Honma T, Ogura Y
Biochim Biophys Acta. 1977 Sep 15;484(1):9-23. doi: 10.1016/0005-2744(77)90109-7.
The reaction mechanism of old yellow enzyme (NADPH:(acceptor) oxidoreductase, EC 1.6.99.1) was kinetically investigated using NADH as substrate. The enzyme was reduced by NADH via a reaction intermediate which has a specific absorption spectrum. This intermediate decomposed to yield a reduced enzyme and NAD+ through an inrreversible first-order reaction step. The reduced enzyme was reoxidized by oxygen through a second-order reaction process. Individual values of elementary rate constants were measured and a computer simulation of the reaction process was carried out. No involvement of free radical of flavin semiquinone in the reaction process could be shown.
以NADH为底物,对老黄色酶(NADPH:(受体)氧化还原酶,EC 1.6.99.1)的反应机制进行了动力学研究。该酶通过具有特定吸收光谱的反应中间体被NADH还原。该中间体通过不可逆的一级反应步骤分解,产生还原态酶和NAD+。还原态酶通过二级反应过程被氧气再氧化。测定了各基元反应速率常数的具体数值,并对反应过程进行了计算机模拟。结果表明,反应过程中黄素半醌自由基未参与其中。