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...
Saved in:
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Published: |
Springer Berlin Heidelberg
2018
|
Subjects: | |
Online Access: | http://eprints.utm.my/id/eprint/86005/ http://dx.doi.org/10.1007/s12539-016-0180-9 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
id |
my.utm.86005 |
---|---|
record_format |
eprints |
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 |
_version_ |
1677781116637937664 |
score |
13.209306 |