Kinetic and spectroscopic studies of the ATP:corrinoid adenosyltransferase PduO from Lactobacillus reuteri: substrate specificity and insights into the mechanism of Co(II)corrinoid reduction.
Kinetic and spectroscopic studies of the ATP:corrinoid adenosyltransferase PduO from Lactobacillus reuteri: substrate specificity and insights into the mechanism of Co(II)corrinoid reduction.
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罗伊氏乳杆菌 ATP:类咕啉腺苷转移酶 PduO 的动力学和光谱研究:底物特异性和 Co(II) 类咕啉还原机制的见解。
DOI:
10.1021/bi800419e
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发表时间:
2008
期刊:
影响因子:
2.9
通讯作者:
Brunold,ThomasC
中科院分区:
文献类型:
--
作者:
Park,Kiyoung;Mera,PaolaE;Escalante-Semerena,JorgeC;Brunold,ThomasC
The PduO-type ATP:corrinoid adenosyltransferase fromLactobacillus reuteri(LrPduO) catalyzes the formation of the essential Co−C bond of adenosylcobalamin (coenzyme B12) by transferring the adenosyl group from cosubstrate ATP to a transient Co1+corrinoid species generated in the enzyme active site. While PduO-type enzymes have previously been believed to be capable of adenosylating only Co1+cobalamin (Co1+Cbl−), our kinetic data obtained in this study provide in vitro evidence thatLrPduO can in fact also utilize the incomplete corrinoid Co1+cobinamide (Co1+Cbi) as an alternative substrate. To explore the mechanism by whichLrPduO overcomes the thermodynamically challenging reduction of its Co2+corrinoid substrates, we have examined how the enzyme active site alters the geometric and electronic properties of Co2+Cbl and Co2+Cbi+by using electronic absorption, magnetic circular dichroism, and electron paramagnetic resonance spectroscopic techniques. Our data reveal that upon binding toLrPduO that was preincubated with ATP, both Co2+corrinoids undergo a partial (∼40−50%) conversion to distinct paramagnetic Co2+species. The spectroscopic signatures of these species are consistent with essentially four-coordinate, square-planar Co2+complexes, based on a comparison with the results obtained in our previous studies of related enzymes. Consequently, it appears that the general strategy employed by adenosyltransferases for effecting Co2+→ Co1+reduction involves the formation of an “activated” Co2+corrinoid intermediate that lacks any significant axial bonding interactions, to stabilize the redox-active, Co 3dz2-based molecular orbital.