Microbacterium oryzae sp. nov., an actinobacterium isolated from rice field soil

A novel aerobic soil actinobacterium (strain MB10T) belonging to the genus Microbacterium was isolated from rice field soil samples collected from Jagatpur, Orissa, India. Cells were Gram-stain positive, short rod-shaped and motile. The strain was oxidase-negative and catalase-positive. Heterotrophi...

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Veröffentlicht in:International journal of systematic and evolutionary microbiology 2013-07, Vol.63 (Pt 7), p.2442-2449
Hauptverfasser: Kumari, Prabla, Bandyopadhyay, Saumya, Das, Subrata K
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Bandyopadhyay, Saumya
Das, Subrata K
description A novel aerobic soil actinobacterium (strain MB10T) belonging to the genus Microbacterium was isolated from rice field soil samples collected from Jagatpur, Orissa, India. Cells were Gram-stain positive, short rod-shaped and motile. The strain was oxidase-negative and catalase-positive. Heterotrophic growth was observed at pH 5.0–11.0 and at 16–37 °C; optimum growth was observed at 28 °C and pH 7.0–9.0. The DNA G+C content was 71.6 mol%. Predominant cellular fatty acids of strain MB10T were iso-C14 : 0, anteiso-C15 : 0, C16 : 0, iso-C16 : 0 and anteiso-C17 : 0. Cell wall sugars were galactose, glucose and rhamnose. The major isoprenoid quinones were MK-9 (10 %), MK-10 (43 %) and MK-11 (36 %). The peptidoglycan represents the peptidoglycan type B2β. The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phospholipid and unknown glycolipids. 16S rRNA gene sequence identity revealed the strain MB10T clustered within the radiation of the genus Microbacterium and showed 99.2 % similarity with Microbacterium barkeri DSM 20145T. However, DNA–DNA similarity study was 37.0 % with Microbacterium barkeri DSM 20145T, the nearest phylogenetic relative. On the basis of phenotypic and chemotaxonomic properties, 16S rRNA gene sequence analysis and DNA–DNA reassociation studies, it is proposed that strain MB10T represents a novel species of the genus Microbacterium, for which the name Microbacterium oryzae sp. nov. is proposed; the type strain is MB10T ( = JCM 16837T = DSM 23396T).
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Cells were Gram-stain positive, short rod-shaped and motile. The strain was oxidase-negative and catalase-positive. Heterotrophic growth was observed at pH 5.0–11.0 and at 16–37 °C; optimum growth was observed at 28 °C and pH 7.0–9.0. The DNA G+C content was 71.6 mol%. Predominant cellular fatty acids of strain MB10T were iso-C14 : 0, anteiso-C15 : 0, C16 : 0, iso-C16 : 0 and anteiso-C17 : 0. Cell wall sugars were galactose, glucose and rhamnose. The major isoprenoid quinones were MK-9 (10 %), MK-10 (43 %) and MK-11 (36 %). The peptidoglycan represents the peptidoglycan type B2β. The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phospholipid and unknown glycolipids. 16S rRNA gene sequence identity revealed the strain MB10T clustered within the radiation of the genus Microbacterium and showed 99.2 % similarity with Microbacterium barkeri DSM 20145T. However, DNA–DNA similarity study was 37.0 % with Microbacterium barkeri DSM 20145T, the nearest phylogenetic relative. 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Cells were Gram-stain positive, short rod-shaped and motile. The strain was oxidase-negative and catalase-positive. Heterotrophic growth was observed at pH 5.0–11.0 and at 16–37 °C; optimum growth was observed at 28 °C and pH 7.0–9.0. The DNA G+C content was 71.6 mol%. Predominant cellular fatty acids of strain MB10T were iso-C14 : 0, anteiso-C15 : 0, C16 : 0, iso-C16 : 0 and anteiso-C17 : 0. Cell wall sugars were galactose, glucose and rhamnose. The major isoprenoid quinones were MK-9 (10 %), MK-10 (43 %) and MK-11 (36 %). The peptidoglycan represents the peptidoglycan type B2β. The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phospholipid and unknown glycolipids. 