nlm:affiliation>Science and Technology Research Institute, Chiang Mai University, Chiang Mai 50200, Thailand.</nlm:affiliation>
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<affiliation><nlm:affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</nlm:affiliation>
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<author><name sortKey="Lumyong, Saisamorn" sort="Lumyong, Saisamorn" uniqKey="Lumyong S" first="Saisamorn" last="Lumyong">Saisamorn Lumyong</name>
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<affiliation><nlm:affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</nlm:affiliation>
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<series><title level="j">International journal of systematic and evolutionary microbiology</title>
<idno type="eISSN">1466-5034</idno>
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<term>Bacterial Typing Techniques (MeSH)</term>
<term>Base Composition (MeSH)</term>
<term>Cell Wall (chemistry)</term>
<term>DNA, Bacterial (genetics)</term>
<term>Diaminopimelic Acid (chemistry)</term>
<term>Fatty Acids (chemistry)</term>
<term>Mycorrhizae (MeSH)</term>
<term>Nucleic Acid Hybridization (MeSH)</term>
<term>Phosphatidylethanolamines (chemistry)</term>
<term>Phylogeny (MeSH)</term>
<term>RNA, Ribosomal, 16S (genetics)</term>
<term>Rhizosphere (MeSH)</term>
<term>Sequence Analysis, DNA (MeSH)</term>
<term>Soil Microbiology (MeSH)</term>
<term>Spores, Fungal (MeSH)</term>
<term>Thailand (MeSH)</term>
<term>Vitamin K 2 (analogs & derivatives)</term>
<term>Vitamin K 2 (chemistry)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="analogs & derivatives" xml:lang="en"><term>Vitamin K 2</term>
</keywords>
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<term>Fatty Acids</term>
<term>Phosphatidylethanolamines</term>
<term>Vitamin K 2</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>DNA, Bacterial</term>
<term>RNA, Ribosomal, 16S</term>
</keywords>
<keywords scheme="MESH" type="geographic" xml:lang="en"><term>Thailand</term>
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<term>Mycorrhizae</term>
<term>Nucleic Acid Hybridization</term>
<term>Phylogeny</term>
<term>Rhizosphere</term>
<term>Sequence Analysis, DNA</term>
<term>Soil Microbiology</term>
<term>Spores, Fungal</term>
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<front><div type="abstract" xml:lang="en">A novel actinomycete, designated strain GLM-1<sup>T</sup>
, was isolated from arbuscular mycorrhizal fungal spores from <i>Funneliformis mosseae</i>
RYA08, collected from <i>Aquilaria crassna</i>
Pierre ex Lec. rhizosphere soil in Klaeng, Rayong Province, Thailand. Morphological characteristics of this strain included long chains of rod-like cells and squarish elements. The cell-wall composition of this novel isolate contained <i>meso</i>
-diaminopimelic acid. The whole-cell diagnostic sugars were arabinose and galactose. The predominant menaquinone was MK-9(H<sub>4</sub>
). The major fatty acids were iso-C<sub>16 : 0</sub>
and iso-C<sub>15 : 0</sub>
. Only phosphatidylethanolamine was detected as a polar lipid. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain GLM-1<sup>T</sup>
was closely related to <i>Amycolatopsis rhabdoformis</i>
SB026<sup>T</sup>
(99.11 %) with a low DNA-DNA hybridization value of 22.6-34.7 %. Genome sequencing revealed a genome size of 10 Mbp. There were obvious distinctions in the average nucleotide identity values between stain GLM-1<sup>T</sup>
and its closely related strains at around 86-93 % (ANIb) and 89-94 % (ANIm). The digital DNA-DNA hybridization values between strain GLM-1<sup>T</sup>
and type strains of phylogenetically related species were 34-55 %. The G+C content of the genomic DNA was 71.8 mol%. Based on these data, strain GLM-1<sup>T</sup>
is considered to represent a novel species of the genus <i>Amycolatopsis</i>
, for which the name <i>Amycolatopsiseburnea</i>
sp. nov. is proposed. The type strain is GLM-1<sup>T</sup>
(=TBRC 9315<sup>T</sup>
=NBRC 113658<sup>T</sup>
