{"title":"<i>Actinomycetospora aeridis</i> sp. nov., <i>Actinomycetospora flava</i> sp. nov. and <i>Actinomycetospora aurantiaca</i> sp. nov., endophytic actinobacteria isolated from wild orchid (<i>Aerides multiflora</i> Roxb).","authors":"Chanwit Suriyachadkun, Wipaporn Ngaemthao, Tawanmol Pujchakarn, Chatsuda Sakdapetsiri, Chanjira Ayawong, Kamonchai Chairote, Suwanee Chunhametha","doi":"10.1099/ijsem.0.006505","DOIUrl":null,"url":null,"abstract":"<p><p>Three novel mycelium-forming actinobacteria, designated OC33-EN06<sup>T</sup>, OC33-EN07<sup>T</sup>, and OC33-EN08<sup>T</sup>, were isolated from wild orchid (<i>Aerides multiflora</i> Roxb), collected from a hill evergreen forest in Northern Thailand. Strains OC33-EN06<sup>T</sup> and OC33-EN07<sup>T</sup> showed the highest 16S rRNA gene similarity with <i>Actinomycetospora lutea</i> TT00-04<sup>T</sup>, 99.17 and 99.45%, respectively. Strain OC33-EN08<sup>T</sup> showed high similarity with four species, namely '<i>Actinomycetospora termitidis</i> Odt1-22<sup>T</sup>' (99.37%), <i>Actinomycetospora chiangmaiensis</i> DSM 45062<sup>T</sup> (99.02%), <i>Actinomycetospora corticicola</i> 014-5<sup>T</sup> (99.02%), and <i>Actinomycetospora soli</i> SF1<sup>T</sup> (98.81%). Comparative genome analysis of OC33-EN06<sup>T</sup>, OC33-EN07<sup>T</sup>, and OC33-EN08<sup>T</sup> with the closely related type strains showed that average nucleotide identity (ANI) based on blast, ANI based on MUMmer, and average amino acid identity values were less than 95% and the digital DNA-DNA hybridization values were less than 70%, all below the thresholds for species demarcation. The digital G+C content of OC33-EN06<sup>T</sup>, OC33-EN07<sup>T</sup>, and OC33-EN08<sup>T</sup> were 74.5, 74, and 74 mol%, respectively. These three strains developed bud-like chains of non-motile cylindrical spores with a smooth surface. The cell-wall peptidoglycan contained <i>meso</i>-diaminopimelic acid. The whole-cell sugars contained ribose, arabinose, and galactose. The predominant menaquinone was MK-8(H<sub>4</sub>). The phospholipid profile included phosphatidylcholine, phosphatidylethanolamine, phosphatidylmethylethanolamine, phosphatidylglycerol, diphosphatidylglycerol, and phosphatidylinositol. Based on comparative analysis of genotypic, phenotypic and chemotaxonomic data, strains OC33-EN06<sup>T</sup> (=TBRC 18349<sup>T</sup>=NBRC 116543<sup>T</sup>), OC33-EN07<sup>T</sup> (=TBRC 18350<sup>T</sup>=NBRC 116544<sup>T</sup>), and OC33-EN08<sup>T</sup> (=TBRC 18318<sup>T</sup>=NBRC 116542<sup>T</sup>) represent the type strains of three novel species of the genus <i>Actinomycetospora</i> for which the names <i>Actinomycetospora aeridis</i> sp. nov., <i>Actinomycetospora flava</i> sp. nov., and <i>Actinomycetospora aurantiaca</i> sp. nov., are proposed.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"74 8","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of systematic and evolutionary microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1099/ijsem.0.006505","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Three novel mycelium-forming actinobacteria, designated OC33-EN06T, OC33-EN07T, and OC33-EN08T, were isolated from wild orchid (Aerides multiflora Roxb), collected from a hill evergreen forest in Northern Thailand. Strains OC33-EN06T and OC33-EN07T showed the highest 16S rRNA gene similarity with Actinomycetospora lutea TT00-04T, 99.17 and 99.45%, respectively. Strain OC33-EN08T showed high similarity with four species, namely 'Actinomycetospora termitidis Odt1-22T' (99.37%), Actinomycetospora chiangmaiensis DSM 45062T (99.02%), Actinomycetospora corticicola 014-5T (99.02%), and Actinomycetospora soli SF1T (98.81%). Comparative genome analysis of OC33-EN06T, OC33-EN07T, and OC33-EN08T with the closely related type strains showed that average nucleotide identity (ANI) based on blast, ANI based on MUMmer, and average amino acid identity values were less than 95% and the digital DNA-DNA hybridization values were less than 70%, all below the thresholds for species demarcation. The digital G+C content of OC33-EN06T, OC33-EN07T, and OC33-EN08T were 74.5, 74, and 74 mol%, respectively. These three strains developed bud-like chains of non-motile cylindrical spores with a smooth surface. The cell-wall peptidoglycan contained meso-diaminopimelic acid. The whole-cell sugars contained ribose, arabinose, and galactose. The predominant menaquinone was MK-8(H4). The phospholipid profile included phosphatidylcholine, phosphatidylethanolamine, phosphatidylmethylethanolamine, phosphatidylglycerol, diphosphatidylglycerol, and phosphatidylinositol. Based on comparative analysis of genotypic, phenotypic and chemotaxonomic data, strains OC33-EN06T (=TBRC 18349T=NBRC 116543T), OC33-EN07T (=TBRC 18350T=NBRC 116544T), and OC33-EN08T (=TBRC 18318T=NBRC 116542T) represent the type strains of three novel species of the genus Actinomycetospora for which the names Actinomycetospora aeridis sp. nov., Actinomycetospora flava sp. nov., and Actinomycetospora aurantiaca sp. nov., are proposed.
期刊介绍:
Published by the Microbiology Society and owned by the International Committee on Systematics of Prokaryotes (ICSP), a committee of the Bacteriology and Applied Microbiology Division of the International Union of Microbiological Societies, International Journal of Systematic and Evolutionary Microbiology is the leading forum for the publication of novel microbial taxa and the ICSP’s official journal of record for prokaryotic names.
The journal welcomes high-quality research on all aspects of microbial evolution, phylogenetics and systematics, encouraging submissions on all prokaryotes, yeasts, microfungi, protozoa and microalgae across the full breadth of systematics including:
Identification, characterisation and culture preservation
Microbial evolution and biodiversity
Molecular environmental work with strong taxonomic or evolutionary content
Nomenclature
Taxonomy and phylogenetics.