Flavivirga spongiicola sp. nov. and Flavivirga abyssicola sp. nov., Isolated from Marine Environments SCIE SCOPUS KCI

DC Field Value Language
dc.contributor.author Yang, Sung Hyun -
dc.contributor.author Park, Mi-Jeong -
dc.contributor.author Oh, Hyun-Myung -
dc.contributor.author Park, Yeong Jun -
dc.contributor.author Kwon, Kae Kyoung -
dc.date.accessioned 2024-02-19T01:30:17Z -
dc.date.available 2024-02-19T01:30:17Z -
dc.date.created 2024-02-19 -
dc.date.issued 2024-01 -
dc.identifier.issn 1225-8873 -
dc.identifier.uri https://sciwatch.kiost.ac.kr/handle/2020.kiost/45389 -
dc.description.abstract Two novel Gram-stain-negative, strictly-aerobic, rod-shaped (1.2 +/- 3.4 mu m x 0.3 +/- 0.7 mu m), and non-motile marine bacterial species, designated MEBiC05379T and MEBiC07777(T), were isolated from a marine sponge Pseudaxinella sp. in Gangneung City and deep-sea sediments of the Ulleung basin in the East Sea of Korea, respectively. The 16S rRNA gene sequence analysis revealed high levels of similarities between these strains and members of the genus Flavivirga (97.0-98.4% sequence identities). Both novel strains revealed as mesophilic, neutrophilic in pH and slightly halophilic. Similar to those of other Flavivirga members, the primary cellular fatty acids of both strains were iso-C-15:0, iso-C-15:1 G, iso-C-15:03-OH, and iso-C-17:0 3-OH, with MEBiC05379(T) and MEBiC07777(T) containing relatively higher proportions of C12:0 and summed feature 3 (C-16:1 omega 7c and/or C-16:1 omega 6c). In both taxa, the major isoprenoid quinone was MK-6. The DNA G + C contents of MEBiC05379(T) and MEBiC07777(T) genomes were 32.62 and 32.46 mol%, respectively. Compared to other members of Flavivirga, both strains exhibited similar DNA G + C ratio and fatty acids pattern, yet enzyme expression and carbon sources utilization pattern were different. Genomes of the genus Flavivirga showed enzyme preferences to fucoidan and sulfated galactans. Considering the monophyly rule, AAI values delineate the genus Flavivirga from adjacent genera calculated to be 76.0-78.7%. Based on the phenotypic, genomic and biochemical data, strains for MEBiC05379T and MEBiC07777T thus represent two novel species in the genus Flavivirga, for which the names Flavivirga spongiicola sp. nov. (MEBiC05379(T) [= KCTC 92527 (T) = JCM 16662 (T)]), and Flavivirga abyssicola sp. nov. (MEBiC07777(T) [= KCTC 92563( T) = JCM 36477 (T)]) are proposed. -
dc.description.uri 1 -
dc.language English -
dc.publisher 한국미생물학회 -
dc.title Flavivirga spongiicola sp. nov. and Flavivirga abyssicola sp. nov., Isolated from Marine Environments -
dc.type Article -
dc.citation.endPage 19 -
dc.citation.startPage 11 -
dc.citation.title The Journal of Microbiology -
dc.citation.volume 62 -
dc.contributor.alternativeName 양성현 -
dc.contributor.alternativeName 박미정 -
dc.contributor.alternativeName 박영준 -
dc.contributor.alternativeName 권개경 -
dc.identifier.bibliographicCitation The Journal of Microbiology, v.62, pp.11 - 19 -
dc.identifier.doi 10.1007/s12275-023-00102-z -
dc.identifier.scopusid 2-s2.0-85184192660 -
dc.identifier.wosid 001158435600001 -
dc.type.docType Article; Early Access -
dc.description.journalClass 1 -
dc.description.isOpenAccess N -
dc.subject.keywordPlus ECKLONIAE SP-NOV -
dc.subject.keywordPlus GEN.-NOV. -
dc.subject.keywordPlus FAMILY FLAVOBACTERIACEAE -
dc.subject.keywordPlus EMENDED DESCRIPTIONS -
dc.subject.keywordPlus EPILITHONIMONAS -
dc.subject.keywordPlus ANNOTATION -
dc.subject.keywordPlus DIVERSITY -
dc.subject.keywordPlus IDENTITY -
dc.subject.keywordPlus MEMBERS -
dc.subject.keywordAuthor Flavivirga spongiicola sp. nov. -
dc.subject.keywordAuthor Flavivirga abyssicola. sp. nov. -
dc.subject.keywordAuthor New Taxa (Bacteroidota) -
dc.relation.journalWebOfScienceCategory Microbiology -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.relation.journalResearchArea Microbiology -
Appears in Collections:
Marine Resources & Environment Research Division > Marine Biotechnology &Bioresource Research Department > 1. Journal Articles
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