School of Environmental Studies, China University of Geosciences (Wuhan), Hubei, 430074, China.
Carl R. Woese Institute for Genomic Biology, University of Illinois Urbana-Champaign, Urbana, Illinois 61801, United States.
Environ Sci Technol. 2020 Aug 18;54(16):10128-10140. doi: 10.1021/acs.est.0c03853. Epub 2020 Aug 6.
Microbial iron reduction is a ubiquitous biogeochemical process driven by diverse microorganisms in a variety of environments. However, it is often difficult to separate the biological from the geochemical controls on bioreduction of Fe(III) oxides. Here, we investigated the primary driving factor(s) that mediate secondary iron mineral formation over a broad range of environmental conditions using a single dissimilatory iron reducer, strain Z6. A total of 17 distinct geochemical conditions were tested with differing pH (6.5-8.5), temperature (22-50 °C), salinity (2-20% NaCl), anions (phosphate and sulfate), electron shuttle (anthraquinone-2,6-disulfonate), and Fe(III) oxide mineralogy (ferrihydrite, lepidocrocite, goethite, hematite, and magnetite). The observed rates and extent of iron reduction differed significantly with between 0.186 and 1.702 mmol L day and Fe(II) production ranging from 6.3% to 83.7% of the initial Fe(III). Using X-ray absorption and scattering techniques (EXAFS and XRD), we identified and assessed the relationship between secondary minerals and the specific environmental conditions. It was inferred that the observed bifurcation of the mineralization pathways may be mediated by differing extents of Fe(II) sorption on the remaining Fe(III) minerals. These results expand our understanding of the controls on biomineralization during microbial iron reduction and aid the development of practical applications.
微生物铁还原是一种普遍存在的生物地球化学过程,由多种微生物在各种环境中驱动。然而,通常很难将生物还原三价铁氧化物的生物控制与地球化学控制分开。在这里,我们使用单一异化铁还原剂 Z6 研究了在广泛的环境条件下介导次生铁矿物形成的主要驱动因素。用 17 种不同的地球化学条件进行了总共 17 种不同的测试,包括不同的 pH 值(6.5-8.5)、温度(22-50°C)、盐度(2-20%NaCl)、阴离子(磷酸盐和硫酸盐)、电子穿梭剂(蒽醌-2,6-二磺酸盐)和三价铁氧化物矿物学(水铁矿、针铁矿、纤铁矿、赤铁矿和磁铁矿)。观察到的铁还原速率和程度差异很大, 介于 0.186 和 1.702 mmol L day之间,Fe(II)的生成量占初始 Fe(III)的 6.3%至 83.7%。使用 X 射线吸收和散射技术(EXAFS 和 XRD),我们确定并评估了次生矿物与特定环境条件之间的关系。推断观察到的矿化途径分叉可能是由剩余三价铁矿物上 Fe(II)吸附程度的不同介导的。这些结果扩展了我们对微生物铁还原过程中生物矿化控制的理解,并有助于实际应用的发展。