A Diferrous-Dinitrosyl Intermediate in the N2O-Generating Pathway of a Deflavinated Flavo-Diiron Protein

详细信息    查看全文

• 作者：Jonathan D. Caranto ; Andrew Weitz ; Nitai Giri ; Michael P. Hendrich ; Donald M. Kurtz ; Jr.
• 刊名：Biochemistry
• 出版年：2014
• 出版时间：September 9, 2014
• 年：2014
• 卷：53
• 期：35
• 页码：5631-5637
• 全文大小：365K
• ISSN：1520-4995

文摘

Flavo-diiron proteins (FDPs) function as anaerobic nitric oxide scavengers in some microorganisms, catalyzing reduction of nitric to nitrous oxide. The FDP from Thermotoga maritima can be prepared in a deflavinated form with an intact diferric site (deflavo-FDP). Hayashi et al. [(2010) Biochemistry 49, 7040鈥?049] reported that reaction of NO with reduced deflavo-FDP produced substoichiometric N₂O. Here we report a multispectroscopic approach to identify the iron species in the reactions of deflavo-FDP with NO. M枚ssbauer spectroscopy identified two distinct ferrous species after reduction of the antiferromagnetically coupled diferric site. Approximately 60% of the total ferrous iron was assigned to a diferrous species associated with the N₂O-generating pathway. This pathway proceeds through successive diferrous-mononitrosyl (S = p>1p>/₂ Fep>IIp>{FeNO}p>7p>) and diferrous-dinitrosyl (S = 0 [{FeNO}p>7p>]₂) species that form within 鈭?00 ms of mixing of the reduced protein with NO. The diferrous-dinitrosyl intermediate converted to an antiferromagnetically coupled diferric species that was spectroscopically indistinguishable from that in the starting deflavinated protein. These diiron species closely resembled those reported for the flavinated FDP [Caranto et al. (2014) J. Am. Chem. Soc. 136, 7981鈥?992], and the time scales of their formation and decay were consistent with the steady state turnover of the flavinated protein. The remaining 鈭?0% of ferrous iron was inactive in N₂O generation but reversibly bound NO to give an S = p>3p>/₂ {FeNO}p>7p> species. The results demonstrate that N₂O formation in FDPs can occur via conversion of S = 0 [{FeNO}p>7p>]₂ to a diferric form without participation of the flavin cofactor.