Katelyn Sparks, Nathan Guy, George Lengyel, Jonathan Franks, Chris Maltman
A polyphasic taxonomic study was carried out on strain T9W2-OT, isolated from the roots of the aquatic plant Salvinia minima. This isolate is rod-shaped, forms yellow/orange pigmented colonies and produces the pigment flexirubin. Nearly complete 16S rRNA gene sequence homology related the strain to Chryseobacterium, with 98.8 and 98.5% similarity to Chryseobacterium profundimaris and Chryseobacterium takakiae, respectively. Average nucleotide identity and digital DNA-DNA hybridization with the closest phylogenetic neighbour of T9W2-OT showed differences at the species level, further confirmed by differences in several physiological characteristics. The main fatty acids are iso C15 : 0, iso C17:1 ω9c, iso C17 : 0 3-OH and summed feature 4 (iso-C15 : 0 2-OH and/or C16:1 ω7c). DNA G+C content is 37.2 mol%. MK-6 is the only menaquinone found, and phosphatidylethanolamine is the dominant polar lipid. Based on the results obtained, this bacterium is assigned to the genus Chryseobacterium as a new species with the name Chryseobacterium salviniae sp. nov., type strain T9W2-OT (=NRRL B-65715T =DSM 118061T).
{"title":"<i>Chryseobacterium salviniae</i> sp. nov., a bacterium isolated from the roots of the aquatic plant <i>Salvinia minima</i>.","authors":"Katelyn Sparks, Nathan Guy, George Lengyel, Jonathan Franks, Chris Maltman","doi":"10.1099/ijsem.0.006644","DOIUrl":"https://doi.org/10.1099/ijsem.0.006644","url":null,"abstract":"<p><p>A polyphasic taxonomic study was carried out on strain T9W2-O<sup>T</sup>, isolated from the roots of the aquatic plant <i>Salvinia minima</i>. This isolate is rod-shaped, forms yellow/orange pigmented colonies and produces the pigment flexirubin. Nearly complete 16S rRNA gene sequence homology related the strain to <i>Chryseobacterium</i>, with 98.8 and 98.5% similarity to <i>Chryseobacterium profundimaris</i> and <i>Chryseobacterium takakiae</i>, respectively. Average nucleotide identity and digital DNA-DNA hybridization with the closest phylogenetic neighbour of T9W2-O<sup>T</sup> showed differences at the species level, further confirmed by differences in several physiological characteristics. The main fatty acids are iso C<sub>15 : 0</sub>, iso C<sub>17:1 ω9c</sub>, iso C<sub>17 : 0</sub> 3-OH and summed feature 4 (iso-C<sub>15 : 0</sub> 2-OH and/or C<sub>16:1 ω7c</sub>). DNA G+C content is 37.2 mol%. MK-6 is the only menaquinone found, and phosphatidylethanolamine is the dominant polar lipid. Based on the results obtained, this bacterium is assigned to the genus <i>Chryseobacterium</i> as a new species with the name <i>Chryseobacterium salviniae</i> sp. nov., type strain T9W2-O<sup>T</sup> (=NRRL B-65715<sup>T</sup> =DSM 118061<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143055906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chun-Yue Chai, Bing-Yan Song, Dan Lu, Cai-Ying Zhang, Feng-Li Hui
Two novel yeast strains, NYNU 236247 and NYNU 23523, were isolated from the leaves of Carpinus turczaninowii Hance, collected in the Tianchi Mountain National Forest Park, Henan Province, central China. Phylogenetic analysis of the D1/D2 domain of the large subunit rRNA gene and the internal transcribed spacer (ITS) region revealed the closest relatives of the strains are three described Pseudobensingtonia species: Ps. fusiformis, Ps. musae and Ps. ingoldii. The novel species differed from the type strains of these three species by 12 to 22 nucleotide substitutions and 1 gap (~2.0-4.0%) in the D1/D2 domain and by 78 to 100 nucleotide mismatches (~12.0-16%) in the ITS region. Physiologically, the novel species differs from Ps. fusiformis and Ps. musae in its ability to assimilate dl-lactate and melezitose and from Ps. ingoldii by its inability to assimilate melibiose, soluble starch and ethanol. Pseudobensingtonia carpini sp. nov. is proposed for those two strains, with the holotype designated as GDMCC 2.483T (MycoBank MB 857072).
