Zhu Hui, Peck Spencer C, Bonnot Florence, van der Donk Wilfred A, Klinman Judith P
Howard Hughes Medical Institute and Department of Chemistry, University of Illinois at Urbana-Champaign , 600 South Mathews Avenue, Urbana, Illinois 61801, United States.
Institute for Genomic Biology, University of Illinois at Urbana-Champaign , 1206 West Gregory Drive, Urbana, Illinois 61801, United States.
J Am Chem Soc. 2015 Aug 26;137(33):10448-51. doi: 10.1021/jacs.5b03907. Epub 2015 Aug 12.
Nonheme iron oxygenases that carry out four-electron oxidations of substrate have been proposed to employ iron(III) superoxide species to initiate this reaction [Paria, S.; Que, L.; Paine, T. K. Angew. Chem. Int. Ed. 2011, 50, 11129]. Here we report experimental evidence in support of this proposal. (18)O KIEs were measured for two recently discovered mononuclear nonheme iron oxygenases: hydroxyethylphosphonate dioxygenase (HEPD) and methylphosphonate synthase (MPnS). Competitive (18)O KIEs measured with deuterated substrates are larger than those measured with unlabeled substrates, which indicates that C-H cleavage must occur before an irreversible reductive step at molecular oxygen. A similar observation was previously used to implicate copper(II) superoxide in the H-abstraction reactions catalyzed by dopamine β-monooxygenase [Tian, G. C.; Klinman, J. P. J. Am. Chem. Soc. 1993, 115, 8891] and peptidylglycine α-hydroxylating monooxygenase [Francisco, W. A.; Blackburn, N. J.; Klinman, J. P. Biochemistry 2003, 42, 1813].
有研究提出,能对底物进行四电子氧化的非血红素铁加氧酶会利用铁(III)超氧物种来引发该反应[帕里亚,S.;奎,L.;佩恩,T. K.《德国应用化学》2011年,第50卷,第11129页]。在此,我们报告支持这一观点的实验证据。我们测定了两种最近发现的单核非血红素铁加氧酶——羟乙基膦酸双加氧酶(HEPD)和甲基膦酸合酶(MPnS)的(18)O动力学同位素效应(KIE)。用氘代底物测得的竞争性(18)O KIE大于用未标记底物测得的结果,这表明在分子氧发生不可逆还原步骤之前,必然发生了C-H键断裂。之前在多巴胺β-单加氧酶[田,G. C.;克林曼,J. P.《美国化学会志》1993年,第115卷,第8891页]和肽基甘氨酸α-羟化单加氧酶[弗朗西斯科,W. A.;布莱克本,N. J.;克林曼,J. P.《生物化学》2003年,第42卷,第1813页]催化的氢原子提取反应中,也曾有类似观察结果暗示铜(II)超氧的参与。