H-NOX from Clostridium botulinum, like H-NOX from Thermoanaerobacter tengcongensis, Binds Oxygen but with a Less Stable Oxyferrous Heme Intermediate.

H-NOX from Clostridium botulinum, like H-NOX from Thermoanaerobacter tengcongensis, Binds Oxygen but with a Less Stable Oxyferrous Heme Intermediate.
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来自肉毒梭菌的H-Nox,例如Themoanaerobacter tengcongensis的H-Nox,结合氧气,但具有较不稳定的氧气血红素中间体。

DOI:
10.1021/acs.biochem.5b00994
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发表时间:
2015-12-08
期刊:
影响因子:
2.9
通讯作者:
Tsai AL
Tsai AL
中科院分区:
生物学3区
文献类型:
--
作者:
Wu G;Liu W;Berka V;Tsai AL

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先前报道了从专性厌氧菌肉毒梭菌(Clostridium botulinum,Cb H-NOX)分离的血红素一氧化氮/氧结合蛋白以飞摩尔KD结合NO(Nioche,P.等人,Science 2004,306,1550-1553)。另一方面,尽管在腾冲嗜热厌氧杆菌H-NOX(Tt H-NOX)中稳定含氧亚铁络合物的关键残基完全保留,但未观察到含氧亚铁Cb H-NOX(同一研究)。在这项研究中,我们重新测量的动力学/亲和力的Cb H-NOX的CO,NO和O2。简单一步平衡结合的KD(CO)为1.6 × 10−7 M。对于第一个六配位NO复合物,Cb H-NOX的KD(NO)为8.0 × 10−11 M,而之前的飞摩尔KD(NO)实际上是其多步NO结合的表观KD。清晰地观察到含氧亚铁Cb H-NOX,其KD(O2)为5.3 × 10−5 M,明显高于Tt H-NOX的KD(O2)= 4.4 × 10−8 M。Cb H-NOX的气态配体结合为“滑动比例尺规则”假设提供了另一个支持性实例(Tsai,A. L.等Antioxid.氧化还原信号。2012,17,1246-1263),并且Cb H-NOX中氢键供体Tyr 139的存在选择性地增强了其对氧的亲和力。
Heme nitric oxide/oxygen binding protein isolated from the obligate anaerobe Clostridium botulinum (Cb H-NOX) was previously reported to bind NO with a femtomolar KD (Nioche, P. et al. Science 2004, 306, 1550–1553). On the other hand, no oxyferrous Cb H-NOX was observed despite full conservation of the key residues that stabilize the oxyferrous complex in the H-NOX from Thermoanaerobacter tengcongensis (Tt H-NOX) (the same study). In this study, we re-measured the kinetics/affinities of Cb H-NOX for CO, NO, and O2. KD(CO) for the simple one-step equilibrium binding was 1.6 × 10−7 M. The KD(NO) of Cb H-NOX was 8.0 × 10−11 M for the first six-coordinate NO complex, and the previous femtomolar KD(NO) was actually an apparent KD for its multiple-step NO binding. An oxyferrous Cb H-NOX was clearly observed with a KD(O2) of 5.3 × 10−5 M, which is significantly higher than Tt H-NOX’s KD(O2) = 4.4 × 10−8 M. The gaseous ligand binding of Cb H-NOX provides another supportive example for the “sliding scale rule” hypothesis (Tsai, A.-L. et al. Antioxid. Redox Signal. 2012, 17, 1246–1263), and the presence of hydrogen bond donor Tyr139 in Cb H-NOX selectively enhanced its affinity for oxygen.
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