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dc.contributor.authorKrálová, Stanislava
dc.contributor.authorSandoval-Powers, Megan
dc.contributor.authorFawwal, Dorelle V.
dc.contributor.authorDegnes, Kristin Fløgstad
dc.contributor.authorLewin, Anna
dc.contributor.authorKlinkenberg, Geir
dc.contributor.authorNguyen, Giang-Son
dc.contributor.authorLiles, Mark R.
dc.contributor.authorWentzel, Alexander
dc.date.accessioned2022-09-13T13:46:32Z
dc.date.available2022-09-13T13:46:32Z
dc.date.created2021-08-23T09:21:33Z
dc.date.issued2021
dc.identifier.citationFrontiers in Microbiology, 2021, 12en_US
dc.identifier.issn1664-302X
dc.identifier.urihttps://hdl.handle.net/11250/3017575
dc.description.abstractMarine environments are home to an extensive number of microorganisms, many of which remain unexplored for taxonomic novelty and functional capabilities. In this study, a slow-growing Streptomyces strain expressing unique genomic and phenotypic characteristics, P38-E01T , was described using a polyphasic taxonomic approach. This strain is part of a collection of over 8,000 marine Actinobacteria isolates collected in the Trondheim fjord of Norway by SINTEF Industry (Trondheim, Norway) and the Norwegian University of Science and Technology (NTNU, Trondheim, Norway). Strain P38-E01T was isolated from the sediments of the Trondheim fjord, and phylogenetic analyses affiliated this strain with the genus Streptomyces, but it was not closely affiliated with other described species. The closest related type strains were Streptomyces daliensis YIM 31724T (98.6%), Streptomyces rimosus subsp. rimosus ATCC 10970T (98.4%), and Streptomyces sclerotialus NRRL ISP-5269T (98.3%). Predominant fatty acids were C16V0 iso, C16V0, and Summed Feature 3, and the predominant respiratory quinones were MK-10(H6), MK-10(H4), and MK9(H4). The main polar lipids were identified as diphosphatidylglycerol, phosphatidylethanolamine, hosphatidylglycerol, and phosphoglycolipid. The whole-cell sugars were glucose, ribose, and in minor amounts, mannose. The cell wall peptidoglycan contained LL-diaminopimelic acid. The draft genome has a size of 6.16 Mb, with a %G C C content of 71.4% and is predicted to contain at least 19 biosynthetic gene clusters encoding diverse secondary metabolites. Strain P38-E01T was found to inhibit the growth of the pathogenic yeast Candida albicans ATCC 90028 and a number of Gram-positive bacterial human and plant pathogens. Metabolites extracted from cultures of P38-E01T were analyzed by mass spectrometry, and it was found that the isolate produced the antifungal compound candicidin. Phenotypic and chemotaxonomic signatures, along with phylogenetic analyses, distinguished isolate P38-E01T from its closest neighbors; thus, this isolate represents a novel species of the genus Streptomyces for which the name Streptomyces tardus sp. nov. (P38-E01T D CCM 9049T D DSM 111582T ) is proposed.en_US
dc.language.isoengen_US
dc.publisherFrontiersen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectbiosynthetic potentialen_US
dc.subjectpolyphasic taxonomyen_US
dc.subjectmarine sedimentsen_US
dc.subjectActinobacteriaen_US
dc.subjectStreptomyces tardus sp. nov.en_US
dc.subjectsystematicsen_US
dc.titleStreptomyces tardus sp. nov.: A Slow-Growing Actinobacterium Producing Candicidin, Isolated From Sediments of the Trondheim Fjorden_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume12en_US
dc.source.journalFrontiers in Microbiologyen_US
dc.identifier.doi10.3389/fmicb.2021.714233
dc.identifier.cristin1927909
dc.relation.projectNorges forskningsråd: 248885en_US
dc.relation.projectNorges forskningsråd: 288057en_US
dc.source.articlenumber714233en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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