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Easily recognized by its iron-mineralized sheaths,\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      was one of the first microorganisms described in the 1800s. Yet it has never been isolated and does not have a complete genome sequence available, so key questions about its physiology remain unresolved. It is debated whether iron oxidation can be used for energy or growth and if\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      is an autotroph, heterotroph, or mixotroph. To address these issues, we sampled\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      -rich mats from three of its typical environments (a stream, wetlands, and a drainage channel) and reconstructed nine high-quality genomes of\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      from metagenomes. These genomes contain iron oxidase genes\n                      <jats:italic>cyc2<\/jats:italic>\n                      and\n                      <jats:italic>mtoA,<\/jats:italic>\n                      showing that\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      has the potential to conserve energy from iron oxidation. Sox genes confer potential to oxidize sulfur for energy. There are genes for both carbon fixation (RuBisCO) and utilization of sugars and organic acids (acetate, lactate, and formate).\n                      <jats:italic>In silico<\/jats:italic>\n                      stoichiometric metabolic models further demonstrated the potential for growth using sugars and organic acids. Metatranscriptomes showed a high expression of genes for iron oxidation; aerobic respiration; and utilization of lactate, acetate, and sugars, as well as RuBisCO, supporting mixotrophic growth in the environment. In summary, our results suggest that\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      has substantial metabolic flexibility. It is adapted to iron-rich, organic carbon-containing wetland niches, where it can thrive as a mixotrophic iron oxidizer by utilizing both iron oxidation and organics for energy generation and both inorganic and organic carbon for cell and sheath production.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>IMPORTANCE<\/jats:title>\n                    <jats:p>\n                      Winogradsky's observations of\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      led him to propose autotrophic iron oxidation as a new microbial metabolism, following his work on autotrophic sulfur-oxidizers. While much culture-based research has ensued, isolation proved elusive, so most work on\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      has been based in the environment and in microcosms. Meanwhile, the autotrophic\n                      <jats:italic>Gallionella<\/jats:italic>\n                      became the model for freshwater microbial iron oxidation, while heterotrophic and mixotrophic iron oxidation is not well-studied. Ecological studies have shown that\n                      <jats:italic>Leptothrix<\/jats:italic>\n                      overtakes\n                      <jats:italic>Gallionella<\/jats:italic>\n                      when dissolved organic carbon content increases, demonstrating distinct niches. This study presents the first near-complete genomes of\n                      <jats:italic>L. ochracea<\/jats:italic>\n                      , which share some features with autotrophic iron oxidizers, while also incorporating heterotrophic metabolisms. These genome, metabolic modeling, and transcriptome results give us a detailed metabolic picture of how the organism may combine lithoautotrophy with organoheterotrophy to promote Fe oxidation and C cycling and drive many biogeochemical processes resulting from microbial growth and iron oxyhydroxide formation in wetlands.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1128\/aem.00599-24","type":"journal-article","created":{"date-parts":[[2024,8,12]],"date-time":"2024-08-12T09:01:43Z","timestamp":1723453303000},"update-policy":"https:\/\/doi.org\/10.1128\/asmj-crossmark-policy-page","source":"Crossref","is-referenced-by-count":20,"title":["<i>Leptothrix ochracea<\/i>\n                    genomes reveal potential for mixotrophic growth on Fe(II) and organic carbon"],"prefix":"10.1128","volume":"90","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7792-3880","authenticated-orcid":false,"given":"Gracee K.","family":"Tothero","sequence":"first","affiliation":[{"name":"Microbiology Graduate Program, University of Delaware, Newark, Delaware, USA"},{"name":"Delaware Biotechnology Institute, Newark, Delaware, USA"},{"name":"Department of Earth Sciences, University of Delaware, Newark, Delaware, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-8464-4553","authenticated-orcid":false,"given":"Rene L.","family":"Hoover","sequence":"additional","affiliation":[{"name":"Microbiology Graduate Program, University of Delaware, Newark, Delaware, USA"},{"name":"Delaware Biotechnology Institute, Newark, Delaware, USA"},{"name":"Department of Earth Sciences, University of Delaware, Newark, Delaware, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5732-4108","authenticated-orcid":false,"given":"Ibrahim F.","family":"Farag","sequence":"additional","affiliation":[{"name":"School of Marine Science and Policy, University of Delaware, Newark, Delaware, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1019-8386","authenticated-orcid":true,"given":"Daniel I.","family":"Kaplan","sequence":"additional","affiliation":[{"name":"Savannah River Ecology Laboratory, University of Georgia, Aiken, South Carolina, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1844-5502","authenticated-orcid":false,"given":"Pamela","family":"Weisenhorn","sequence":"additional","affiliation":[{"name":"Argonne National Laboratory, Lemont, Illinois, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1737-356X","authenticated-orcid":false,"given":"David","family":"Emerson","sequence":"additional","affiliation":[{"name":"Bigelow Laboratory for Ocean Sciences, East Boothbay, Maine, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-1810-4994","authenticated-orcid":true,"given":"Clara S.","family":"Chan","sequence":"additional","affiliation":[{"name":"Microbiology Graduate Program, University of Delaware, Newark, Delaware, USA"},{"name":"Delaware Biotechnology Institute, Newark, Delaware, USA"},{"name":"Department of Earth Sciences, University of Delaware, Newark, Delaware, USA"},{"name":"School of Marine Science and Policy, University of Delaware, Newark, Delaware, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"235","reference":[{"key":"e_1_3_4_2_2","doi-asserted-by":"publisher","DOI":"10.5962\/bhl.title.124909"},{"key":"e_1_3_4_3_2","doi-asserted-by":"publisher","DOI":"10.5962\/bhl.title.4746"},{"key":"e_1_3_4_4_2","first-page":"261","article-title":"Uber eisenbakterien","volume":"46","author":"Winogradsky S","year":"1888","unstructured":"Winogradsky S. 1888. 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