Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis

Cyclodextrin glycosyltransferase (CGTase) has always played a significant role in the production of cyclodextrin through the cyclization reaction. The wide application of this valuable protein demands a better understanding, leading to a comprehensive insilico analysis of CGTase. The analysis focu...

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Main Authors: Nik-Pa, Nik Ida Mardiana, Mohamad Sobri, Mohamad Farhan, Zolkefli, Nurhasliza, Abd-Aziz, Suraini, Ibrahim, Mohamad Faizal, Mohamed Alitheen, Noorjahan Banu, Ramli, Norhayati
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Published: The Malaysian Society for Biochemistry & Molecular Biology 2023
Online Access:http://psasir.upm.edu.my/id/eprint/107212/
https://msbmb2010.wixsite.com/mjbmb
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spelling my.upm.eprints.1072122024-10-17T02:06:59Z http://psasir.upm.edu.my/id/eprint/107212/ Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis Nik-Pa, Nik Ida Mardiana Mohamad Sobri, Mohamad Farhan Zolkefli, Nurhasliza Abd-Aziz, Suraini Ibrahim, Mohamad Faizal Mohamed Alitheen, Noorjahan Banu Ramli, Norhayati Cyclodextrin glycosyltransferase (CGTase) has always played a significant role in the production of cyclodextrin through the cyclization reaction. The wide application of this valuable protein demands a better understanding, leading to a comprehensive insilico analysis of CGTase. The analysis focused on the functional domain composition of the recombinant CGT-BS protein by comparing it with several other CGTase proteins from different Bacillus spp. A three-dimensional (3-D) model was constructed to predict the active, substrate binding and cyclization sites of the CGT-BS protein. Structural function prediction revealed the active site within domain A at the wide end of the (β/α)8-barrel, with Asp 268, Glu 296 and Asp 357 as the catalytic residues. Additionally, the reaction site for cyclization was identified in domain B at Tyr 234. In comparison to maltose binding sites (MBS) 1 and 2 which are associated with raw starch binding activity, a comparable role is deduced for the MBS identified on the surface of the Domain E protein. We additionally observed that the residues Tyr 139, Arg 266 and Asp 367, located at the substrate binding cleft of the catalytic site, exhibited heightened hydrophobicity and concurrent cyclization activity. The successful extracellular expression of the CGT-BS protein is also anticipated to be facilitated by the presence of a functional signal peptide. In conclusion, our in-depth insilico analysis unveils critical insights into the structural and functional aspects of CGTBS protein, laying the groundwork for further exploration of its catalytic mechanisms and potential applications in cyclodextrin synthesis. The Malaysian Society for Biochemistry & Molecular Biology 2023 Article PeerReviewed Nik-Pa, Nik Ida Mardiana and Mohamad Sobri, Mohamad Farhan and Zolkefli, Nurhasliza and Abd-Aziz, Suraini and Ibrahim, Mohamad Faizal and Mohamed Alitheen, Noorjahan Banu and Ramli, Norhayati (2023) Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis. Malaysian Journal of Biochemistry & Molecular Biology, 26 (2). pp. 45-54. ISSN 2600-9005 https://msbmb2010.wixsite.com/mjbmb
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
description Cyclodextrin glycosyltransferase (CGTase) has always played a significant role in the production of cyclodextrin through the cyclization reaction. The wide application of this valuable protein demands a better understanding, leading to a comprehensive insilico analysis of CGTase. The analysis focused on the functional domain composition of the recombinant CGT-BS protein by comparing it with several other CGTase proteins from different Bacillus spp. A three-dimensional (3-D) model was constructed to predict the active, substrate binding and cyclization sites of the CGT-BS protein. Structural function prediction revealed the active site within domain A at the wide end of the (β/α)8-barrel, with Asp 268, Glu 296 and Asp 357 as the catalytic residues. Additionally, the reaction site for cyclization was identified in domain B at Tyr 234. In comparison to maltose binding sites (MBS) 1 and 2 which are associated with raw starch binding activity, a comparable role is deduced for the MBS identified on the surface of the Domain E protein. We additionally observed that the residues Tyr 139, Arg 266 and Asp 367, located at the substrate binding cleft of the catalytic site, exhibited heightened hydrophobicity and concurrent cyclization activity. The successful extracellular expression of the CGT-BS protein is also anticipated to be facilitated by the presence of a functional signal peptide. In conclusion, our in-depth insilico analysis unveils critical insights into the structural and functional aspects of CGTBS protein, laying the groundwork for further exploration of its catalytic mechanisms and potential applications in cyclodextrin synthesis.
format Article
author Nik-Pa, Nik Ida Mardiana
Mohamad Sobri, Mohamad Farhan
Zolkefli, Nurhasliza
Abd-Aziz, Suraini
Ibrahim, Mohamad Faizal
Mohamed Alitheen, Noorjahan Banu
Ramli, Norhayati
spellingShingle Nik-Pa, Nik Ida Mardiana
Mohamad Sobri, Mohamad Farhan
Zolkefli, Nurhasliza
Abd-Aziz, Suraini
Ibrahim, Mohamad Faizal
Mohamed Alitheen, Noorjahan Banu
Ramli, Norhayati
Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
author_facet Nik-Pa, Nik Ida Mardiana
Mohamad Sobri, Mohamad Farhan
Zolkefli, Nurhasliza
Abd-Aziz, Suraini
Ibrahim, Mohamad Faizal
Mohamed Alitheen, Noorjahan Banu
Ramli, Norhayati
author_sort Nik-Pa, Nik Ida Mardiana
title Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
title_short Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
title_full Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
title_fullStr Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
title_full_unstemmed Deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
title_sort deciphering the molecular landscape: in-silico analysis of cyclodextrin glycosyltransferase for enhanced enzyme functionality and cyclodextrin synthesis
publisher The Malaysian Society for Biochemistry & Molecular Biology
publishDate 2023
url http://psasir.upm.edu.my/id/eprint/107212/
https://msbmb2010.wixsite.com/mjbmb
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