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利用双氮同位素分馏解析 BoFeN1 菌株介导的硝酸盐还原异化铁氧化过程中的新机制

Novel Insight into Microbially Mediated Nitrate-Reducing Fe(II) Oxidation by sp. Strain BoFeN1 Using Dual N-O Isotope Fractionation.

机构信息

National-Regional Joint Engineering Research Center for Soil Pollution Control and Remediation in South China, Guangdong Key Laboratory of Integrated Agroenvironmental Pollution Control and Management, Institute of Eco-environmental and Soil Sciences, Guangdong Academy of Sciences, Guangzhou 510650, China.

School of Biological and Chemical Engineering, Panzhihua University, Panzhihua 6170000, China.

出版信息

Environ Sci Technol. 2023 Aug 22;57(33):12546-12555. doi: 10.1021/acs.est.3c02329. Epub 2023 Aug 3.

Abstract

Microbially mediated nitrate reduction coupled with Fe(II) oxidation (NRFO) plays an important role in the Fe/N interactions in pH-neutral anoxic environments. However, the relative contributions of the chemical and microbial processes to NRFO are still unclear. In this study, N-O isotope fractionation during NRFO was investigated. The ratios of O and N isotope enrichment factors (ε:ε)-NO indicated that the main nitrate reductase functioning in sp. strain BoFeN1 was membrane-bound dissimilatory nitrate reductase (Nar). N-O isotope fractionation during chemodenitrification [Fe(II) + NO], microbial nitrite reduction (cells + NO), and the coupled process [cells + NO + Fe(II)] was explored. The ratios of (ε:ε)-NO were 0.58 ± 0.05 during chemodenitrification and -0.41 ± 0.11 during microbial nitrite reduction, indicating that N-O isotopes can be used to distinguish chemical from biological reactions. The (ε:ε)-NO of 0.70 ± 0.05 during the coupled process was close to that obtained for chemodenitrification, indicating that chemodenitrification played a more important role than biological reactions during the coupled process. The results of kinetic modeling showed that the relative contribution of chemodenitrification was 99.3% during the coupled process, which was consistent with that of isotope fractionation. This study provides a better understanding of chemical and biological mechanisms of NRFO using N-O isotopes and kinetic modeling.

摘要

微生物介导的硝酸盐还原耦合铁(II)氧化(NRFO)在中性缺氧环境中的铁/氮相互作用中起着重要作用。然而,化学和微生物过程对 NRFO 的相对贡献仍不清楚。在本研究中,研究了 NRFO 过程中的 N-O 同位素分馏。O 和 N 同位素富集因子(ε:ε)-NO 的比值表明,在 sp. 菌株 BoFeN1 中起主要作用的硝酸盐还原酶是膜结合异化硝酸盐还原酶(Nar)。研究了化学反硝化[Fe(II) + NO]、微生物亚硝酸盐还原(细胞+NO)和耦合过程[细胞+NO+Fe(II)]中的 N-O 同位素分馏。化学反硝化和微生物亚硝酸盐还原过程中(ε:ε)-NO 的比值分别为 0.58 ± 0.05 和-0.41 ± 0.11,表明 N-O 同位素可用于区分化学和生物反应。耦合过程中(ε:ε)-NO 的值为 0.70 ± 0.05,接近化学反硝化的值,表明在耦合过程中,化学反硝化比生物反应起更重要的作用。动力学模型的结果表明,在耦合过程中,化学反硝化的相对贡献为 99.3%,与同位素分馏的结果一致。本研究通过 N-O 同位素和动力学模型,为更好地理解 NRFO 的化学和生物学机制提供了依据。

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