{"title":"<i>Pseudobensingtonia carpini</i> sp. nov., a novel yeast species isolated from plant leaves in China.","authors":"Chun-Yue Chai, Bing-Yan Song, Dan Lu, Cai-Ying Zhang, Feng-Li Hui","doi":"10.1099/ijsem.0.006642","DOIUrl":"https://doi.org/10.1099/ijsem.0.006642","url":null,"abstract":"<p><p>Two novel yeast strains, NYNU 236247 and NYNU 23523, were isolated from the leaves of <i>Carpinus turczaninowii</i> Hance, collected in the Tianchi Mountain National Forest Park, Henan Province, central China. Phylogenetic analysis of the D1/D2 domain of the large subunit rRNA gene and the internal transcribed spacer (ITS) region revealed the closest relatives of the strains are three described <i>Pseudobensingtonia</i> species: <i>Ps. fusiformis</i>, <i>Ps. musae</i> and <i>Ps. ingoldii</i>. The novel species differed from the type strains of these three species by 12 to 22 nucleotide substitutions and 1 gap (~2.0-4.0%) in the D1/D2 domain and by 78 to 100 nucleotide mismatches (~12.0-16%) in the ITS region. Physiologically, the novel species differs from <i>Ps. fusiformis</i> and <i>Ps. musae</i> in its ability to assimilate dl-lactate and melezitose and from <i>Ps. ingoldii</i> by its inability to assimilate melibiose, soluble starch and ethanol. <i>Pseudobensingtonia carpini</i> sp. nov. is proposed for those two strains, with the holotype designated as GDMCC 2.483<sup>T</sup> (MycoBank MB 857072).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142970861","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A thorough polyphasic taxonomic study, integrating genome-based taxonomic approaches, was carried out to characterize the RB5T strain isolated from root nodules of Retama monosperma growing on the coastal dunes of Bousfer Beach (Oran, Algeria). The 16S rRNA gene sequence analysis revealed that strain RB5T had the highest similarity to Pseudomonas granadensis LMG27940T (98.94%) and Pseudomonas gozinkensis IzPS32dT (98.73%). Phylogenetic studies, including both 16S rRNA gene sequence and multilocus sequence analysis using 16S rRNA, gyrB and rpoD housekeeping genes, positioned RB5T in a distinct branch alongside its closest relative, P. granadensis LMG27940T. Phylogenomic analysis using the Bac120 marker set and Type (Strain) Genome Server confirmed the unique position of RB5T and its close relationship with P. granadensis LMG27940T. Similarly, genomic comparisons using average nucleotide identity based on blast (ANIb) and digital DNA-DNA hybridization (dDDH) revealed values of 92.85 and 59.3%, respectively, when compared with its closest relative, P. granadensis LMG27940T. Both values fall below the established species delimitation thresholds of 95-96% for ANIb and 70% for dDDH, providing strong genomic evidence that strain RB5T represents a novel species. Further average nucleotide identity comparisons with unclassified Pseudomonas spp. (384 genomes) and metagenomic-derived genomes from the Genome Taxonomy Database (GTDB) showed values between 84.27 and 89.2%, indicating that strain RB5T belongs to a unique evolutionary line. The genome of RB5T, with a size of 6 311 310 bp and a G+C content of 60%, harbours several key genes associated with plant growth-promoting traits, making it a promising candidate for sustainable agriculture. Phenotypically, RB5T strain is an aerobic, rod-shaped, Gram-negative, non-spore-forming bacterium that is motile with a single polar flagellum. It grows under a wide range of temperature (4-42 °C) and pH (5-10) conditions and tolerates up to 6% (w/v) NaCl. The main cellular fatty acid composition of RB5T includes C16:0, C17:0 cyclo and the summed features 3 consisting of C16:1 ω7c/C16:1 ω6c. Based on the phylogenetic, phenotypic, chemotaxonomic and genome comparison analyses, strain RB5T was identified as a novel species of the genus Pseudomonas, for which the name Pseudomonas retamae sp. nov. is proposed. The type strain is RB5T (=DSM 117471T=LMG 33633T=CIP 112482T).
{"title":"<i>Pseudomonas retamae</i> sp. nov., a novel endophytic bacterium with plant growth-promoting potential, isolated from root nodules of <i>Retama monosperma</i> in Northwestern Algeria.","authors":"Nawel Selami, Fatima El-Houaria Zitouni-Haouar, Chahira Zerouki, Chahrazed Aibeche, Nassima Draou, Omar Khelil, Slimane Choubane, Makaoui Maatallah, Ikram Madani, Khadidja Ouenzar, Assia Zemmour, Mohamed Kerkoud, Bacem Mnasri, Bouziane Moumen, Cécile Vriet, Abderrezak Djabeur","doi":"10.1099/ijsem.0.006646","DOIUrl":"https://doi.org/10.1099/ijsem.0.006646","url":null,"abstract":"<p><p>A thorough polyphasic taxonomic study, integrating genome-based taxonomic approaches, was carried out to characterize the RB5<sup>T</sup> strain isolated from root nodules of <i>Retama monosperma</i> growing on the coastal dunes of Bousfer Beach (Oran, Algeria). The 16S rRNA gene sequence analysis revealed that strain RB5<sup>T</sup> had the highest similarity to <i>Pseudomonas granadensis</i> LMG27940<sup>T</sup> (98.94%) and <i>Pseudomonas gozinkensis</i> IzPS32d<sup>T</sup> (98.73%). Phylogenetic studies, including both 16S rRNA gene sequence and multilocus sequence analysis using 16S <i>rRNA</i>, <i>gyrB</i> and <i>rpoD</i> housekeeping genes, positioned RB5<sup>T</sup> in a distinct branch alongside its closest