{"title":"磷微杆菌,一种从磷矿中分离出来的放线菌。","authors":"Huan Ma, Jing Zhen, Fei Feng, Shujing Quan, Hong Hu, Gao Lei, Wentao Diao, Dehai Liu, Shanshan Li, Lei Li, Xueyan Wang, Fuhong Xie","doi":"10.1099/ijsem.0.006849","DOIUrl":null,"url":null,"abstract":"<p><p>Two Gram-staining-positive, non-motile and non-spore-forming bacterial strains, designated as 9H2<sup>T</sup> and YDN13, were isolated from a phosphate mine in Yunnan Province, China. Phylogenetic analyses based on 16S rRNA gene sequences indicated that strains 9H2<sup>T</sup> and YDN13 belong to the genus <i>Microbacterium</i>. Results show that strains 9H2<sup>T</sup> and YDN13 occupied a distinct position within the genus <i>Microbacterium</i> and showed the highest 16S rRNA gene sequence similarity of 97.6% with the type strains of <i>Microbacterium thalassium</i> CCTCC AB 2020140<sup>T</sup>, followed by 97.5% with <i>Microbacterium hydrocarboxydans</i> DSM 16089<sup>T</sup> and 97.3% with <i>Microbacterium stercoris</i> CCTCC AA 2018028<sup>T</sup>. In the phylogenetic trees based on 16S rRNA gene sequences, strains 9H2<sup>T</sup> and YDN13 were closely related to <i>M. stercoris</i> CCTCC AA 2018028<sup>T</sup> and <i>Microbacterium sediminicola</i> YM 10-847<sup>T</sup>. Strains 9H2<sup>T</sup> and YDN13 showed the highest values of an orthologous average nucleotide identity (84%) and a digital DNA-DNA hybridization (49%) with <i>M. stercoris</i> CCTCC AA 2018028<sup>T</sup>, followed by an orthologous average nucleotide identity of 76.0% and a digital DNA-DNA hybridization value of 17.9% with <i>M. thalassium</i> CCTCC AB 2020140<sup>T</sup>. The respiratory menaquinones were MK-11, MK-12, MK-10 and MK-13. The major fatty acid profile contained anteiso-C<sub>15 : 0</sub>, iso-C<sub>16 : 0</sub> and anteiso-C<sub>17 : 0</sub>. The polar lipids contained diphosphatidylglycerol, phosphatidylglycerol, three unidentified phospholipids and one unidentified glycolipid. The whole-cell sugars included galactose and glucose. The peptidoglycan hydrolysate contained glutamate, glycine, ornithine and alanine. The DNA G+C contents were 71.1 mol%. Phenotypic, phylogenetic, chemotaxonomic and genomic analyses revealed that strains 9H2<sup>T</sup> and YDN13 represent a novel species of <i>Microbacterium</i>, for which the name <i>Microbacterium phosphatis</i> sp. nov. was proposed. The type strain is 9H2<sup>T</sup> (MCCC 1K08680<sup>T</sup>=KCTC 59053<sup>T</sup>=CGMCC 1.60061<sup>T</sup>).</p>","PeriodicalId":14390,"journal":{"name":"International journal of systematic and evolutionary microbiology","volume":"75 8","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Microbacterium phosphatis</i> sp. nov., an actinomycete isolated from a phosphate mine.\",\"authors\":\"Huan Ma, Jing Zhen, Fei Feng, Shujing Quan, Hong Hu, Gao Lei, Wentao Diao, Dehai Liu, Shanshan Li, Lei Li, Xueyan Wang, Fuhong Xie\",\"doi\":\"10.1099/ijsem.0.006849\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Two Gram-staining-positive, non-motile and non-spore-forming bacterial strains, designated as 9H2<sup>T</sup> and YDN13, were isolated from a phosphate mine in Yunnan Province, China. Phylogenetic analyses based on 16S rRNA gene sequences indicated that strains 9H2<sup>T</sup> and YDN13 belong to the genus <i>Microbacterium</i>. Results show that strains 9H2<sup>T</sup> and YDN13 occupied a distinct position within the genus <i>Microbacterium</i> and showed the highest 16S rRNA gene sequence similarity of 97.6% with the type strains of <i>Microbacterium thalassium</i> CCTCC AB 2020140<sup>T</sup>, followed by 97.5% with <i>Microbacterium hydrocarboxydans</i> DSM 16089<sup>T</sup> and 97.3% with <i>Microbacterium stercoris</i> CCTCC AA 2018028<sup>T</sup>. In the phylogenetic trees based on 16S rRNA gene sequences, strains 9H2<sup>T</sup> and YDN13 were closely related to <i>M. stercoris</i> CCTCC AA 2018028<sup>T</sup> and <i>Microbacterium sediminicola</i> YM 10-847<sup>T</sup>. Strains 9H2<sup>T</sup> and YDN13 showed the highest values of an orthologous average nucleotide identity (84%) and a digital DNA-DNA hybridization (49%) with <i>M. stercoris</i> CCTCC AA 2018028<sup>T</sup>, followed by an orthologous average nucleotide identity of 76.0% and a digital DNA-DNA hybridization value of 17.9% with <i>M. thalassium</i> CCTCC AB 2020140<sup>T</sup>. The respiratory menaquinones were MK-11, MK-12, MK-10 and MK-13. The major fatty acid profile contained anteiso-C<sub>15 : 0</sub>, iso-C<sub>16 : 0</sub> and anteiso-C<sub>17 : 0</sub>. The polar lipids contained diphosphatidylglycerol, phosphatidylglycerol, three unidentified phospholipids and one unidentified glycolipid. The whole-cell sugars included galactose and glucose. The peptidoglycan hydrolysate contained glutamate, glycine, ornithine and alanine. The DNA G+C contents were 71.1 mol%. 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引用次数: 0
摘要
从云南某磷矿中分离到两株革兰氏染色阳性、不运动、不形成孢子的细菌9H2T和YDN13。基于16S rRNA基因序列的系统发育分析表明,菌株9H2T和YDN13属于微杆菌属。结果表明,菌株9H2T和YDN13在微杆菌属中占据明显的位置,与地中海微杆菌CCTCC AB 2020140T的16S rRNA基因序列相似性最高,为97.6%,与羧微杆菌DSM 16089T的相似性为97.5%,与粪微杆菌CCTCC AA 2018028T的相似性为97.3%。在基于16S rRNA基因序列的系统发育树中,菌株9H2T和YDN13与M. stercoris CCTCC AA 2018028T和Microbacterium sediminicola YM 10-847T亲缘关系较近。菌株9H2T和YDN13与m.s stercoris CCTCC AA 2018028T同源性最高(84%),数字DNA-DNA杂交(49%),其次是m.s thalassium CCTCC AB 2020140T同源性平均76.0%,数字DNA-DNA杂交值为17.9%。呼吸性萘醌类药物为MK-11、MK-12、MK-10和MK-13。主要脂肪酸谱为前iso- c15: 0、前iso-C16: 0和前iso- c17: 0。极性脂质含有二磷脂酰甘油、磷脂酰甘油、三种未识别的磷脂和一种未识别的糖脂。全细胞糖包括半乳糖和葡萄糖。肽聚糖水解产物含有谷氨酸、甘氨酸、鸟氨酸和丙氨酸。DNA G+C含量为71.1 mol%。表型、系统发育、化学分类和基因组学分析表明,菌株9H2T和YDN13是一种新的微细菌,并建议将其命名为微细菌磷酸盐sp. 11。型应变为9H2T (MCCC 1K08680T=KCTC 59053T=CGMCC 1.60061T)。
Microbacterium phosphatis sp. nov., an actinomycete isolated from a phosphate mine.
Two Gram-staining-positive, non-motile and non-spore-forming bacterial strains, designated as 9H2T and YDN13, were isolated from a phosphate mine in Yunnan Province, China. Phylogenetic analyses based on 16S rRNA gene sequences indicated that strains 9H2T and YDN13 belong to the genus Microbacterium. Results show that strains 9H2T and YDN13 occupied a distinct position within the genus Microbacterium and showed the highest 16S rRNA gene sequence similarity of 97.6% with the type strains of Microbacterium thalassium CCTCC AB 2020140T, followed by 97.5% with Microbacterium hydrocarboxydans DSM 16089T and 97.3% with Microbacterium stercoris CCTCC AA 2018028T. In the phylogenetic trees based on 16S rRNA gene sequences, strains 9H2T and YDN13 were closely related to M. stercoris CCTCC AA 2018028T and Microbacterium sediminicola YM 10-847T. Strains 9H2T and YDN13 showed the highest values of an orthologous average nucleotide identity (84%) and a digital DNA-DNA hybridization (49%) with M. stercoris CCTCC AA 2018028T, followed by an orthologous average nucleotide identity of 76.0% and a digital DNA-DNA hybridization value of 17.9% with M. thalassium CCTCC AB 2020140T. The respiratory menaquinones were MK-11, MK-12, MK-10 and MK-13. The major fatty acid profile contained anteiso-C15 : 0, iso-C16 : 0 and anteiso-C17 : 0. The polar lipids contained diphosphatidylglycerol, phosphatidylglycerol, three unidentified phospholipids and one unidentified glycolipid. The whole-cell sugars included galactose and glucose. The peptidoglycan hydrolysate contained glutamate, glycine, ornithine and alanine. The DNA G+C contents were 71.1 mol%. Phenotypic, phylogenetic, chemotaxonomic and genomic analyses revealed that strains 9H2T and YDN13 represent a novel species of Microbacterium, for which the name Microbacterium phosphatis sp. nov. was proposed. The type strain is 9H2T (MCCC 1K08680T=KCTC 59053T=CGMCC 1.60061T).
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.