Rikuan Zheng, Chong Wang, Rui Liu, Ruining Cai, Chaomin Sun
{"title":"对深海 Planctomycetes 细菌中首个厌氧培养代表的生理和代谢深入研究","authors":"Rikuan Zheng, Chong Wang, Rui Liu, Ruining Cai, Chaomin Sun","doi":"https://doi.org/10.7554/elife.89874.3","DOIUrl":null,"url":null,"abstract":"<i>Planctomycetes</i> bacteria are ubiquitously distributed across various biospheres and play key roles in global element cycles. However, few deep-sea <i>Planctomycetes</i> members have been cultivated, limiting our understanding of <i>Planctomycetes</i> in the deep biosphere. Here, we have successfully cultured a novel strain of <i>Planctomycetes</i> (strain ZRK32) from a deep-sea cold seep sediment. Our genomic, physiological, and phylogenetic analyses indicate that strain ZRK32 is a novel species, which we propose be named: <i>Poriferisphaera heterotrophicis</i>. We show that strain ZRK32 replicates using a budding mode of division. Based on the combined results from growth assays and transcriptomic analyses, we found that rich nutrients, or supplementation with NO<sub>3</sub><sup>-</sup> or NH<sub>4</sub><sup>+</sup> promoted the growth of strain ZRK32 by facilitating energy production through the tricarboxylic acid cycle and the Embden-Meyerhof-Parnas glycolysis pathway. Moreover, supplementation with NO<sub>3</sub><sup>-</sup> or NH<sub>4</sub><sup>+</sup> induced strain ZRK32 to release a bacteriophage in a chronic manner, without host cell lysis. This bacteriophage then enabled strain ZRK32, and another marine bacterium that we studied, to metabolize nitrogen through the function of auxiliary metabolic genes. Overall, these findings expand our understanding of deep-sea <i>Planctomycetes</i> bacteria, while highlighting their ability to metabolize nitrogen when reprogrammed by chronic viruses.","PeriodicalId":11640,"journal":{"name":"eLife","volume":"84 1","pages":""},"PeriodicalIF":6.4000,"publicationDate":"2024-01-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Physiological and metabolic insights into the first cultured anaerobic representative of deep-sea Planctomycetes bacteria\",\"authors\":\"Rikuan Zheng, Chong Wang, Rui Liu, Ruining Cai, Chaomin Sun\",\"doi\":\"https://doi.org/10.7554/elife.89874.3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<i>Planctomycetes</i> bacteria are ubiquitously distributed across various biospheres and play key roles in global element cycles. However, few deep-sea <i>Planctomycetes</i> members have been cultivated, limiting our understanding of <i>Planctomycetes</i> in the deep biosphere. Here, we have successfully cultured a novel strain of <i>Planctomycetes</i> (strain ZRK32) from a deep-sea cold seep sediment. Our genomic, physiological, and phylogenetic analyses indicate that strain ZRK32 is a novel species, which we propose be named: <i>Poriferisphaera heterotrophicis</i>. We show that strain ZRK32 replicates using a budding mode of division. Based on the combined results from growth assays and transcriptomic analyses, we found that rich nutrients, or supplementation with NO<sub>3</sub><sup>-</sup> or NH<sub>4</sub><sup>+</sup> promoted the growth of strain ZRK32 by facilitating energy production through the tricarboxylic acid cycle and the Embden-Meyerhof-Parnas glycolysis pathway. Moreover, supplementation with NO<sub>3</sub><sup>-</sup> or NH<sub>4</sub><sup>+</sup> induced strain ZRK32 to release a bacteriophage in a chronic manner, without host cell lysis. This bacteriophage then enabled strain ZRK32, and another marine bacterium that we studied, to metabolize nitrogen through the function of auxiliary metabolic genes. Overall, these findings expand our understanding of deep-sea <i>Planctomycetes</i> bacteria, while highlighting their ability to metabolize nitrogen when reprogrammed by chronic viruses.\",\"PeriodicalId\":11640,\"journal\":{\"name\":\"eLife\",\"volume\":\"84 1\",\"pages\":\"\"},\"PeriodicalIF\":6.4000,\"publicationDate\":\"2024-01-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"eLife\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/https://doi.org/10.7554/elife.89874.3\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"eLife","FirstCategoryId":"99","ListUrlMain":"https://doi.org/https://doi.org/10.7554/elife.89874.3","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOLOGY","Score":null,"Total":0}
Physiological and metabolic insights into the first cultured anaerobic representative of deep-sea Planctomycetes bacteria
Planctomycetes bacteria are ubiquitously distributed across various biospheres and play key roles in global element cycles. However, few deep-sea Planctomycetes members have been cultivated, limiting our understanding of Planctomycetes in the deep biosphere. Here, we have successfully cultured a novel strain of Planctomycetes (strain ZRK32) from a deep-sea cold seep sediment. Our genomic, physiological, and phylogenetic analyses indicate that strain ZRK32 is a novel species, which we propose be named: Poriferisphaera heterotrophicis. We show that strain ZRK32 replicates using a budding mode of division. Based on the combined results from growth assays and transcriptomic analyses, we found that rich nutrients, or supplementation with NO3- or NH4+ promoted the growth of strain ZRK32 by facilitating energy production through the tricarboxylic acid cycle and the Embden-Meyerhof-Parnas glycolysis pathway. Moreover, supplementation with NO3- or NH4+ induced strain ZRK32 to release a bacteriophage in a chronic manner, without host cell lysis. This bacteriophage then enabled strain ZRK32, and another marine bacterium that we studied, to metabolize nitrogen through the function of auxiliary metabolic genes. Overall, these findings expand our understanding of deep-sea Planctomycetes bacteria, while highlighting their ability to metabolize nitrogen when reprogrammed by chronic viruses.
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