{"title":"对Kocuria的基因组分析:五种产生iaa的极端微生物的分类修订和鉴定。","authors":"Cong-Jian Li, Zhu-Ming Jiang, Xiao-Yang Zhi, Hua-Hong Chen, Li-Yan Yu, Guang-Fu Li, Yu-Qin Zhang","doi":"10.3389/fmicb.2025.1547983","DOIUrl":null,"url":null,"abstract":"<p><p>Desert ecosystems have increasingly piqued the interest of microbiologists seeking novel bioactive compounds, as they are viewed as a largely uncharted reservoir of extremophiles with remarkable resilience to severe conditions. The genus <i>Kocuria</i>, belonging to the phylum <i>Actinomycetota</i>, is particularly notable for its documented capacity to flourish in such extreme environmental conditions. In this study, a total of 21 <i>Kocuria</i> strains were isolated from various ecosystems. Using polyphasic taxonomy approaches, eight strains from desert soils (CPCC 205273<sup>T</sup>, CPCC 205300, CPCC 205290, CPCC 205236<sup>T</sup>, CPCC 205293, CPCC 205292<sup>T</sup>, CPCC 205315<sup>T</sup>, CPCC 205268<sup>T</sup>) were identified representing five new species of the genus <i>Kocuria</i>. Strains CPCC 205281 and CPCC 205293 were identified as siblings of strain CPCC 205236<sup>T</sup>, while strains CPCC 205290 and CPCC 205300 were identified as siblings of strain CPCC 205273<sup>T</sup>. Additionally, <i>K. polaris</i> and <i>K</i>. <i>indcia</i> were determined to be the later heterotypic synonym of <i>K. rosea</i> and <i>K. marina</i>, respectively. Genomic analysis and physiological assays demonstrated that these previously uncharacterized strains were tolerant to high-level salt concentration and UV radiation, key survival traits in desert environments. The fermentation analysis revealed that most strains produced high-level contents of indole-3-acetic acid (IAA), although the complete gene sets for IAA biosynthesis were found in only one strain. Comparative genome analysis further showed that genes related to carbohydrate metabolism and transports were significantly enriched in desert-derived <i>Kocuria</i> strains, indicating adaptation to desert habitats. Collectively, our findings enhance our understanding of <i>Kocuria</i> taxonomy and highlight their genetic adaptation strategies to extreme environments, with potential biotechnological applications.</p>","PeriodicalId":12466,"journal":{"name":"Frontiers in Microbiology","volume":"16 ","pages":"1547983"},"PeriodicalIF":4.0000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12149201/pdf/","citationCount":"0","resultStr":"{\"title\":\"Genomic insights into <i>Kocuria</i>: taxonomic revision and identification of five IAA-producing extremophiles.\",\"authors\":\"Cong-Jian Li, Zhu-Ming Jiang, Xiao-Yang Zhi, Hua-Hong Chen, Li-Yan Yu, Guang-Fu Li, Yu-Qin Zhang\",\"doi\":\"10.3389/fmicb.2025.1547983\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Desert ecosystems have increasingly piqued the interest of microbiologists seeking novel bioactive compounds, as they are viewed as a largely uncharted reservoir of extremophiles with remarkable resilience to severe conditions. The genus <i>Kocuria</i>, belonging to the phylum <i>Actinomycetota</i>, is particularly notable for its documented capacity to flourish in such extreme environmental conditions. In this study, a total of 21 <i>Kocuria</i> strains were isolated from various ecosystems. Using polyphasic taxonomy approaches, eight strains from desert soils (CPCC 205273<sup>T</sup>, CPCC 205300, CPCC 205290, CPCC 205236<sup>T</sup>, CPCC 205293, CPCC 205292<sup>T</sup>, CPCC 205315<sup>T</sup>, CPCC 205268<sup>T</sup>) were identified representing five new species of the genus <i>Kocuria</i>. Strains CPCC 205281 and CPCC 205293 were identified as siblings of strain CPCC 205236<sup>T</sup>, while strains CPCC 205290 and CPCC 205300 were identified as siblings of strain CPCC 205273<sup>T</sup>. Additionally, <i>K. polaris</i> and <i>K</i>. <i>indcia</i> were determined to be the later heterotypic synonym of <i>K. rosea</i> and <i>K. marina</i>, respectively. Genomic analysis and physiological assays demonstrated that these previously uncharacterized strains were tolerant to high-level salt concentration and UV radiation, key survival traits in desert environments. The fermentation analysis revealed that most strains produced high-level contents of indole-3-acetic acid (IAA), although the complete gene sets for IAA biosynthesis were found in only one strain. Comparative genome analysis further showed that genes related to carbohydrate metabolism and transports were significantly enriched in desert-derived <i>Kocuria</i> strains, indicating adaptation to desert habitats. Collectively, our findings enhance our understanding of <i>Kocuria</i> taxonomy and highlight their genetic adaptation strategies to extreme environments, with potential biotechnological applications.</p>\",\"PeriodicalId\":12466,\"journal\":{\"name\":\"Frontiers in Microbiology\",\"volume\":\"16 \",\"pages\":\"1547983\"},\"PeriodicalIF\":4.0000,\"publicationDate\":\"2025-05-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12149201/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3389/fmicb.2025.1547983\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3389/fmicb.2025.1547983","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Genomic insights into Kocuria: taxonomic revision and identification of five IAA-producing extremophiles.
Desert ecosystems have increasingly piqued the interest of microbiologists seeking novel bioactive compounds, as they are viewed as a largely uncharted reservoir of extremophiles with remarkable resilience to severe conditions. The genus Kocuria, belonging to the phylum Actinomycetota, is particularly notable for its documented capacity to flourish in such extreme environmental conditions. In this study, a total of 21 Kocuria strains were isolated from various ecosystems. Using polyphasic taxonomy approaches, eight strains from desert soils (CPCC 205273T, CPCC 205300, CPCC 205290, CPCC 205236T, CPCC 205293, CPCC 205292T, CPCC 205315T, CPCC 205268T) were identified representing five new species of the genus Kocuria. Strains CPCC 205281 and CPCC 205293 were identified as siblings of strain CPCC 205236T, while strains CPCC 205290 and CPCC 205300 were identified as siblings of strain CPCC 205273T. Additionally, K. polaris and K. indcia were determined to be the later heterotypic synonym of K. rosea and K. marina, respectively. Genomic analysis and physiological assays demonstrated that these previously uncharacterized strains were tolerant to high-level salt concentration and UV radiation, key survival traits in desert environments. The fermentation analysis revealed that most strains produced high-level contents of indole-3-acetic acid (IAA), although the complete gene sets for IAA biosynthesis were found in only one strain. Comparative genome analysis further showed that genes related to carbohydrate metabolism and transports were significantly enriched in desert-derived Kocuria strains, indicating adaptation to desert habitats. Collectively, our findings enhance our understanding of Kocuria taxonomy and highlight their genetic adaptation strategies to extreme environments, with potential biotechnological applications.
期刊介绍:
Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.