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首页> 外文期刊>Biochemistry >Remarkable Aliphatic Hydroxylation by the Diiron Enzyme Toluene 4-Monooxygenase in Reactions with Radical or Cation Diagnostic Probes Norcarane,1,1-Dimethylcyclopropane,and 1,1-Diethylcyclopropane
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Remarkable Aliphatic Hydroxylation by the Diiron Enzyme Toluene 4-Monooxygenase in Reactions with Radical or Cation Diagnostic Probes Norcarane,1,1-Dimethylcyclopropane,and 1,1-Diethylcyclopropane

机译:Diiron酶甲苯4-单加氧酶与自由基或阳离子诊断探针Norcarane,1,1-Dimethylcyclopropane和1,1-Diethylcyclopropane的反应中显着的脂肪羟基化作用

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摘要

Toluene 4-monooxygenase(T4MO)catalyzes the hydroxylation of toluene to yield 96% p-cresol.This diiron enzyme complex was used to oxidize norcarane(bicyclo[4.1.0]heptane),1,1-dimethylcyclo-propane,and 1,1-diethylcyclopropane,substrate analogues that can undergo diagnostic reactions upon the production of transient radical or cationic intermediates.Norcarane closely matches the shape and volume of the natural substrate toluene.Reaction of isoforms of the hydroxylase component of T4MO(T4moH)with different regiospecificities for toluene hydroxylation(k_(cat)approx=1.9-2.3 s~(-1)and coupling efficiency approx=81-96%)revealed similar catalytic parameters for norcarane oxidation(k_(cat)approx=0.3-0.5 s~(-1)and coupling efficiency approx=72%).The products included variable amounts of the un-rearranged isomeric norcaranols and cyclohex-2-enyl methanol,a product attributed to rearrangement of a radical oxidation intermediate.A ring-expansion product derived from the norcaranyl C-2 cation,cyclohept-3-enol,was not produced by either the natural enzyme or any of the T4moH isoforms tested.Comparative studies of 1,1-dimethylcyclopropane and 1,1-diethylcyclopropane,diagnostic substrates with differences in size and with approx50-fold slower k_(cat)values,gave products consistent with both radical rearrangement and cation ring expansion.Examination of the isotopic enrichment of the incorporated O-atoms for all products revealed high-fidelity incorporation of an O-atom from O_2 in the un-rearranged and radical-rearranged products,while the O-atom found in the cation ring-expansion products was predominantly obtained by reaction with H_2O.The results show a divergence of radical and cation pathways for T4moH-mediated hydroxylation that can be dissected by diagnostic substrate probe rearrangements and by changes in the source of oxygen used for substrate oxygenation.
机译:甲苯4-单加氧酶(T4MO)催化甲苯的羟基化反应,生成96%的对甲酚。该二铁酶配合物用于氧化正烷(双环[4.1.0]庚烷),1,1-二甲基环丙烷和1, 1-二乙基环丙烷,底物类似物,可在产生瞬时自由基或阳离子中间体时发生诊断反应。正烷与天然底物甲苯的形状和体积紧密匹配.T4MO(T4moH)羟化酶组分的同工型具有不同的区域特异性甲苯羟化反应(k_(cat)约= 1.9-2.3 s〜(-1)和偶联效率约= 81-96%)显示出类似的催化参数,用于正烷烷氧化(k_(cat)约= 0.3-0.5 s〜(-1) ),偶合效率约为72%)。产物包括可变数量的未重排异构正烷醇和环己-2-烯基甲醇,这归因于自由基氧化中间体的重排。正戊烷衍生的扩环产物C-2阳离子环天然酶或任何T4moH同工型均未产生pt-3-烯醇.1,1-二甲基环丙烷和1,1-二乙基环丙烷的诊断性底物的比较研究,诊断底物大小不同且k_慢约50倍(cat)值,得到与自由基重排和阳离子环膨胀都一致的产物。对所有产品中掺入的O原子的同位素富集的检查表明,高保真地从未重排和自由基的O_2中引入了O_2 -重排产物,而在阳离子扩环产物中发现的O-原子主要是通过与H_2O反应获得的。结果表明,T4moH介导的羟基化反应的自由基和阳离子途径存在差异,可以通过诊断底物探针的重排和通过改变用于底物氧合的氧源。

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