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首页> 外文期刊>The Biochemical Journal >Characterization of Medicago truncatula (barrel medic) hydroperoxide lyase (CYP74C3), a water-soluble detergent-free cytochrome P450 monomer whose biological activity is defined by monomer-micelle association
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Characterization of Medicago truncatula (barrel medic) hydroperoxide lyase (CYP74C3), a water-soluble detergent-free cytochrome P450 monomer whose biological activity is defined by monomer-micelle association

机译:苜蓿(藜(桶状)氢过氧化物裂解酶(CYP74C3)的表征,一种水溶性无洗涤剂的细胞色素P450单体,其生物活性由单体-胶束缔合定义

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We describe the detailed biochemical characterization of CYP74C3 (cytochrome P450 subfamily 740), a recombinant plant cytochrome P450 enzyme with HPL (hydroperoxide lyase) activity from Medicago truncatula (barrel medic). Steady-state kinetic parameters, substrate and product specificities, RZ (Reinheitszahl or purity index), molar absorption coefficient, haem content, and new ligands for an HPL are reported. We show on the basis of gel filtration, sedimentation velocity (sedimentation coefficient distribution) and sedimentation equilibrium (molecular mass) analyses that CYP74C3 has low enzyme activity as a detergent-free, water-soluble, monomer. The enzyme activity can be completely restored by re-activation with detergent micelles, but not detergent monomers. Corresponding changes in the spin state equilibrium, and probably co-ordination of the haem iron, are novel for cytochrome P450 enzymes and suggest that detergent micelles have a subtle effect on protein conformation, rather than substrate presentation, which is sufficient to improve substrate binding and catalytic-centre activity by an order of magnitude. The k(cat)/K-m of up to 1.6 x 10(8) M-1 center dot s(-1) is among the highest recorded. which is remarkable for an enzyme whose reaction mechanism involves the scission of a C-C bond. We carried out both kinetic and biophysical studies to demonstrate that this effect is a result of the formation of a complex between a protein monomer and a single detergent micelle. Association with a detergent micelle rather than oligomeric state represents a new mechanism of activation for membrane-associated cytochrome P450 enzymes. Highly concentrated and monodispersed samples of detergent-free CYP74C3 protein may be well suited for the purposes of crystallization and structural resolution of the first plant cytochrome P450 enzyme.
机译:我们描述了CYP74C3(细胞色素P450亚家族740)的详细生化特征,CYP74C3是一种重组植物细胞色素P450酶,具有从紫花苜蓿(桶形药用)中的HPL(氢过氧化物裂解酶)活性。报告了稳态动力学参数,底物和产物的特异性,RZ(Reinheitszahl或纯度指数),摩尔吸收系数,血红素含量和HPL的新配体。我们通过凝胶过滤,沉降速度(沉降系数分布)和沉降平衡(分子量)分析表明,CYP74C3作为无洗涤剂的水溶性单体具有较低的酶活性。通过用去污剂胶束而不是去污剂单体的再活化可以完全恢复酶的活性。自旋态平衡的相应变化以及可能与血红素铁的配位关系对于细胞色素P450酶而言是新颖的,并表明去污剂胶束对蛋白质构象具有微妙的作用,而不是对底物呈递具有微妙的作用,这足以改善底物的结合和催化中心活性提高了一个数量级。最高记录为1.6 x 10(8)M-1中心点s(-1)的k(cat)/ K-m。对于反应机理涉及C-C键断裂的酶而言,这是非常了不起的。我们进行了动力学和生物物理研究,以证明这种效果是蛋白质单体和单个去污胶束之间形成复合物的结果。与去污剂胶束而不是低聚状态的结合代表了与膜相关的细胞色素P450酶激活的新机制。不含去污剂的CYP74C3蛋白的高度浓缩和单分散的样品可能非常适合第一种植物细胞色素P450酶的结晶和结构拆分。

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