基于二醇的深溶解剂中的乳糖酶稳定性和活性:实验和计算研究.
Madushmita Hatimuria1, Jyoti Vishwakarma2, Akshara Mohan1
1Department of Chemistry, School of Chemical Sciences, Central University of Karnataka, Kadaganchi, Karnataka, 585367, India.
International journal of biological macromolecules
|December 18, 2025
概括
深度水溶剂 (DES) 可以增强乳糖酶的活性和稳定性. 基于贝他因的DES具有特定的聚醇结构,如贝他因:1,2-二醇,对可持续生物催化最有希望.
科学领域:
- 生物催化剂是一种生物催化剂.
- 绿色化学 绿色化学
- 酶工程是什么? 酶工程是什么?
背景情况:
- 乳糖酶是一种有价值的氧化还原酶酶,具有广泛的工业应用.
- 工业条件往往会损害湖活动和稳定性.
- 目前用于提高乳性能的方法可能是复杂的和不可持续的.
研究的目的:
- 为了研究深层欧性溶剂 (DES) 结构对乳糖酶活性和稳定性的影响.
- 为了确定最佳的DES配方,以提高laccase的性能.
- 为设计可持续的生物催化剂DES辅溶剂提供一个框架.
主要方法:
- 合成并测试了15种以贝他因和胆化物为基础的DES,具有不同的二醇.
- 在不同的DES中评估了乳糖酶活性和热稳定性.
- 利用分子对接和分子动力学 (MD) 模拟来理解相互作用.
主要成果:
- 贝他因衍生的二醇基DES显著增强了乳糖酶活性和稳定性.
- 1:4的M比例的DES成分被证明是最佳的laccase活动.
- 与贝他因:1,3-二醇DES相比,贝他因:1,2-二醇DES表现出更高的性能.
- 计算模拟证实了稳定键并保持了酶结构.
结论:
- 在DES中聚醇的结构特征极大地影响了乳酶调制.
- 基于贝他因的DES提供了一种可持续的方法来改善乳酶生物催化剂.
- 这项研究为工业酶应用的DES的合理设计提供了见解.
相关概念视频
Stability of Conjugated Dienes
4.1K
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
4.1K
Preparation of Diols and Pinacol Rearrangement
4.1K
Compounds bearing two hydroxyl groups are known as diols. When the hydroxyl groups are located on adjacent carbon atoms, the diols are called vicinal diols or glycols. Under acidic conditions, vicinal diols undergo a specific reaction called pinacol rearrangement.
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
4.1K
Types of Enols and Enolates
3.4K
Aldehydes and ketones form enols, although only about 1% of the enol is present at the equilibrium for simple monocarbonyl compounds. The enol form is undetectable for acetaldehyde, present as only 1.5 × 10−4 % of acetone, and present as only 1.2% of cyclohexanone. Two kinds of regioisomeric enols are possible for unsymmetrical ketones, and their net composition is 1% at equilibrium. This instability is due to the lower bond energy of C=C than the C=O group. The additional...
3.4K
Solvating Effects
8.4K
An understanding of the solvating effect helps rationalize the relation between solvation and acidity of the compound. In addition, this also explains the relative stability of conjugate bases for compounds with different pKa values. This lesson details, in-depth, the principle of solvating effects. The strength of an acid and the stability of its corresponding conjugate base are determined using pKa values. This observed relationship is a consequence of solvation, which is the interaction...
8.4K
Solvents
69.4K
A solvent is a substance, most often a liquid, that can dissolve other substances. Here, the substance being dissolved is called a solute. When a solvent and a solute combine, they form a solution - a homogenous mixture of both the solvent and the solute. Water is a universal biological solvent. Its polar structure allows it to dissolve many other polar compounds. The ability of water to dissolve is governed by a balance between water molecules binding to each other and binding to the solute.
A...
A...
69.4K
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
7.2K
Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
7.2K


