Anderson R F, Patel K B, Stratford M R
Gray Laboratory of the Cancer Research Campaign, Mount Vernon Hospital, Northwood, Middlesex, United Kingdom.
J Biol Chem. 1990 Feb 5;265(4):1952-7.
The absorption spectra of the hydroxycyclohexadienyl radicals formed upon the addition of OH radicals to six substrates for phenol hydroxylase have been determined using pulse radiolysis. Combining the radical spectra of thiophenol (lambda max, 390 nm; epsilon, 10,500 M-1 cm-1) and resorcinol (lambda max, 340 nm; epsilon, 4,100 M-1 cm-1) with their respective published spectra of enzyme-bound reduced flavin that is substituted in the C(4a) position of the dihydroflavin ring gave composite spectra that closely match the spectra formed concomitantly with the introduction of an oxygen atom into the substrates, the so-called Intermediate II species. A similar procedure for the substrates hydroquinone, 3-aminophenol, 3-chlorophenol, and 3-methylphenol yielded spectra that are also consistent with the known characteristics of their Intermediate II species. These spectral results give further support to the proposed biradical mechanism (Anderson, R.F., Patel, K. B., and Stratford, M. R. L. (1987) J. Biol. Chem. 262, 17475-17479) for the functioning of this class of flavoprotein hydroxylases.
利用脉冲辐解技术测定了羟基自由基加成到六种苯酚羟化酶底物上形成的羟基环己二烯基自由基的吸收光谱。将苯硫酚(最大吸收波长λmax为390 nm;摩尔吸光系数ε为10,500 M-1·cm-1)和间苯二酚(λmax为340 nm;ε为4,100 M-1·cm-1)的自由基光谱与其各自已发表的在二氢黄素环C(4a)位置被取代的酶结合还原黄素光谱相结合,得到的复合光谱与将一个氧原子引入底物时同时形成的光谱,即所谓的中间体II物种,紧密匹配。对底物对苯二酚、3-氨基苯酚、3-氯苯酚和3-甲基苯酚采用类似方法得到的光谱也与它们的中间体II物种的已知特征一致。这些光谱结果进一步支持了所提出的关于这类黄素蛋白羟化酶作用机制的双自由基机制(安德森,R.F.,帕特尔,K.B.,和斯特拉特福,M.R.L.(1987年)《生物化学杂志》262,17475 - 17479)。