纤维素酶Cel48F的分子动力学和元动力学模拟。

Q2 Biochemistry, Genetics and Molecular Biology
Enzyme Research Pub Date : 2014-01-01 Epub Date: 2014-05-21 DOI:10.1155/2014/692738
Osmair Vital de Oliveira
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引用次数: 5

摘要

采用分子动力学和元动力学技术对纤维素酶cel48f -糖进行了研究。纤维素酶是一种将纤维素纤维分解成小糖单位的酶,在第二代酒精生产中有潜在的用途。在MD模拟中,平衡后的Cel48F的整体结构沿轨迹没有明显变化,均方根偏差保持在0.15 nm以下。在整个模拟过程中,观察到一组15个残基通过氢键与糖链相互作用。用元动力学方法测定了各链在Cel48F催化通道中的解离自由能(ΔGdiss.)。的ΔGdiss。进入和离开野生型Cel48F腔的链值分别为13.9和62.1 kcal/mol。我们还将E542和Q543突变为丙氨酸残基,得到ΔGdiss。分别为41.8和45.9 kcal/mol。这些突变被发现促进了糖链在Cel48F通道上的顺利解离。在Cel48F通道入口处,三个残基突变为丙氨酸:T110、T213和L274。与T110A-Cel48F相反,突变体T213-Cel48F和L274-Cel48F阻止糖链穿过离开位点。本研究结果可为改进Cel48F处理的诱变研究提供指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Molecular Dynamics and Metadynamics Simulations of the Cellulase Cel48F.

Molecular Dynamics and Metadynamics Simulations of the Cellulase Cel48F.

Molecular Dynamics and Metadynamics Simulations of the Cellulase Cel48F.

Molecular Dynamics and Metadynamics Simulations of the Cellulase Cel48F.

Molecular dynamics (MD) and metadynamics techniques were used to study the cellulase Cel48F-sugar. Cellulase is enzyme that breaks cellulose fibers into small sugar units and is potentially useful in second generation alcohol production. In MD simulations, the overall structure of equilibrated Cel48F did not significantly change along the trajectory, retaining root mean square deviation below 0.15 nm. A set of 15 residues interacting with the sugar chains via hydrogen bonding throughout the simulation was observed. The free energy of dissociation (ΔGdiss.) of the chains in the catalytic tunnel of Cel48F was determined by metadynamics. The ΔGdiss. values of the chains entering and leaving the wild-type Cel48F cavity were 13.9 and 62.1 kcal/mol, respectively. We also mutated the E542 and Q543 to alanine residue and obtained ΔGdiss. of 41.8 and 45.9 kcal/mol, respectively. These mutations were found to facilitate smooth dissociation of the sugar chain across the Cel48F tunnel. At the entry of the Cel48F tunnel, three residues were mutated to alanine: T110, T213, and L274. Contrary to the T110A-Cel48F, the mutants T213-Cel48F and L274-Cel48F prevented the sugar chain from passing across the leaving site. The present results can be a guideline in mutagenesis studies to improve processing by Cel48F.

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来源期刊
Enzyme Research
Enzyme Research Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
4.60
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