16S rRNA gene sequence identity revealed the strain MB10T clustered within the radiation of the genus Microbacterium and showed 99.2 % similarity with Microbacterium barkeri DSM 20145T. However, DNA–DNA similarity study was 37.0 % with Microbacterium barkeri DSM 20145T, the nearest phylogenetic relative. On the basis of phenotypic and chemotaxonomic properties, 16S rRNA gene sequence analysis and DNA–DNA reassociation studies, it is proposed that strain MB10T represents a novel species of the genus Microbacterium, for which the name Microbacterium oryzae sp. nov. is proposed; the type strain is MB10T ( = JCM 16837T = DSM 23396T).</description><subject>Actinomycetales - classification</subject><subject>Actinomycetales - genetics</subject><subject>Actinomycetales - isolation &amp; purification</subject><subject>agricultural soils</subject><subject>Bacterial Typing Techniques</subject><subject>Base Composition</subject><subject>cell walls</subject><subject>chemotaxonomy</subject><subject>DNA</subject><subject>DNA, Bacterial - genetics</subject><subject>fatty acids</subject><subject>Fatty Acids - analysis</subject><subject>galactose</subject><subject>glucose</subject><subject>glycolipids</subject><subject>India</subject><subject>Microbacterium barkeri</subject><subject>microbiology</subject><subject>Molecular Sequence Data</subject><subject>Nucleic Acid Hybridization</subject><subject>nucleotide sequences</subject><subject>Oryza - microbiology</subject><subject>peptidoglycans</subject><subject>phospholipids</subject><subject>Phospholipids - analysis</subject><subject>Phylogeny</subject><subject>quinones</subject><subject>Quinones - analysis</subject><subject>rhamnose</subject><subject>ribosomal RNA</subject><subject>RNA, Ribosomal, 16S - genetics</subject><subject>sequence analysis</subject><subject>Sequence Analysis, DNA</subject><subject>Soil Microbiology</subject><subject>soil sampling</subject><issn>1466-5034</issn><issn>1466-5026</issn><issn>1466-5034</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkMtLAzEQh4MotlavHjVHD-46eewjRym-oKKgPYfsbiIpu5uadIX615uyKj3NMPPNwO9D6JxASkCIG7sKKaTA87KABA7QlPA8TzJg_HCvn6CTEFYAcQBwjCaUUWA55VP0-mxr7ypVb7S3Q4ed334rjcM6xb37Sq-x6nFc2n6PscG1aqMbbLzrsLe1xsbqtsHB2fYUHRnVBn32W2doeX_3Pn9MFi8PT_PbRVIzIjZJRVWjKCvKpuSCKkPKiueZaYAUoo5peE6aqshMoblRtcgzVmaC6awSihHOGZuhq_Hv2rvPQYeN7GyodduqXrshSMKEgCwHQSOajmhMGoLXRq697ZTfSgJyZ1FGixLkaFFCPLj4_T1UnW7-8T9tEbgcAaOcVB_eBrl8o0CynWIOlLEfUHZ2CQ</recordid><startdate>20130701</startdate><enddate>20130701</enddate><creator>Kumari, Prabla</creator><creator>Bandyopadhyay, Saumya</creator><creator>Das, Subrata K</creator><general>International Union of Microbiological Societies</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></search><sort><creationdate>20130701</creationdate><title>Microbacterium oryzae sp. nov., an actinobacterium isolated from rice field soil</title><author>Kumari, Prabla ; Bandyopadhyay, Saumya ; Das, Subrata K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c319t-b2ada2378d8492af18b465fd0179c468461db75f7e4fac96538593e5b9a314433</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Actinomycetales - classification</topic><topic>Actinomycetales - genetics</topic><topic>Actinomycetales - isolation &amp; purification</topic><topic>agricultural soils</topic><topic>Bacterial Typing Techniques</topic><topic>Base Composition</topic><topic>cell walls</topic><topic>chemotaxonomy</topic><topic>DNA</topic><topic>DNA, Bacterial - genetics</topic><topic>fatty acids</topic><topic>Fatty Acids - analysis</topic><topic>galactose</topic><topic>glucose</topic><topic>glycolipids</topic><topic>India</topic><topic>Microbacterium barkeri</topic><topic>microbiology</topic><topic>Molecular Sequence Data</topic><topic>Nucleic Acid