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Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques

Bibliographic Details
Main Author: Chan, Kam Khong
Publication Date: 2024
Other Authors: Pereira, Ana F., Valente, Ana I., Tavares, Ana P. M., Coutinho, João A. P., Ooi, Chien Wei
Format: Article
Language: eng
Source: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Download full: http://hdl.handle.net/10773/42300
Summary: Laccases hold great potential for biotechnological applications, particularly in environmental pollutant remediation. Laccase activity is governed by the solvent environment, and ionic liquids (ILs) emerge as a versatile solvent for activation or stabilization of enzymes. Herein, effects of cholinium-based ILs formulated with carboxylic acids, inorganic acid, and amino acids as anionic species, on the catalytic activity of laccase from Trametes versicolor were investigated by experimental and computational approaches. Experimental results showed that laccase activity was enhanced by 21.39 % in 0.5 M cholinium dihydrogen citrate ([Cho][DHC]), in relation to the laccase activity in phosphate buffer medium. However, cholinium aminoate ILs negatively affected laccase activity, as evidenced by the partial deactivation of laccase in both cholinium glycinate and cholinium phenylalaninate, at concentrations of 0.1 M and 0.5 M, respectively. Molecular dynamics studies revealed that the enhancement of laccase activity in [Cho][DHC] might be attributed to the highly stabilized and compact structure of laccase, facilitating a better internal electron transfer during the laccase-substrate interactions. Enhanced catalytic performance of laccase in [Cho][DHC] was postulated to be driven by the high accumulation level of dihydrogen citrate anions around laccase's surface. [Cho][DHC] holds great promise as a cosolvent in laccase-catalyzed biochemical reactions.
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spelling Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniquesLaccaseMolecular dynamics simulationIonic liquidsLaccases hold great potential for biotechnological applications, particularly in environmental pollutant remediation. Laccase activity is governed by the solvent environment, and ionic liquids (ILs) emerge as a versatile solvent for activation or stabilization of enzymes. Herein, effects of cholinium-based ILs formulated with carboxylic acids, inorganic acid, and amino acids as anionic species, on the catalytic activity of laccase from Trametes versicolor were investigated by experimental and computational approaches. Experimental results showed that laccase activity was enhanced by 21.39 % in 0.5 M cholinium dihydrogen citrate ([Cho][DHC]), in relation to the laccase activity in phosphate buffer medium. However, cholinium aminoate ILs negatively affected laccase activity, as evidenced by the partial deactivation of laccase in both cholinium glycinate and cholinium phenylalaninate, at concentrations of 0.1 M and 0.5 M, respectively. Molecular dynamics studies revealed that the enhancement of laccase activity in [Cho][DHC] might be attributed to the highly stabilized and compact structure of laccase, facilitating a better internal electron transfer during the laccase-substrate interactions. Enhanced catalytic performance of laccase in [Cho][DHC] was postulated to be driven by the high accumulation level of dihydrogen citrate anions around laccase's surface. [Cho][DHC] holds great promise as a cosolvent in laccase-catalyzed biochemical reactions.Elsevier2024-09-04T16:36:10Z2024-10-01T00:00:00Z2024-10info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/42300eng0141-813010.1016/j.ijbiomac.2024.134443Chan, Kam KhongPereira, Ana F.Valente, Ana I.Tavares, Ana P. M.Coutinho, João A. P.Ooi, Chien Weiinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-09-09T01:47:07Zoai:ria.ua.pt:10773/42300Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T18:49:17.166486Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
title Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
spellingShingle Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
Chan, Kam Khong
Laccase
Molecular dynamics simulation
Ionic liquids
title_short Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
title_full Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
title_fullStr Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
title_full_unstemmed Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
title_sort Investigation of laccase activity in cholinium-based ionic liquids using experimental and molecular dynamics techniques
author Chan, Kam Khong
author_facet Chan, Kam Khong
Pereira, Ana F.
Valente, Ana I.
Tavares, Ana P. M.
Coutinho, João A. P.
Ooi, Chien Wei
author_role author
author2 Pereira, Ana F.
Valente, Ana I.
Tavares, Ana P. M.
Coutinho, João A. P.
Ooi, Chien Wei
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Chan, Kam Khong
Pereira, Ana F.
Valente, Ana I.
Tavares, Ana P. M.
Coutinho, João A. P.
Ooi, Chien Wei
dc.subject.por.fl_str_mv Laccase
Molecular dynamics simulation
Ionic liquids
topic Laccase
Molecular dynamics simulation
Ionic liquids
description Laccases hold great potential for biotechnological applications, particularly in environmental pollutant remediation. Laccase activity is governed by the solvent environment, and ionic liquids (ILs) emerge as a versatile solvent for activation or stabilization of enzymes. Herein, effects of cholinium-based ILs formulated with carboxylic acids, inorganic acid, and amino acids as anionic species, on the catalytic activity of laccase from Trametes versicolor were investigated by experimental and computational approaches. Experimental results showed that laccase activity was enhanced by 21.39 % in 0.5 M cholinium dihydrogen citrate ([Cho][DHC]), in relation to the laccase activity in phosphate buffer medium. However, cholinium aminoate ILs negatively affected laccase activity, as evidenced by the partial deactivation of laccase in both cholinium glycinate and cholinium phenylalaninate, at concentrations of 0.1 M and 0.5 M, respectively. Molecular dynamics studies revealed that the enhancement of laccase activity in [Cho][DHC] might be attributed to the highly stabilized and compact structure of laccase, facilitating a better internal electron transfer during the laccase-substrate interactions. Enhanced catalytic performance of laccase in [Cho][DHC] was postulated to be driven by the high accumulation level of dihydrogen citrate anions around laccase's surface. [Cho][DHC] holds great promise as a cosolvent in laccase-catalyzed biochemical reactions.
publishDate 2024
dc.date.none.fl_str_mv 2024-09-04T16:36:10Z
2024-10-01T00:00:00Z
2024-10
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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format article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/42300
url http://hdl.handle.net/10773/42300
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0141-8130
10.1016/j.ijbiomac.2024.134443
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dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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collection Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
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