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“Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation

[Image: see text] By mimicking the water structure to improve the enzyme activity, we designed imidazolium (Im)-based ionic liquids (ILs) functionalized with both ether and tert-alcohol groups (e.g., [CH(3)(OCH(2)CH(2))(n)-Im-t-BuOH][Tf(2)N]). This unique combination of the “water-like” structure en...

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Detalles Bibliográficos
Autores principales: Zhao, Hua, Harter, Glenn A., Martin, Caden J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2019
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751713/
https://www.ncbi.nlm.nih.gov/pubmed/31552369
http://dx.doi.org/10.1021/acsomega.9b02118
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author Zhao, Hua
Harter, Glenn A.
Martin, Caden J.
author_facet Zhao, Hua
Harter, Glenn A.
Martin, Caden J.
author_sort Zhao, Hua
collection PubMed
description [Image: see text] By mimicking the water structure to improve the enzyme activity, we designed imidazolium (Im)-based ionic liquids (ILs) functionalized with both ether and tert-alcohol groups (e.g., [CH(3)(OCH(2)CH(2))(n)-Im-t-BuOH][Tf(2)N]). This unique combination of the “water-like” structure enabled very high transesterification (synthetic) activities for immobilized lipase B from Candida antarctica, which are up to 2–4 folds higher than nonfunctionalized “classical” ionic liquids (such as [BMIM][Tf(2)N]) and up to 40–100% higher than diisopropyl ether and tert-butanol. Fluorescence emission spectra confirmed the general protein structural preservation in these tailored ionic solvents. In addition, functionalized ILs showed high thermal stabilities, which are comparable with diisopropyl ether but much higher than tert-butanol.
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spelling pubmed-67517132019-09-24 “Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation Zhao, Hua Harter, Glenn A. Martin, Caden J. ACS Omega [Image: see text] By mimicking the water structure to improve the enzyme activity, we designed imidazolium (Im)-based ionic liquids (ILs) functionalized with both ether and tert-alcohol groups (e.g., [CH(3)(OCH(2)CH(2))(n)-Im-t-BuOH][Tf(2)N]). This unique combination of the “water-like” structure enabled very high transesterification (synthetic) activities for immobilized lipase B from Candida antarctica, which are up to 2–4 folds higher than nonfunctionalized “classical” ionic liquids (such as [BMIM][Tf(2)N]) and up to 40–100% higher than diisopropyl ether and tert-butanol. Fluorescence emission spectra confirmed the general protein structural preservation in these tailored ionic solvents. In addition, functionalized ILs showed high thermal stabilities, which are comparable with diisopropyl ether but much higher than tert-butanol. American Chemical Society 2019-09-04 /pmc/articles/PMC6751713/ /pubmed/31552369 http://dx.doi.org/10.1021/acsomega.9b02118 Text en Copyright © 2019 American Chemical Society This is an open access article published under a Creative Commons Non-Commercial No Derivative Works (CC-BY-NC-ND) Attribution License (http://pubs.acs.org/page/policy/authorchoice_ccbyncnd_termsofuse.html) , which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.
spellingShingle Zhao, Hua
Harter, Glenn A.
Martin, Caden J.
“Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation
title “Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation
title_full “Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation
title_fullStr “Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation
title_full_unstemmed “Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation
title_short “Water-like” Dual-Functionalized Ionic Liquids for Enzyme Activation
title_sort “water-like” dual-functionalized ionic liquids for enzyme activation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6751713/
https://www.ncbi.nlm.nih.gov/pubmed/31552369
http://dx.doi.org/10.1021/acsomega.9b02118
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