relative, <i>P. granadensis</i> LMG27940<sup>T</sup>. Phylogenomic analysis using the Bac120 marker set and Type (Strain) Genome Server confirmed the unique position of RB5<sup>T</sup> and its close relationship with <i>P. granadensis</i> LMG27940<sup>T</sup>. Similarly, genomic comparisons using average nucleotide identity based on blast (ANIb) and digital DNA-DNA hybridization (dDDH) revealed values of 92.85 and 59.3%, respectively, when compared with its closest relative, <i>P. granadensis</i> LMG27940<sup>T</sup>. Both values fall below the established species delimitation thresholds of 95-96% for ANIb and 70% for dDDH, providing strong genomic evidence that strain RB5<sup>T</sup> represents a novel species. Further average nucleotide identity comparisons with unclassified <i>Pseudomonas</i> spp. (384 genomes) and metagenomic-derived genomes from the Genome Taxonomy Database (GTDB) showed values between 84.27 and 89.2%, indicating that strain RB5<sup>T</sup> belongs to a unique evolutionary line. The genome of RB5<sup>T</sup>, with a size of 6 311 310 bp and a G+C content of 60%, harbours several key genes associated with plant growth-promoting traits, making it a promising candidate for sustainable agriculture. Phenotypically, RB5<sup>T</sup> strain is an aerobic, rod-shaped, Gram-negative, non-spore-forming bacterium that is motile with a single polar flagellum. It grows under a wide range of temperature (4-42 °C) and pH (5-10) conditions and tolerates up to 6% (w/v) NaCl. The main cellular fatty acid composition of RB5<sup>T</sup> includes C<sub>16:0</sub>, C<sub>17:0</sub> cyclo and the summed features 3 consisting of C<sub>16:1</sub> ω7c/<sub>C16:1</sub> ω6c. Based on the phylogenetic, phenotypic, chemotaxonomic and genome comparison analyses, strain RB5<sup>T</sup> was identified as a novel species of the genus <i>Pseudomonas</i>, for which the name <i>Pseudomonas retamae</i> sp. nov. is proposed. The type strain is RB5<sup>T</sup> (=DSM 117471<sup>T</sup>=LMG 33633<sup>T</sup>=CIP 112482<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142983524","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Following a proposal to emend Recommendation 6(7), Rule 64 and Appendix 9, Section D of the International Code of Nomenclature of Prokaryotes to regulate the formation of prokaryote names from personal names, I hereby report the outcome of the ballot on this proposal by the members of the International Committee on Systematics of Prokaryotes.
{"title":"Emendation of Recommendation 6(7), Rule 64 and Appendix 9 Section D of the International Code of Nomenclature of Prokaryotes to regulate the formation of prokaryote names from personal names.","authors":"Aharon Oren","doi":"10.1099/ijsem.0.006626","DOIUrl":"10.1099/ijsem.0.006626","url":null,"abstract":"<p><p>Following a proposal to emend Recommendation 6(7), Rule 64 and Appendix 9, Section D of the International Code of Nomenclature of Prokaryotes to regulate the formation of prokaryote names from personal names, I hereby report the outcome of the ballot on this proposal by the members of the International Committee on Systematics of Prokaryotes.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142921789","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Yi Li, Jiaojiao Wang, Chunyuan Wu, Jian He, Qinfen Li, Xiao Deng, Huadong Tan
A bacterial strain, designated as A6T, was isolated from the rhizosphere soil of a healthy muskmelon in Wenchang, Hainan Province, China. The cells of strain A6T were Gram-negative, aerobic, short rod and motile with a single polar flagellum. Strain A6T could tolerate up to 55.0 mM Al3+ and inhibited the growth of Fusarium oxysporum f. sp. melonis, which is the pathogen of muskmelon Fusarium wilt. Growth occurred at 15-37 ℃ (optimum at 30 ℃), pH 4.5-8.0 (optimum pH 6.5) and with 0-3.0 % NaCl (w/v; optimum, 0.5%). Strain A6T shared the highest 16S rRNA gene sequence similarities with Dyella lutea SaT (98.0%), followed by Dyella thiooxydans ATSB10T (98.0%), Frateuria edaphi 5GH9-34T (97.9%), Dyella nitratireducens DHG59T (97.7%), Frateuria defendens DHoT (97.7%) and Frateuria soli 5GH9-11T (97.7%). Phylogenetic trees based on 16S rRNA gene and genomic sequences indicated that strain A6T belonged to the genus Dyella and formed a subclade with Dyella lutea SaT and Dyella thiooxydans ATSB10T. The average nucleotide identity (ANI), average amino acid identity (AAI) and digital DNA-DNA hybridization (dDDH) values between A6T and its closely related type strains were 78.8-80.8 %, 70.0-71.7 % and 20.5-22.1 %, respectively. The sole respiratory quinone was ubiquinone-8 (Q-8). The polar lipid profile consisted of diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylethanolamine (PE), two unidentified aminophospholipids (APL1-2) and three unidentified phospholipids (PL1-3). The major cellular fatty acids (≥5 %) were iso-C17 : 0, C16 : 0, summed feature 9 (iso-C17 : 1ω9c and/or C16 : 0 10-methyl), iso-C15 : 0, iso-C16 : 0 and anteiso-C17 : 0. The genome size of strain A6T was 3.7 Mb with a DNA G+C content of 65.1%. Based on the phenotypic, phylogenetic, genotypic and chemotaxonomic features, strain A6T represents a novel species in the genus Dyella, for which Dyella aluminiiresistens A6T sp. nov. is proposed. The type strain is A6T (= GDMCC 1.4640T = KCTC 92542T).
