Reversible Interconversion of Nitrate and Nitrite Catalyzed by Periplasmic Nitrate Reductase from Campylobacter jejuni

IF 14.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Nitai C. Giri, Lahiru Wedasingha, Nicholas Manicke, Maciej Szaleniec, Partha Basu
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Abstract

The periplasmic nitrate reductase catalytic subunit (NapA) belongs to the DMSO reductase (DMSOR) family of the molybdenum cofactor (Moco) containing enzymes and catalyzes nitrate reduction to nitrite. Some members of the DMSOR family (e.g., DMSO reductase, formate dehydrogenase, nitrite oxidoreductase, and arsenate reductase) catalyze the reversible interconversion of the substrate and product with varying efficiency. Here, we demonstrate that NapA not only can reduce nitrate to nitrite but also can also oxidize nitrite to nitrate. At least three mechanisms involving the oxygen atom transfer (OAT) process have been proposed for NapA-catalyzed nitrate reduction. NapA can also oxidize nitrite via an OAT process. However, there is no experimental evidence for any of these OAT processes using isolated pure enzymes so far. Here, we provide the first experimental evidence for OAT reactions in both forward (i.e., nitrate reduction) and backward (i.e., nitrite oxidation) reactions catalyzed by NapA using isotope labeling, mass spectrometry, and NMR experiments. Finally, we propose a mechanistic scheme supported by experiment and computation consistent with atom transfer as the rate-limiting step.

Abstract Image

质外硝酸还原酶催化亚基(NapA)属于含钼辅助因子(Moco)酶的 DMSO 还原酶(DMSOR)家族,可催化硝酸盐还原为亚硝酸盐。DMSOR 家族的一些成员(如 DMSO 还原酶、甲酸脱氢酶、亚硝酸盐氧化还原酶和砷酸还原酶)催化底物和产物的可逆相互转化,但效率各不相同。在这里,我们证明了 NapA 不仅能将硝酸盐还原成亚硝酸盐,还能将亚硝酸盐氧化成硝酸盐。关于 NapA 催化硝酸盐还原,至少有三种涉及氧原子转移(OAT)过程的机制。NapA 也能通过 OAT 过程氧化亚硝酸盐。然而,迄今为止还没有使用分离的纯酶对这些 OAT 过程进行实验证明。在这里,我们利用同位素标记、质谱分析和核磁共振实验,首次提供了由 NapA 催化的正向(即硝酸盐还原)和反向(即亚硝酸盐氧化)反应中的 OAT 反应的实验证据。最后,我们提出了以原子转移为限速步骤的机理方案,该方案得到了实验和计算的支持。
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来源期刊
CiteScore
24.40
自引率
6.00%
发文量
2398
审稿时长
1.6 months
期刊介绍: The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.
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