<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Molinas M</submitter><funding>Swiss National Science Foundation</funding><funding>European Research Council</funding><pagination>7537-7546</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10193582</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>57(19)</volume><pubmed_abstract>The biological reduction of soluble U(VI) complexes to form immobile U(IV) species has been proposed to remediate contaminated sites. It is well established that multiheme &lt;i>c&lt;/i>-type cytochromes (MHCs) are key mediators of electron transfer to aqueous phase U(VI) complexes for bacteria such as &lt;i>Shewanella oneidensis&lt;/i> MR-1. Recent studies have confirmed that the reduction proceeds via a first electron transfer forming pentavalent U(V) species that readily disproportionate. However, in the presence of the stabilizing aminocarboxylate ligand, dpaea&lt;sup>2-&lt;/sup> (dpaeaH&lt;sub>2&lt;/sub>═bis(pyridyl-6-methyl-2-carboxylate)-ethylamine), biologically produced U(V) persisted in aqueous solution at pH 7. We aim to pinpoint the role of MHC in the reduction of U(V)-dpaea and to establish the mecha</pubmed_abstract><journal>Environmental science &amp; technology</journal><pubmed_title>Mechanism of Reduction of Aqueous U(V)-dpaea and Solid-Phase U(VI)-dpaea Complexes: The Role of Multiheme &lt;i>c&lt;/i>-Type Cytochromes.</pubmed_title><pmcid>PMC10193582</pmcid><funding_grant_id>200021E-164209</funding_grant_id><funding_grant_id>725675</funding_grant_id><pubmed_authors>Meibom KL</pubmed_authors><pubmed_authors>Mazzanti M</pubmed_authors><pubmed_authors>Bernier-Latmani R</pubmed_authors><pubmed_authors>Faizova R</pubmed_authors><pubmed_authors>Molinas M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Mechanism of Reduction of Aqueous U(V)-dpaea and Solid-Phase U(VI)-dpaea Complexes: The Role of Multiheme &lt;i>c&lt;/i>-Type Cytochromes.</name><description>The biological reduction of soluble U(VI) complexes to form immobile U(IV) species has been proposed to remediate contaminated sites. It is well established that multiheme &lt;i>c&lt;/i>-type cytochromes (MHCs) are key mediators of electron transfer to aqueous phase U(VI) complexes for bacteria such as &lt;i>Shewanella oneidensis&lt;/i> MR-1. Recent studies have confirmed that the reduction proceeds via a first electron transfer forming pentavalent U(V) species that readily disproportionate. However, in the presence of the stabilizing aminocarboxylate ligand, dpaea&lt;sup>2-&lt;/sup> (dpaeaH&lt;sub>2&lt;/sub>═bis(pyridyl-6-methyl-2-carboxylate)-ethylamine), biologically produced U(V) persisted in aqueous solution at pH 7. We aim to pinpoint the role of MHC in the reduction of U(V)-dpaea and to establish the mecha</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 May</publication><modification>2025-04-21T22:43:23.418Z</modification><creation>2025-04-05T18:54:33.142Z</creation></dates><accession>S-EPMC10193582</accession><cross_references><pubmed>37133831</pubmed><doi>10.1021/acs.est.3c00666</doi></cross_references></HashMap>