Ju-Young Hong, Jung-Hun Jo, Se-Yoon Chun, Wan-Taek Im
{"title":"Isolation and characterization of <i>Novosphingobium aquae</i> sp. nov. and <i>Novosphingobium anseongense</i> sp. nov.<i>,</i> isolated from freshwater.","authors":"Ju-Young Hong, Jung-Hun Jo, Se-Yoon Chun, Wan-Taek Im","doi":"10.1099/ijsem.0.006688","DOIUrl":null,"url":null,"abstract":"<p><p>Two novel Gram-stain-negative, aerobic, heterotrophic, non-motile bacterial strains, designated as AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup>, were isolated from freshwater in South Korea. To determine their taxonomic positions, the strains were thoroughly characterized. Genomic analyses, based on 16S rRNA gene and draft genome sequence data, revealed that the two novel isolates, AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup>, belonged to the genus <i>Novosphingobium</i>. AS3R-12<sup>T</sup> showed the highest 16S rRNA gene similarity (97.7%) with <i>Novosphingobium flavum</i> UCT-28<sup>T</sup>. In addition, PS1R-30<sup>T</sup> showed 97.9% 16S rRNA gene similarity with <i>Novosphingobium lentum</i> NBRC 107847<sup>T</sup>. The draft genome of strains AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup> consisted of 4 149 275 and 4 969 838 bps, with DNA G+C content of 63.1 and 66.1 mol%, respectively. The average nucleotide identity between two strains and other related species was below 76.2%, and the digital DNA-DNA hybridization values with closely related species were below 20.8%, both lower than the species delineation threshold. Strains AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup> contained the ubiquinone Q-10 as the major quinone and displayed a polyamine pattern with spermidine as the predominant polyamine. Additionally, their major fatty acids were characterized by C<sub>16:1</sub> <i> ω7c</i>/C<sub>16:1</sub> <i> ω6c</i> (summed feature 3) and C<sub>18:1</sub> <i> ω7c</i>/C<sub>18:1</sub> <i> ω6c</i> (summed feature 8). The major polar lipids of AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup> were diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylethanolamine (PE), sphingoglycolipid (SGL) and phosphatidylcholine (PC). Moreover, physiological and biochemical results allowed the phenotypic and genotypic differentiation of strains AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup> from their closest and other species of the genus <i>Novosphingobium</i> with validly published names. Therefore, AS3R-12<sup>T</sup> and PS1R-30<sup>T</sup> represented novel species of the genus <i>Novosphingobium</i>, for which the names <i>Novosphingobium aquae</i> sp. nov. (type strain AS3R-12<sup>T</sup>=KACC 23096<sup>T</sup>=LMG 32950<sup>T</sup>) and <i>Novosphingobium anseongense</i> sp. nov. (type strain PS1R-30<sup>T</sup>=KACC 23097<sup>T</sup>=LMG 32951<sup>T</sup>) are proposed.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 2","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-02-01","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.0.006688","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
Two novel Gram-stain-negative, aerobic, heterotrophic, non-motile bacterial strains, designated as AS3R-12T and PS1R-30T, were isolated from freshwater in South Korea. To determine their taxonomic positions, the strains were thoroughly characterized. Genomic analyses, based on 16S rRNA gene and draft genome sequence data, revealed that the two novel isolates, AS3R-12T and PS1R-30T, belonged to the genus Novosphingobium. AS3R-12T showed the highest 16S rRNA gene similarity (97.7%) with Novosphingobium flavum UCT-28T. In addition, PS1R-30T showed 97.9% 16S rRNA gene similarity with Novosphingobium lentum NBRC 107847T. The draft genome of strains AS3R-12T and PS1R-30T consisted of 4 149 275 and 4 969 838 bps, with DNA G+C content of 63.1 and 66.1 mol%, respectively. The average nucleotide identity between two strains and other related species was below 76.2%, and the digital DNA-DNA hybridization values with closely related species were below 20.8%, both lower than the species delineation threshold. Strains AS3R-12T and PS1R-30T contained the ubiquinone Q-10 as the major quinone and displayed a polyamine pattern with spermidine as the predominant polyamine. Additionally, their major fatty acids were characterized by C16:1 ω7c/C16:1 ω6c (summed feature 3) and C18:1 ω7c/C18:1 ω6c (summed feature 8). The major polar lipids of AS3R-12T and PS1R-30T were diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylethanolamine (PE), sphingoglycolipid (SGL) and phosphatidylcholine (PC). Moreover, physiological and biochemical results allowed the phenotypic and genotypic differentiation of strains AS3R-12T and PS1R-30T from their closest and other species of the genus Novosphingobium with validly published names. Therefore, AS3R-12T and PS1R-30T represented novel species of the genus Novosphingobium, for which the names Novosphingobium aquae sp. nov. (type strain AS3R-12T=KACC 23096T=LMG 32950T) and Novosphingobium anseongense sp. nov. (type strain PS1R-30T=KACC 23097T=LMG 32951T) 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.