).</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" IndexingMethod="Curated" Owner="NLM"><PMID Version="1">31433288</PMID>
<DateCompleted><Year>2019</Year>
<Month>11</Month>
<Day>11</Day>
</DateCompleted>
<DateRevised><Year>2020</Year>
<Month>01</Month>
<Day>08</Day>
</DateRevised>
<Article PubModel="Print"><Journal><ISSN IssnType="Electronic">1466-5034</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>69</Volume>
<Issue>11</Issue>
<PubDate><Year>2019</Year>
<Month>Nov</Month>
</PubDate>
</JournalIssue>
<Title>International journal of systematic and evolutionary microbiology</Title>
<ISOAbbreviation>Int J Syst Evol Microbiol</ISOAbbreviation>
</Journal>
<ArticleTitle><i>Amycolatopsis eburnea</i>
sp. nov., an actinomycete associated with arbuscular mycorrhizal fungal spores.</ArticleTitle>
<Pagination><MedlinePgn>3603-3608</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1099/ijsem.0.003669</ELocationID>
<Abstract><AbstractText>A novel actinomycete, designated strain GLM-1<sup>T</sup>
, was isolated from arbuscular mycorrhizal fungal spores from <i>Funneliformis mosseae</i>
RYA08, collected from <i>Aquilaria crassna</i>
Pierre ex Lec. rhizosphere soil in Klaeng, Rayong Province, Thailand. Morphological characteristics of this strain included long chains of rod-like cells and squarish elements. The cell-wall composition of this novel isolate contained <i>meso</i>
-diaminopimelic acid. The whole-cell diagnostic sugars were arabinose and galactose. The predominant menaquinone was MK-9(H<sub>4</sub>
). The major fatty acids were iso-C<sub>16 : 0</sub>
and iso-C<sub>15 : 0</sub>
. Only phosphatidylethanolamine was detected as a polar lipid. Phylogenetic analysis based on 16S rRNA gene sequences showed that strain GLM-1<sup>T</sup>
was closely related to <i>Amycolatopsis rhabdoformis</i>
SB026<sup>T</sup>
(99.11 %) with a low DNA-DNA hybridization value of 22.6-34.7 %. Genome sequencing revealed a genome size of 10 Mbp. There were obvious distinctions in the average nucleotide identity values between stain GLM-1<sup>T</sup>
and its closely related strains at around 86-93 % (ANIb) and 89-94 % (ANIm). The digital DNA-DNA hybridization values between strain GLM-1<sup>T</sup>
and type strains of phylogenetically related species were 34-55 %. The G+C content of the genomic DNA was 71.8 mol%. Based on these data, strain GLM-1<sup>T</sup>
is considered to represent a novel species of the genus <i>Amycolatopsis</i>
, for which the name <i>Amycolatopsiseburnea</i>
sp. nov. is proposed. The type strain is GLM-1<sup>T</sup>
(=TBRC 9315<sup>T</sup>
=NBRC 113658<sup>T</sup>
).</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Chaiya</LastName>
<ForeName>Leardwiriyakool</ForeName>
<Initials>L</Initials>
<AffiliationInfo><Affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Matsumoto</LastName>
<ForeName>Atsuko</ForeName>
<Initials>A</Initials>
<AffiliationInfo><Affiliation>Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Wink</LastName>
<ForeName>Joachim</ForeName>
<Initials>J</Initials>
<AffiliationInfo><Affiliation>Microbial Strain Collection, Helmholtz Centre for Infection Research (HZI), 38124, Braunschweig, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Inahashi</LastName>
<ForeName>Yuki</ForeName>
<Initials>Y</Initials>
<AffiliationInfo><Affiliation>Graduate School of Infection Control Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Kitasato Institute for Life Sciences, Kitasato University, 5-9-1 Shirokane, Minato-ku, Tokyo 108-8641, Japan.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Risdian</LastName>
<ForeName>Chandra</ForeName>
<Initials>C</Initials>
<AffiliationInfo><Affiliation>Research Unit for Clean Technology, Indonesian Institute of Sciences (LIPI), Bandung 40135, Indonesia.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Microbial Strain Collection, Helmholtz Centre for Infection Research (HZI), 38124, Braunschweig, Germany.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Pathom-Aree</LastName>
<ForeName>Wasu</ForeName>
<Initials>W</Initials>
