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吡啶基离子液体的合成及其在甲醇-水溶剂体系中提高脂肪酶稳定性的应用。

Synthesis of pyridinium-based ionic liquids and their application to improve lipase stability in a methanol-water solvent system.

作者信息

Hendra Cipta Oktavianus, Alni Anita, Hertadi Rukman

机构信息

Department of Chemistry, Bandung Institute of Technology, Bandung, Indonesia.

出版信息

Turk J Chem. 2022 Oct 31;47(2):307-320. doi: 10.55730/1300-0527.3539. eCollection 2023.

DOI:10.55730/1300-0527.3539
PMID:37528930
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10388036/
Abstract

This paper studied the effect of pyridinium-based ionic liquids as cosolvents in a methanol-water solvent system on the hydrolytic activity of lipase. These ionic liquids were successfully synthesized using imidazolium-based ionic liquid synthesizing methods with a certain adjustment. The hydrolytic activity of lipase was analyzed using 4-nitrophenol acetate (pNPA) and 4-nitrophenol palmitate (pNPP) as substrates. The addition of ionic liquids had no significant effect on the hydrolytic activity of lipase in a water solvent, and it had a greater effect in methanol. The addition of [C6Py] Br ionic liquid as a methanol cosolvent (methanol: ionic liquid, 10:5) could increase the hydrolytic activity of lipase. The use of ionic liquid as a cosolvent could increase the hydrolytic activity of lipase by about 15.61% while using pNPP as a substrate in the methanol system. A molecular dynamics study for the interaction between lipase and ionic liquids supported the experimental results. The ionic liquid using bromide as an anion provided more stability on lipase conformation. It tends to form the short-range interaction between the lipase and bromide anion.

摘要

本文研究了吡啶基离子液体作为共溶剂在甲醇 - 水溶剂体系中对脂肪酶水解活性的影响。这些离子液体采用咪唑基离子液体合成方法并做了一定调整后成功合成。以乙酸对硝基苯酯(pNPA)和棕榈酸对硝基苯酯(pNPP)为底物分析脂肪酶的水解活性。在水溶剂中添加离子液体对脂肪酶的水解活性没有显著影响,而在甲醇中影响较大。添加[C6Py]Br离子液体作为甲醇共溶剂(甲醇:离子液体,10:5)可提高脂肪酶的水解活性。在甲醇体系中以pNPP为底物时,使用离子液体作为共溶剂可使脂肪酶的水解活性提高约15.61%。对脂肪酶与离子液体之间相互作用的分子动力学研究支持了实验结果。以溴化物作为阴离子的离子液体对脂肪酶构象提供了更高的稳定性。它倾向于在脂肪酶和溴离子之间形成短程相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/b45782dad309/turkjchem-47-2-307f14.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/8f71f91e7d28/turkjchem-47-2-307f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/3cc8b9191ac1/turkjchem-47-2-307f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/bb95322a417a/turkjchem-47-2-307f12.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/cab7d9375da9/turkjchem-47-2-307f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/de02f8063f9b/turkjchem-47-2-307f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/7e7b50081132/turkjchem-47-2-307f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/9fd7465818ad/turkjchem-47-2-307f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/06f935eae90d/turkjchem-47-2-307f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/e4b42df1e88b/turkjchem-47-2-307f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/662938e4ec9f/turkjchem-47-2-307f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/2db2e95892f2/turkjchem-47-2-307f8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/0b81d1ad3935/turkjchem-47-2-307f9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/8f71f91e7d28/turkjchem-47-2-307f10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/3cc8b9191ac1/turkjchem-47-2-307f11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/bb95322a417a/turkjchem-47-2-307f12.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/bd94758f04f3/turkjchem-47-2-307f13.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ac7/10388036/b45782dad309/turkjchem-47-2-307f14.jpg

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