{"title":"<i>Dyella aluminiiresistens</i> sp. nov., a Al<sup>3+</sup>-tolerant bacterium with the ability to inhibit <i>Fusarium oxysporum</i> f. sp. <i>melonis</i> isolated from rhizosphere soil of muskmelon.","authors":"Yi Li, Jiaojiao Wang, Chunyuan Wu, Jian He, Qinfen Li, Xiao Deng, Huadong Tan","doi":"10.1099/ijsem.0.006611","DOIUrl":"10.1099/ijsem.0.006611","url":null,"abstract":"<p><p>A bacterial strain, designated as A6<sup>T</sup>, was isolated from the rhizosphere soil of a healthy muskmelon in Wenchang, Hainan Province, China. The cells of strain A6<sup>T</sup> were Gram-negative, aerobic, short rod and motile with a single polar flagellum. Strain A6<sup>T</sup> could tolerate up to 55.0 mM Al<sup>3+</sup> and inhibited the growth of <i>Fusarium oxysporum</i> f. sp. <i>melonis,</i> which is the pathogen of muskmelon <i>Fusarium wilt</i>. Growth occurred at 15-37 ℃ (optimum at 30 ℃), pH 4.5-8.0 (optimum pH 6.5) and with 0-3.0 % NaCl (w/v; optimum, 0.5%). Strain A6<sup>T</sup> shared the highest 16S rRNA gene sequence similarities with <i>Dyella lutea</i> Sa<sup>T</sup> (98.0%), followed by <i>Dyella thiooxydans</i> ATSB10<sup>T</sup> (98.0%), <i>Frateuria edaphi</i> 5GH9-34<sup>T</sup> (97.9%), <i>Dyella nitratireducens</i> DHG59<sup>T</sup> (97.7%), <i>Frateuria defendens</i> DHo<sup>T</sup> (97.7%) and <i>Frateuria soli</i> 5GH9-11<sup>T</sup> (97.7%). Phylogenetic trees based on 16S rRNA gene and genomic sequences indicated that strain A6<sup>T</sup> belonged to the genus <i>Dyella</i> and formed a subclade with <i>Dyella lutea</i> Sa<sup>T</sup> and <i>Dyella thiooxydans</i> ATSB10<sup>T</sup>. The average nucleotide identity (ANI), average amino acid identity (AAI) and digital DNA-DNA hybridization (dDDH) values between A6<sup>T</sup> and its closely related type strains were 78.8-80.8 %, 70.0-71.7 % and 20.5-22.1 %, respectively. The sole respiratory quinone was ubiquinone-8 (Q-8). The polar lipid profile consisted of diphosphatidylglycerol (DPG), phosphatidylglycerol (PG), phosphatidylethanolamine (PE), two unidentified aminophospholipids (APL1-2) and three unidentified phospholipids (PL1-3). The major cellular fatty acids (≥5 %) were iso-C<sub>17 : 0</sub>, C<sub>16 : 0</sub>, summed feature 9 (iso-C<sub>17 : 1</sub> <i>ω</i>9<i>c</i> and/or C<sub>16 : 0</sub> 10-methyl), iso-C<sub>15 : 0</sub>, iso-C<sub>16 : 0</sub> and anteiso-C<sub>17 : 0</sub>. The genome size of strain A6<sup>T</sup> was 3.7 Mb with a DNA G+C content of 65.1%. Based on the phenotypic, phylogenetic, genotypic and chemotaxonomic features, strain A6<sup>T</sup> represents a novel species in the genus <i>Dyella</i>, for which <i>Dyella aluminiiresistens</i> A6<sup>T</sup> sp. nov. is proposed. The type strain is A6<sup>T</sup> (= GDMCC 1.4640<sup>T</sup> = KCTC 92542<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142931781","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A novel bacterium, designated 19SA41, was isolated from the air of the Icelandic volcanic island Surtsey. Cells of strain 19SA41 are Gram-stain-negative, strictly aerobic, non-motile rods and form pale yellow-pigmented colonies. The strain grows at 4-30 °C (optimum, 22 °C), at pH 6-10 (optimum, pH 7.5) and with 0-4% NaCl (optimum, 0.5%). Phylogenetic analyses based on 16S rRNA gene sequences showed that 19SA41 belonged to the genus Flavobacterium and is most similar to Flavobacterium xinjiangense DSM 19743T, with a sequence similarity of 96.52%. The new strain contained iso-C15 : 0 (22%) and summed feature 3 (C16∶1ω6c/C16∶1ω7c) (20%) as the predominant fatty acids. The major respiratory quinone was menaquinone-6 (100%). The polar lipid profile consisted of phosphatidylethanolamine and several uncharacterized amino lipids, glycolipids and lipids. The genome of the new strain was 4.01 Mbp, and its G+C content was 33.2 mol%. Based on characterization and comparative results, using a polyphasic taxonomic approach, we propose that the new isolate represents a novel species of the genus Flavobacterium with the name Flavobacterium aerium sp. nov. The type strain is ISCaR-07695T (=DSM 116640T =UBOOC-M-3567T).