<AffiliationInfo><Affiliation>Center of Excellence in Microbial Diversity and Sustainable Utilization, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Science and Technology Research Institute, Chiang Mai University, Chiang Mai 50200, Thailand.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>Lumyong</LastName>
<ForeName>Saisamorn</ForeName>
<Initials>S</Initials>
<AffiliationInfo><Affiliation>The Royal Society of Thailand, Academy of Science, Bangkok 10300, Thailand.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Center of Excellence in Microbial Diversity and Sustainable Utilization, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand.</Affiliation>
</AffiliationInfo>
<AffiliationInfo><Affiliation>Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand.</Affiliation>
</AffiliationInfo>
</Author>
</AuthorList>
<Language>eng</Language>
<PublicationTypeList><PublicationType UI="D016428">Journal Article</PublicationType>
</PublicationTypeList>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Int J Syst Evol Microbiol</MedlineTA>
<NlmUniqueID>100899600</NlmUniqueID>
<ISSNLinking>1466-5026</ISSNLinking>
</MedlineJournalInfo>
<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D004269">DNA, Bacterial</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D005227">Fatty Acids</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D010714">Phosphatidylethanolamines</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D012336">RNA, Ribosomal, 16S</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>11032-49-8</RegistryNumber>
<NameOfSubstance UI="D024482">Vitamin K 2</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>39382-08-6</RegistryNumber>
<NameOfSubstance UI="C483858">phosphatidylethanolamine</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>523-39-7</RegistryNumber>
<NameOfSubstance UI="C073355">menaquinone 9</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>583-93-7</RegistryNumber>
<NameOfSubstance UI="D003960">Diaminopimelic Acid</NameOfSubstance>
</Chemical>
</ChemicalList>
<CitationSubset>IM</CitationSubset>
<MeshHeadingList><MeshHeading><DescriptorName UI="D039903" MajorTopicYN="N">Actinobacteria</DescriptorName>
<QualifierName UI="Q000145" MajorTopicYN="Y">classification</QualifierName>
<QualifierName UI="Q000302" MajorTopicYN="N">isolation & purification</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D015373" MajorTopicYN="N">Bacterial Typing Techniques</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D001482" MajorTopicYN="N">Base Composition</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D002473" MajorTopicYN="N">Cell Wall</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D004269" MajorTopicYN="N">DNA, Bacterial</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D003960" MajorTopicYN="N">Diaminopimelic Acid</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D005227" MajorTopicYN="N">Fatty Acids</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D038821" MajorTopicYN="Y">Mycorrhizae</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D009693" MajorTopicYN="N">Nucleic Acid Hybridization</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010714" MajorTopicYN="N">Phosphatidylethanolamines</DescriptorName>
<QualifierName UI="Q000737" MajorTopicYN="N">chemistry</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D010802" MajorTopicYN="Y">Phylogeny</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012336" MajorTopicYN="N">RNA, Ribosomal, 16S</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D058441" MajorTopicYN="N">Rhizosphere</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D012988" MajorTopicYN="Y">Soil Microbiology</DescriptorName>
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<KeywordList Owner="NOTNLM"><Keyword MajorTopicYN="N">Amycolatopsis eburnea</Keyword>
<Keyword MajorTopicYN="N">Arbuscular mycorrhiza fungi</Keyword>
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<ArticleIdList><ArticleId IdType="pubmed">31433288</ArticleId>
<ArticleId IdType="doi">10.1099/ijsem.0.003669</ArticleId>
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