Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12

We report a detailed structural analysis of the psychrophilic exo-β-1,3-glucanase (GaExg55) from Glaciozyma antarctica PI12. This study elucidates the structural basis of exo-1,3-β-1,3-glucanase from this psychrophilic yeast. The structural prediction of GaExg55 remains a challenge because of its lo...

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Main Authors: Mohammadi, Salimeh, Parvizpour, Sepideh, Razmara, Jafar, Abu Bakar, Farah Diba, Md. Illias, Rosli, Mahadi, Nor Muhammad, Abdul Murad, Abdul Munir
Format: Article
Published: Springer Berlin Heidelberg 2018
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Online Access:http://eprints.utm.my/id/eprint/86005/
http://dx.doi.org/10.1007/s12539-016-0180-9
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spelling my.utm.860052020-08-30T08:49:25Z http://eprints.utm.my/id/eprint/86005/ Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12 Mohammadi, Salimeh Parvizpour, Sepideh Razmara, Jafar Abu Bakar, Farah Diba Md. Illias, Rosli Mahadi, Nor Muhammad Abdul Murad, Abdul Munir TP Chemical technology We report a detailed structural analysis of the psychrophilic exo-β-1,3-glucanase (GaExg55) from Glaciozyma antarctica PI12. This study elucidates the structural basis of exo-1,3-β-1,3-glucanase from this psychrophilic yeast. The structural prediction of GaExg55 remains a challenge because of its low sequence identity (37 %). A 3D model was constructed for GaExg55. Threading approach was employed to determine a suitable template and generate optimal target–template alignment for establishing the model using MODELLER9v15. The primary sequence analysis of GaExg55 with other mesophilic exo-1,3-β-glucanases indicated that an increased flexibility conferred to the enzyme by a set of amino acids substitutions in the surface and loop regions of GaExg55, thereby facilitating its structure to cold adaptation. A comparison of GaExg55 with other mesophilic exo-β-1,3-glucanases proposed that the catalytic activity and structural flexibility at cold environment were attained through a reduced amount of hydrogen bonds and salt bridges, as well as an increased exposure of the hydrophobic side chains to the solvent. A molecular dynamics simulation was also performed using GROMACS software to evaluate the stability of the GaExg55 structure at varying low temperatures. The simulation result confirmed the above findings for cold adaptation of the psychrophilic GaExg55. Furthermore, the structural analysis of GaExg55 with large catalytic cleft and wide active site pocket confirmed the high activity of GaExg55 to hydrolyze polysaccharide substrates. Springer Berlin Heidelberg 2018-03 Article PeerReviewed Mohammadi, Salimeh and Parvizpour, Sepideh and Razmara, Jafar and Abu Bakar, Farah Diba and Md. Illias, Rosli and Mahadi, Nor Muhammad and Abdul Murad, Abdul Munir (2018) Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12. Interdisciplinary Sciences: Computational Life Sciences, 10 (1). pp. 157-168. ISSN 1913-2751 http://dx.doi.org/10.1007/s12539-016-0180-9
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic TP Chemical technology
spellingShingle TP Chemical technology
Mohammadi, Salimeh
Parvizpour, Sepideh
Razmara, Jafar
Abu Bakar, Farah Diba
Md. Illias, Rosli
Mahadi, Nor Muhammad
Abdul Murad, Abdul Munir
Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12
description We report a detailed structural analysis of the psychrophilic exo-β-1,3-glucanase (GaExg55) from Glaciozyma antarctica PI12. This study elucidates the structural basis of exo-1,3-β-1,3-glucanase from this psychrophilic yeast. The structural prediction of GaExg55 remains a challenge because of its low sequence identity (37 %). A 3D model was constructed for GaExg55. Threading approach was employed to determine a suitable template and generate optimal target–template alignment for establishing the model using MODELLER9v15. The primary sequence analysis of GaExg55 with other mesophilic exo-1,3-β-glucanases indicated that an increased flexibility conferred to the enzyme by a set of amino acids substitutions in the surface and loop regions of GaExg55, thereby facilitating its structure to cold adaptation. A comparison of GaExg55 with other mesophilic exo-β-1,3-glucanases proposed that the catalytic activity and structural flexibility at cold environment were attained through a reduced amount of hydrogen bonds and salt bridges, as well as an increased exposure of the hydrophobic side chains to the solvent. A molecular dynamics simulation was also performed using GROMACS software to evaluate the stability of the GaExg55 structure at varying low temperatures. The simulation result confirmed the above findings for cold adaptation of the psychrophilic GaExg55. Furthermore, the structural analysis of GaExg55 with large catalytic cleft and wide active site pocket confirmed the high activity of GaExg55 to hydrolyze polysaccharide substrates.
format Article
author Mohammadi, Salimeh
Parvizpour, Sepideh
Razmara, Jafar
Abu Bakar, Farah Diba
Md. Illias, Rosli
Mahadi, Nor Muhammad
Abdul Murad, Abdul Munir
author_facet Mohammadi, Salimeh
Parvizpour, Sepideh
Razmara, Jafar
Abu Bakar, Farah Diba
Md. Illias, Rosli
Mahadi, Nor Muhammad
Abdul Murad, Abdul Munir
author_sort Mohammadi, Salimeh
title Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12
title_short Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12
title_full Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12
title_fullStr Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12
title_full_unstemmed Structure prediction of a novel Exo-ß-1,3-Glucanase: Insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica PI12
title_sort structure prediction of a novel exo-ß-1,3-glucanase: insights into the cold adaptation of psychrophilic yeast glaciozyma antarctica pi12
publisher Springer Berlin Heidelberg
publishDate 2018
url http://eprints.utm.my/id/eprint/86005/
http://dx.doi.org/10.1007/s12539-016-0180-9
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