{"title":"<i>Flavobacterium aerium</i> sp. nov., a bacterium isolated from the air of the Icelandic volcanic island Surtsey.","authors":"Aurélien Daussin, Pauline Vannier, Marine Ménager, Émilien Mater, Viggó Þór Marteinsson","doi":"10.1099/ijsem.0.006647","DOIUrl":"10.1099/ijsem.0.006647","url":null,"abstract":"<p><p>A novel bacterium, designated 19SA41, was isolated from the air of the Icelandic volcanic island Surtsey. Cells of strain 19SA41 are Gram-stain-negative, strictly aerobic, non-motile rods and form pale yellow-pigmented colonies. The strain grows at 4-30 °C (optimum, 22 °C), at pH 6-10 (optimum, pH 7.5) and with 0-4% NaCl (optimum, 0.5%). Phylogenetic analyses based on 16S rRNA gene sequences showed that 19SA41 belonged to the genus <i>Flavobacterium</i> and is most similar to <i>Flavobacterium xinjiangense</i> DSM 19743<sup>T</sup>, with a sequence similarity of 96.52%. The new strain contained iso-C<sub>15 : 0</sub> (22%) and summed feature 3 (C<sub>16∶1</sub>ω6c/C<sub>16∶1</sub>ω7c) (20%) as the predominant fatty acids. The major respiratory quinone was menaquinone-6 (100%). The polar lipid profile consisted of phosphatidylethanolamine and several uncharacterized amino lipids, glycolipids and lipids. The genome of the new strain was 4.01 Mbp, and its G+C content was 33.2 mol%. Based on characterization and comparative results, using a polyphasic taxonomic approach, we propose that the new isolate represents a novel species of the genus <i>Flavobacterium</i> with the name <i>Flavobacterium aerium</i> sp. nov. The type strain is ISCaR-07695<sup>T</sup> (=DSM 116640<sup>T</sup> =UBOOC-M-3567<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11756700/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143023405","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A Gram-stain-positive, facultatively anaerobic, rod-shaped strain, designated SPB1-3T, was isolated from tree bark. This strain exhibited heterofermentative production of dl-lactic acid from glucose. Optimal growth was observed at 25-40 °C, pH 4.0-7.0, and in the presence of 3% (w/v) NaCl. The cell wall peptidoglycan contained lysine and aspartic acid. The predominant fatty acids identified were C16:0 and the Summed feature 7 (C19 :1 ω7c/C19:1 ω6c and/or C19:1 ω6c/ω7c/19cy). The polar lipid profile included phosphatidylglycerol, diphosphatidylglycerol and phosphatidylinositol, along with two unidentified phospholipids, two unidentified amino lipids and two unidentified lipids. Phylogenetic analysis based on 16S rRNA gene sequences positioned strain SPB1-3T within the genus Lentilactobacillus, showing a close relation to Lentilactobacillus kosonis NBRC 111893T (99.86%) and Lentilactobacillus curieae CCTCC M 2011381T (98.65%). The whole genome of strain SPB1-3T comprised 1 932 998 base pairs with 1955 coding genes and a DNA G+C content of 37.8%. Digital DNA-DNA hybridization between strain SPB1-3T and closely related type strains ranged from 19.50 to 27.20%. The average nucleotide identity ranged from 84.21 to 85.56%, and the average amino acid identity ranged from 57.25 to 85.99%, both falling below the established thresholds for species delineation. Strain SPB1-3T was clearly distinguishable from related Lentilactobacillus species based on its phenotypic and chemotaxonomic characteristics, 16S rRNA gene sequence similarity and whole genome analysis. Additionally, the strain exhibited radical scavenging activity at 66.92% and demonstrated 82.32% inhibition in the tyrosinase inhibitory assay. These findings support the classification of strain SPB1-3T as a novel species within the genus Lentilactobacillus, for which the name Lentilactobacillus terminaliae sp. nov. is proposed. The type strain is SPB1-3T (=JCM 35081T=TISTR 10005T).
