Rollema H S, Raap A, de Bruin S H
Eur J Biochem. 1978 Feb 1;83(1):313-7. doi: 10.1111/j.1432-1033.1978.tb12096.x.
The kinetics of carbon monoxide binding following fast reduction of the valency hybrids alpha2+betaCO2 and alphaCO2beta+2 by hydrated electrons have been studied at different degrees of reduction. The results show that at pH 6.0 and 7.0 reduction of one heme group yields a species which reacts fast with carbon monoxide (rate constant of the order of 10(6) M-1S-1). At pH 6.0 the intermediates alphaCO2beta2 and alpha2betaCO2 bind carbon monoxide with a rate characteristic of the T state. At pH 7.0 alphaCO2beta2 is for the greater part in the T state, while in the case of alpha2betaCO2 the R and the T state are about equally populated.
通过水合电子快速还原价态杂合物α2 + βCO2和αCO2β + 2后,研究了一氧化碳结合的动力学,研究是在不同还原程度下进行的。结果表明,在pH值为6.0和7.0时,一个血红素基团的还原产生一种能与一氧化碳快速反应的物质(速率常数约为10(6) M-1S-1)。在pH值为6.0时,中间体αCO2β2和α2βCO2以T态特征速率结合一氧化碳。在pH值为7.0时,αCO2β2大部分处于T态,而对于α2βCO2,R态和T态的占据程度大致相同。