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去甲蒈烯酶催化氧化产物。

Products from enzyme-catalyzed oxidations of norcarenes.

作者信息

Newcomb Martin, Lansakara-P Dharmika S P, Kim Hye-Yeong, Chandrasena R Esala P, Lippard Stephen J, Beauvais Laurance G, Murray Leslie J, Izzo Viviana, Hollenberg Paul F, Coon Minor J

机构信息

Department of Chemistry, University of Illinois at Chicago, 845 West Taylor Street, Chicago, IL 60607, USA.

出版信息

J Org Chem. 2007 Feb 16;72(4):1128-33. doi: 10.1021/jo061865j.

Abstract

Recent studies revealed that norcarane (bicyclo[4.1.0]heptane) is oxidized to 2-norcarene (bicyclo[4.1.0]-hept-2-ene) and 3-norcarene (bicyclo[4.1.0]hept-3-ene) by iron-containing enzymes and that secondary oxidation products from the norcarenes complicate mechanistic probe studies employing norcarane as the substrate (Newcomb, M.; Chandrasena, R. E. P.; Lansakara-P., D. S. P.; Kim, H.-Y.; Lippard, S. J.; Beauvais, L. G.; Murray, L. J.; Izzo, V.; Hollenberg, P. F.; Coon, M. J. J. Org. Chem. 2007, 72, 1121-1127). In the present work, the product profiles from the oxidations of 2-norcarene and 3-norcarene by several enzymes were determined. Most of the products were identified by GC and GC-mass spectral comparison to authentic samples produced independently; in some cases, stereochemical assignments were made or confirmed by 2D NMR analysis of the products. The enzymes studied in this work were four cytochrome P450 enzymes, CYP2B1, CYPDelta2E1, CYPDelta2E1 T303A, and CYPDelta2B4, and three diiron-containing enzymes, soluble methane monooxygenase (sMMO) from Methylococcus capsulatus (Bath), toluene monooxygenase (ToMO) from Pseudomonas stutzeri OX1, and phenol hydroxylase (PH) from Pseudomonas stutzeri OX1. The oxidation products from the norcarenes identified in this work are 2-norcaranone, 3-norcaranone, syn- and anti-2-norcarene oxide, syn- and anti-3-norcarene oxide, syn- and anti-4-hydroxy-2-norcarene, syn- and anti-2-hydroxy-3-norcarene, 2-oxo-3-norcarene, 4-oxo-2-norcarene, and cyclohepta-3,5-dienol. Two additional, unidentified oxidation products were observed in low yields in the oxidations. In matched oxidations, 3-norcarene was a better substrate than 2-norcarene in terms of turnover by factors of 1.5-15 for the enzymes studied here. The oxidation products found in enzyme-catalyzed oxidations of the norcarenes are useful for understanding the complex product mixtures obtained in norcarane oxidations.

摘要

最近的研究表明,降蒈烷(双环[4.1.0]庚烷)可被含铁酶氧化为2-降蒈烯(双环[4.1.0]庚-2-烯)和3-降蒈烯(双环[4.1.0]庚-3-烯),并且降蒈烯的二次氧化产物使以降蒈烷为底物的机理探针研究变得复杂(纽科姆,M.;钱德拉塞纳,R. E. P.;兰萨克ara-P.,D. S. P.;金,H.-Y.;利帕德,S. J.;博韦,L. G.;默里,L. J.;伊佐,V.;霍伦贝格,P. F.;库恩,M. J.《有机化学杂志》2007年,72卷,1121 - 1127页)。在本研究中,测定了几种酶催化氧化2-降蒈烯和3-降蒈烯的产物谱。大多数产物通过气相色谱(GC)以及与独立制备的标准样品进行气相色谱 - 质谱(GC - 质谱)比较来鉴定;在某些情况下,通过对产物进行二维核磁共振(2D NMR)分析来确定或确认立体化学归属。本研究中所研究的酶包括四种细胞色素P450酶,即CYP2B1、CYPDelta2E1、CYPDelta2E1 T303A和CYPDelta2B4,以及三种含双铁的酶,来自荚膜甲基球菌(巴斯)的可溶性甲烷单加氧酶(sMMO)、来自施氏假单胞菌OX1的甲苯单加氧酶(ToMO)和来自施氏假单胞菌OX1的苯酚羟化酶(PH)。在本研究中鉴定出的降蒈烯氧化产物有2-降蒈酮、3-降蒈酮、顺式和反式-2-降蒈烯氧化物、顺式和反式-3-降蒈烯氧化物、顺式和反式-4-羟基-2-降蒈烯、顺式和反式-2-羟基-3-降蒈烯、2-氧代-3-降蒈烯、4-氧代-2-降蒈烯以及环庚-3,5-二烯醇。在氧化反应中还观察到另外两种未鉴定的低产率氧化产物。在相应的氧化反应中,就这里所研究的酶的周转率而言,3-降蒈烯比2-降蒈烯是更好的底物,前者是后者的1.5 - 15倍。降蒈烯在酶催化氧化反应中得到的氧化产物有助于理解降蒈烷氧化反应中获得的复杂产物混合物。

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Products from enzyme-catalyzed oxidations of norcarenes.去甲蒈烯酶催化氧化产物。
J Org Chem. 2007 Feb 16;72(4):1128-33. doi: 10.1021/jo061865j.

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