{"title":"<i>Lentilactobacillus terminaliae</i> sp. nov., isolated from tree bark (<i>Terminalia ivorensis</i> Chev.) and its antioxidant activity.","authors":"Sukanya Phuengjayaem, Engkarat Kingkaew, Nitcha Chamroensaksri, Wongsakorn Phongsopitanun, Somboon Tanasupawat","doi":"10.1099/ijsem.0.006649","DOIUrl":"https://doi.org/10.1099/ijsem.0.006649","url":null,"abstract":"<p><p>A Gram-stain-positive, facultatively anaerobic, rod-shaped strain, designated SPB1-3<sup>T</sup>, was isolated from tree bark. This strain exhibited heterofermentative production of dl-lactic acid from glucose. Optimal growth was observed at 25-40 °C, pH 4.0-7.0, and in the presence of 3% (w/v) NaCl. The cell wall peptidoglycan contained lysine and aspartic acid. The predominant fatty acids identified were C<sub>16:0</sub> and the Summed feature 7 (C<sub>19 :1</sub> <i> ω</i>7c/C<sub>19:1</sub> <i> ω6</i>c and/or C<sub>19:1</sub> <i> ω</i>6c/<i>ω</i>7c/19cy). The polar lipid profile included phosphatidylglycerol, diphosphatidylglycerol and phosphatidylinositol, along with two unidentified phospholipids, two unidentified amino lipids and two unidentified lipids. Phylogenetic analysis based on 16S rRNA gene sequences positioned strain SPB1-3<sup>T</sup> within the genus <i>Lentilactobacillus</i>, showing a close relation to <i>Lentilactobacillus kosonis</i> NBRC 111893<sup>T</sup> (99.86%) and <i>Lentilactobacillus curieae</i> CCTCC M 2011381<sup>T</sup> (98.65%). The whole genome of strain SPB1-3<sup>T</sup> comprised 1 932 998 base pairs with 1955 coding genes and a DNA G+C content of 37.8%. Digital DNA-DNA hybridization between strain SPB1-3<sup>T</sup> and closely related type strains ranged from 19.50 to 27.20%. The average nucleotide identity ranged from 84.21 to 85.56%, and the average amino acid identity ranged from 57.25 to 85.99%, both falling below the established thresholds for species delineation. Strain SPB1-3<sup>T</sup> was clearly distinguishable from related <i>Lentilactobacillus</i> species based on its phenotypic and chemotaxonomic characteristics, 16S rRNA gene sequence similarity and whole genome analysis. Additionally, the strain exhibited radical scavenging activity at 66.92% and demonstrated 82.32% inhibition in the tyrosinase inhibitory assay. These findings support the classification of strain SPB1-3<sup>T</sup> as a novel species within the genus <i>Lentilactobacillus</i>, for which the name <i>Lentilactobacillus terminaliae</i> sp. nov. is proposed. The type strain is SPB1-3<sup>T</sup> (=JCM 35081<sup>T</sup>=TISTR 10005<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143052535","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Irina A Bryantseva, John A Kyndt, Johannes F Imhoff
A new alkaliphilic strain of a purple sulphur bacterium designated as Um2 (=KCTC 25734=VKM B-3893=UQM 41073) with bacteriochlorophyll b and internal photosynthetic membranes of tubular type was isolated from the Umhei hydrothermal system (40 °C, pH 9.3 and salinity 0.42 g l-1) located in the Baikal rift zone (Russia). Based on morphological and physiological characteristics, this bacterium was classified as Thioalkalicoccus limnaeus. The 16S rRNA gene sequence similarity of strain Um2 was 96.69% with the type strain of Tac. limnaeus A26T, 95.41% with 'Thioflavicoccus mobilis' 8321T and 95.34% with Thiococcus pfennigii 4250. The level of similarity of the ribulose 1,5-bisphosphate carboxylase sequences of strain Um2 and known strains of Thioalkalicoccus showed that they belong to the same species. Comparison of the genome nt sequences of strain Um2 revealed that the new isolate was remote from all other described Chromatiaceae species both in digital DNA-DNA hybridization (21.5%) and in average nt identity (76.7%) at the genus level. However, a genome nt sequence had not been determined for any of the known Thioalkalicoccus strains; therefore, the first genome sequence of a member of the genus Thioalkalicoccus is presented here. Tac. limnaeus Um2 is proposed as the neotype, as strain A26T has been lost from culture collections.