Hybridization</topic><topic>nucleotide sequences</topic><topic>Oryza - microbiology</topic><topic>peptidoglycans</topic><topic>phospholipids</topic><topic>Phospholipids - analysis</topic><topic>Phylogeny</topic><topic>quinones</topic><topic>Quinones - analysis</topic><topic>rhamnose</topic><topic>ribosomal RNA</topic><topic>RNA, Ribosomal, 16S - genetics</topic><topic>sequence analysis</topic><topic>Sequence Analysis, DNA</topic><topic>Soil Microbiology</topic><topic>soil sampling</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kumari, Prabla</creatorcontrib><creatorcontrib>Bandyopadhyay, Saumya</creatorcontrib><creatorcontrib>Das, Subrata K</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><jtitle>International journal of systematic and evolutionary microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kumari, Prabla</au><au>Bandyopadhyay, Saumya</au><au>Das, Subrata K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbacterium oryzae sp. nov., an actinobacterium isolated from rice field soil</atitle><jtitle>International journal of systematic and evolutionary microbiology</jtitle><addtitle>Int J Syst Evol Microbiol</addtitle><date>2013-07-01</date><risdate>2013</risdate><volume>63</volume><issue>Pt 7</issue><spage>2442</spage><epage>2449</epage><pages>2442-2449</pages><issn>1466-5034</issn><issn>1466-5026</issn><eissn>1466-5034</eissn><abstract>A novel aerobic soil actinobacterium (strain MB10T) belonging to the genus Microbacterium was isolated from rice field soil samples collected from Jagatpur, Orissa, India. Cells were Gram-stain positive, short rod-shaped and motile. The strain was oxidase-negative and catalase-positive. Heterotrophic growth was observed at pH 5.0–11.0 and at 16–37 °C; optimum growth was observed at 28 °C and pH 7.0–9.0. The DNA G+C content was 71.6 mol%. Predominant cellular fatty acids of strain MB10T were iso-C14 : 0, anteiso-C15 : 0, C16 : 0, iso-C16 : 0 and anteiso-C17 : 0. Cell wall sugars were galactose, glucose and rhamnose. The major isoprenoid quinones were MK-9 (10 %), MK-10 (43 %) and MK-11 (36 %). The peptidoglycan represents the peptidoglycan type B2β. The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, phospholipid and unknown glycolipids. 16S rRNA gene sequence identity revealed the strain MB10T clustered within the radiation of the genus Microbacterium and showed 99.2 % similarity with Microbacterium barkeri DSM 20145T. However, DNA–DNA similarity study was 37.0 % with Microbacterium barkeri DSM 20145T, the nearest phylogenetic relative. On the basis of phenotypic and chemotaxonomic properties, 16S rRNA gene sequence analysis and DNA–DNA reassociation studies, it is proposed that strain MB10T represents a novel species of the genus Microbacterium, for which the name Microbacterium oryzae sp. nov. is proposed; the type strain is MB10T ( = JCM 16837T = DSM 23396T).</abstract><cop>England</cop><pub>International Union of Microbiological Societies</pub><pmid>23203624</pmid><doi>10.1099/ijs.0.046870-0</doi><tpages>8</tpages></addata></record>
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subjects Actinomycetales - classification
Actinomycetales - genetics
Actinomycetales - isolation & purification
agricultural soils
Bacterial Typing Techniques
Base Composition
cell walls
chemotaxonomy
DNA
DNA, Bacterial - genetics
fatty acids
Fatty Acids - analysis
galactose
glucose
glycolipids
India
Microbacterium barkeri
microbiology
Molecular Sequence Data
Nucleic Acid Hybridization
nucleotide sequences
Oryza - microbiology
peptidoglycans
phospholipids
Phospholipids - analysis
Phylogeny
quinones
Quinones - analysis
rhamnose
ribosomal RNA
RNA, Ribosomal, 16S - genetics
sequence analysis
Sequence Analysis, DNA
Soil Microbiology
soil sampling
title Microbacterium oryzae sp. nov., an actinobacterium isolated from rice field soil
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