{"title":"水生环境中由单一光养细菌介导的铁循环。","authors":"Kai-Li Wang, Xin Ma, Dao-Bo Li, Yan-Ling Qi, Zheng-Shuang Hua, Tian Tian, Dong-Feng Liu, Di Min, Wen-Wei Li, Gui-Xiang Huang, Han-Qing Yu","doi":"10.34133/research.0528","DOIUrl":null,"url":null,"abstract":"<p><p>Redox cycling of iron plays a pivotal role in both nutrient acquisition by living organisms and the geochemical cycling of elements in aquatic environments. In nature, iron cycling is mediated by microbial Fe(II)-oxidizers and Fe(III)-reducers or through the interplay of biotic and abiotic iron transformation processes. Here, we unveil a specific iron cycling process driven by one single phototrophic species, <i>Rhodobacter ferrooxidans</i> SW2. It exhibits the capability to reduce Fe(III) during bacterial cultivation. A <i>c</i>-type cytochrome is identified with Fe(III)-reducing activity, implying the linkage of Fe(III) reduction with the electron transport system. <i>R. ferrooxidans</i> SW2 can mediate iron redox transformation, depending on the availability of light and/or organic substrates. Iron cycling driven by anoxygenic photoferrotrophs is proposed to exist worldwide in modern and ancient environments. Our work not only enriches the theoretical basis of iron cycling in nature but also implies multiple roles of anoxygenic photoferrotrophs in iron transformation processes.</p>","PeriodicalId":21120,"journal":{"name":"Research","volume":"7 ","pages":"0528"},"PeriodicalIF":11.0000,"publicationDate":"2024-11-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11570789/pdf/","citationCount":"0","resultStr":"{\"title\":\"Single Phototrophic Bacterium-Mediated Iron Cycling in Aquatic Environments.\",\"authors\":\"Kai-Li Wang, Xin Ma, Dao-Bo Li, Yan-Ling Qi, Zheng-Shuang Hua, Tian Tian, Dong-Feng Liu, Di Min, Wen-Wei Li, Gui-Xiang Huang, Han-Qing Yu\",\"doi\":\"10.34133/research.0528\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Redox cycling of iron plays a pivotal role in both nutrient acquisition by living organisms and the geochemical cycling of elements in aquatic environments. In nature, iron cycling is mediated by microbial Fe(II)-oxidizers and Fe(III)-reducers or through the interplay of biotic and abiotic iron transformation processes. Here, we unveil a specific iron cycling process driven by one single phototrophic species, <i>Rhodobacter ferrooxidans</i> SW2. It exhibits the capability to reduce Fe(III) during bacterial cultivation. A <i>c</i>-type cytochrome is identified with Fe(III)-reducing activity, implying the linkage of Fe(III) reduction with the electron transport system. <i>R. ferrooxidans</i> SW2 can mediate iron redox transformation, depending on the availability of light and/or organic substrates. Iron cycling driven by anoxygenic photoferrotrophs is proposed to exist worldwide in modern and ancient environments. Our work not only enriches the theoretical basis of iron cycling in nature but also implies multiple roles of anoxygenic photoferrotrophs in iron transformation processes.</p>\",\"PeriodicalId\":21120,\"journal\":{\"name\":\"Research\",\"volume\":\"7 \",\"pages\":\"0528\"},\"PeriodicalIF\":11.0000,\"publicationDate\":\"2024-11-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11570789/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Research\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://doi.org/10.34133/research.0528\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"Multidisciplinary\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Research","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.34133/research.0528","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"Multidisciplinary","Score":null,"Total":0}
引用次数: 0
摘要
铁的氧化还原循环在生物获取养分和水生环境中元素的地球化学循环中都起着关键作用。在自然界中,铁的循环是由微生物铁(II)氧化剂和铁(III)还原剂或通过生物和非生物铁转化过程的相互作用促成的。在这里,我们揭示了一种由单一光营养物种铁氧化罗杆菌 SW2 驱动的特殊铁循环过程。它具有在细菌培养过程中还原铁(III)的能力。发现了一种具有还原铁(III)活性的 c 型细胞色素,这意味着还原铁(III)与电子传递系统有关。R. ferrooxidans SW2 能介导铁的氧化还原转化,这取决于光和/或有机底物的可用性。由含氧光铁氧体驱动的铁循环被认为存在于世界各地的现代和远古环境中。我们的研究不仅丰富了自然界铁循环的理论基础,而且暗示了无氧光铁氧体在铁转化过程中的多重作用。
Single Phototrophic Bacterium-Mediated Iron Cycling in Aquatic Environments.
Redox cycling of iron plays a pivotal role in both nutrient acquisition by living organisms and the geochemical cycling of elements in aquatic environments. In nature, iron cycling is mediated by microbial Fe(II)-oxidizers and Fe(III)-reducers or through the interplay of biotic and abiotic iron transformation processes. Here, we unveil a specific iron cycling process driven by one single phototrophic species, Rhodobacter ferrooxidans SW2. It exhibits the capability to reduce Fe(III) during bacterial cultivation. A c-type cytochrome is identified with Fe(III)-reducing activity, implying the linkage of Fe(III) reduction with the electron transport system. R. ferrooxidans SW2 can mediate iron redox transformation, depending on the availability of light and/or organic substrates. Iron cycling driven by anoxygenic photoferrotrophs is proposed to exist worldwide in modern and ancient environments. Our work not only enriches the theoretical basis of iron cycling in nature but also implies multiple roles of anoxygenic photoferrotrophs in iron transformation processes.
期刊介绍:
Research serves as a global platform for academic exchange, collaboration, and technological advancements. This journal welcomes high-quality research contributions from any domain, with open arms to authors from around the globe.
Comprising fundamental research in the life and physical sciences, Research also highlights significant findings and issues in engineering and applied science. The journal proudly features original research articles, reviews, perspectives, and editorials, fostering a diverse and dynamic scholarly environment.