{"title":"First genome sequence of a purple sulphur bacterium of the genus <i>Thioalkalicoccus</i>, its characterization as a new isolate of <i>Thioalkalicoccus limnaeus</i> and proposal of strain Um2 as neotype of this species.","authors":"Irina A Bryantseva, John A Kyndt, Johannes F Imhoff","doi":"10.1099/ijsem.0.006657","DOIUrl":"https://doi.org/10.1099/ijsem.0.006657","url":null,"abstract":"<p><p>A new alkaliphilic strain of a purple sulphur bacterium designated as Um2 (=KCTC 25734=VKM B-3893=UQM 41073) with bacteriochlorophyll <i>b</i> and internal photosynthetic membranes of tubular type was isolated from the Umhei hydrothermal system (40 °C, pH 9.3 and salinity 0.42 g l<sup>-1</sup>) located in the Baikal rift zone (Russia). Based on morphological and physiological characteristics, this bacterium was classified as <i>Thioalkalicoccus limnaeus</i>. The 16S rRNA gene sequence similarity of strain Um2 was 96.69% with the type strain of <i>Tac. limnaeus</i> A26<sup>T</sup>, 95.41% with '<i>Thioflavicoccus mobilis</i>' 8321<sup>T</sup> and 95.34% with <i>Thiococcus pfennigii</i> 4250. The level of similarity of the ribulose 1,5-bisphosphate carboxylase sequences of strain Um2 and known strains of <i>Thioalkalicoccus</i> showed that they belong to the same species. Comparison of the genome nt sequences of strain Um2 revealed that the new isolate was remote from all other described <i>Chromatiaceae</i> species both in digital DNA-DNA hybridization (21.5%) and in average nt identity (76.7%) at the genus level. However, a genome nt sequence had not been determined for any of the known <i>Thioalkalicoccus</i> strains; therefore, the first genome sequence of a member of the genus <i>Thioalkalicoccus</i> is presented here. <i>Tac. limnaeus</i> Um2 is proposed as the neotype, as strain A26<sup>T</sup> has been lost from culture collections.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143065695","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A novel Pseudonocardia strain DW16-2T, isolated from duckweed (Spirodela polyrhiza), was taxonomically studied in detail. The analysis based on its 16S rRNA gene sequence revealed that the strain was most closely related to Pseudonocardia carboxydivorans Y8T (98.8%), followed by Pseudonocardia tropica YIM 61452T (98.7%), Pseudonocardia antarctica DVS 5a1T (98.7%) and Pseudonocardia alni DSM 44104T (98.7%). The average nucleotide identity (ANI) based on blast and digital DNA-DNA hybridization (dDDH) relatedness values between strain DW16-2T and their closest type strains were below the threshold values for identifying a novel species. Morphological, physiological and chemotaxonomic features of strain DW16-2T were typical for the genus Pseudonocardia by forming extensively branched substrate mycelium and aerial mycelium that fragmented into rod-shaped spore, with a smooth surface. The whole-cell hydrolysates of strain DW16-2T contained meso-diaminopimelic acid as the diagnostic diamino acid, and the whole-cell sugars were arabinose, galactose, glucose and a trace amount of ribose. The polar lipids contained phosphatidylethanolamine, phosphatidylcholine, phosphatidylglycerol and unidentified phospholipids. The menaquinone (MK) was MK-8(H4). The cellular fatty acids (>5 %) were iso-C16 : 0, iso-C16 : 1 H, summed feature 3: C16 : 1 ω7c/C16 : 1 ω6c; C16 : 1 ω6c/C16 : 1 ω7c, C17 : 1 ω8c and anteiso-C17 : 0. Characterization based on chemotaxonomic, phenotypic, genotypic and phylogenetic evidence demonstrated that strain DW16-2T represents a novel species of the genus Pseudonocardia, for which the name Pseudonocardia spirodelae sp. nov. (type strain DW16-2T = TBRC 16418T = NBRC 115857T) is proprosed. In addition, the comparison of the whole genome sequences suggested that P. alni and P. antarctica belong to the same species and P. carboxydivorans is a subspecies of P. alni. Therefore, it is proposed that P. antarctica Prabahar et al. 2004 is reclassified as a later heterotypic synonym of P. alni (Evtushenko et al. 1989) Warwick et al. 1994, and P. carboxydivorans Park et al. 2008 is proposed as a subspecies of P. alni (Evtushenko et al. 1989) Warwick et al. 1994.
对从浮萍(Spirodela polyrhiza)中分离得到的一株伪心菌DW16-2T进行了详细的分类研究。16S rRNA基因序列分析显示,该菌株与pseudocardidia carboxydivorans Y8T亲缘关系最密切(98.8%),其次为pseudocardidia tropica YIM 61452T(98.7%)、pseudoncardidia antarctica DVS 5a1T(98.7%)和pseudoncardidia alni DSM 44104T(98.7%)。菌株DW16-2T与其最近型菌株的平均核苷酸同源性(ANI)和数字DNA-DNA杂交(dDDH)亲缘性值均低于鉴定新种的阈值。菌株DW16-2T在形态、生理和化学分类上具有假心草属的典型特征,形成分枝广泛的底生菌丝和气生菌丝,并破碎成杆状孢子,表面光滑。菌株DW16-2T全细胞水解产物中诊断二氨基戊酸,全细胞糖为阿拉伯糖、半乳糖、葡萄糖和微量核糖。极性脂质含有磷脂酰乙醇胺、磷脂酰胆碱、磷脂酰甘油和未识别的磷脂。甲基萘醌(MK)为MK-8(H4)。细胞脂肪酸(bbb5 %)分别为iso-C16: 0, iso-C16: 1 H,总特征3:C16: 1 ω7c/C16: 1 ω6c;C16: 1ω6 c / C16: 1ω7 c, C17: 1ω8 c和anteiso-C17: 0。基于化学分类、表型、基因型和系统发育证据的鉴定表明,菌株DW16-2T是Pseudonocardia属的一个新种,并建议将其命名为Pseudonocardia spirodelae ps . nov(型菌株DW16-2T = TBRC 16418T = NBRC 115857T)。此外,全基因组序列比较表明,P. alni和P. antarctica属于同一种,P. carboxydivorans是P. alni的一个亚种。因此,有人建议将P. antarctica Prabahar et al. 2004重新归类为P. alni (Evtushenko et al. 1989)的后异型同义词(Warwick et al. 1994),并提出P. carboxydivorans Park et al. 2008作为P. alni的一个亚种(Evtushenko et al. 1989) Warwick et al. 1994。
