Significance Under anoxic conditions, various microorganisms couple the oxidation of organic carbon to the reduction of solid ferric iron oxide phases using extracellular electron shuttles (EES). Determining the contribution of… Click to show full abstract
Significance Under anoxic conditions, various microorganisms couple the oxidation of organic carbon to the reduction of solid ferric iron oxide phases using extracellular electron shuttles (EES). Determining the contribution of this widespread terminal electron accepting process to total anaerobic respiration has proven challenging because of large variations in observed ferric iron reduction rates. This study demonstrates that rates of ferric iron oxide reduction by EES can be rationalized based on a unifying relationship that links rates to the thermodynamic driving force for the least favorable electron transfer from the EES to ferric iron. The relationship derived herein allows for a generalized and precise assessment of the contribution of EES-facilitated ferric iron oxide reduction to organic matter decomposition in anoxic environments. Anaerobic microbial respiration in suboxic and anoxic environments often involves particulate ferric iron (oxyhydr-)oxides as terminal electron acceptors. To ensure efficient respiration, a widespread strategy among iron-reducing microorganisms is the use of extracellular electron shuttles (EES) that transfer two electrons from the microbial cell to the iron oxide surface. Yet, a fundamental understanding of how EES–oxide redox thermodynamics affect rates of iron oxide reduction remains elusive. Attempts to rationalize these rates for different EES, solution pH, and iron oxides on the basis of the underlying reaction free energy of the two-electron transfer were unsuccessful. Here, we demonstrate that broadly varying reduction rates determined in this work for different iron oxides and EES at varying solution chemistry as well as previously published data can be reconciled when these rates are instead related to the free energy of the less exergonic (or even endergonic) first of the two electron transfers from the fully, two-electron reduced EES to ferric iron oxide. We show how free energy relationships aid in identifying controls on microbial iron oxide reduction by EES, thereby advancing a more fundamental understanding of anaerobic respiration using iron oxides.
               
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