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Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications

Cellulases involved in the hydrolysis of cellulose and plays a vital role in different industries like textile, detergent paper and Feed industry. Cellulases have been a prospective target for research by both the academic and industrial sectors because of the intricacy of the enzyme system and the...

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Autores principales: Nisar, Kinza, Abdullah, Roheena, Kaleem, Afshan, Iqtedar, Mehwish, Aftab, Mahwish, Saleem, Faiza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649386/
https://www.ncbi.nlm.nih.gov/pubmed/36389206
http://dx.doi.org/10.1016/j.sjbs.2022.103483
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author Nisar, Kinza
Abdullah, Roheena
Kaleem, Afshan
Iqtedar, Mehwish
Aftab, Mahwish
Saleem, Faiza
author_facet Nisar, Kinza
Abdullah, Roheena
Kaleem, Afshan
Iqtedar, Mehwish
Aftab, Mahwish
Saleem, Faiza
author_sort Nisar, Kinza
collection PubMed
description Cellulases involved in the hydrolysis of cellulose and plays a vital role in different industries like textile, detergent paper and Feed industry. Cellulases have been a prospective target for research by both the academic and industrial sectors because of the intricacy of the enzyme system and the enormous industrial potential. In the present work Thermomyces dupontii, which had previously been isolated and recorded as a promising cellulase producer were used. Both endoglucanases and betaglucosidases were purified to its homogeneity by ammonium sulfate followed by anion exchange and gel filtration chromatography. The recovery and purification fold for endoglucanases and betaglucosidases were 13.7, 10.7 % and 5.9, 2.7, respectively. The molecular weight of endoglucanases and betaglucosidases were estimated as 37 and 66 kDa on SDS-PAGE. Upon kinetic analysis the purified endoglucanases and betaglucosidases showed Km 0.63; 28.56 mg/ml and Vmax 82; 80 U/ml/min, respectively. Characterization revealed that enzyme was found to be acidophilic cellulase having optimal pH of 5.5 and 70 ⁰C. Furthermore, cellulases were accelerated in the presence of Ca(2+) and EDTA. The cellulases had activation energy (Ea) of −44.55; −50.02 kJ/mol for carboxy-methyl-cellulose hydrolysis and Enthalpy (ΔH) 42.20; 47.70 kJ/mol and entropy ΔS −5.1 and −5.7 kJ/mol for EG and BGL, respectively. In addition to this the enzyme had a secondary structure of protein as represented by FTIR spectrum The current study suggested that purified cellulases can be used as a detergent additive to improve washing. Furthermore, it shows the biostoning ability when applied on jean fabric.
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spelling pubmed-96493862022-11-15 Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications Nisar, Kinza Abdullah, Roheena Kaleem, Afshan Iqtedar, Mehwish Aftab, Mahwish Saleem, Faiza Saudi J Biol Sci Original Article Cellulases involved in the hydrolysis of cellulose and plays a vital role in different industries like textile, detergent paper and Feed industry. Cellulases have been a prospective target for research by both the academic and industrial sectors because of the intricacy of the enzyme system and the enormous industrial potential. In the present work Thermomyces dupontii, which had previously been isolated and recorded as a promising cellulase producer were used. Both endoglucanases and betaglucosidases were purified to its homogeneity by ammonium sulfate followed by anion exchange and gel filtration chromatography. The recovery and purification fold for endoglucanases and betaglucosidases were 13.7, 10.7 % and 5.9, 2.7, respectively. The molecular weight of endoglucanases and betaglucosidases were estimated as 37 and 66 kDa on SDS-PAGE. Upon kinetic analysis the purified endoglucanases and betaglucosidases showed Km 0.63; 28.56 mg/ml and Vmax 82; 80 U/ml/min, respectively. Characterization revealed that enzyme was found to be acidophilic cellulase having optimal pH of 5.5 and 70 ⁰C. Furthermore, cellulases were accelerated in the presence of Ca(2+) and EDTA. The cellulases had activation energy (Ea) of −44.55; −50.02 kJ/mol for carboxy-methyl-cellulose hydrolysis and Enthalpy (ΔH) 42.20; 47.70 kJ/mol and entropy ΔS −5.1 and −5.7 kJ/mol for EG and BGL, respectively. In addition to this the enzyme had a secondary structure of protein as represented by FTIR spectrum The current study suggested that purified cellulases can be used as a detergent additive to improve washing. Furthermore, it shows the biostoning ability when applied on jean fabric. Elsevier 2022-12 2022-10-31 /pmc/articles/PMC9649386/ /pubmed/36389206 http://dx.doi.org/10.1016/j.sjbs.2022.103483 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Nisar, Kinza
Abdullah, Roheena
Kaleem, Afshan
Iqtedar, Mehwish
Aftab, Mahwish
Saleem, Faiza
Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications
title Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications
title_full Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications
title_fullStr Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications
title_full_unstemmed Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications
title_short Purification, characterization and thermodynamic analysis of cellulases produced from Thermomyces dupontii and its industrial applications
title_sort purification, characterization and thermodynamic analysis of cellulases produced from thermomyces dupontii and its industrial applications
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9649386/
https://www.ncbi.nlm.nih.gov/pubmed/36389206
http://dx.doi.org/10.1016/j.sjbs.2022.103483
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