{"title":"<i>Pseudonocardia spirodelae</i> sp. nov., isolated from duckweed and formal proposal to reclassify <i>Pseudonocardia antarctica</i> as a later heterotypic synonym of <i>Pseudonocardia alni</i> and reclassify <i>Pseudonocardia carboxydivorans</i> as <i>Pseudonocardia alni</i> subsp. <i>carboxydivorans</i>.","authors":"Waranya Butdee, Yuparat Saimee, Chanwit Suriyachadkun, Kannika Duangmal","doi":"10.1099/ijsem.0.006608","DOIUrl":"10.1099/ijsem.0.006608","url":null,"abstract":"<p><p>A novel <i>Pseudonocardia</i> strain DW16-2<sup>T</sup>, isolated from duckweed (<i>Spirodela polyrhiza</i>), was taxonomically studied in detail. The analysis based on its 16S rRNA gene sequence revealed that the strain was most closely related to <i>Pseudonocardia carboxydivorans</i> Y8<sup>T</sup> (98.8%), followed by <i>Pseudonocardia tropica</i> YIM 61452<sup>T</sup> (98.7%), <i>Pseudonocardia antarctica</i> DVS 5a1<sup>T</sup> (98.7%) and <i>Pseudonocardia alni</i> DSM 44104<sup>T</sup> (98.7%). The average nucleotide identity (ANI) based on blast and digital DNA-DNA hybridization (dDDH) relatedness values between strain DW16-2<sup>T</sup> and their closest type strains were below the threshold values for identifying a novel species. Morphological, physiological and chemotaxonomic features of strain DW16-2<sup>T</sup> were typical for the genus <i>Pseudonocardia</i> by forming extensively branched substrate mycelium and aerial mycelium that fragmented into rod-shaped spore, with a smooth surface. The whole-cell hydrolysates of strain DW16-2<sup>T</sup> contained <i>meso</i>-diaminopimelic acid as the diagnostic diamino acid, and the whole-cell sugars were arabinose, galactose, glucose and a trace amount of ribose. The polar lipids contained phosphatidylethanolamine, phosphatidylcholine, phosphatidylglycerol and unidentified phospholipids. The menaquinone (MK) was MK-8(H<sub>4</sub>). The cellular fatty acids (>5 %) were <i>iso</i>-C<sub>16 : 0</sub>, <i>iso</i>-C<sub>16 : 1</sub> H, summed feature 3: C<sub>16 : 1</sub> ω7c/C<sub>16 : 1</sub> ω6c; C<sub>16 : 1</sub> ω6c/C<sub>16 : 1</sub> ω7c, C<sub>17 : 1</sub> ω8c and <i>anteiso</i>-C<sub>17 : 0</sub>. Characterization based on chemotaxonomic, phenotypic, genotypic and phylogenetic evidence demonstrated that strain DW16-2<sup>T</sup> represents a novel species of the genus <i>Pseudonocardia</i>, for which the name <i>Pseudonocardia spirodelae</i> sp. nov. (type strain DW16-2<sup>T</sup> = TBRC 16418<sup>T</sup> = NBRC 115857<sup>T</sup>) is proprosed. In addition, the comparison of the whole genome sequences suggested that <i>P. alni</i> and <i>P. antarctica</i> belong to the same species and <i>P. carboxydivorans</i> is a subspecies of <i>P. alni</i>. Therefore, it is proposed that <i>P. antarctica</i> Prabahar <i>et al</i>. 2004 is reclassified as a later heterotypic synonym of <i>P. alni</i> (Evtushenko <i>et al</i>. 1989) Warwick <i>et al</i>. 1994, and <i>P. carboxydivorans</i> Park <i>et al</i>. 2008 is proposed as a subspecies of <i>P. alni</i> (Evtushenko <i>et al</i>. 1989) Warwick <i>et al</i>. 1994.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142921785","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A hybrid in-person and online open plenary meeting of the International Committee on Systematics of Prokaryotes (ICSP) was held on 22 October 2024 at the Consiglio Nazionale delle Ricerche, Sesto Fiorentino, Florence, Italy, and via Teams just prior to the IUMS 2024 Congress. To comply with Articles 4(d) and 5(d) (1) of the statutes of the ICSP, the minutes of this meeting are published here.
国际原核生物系统学委员会(ICSP)于2024年10月22日在意大利佛罗伦萨Sesto Fiorentino的Consiglio Nazionale delle Ricerche举行了现场和在线混合公开全体会议,并在IUMS 2024年大会之前通过团队举行了会议。为遵守国际科学技术委员会章程第4(d)条和第5(d)(1)条的规定,会议记录在此公布。
{"title":"International Committee on Systematics of Prokaryotes: minutes of the open plenary meeting, Tuesday, 22 October 2024, Sesto Fiorentino, Florence, Italy, and via Teams.","authors":"Aharon Oren","doi":"10.1099/ijsem.0.006621","DOIUrl":"10.1099/ijsem.0.006621","url":null,"abstract":"<p><p>A hybrid in-person and online open plenary meeting of the International Committee on Systematics of Prokaryotes (ICSP) was held on 22 October 2024 at the Consiglio Nazionale delle Ricerche, Sesto Fiorentino, Florence, Italy, and via Teams just prior to the IUMS 2024 Congress. To comply with Articles 4(d) and 5(d) (1) of the statutes of the ICSP, the minutes of this meeting are published here.</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 1","pages":""},"PeriodicalIF":2.0,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142921793","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}