Cloning and expression of pullulanase gene from locally isolated bacillus SP

Bacterial pullulanase represents one of th e starch-degrading enzymes that are widely used in the starch processing indu stry along with amylases. Amylases hydrolyze a -(1,4 )-glycosidic linkage in starch to produce a mixture of glucose , maltooligo sacchari de and limited a-dextrin. All the r...

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Main Authors: Nik Mahmood, Nik Azmi, Md. Illias, Rosli, Md. Salleh, Madihah, Hassan, Osman, Kamaruddin, Kamarulzaman, Shahab, Neelam
Format: Monograph
Language:en
Published: Universiti Teknologi Malaysia 2006
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Online Access:http://eprints.utm.my/2754/1/74189.pdf
http://eprints.utm.my/2754/
https://www.researchgate.net/publication/254655826_Cloning_and_Expression_of_Pullulanase_a_Gene_from_Locally_Isolated_Bacillus
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author Nik Mahmood, Nik Azmi
Md. Illias, Rosli
Md. Salleh, Madihah
Hassan, Osman
Kamaruddin, Kamarulzaman
Shahab, Neelam
author_facet Nik Mahmood, Nik Azmi
Md. Illias, Rosli
Md. Salleh, Madihah
Hassan, Osman
Kamaruddin, Kamarulzaman
Shahab, Neelam
author_sort Nik Mahmood, Nik Azmi
building UTM Library
collection Institutional Repository
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
continent Asia
country Malaysia
description Bacterial pullulanase represents one of th e starch-degrading enzymes that are widely used in the starch processing indu stry along with amylases. Amylases hydrolyze a -(1,4 )-glycosidic linkage in starch to produce a mixture of glucose , maltooligo sacchari de and limited a-dextrin. All the remaining a -(1,6)-glycosid ic branches in the products are hydrolyzed by p ullulanase. This is an advantage t o improve glucose production by coupling pullulanase and amylase in the p rocess. As such, many pullulana e enzyme has been isolated and one has been showing optimum pH of 10-10.5 which is suitable for use in dishwasher detergent additive in removal of star ch stain. We have recently iso lated a few bacterias that have shown potentially pullulanase producers by the holo-zone in pullulan-plate assay. One of them, we named Bacillus –1 sho ws a bigger holo-zone among others, Bacillus- 1 is highly active in pH more than 7. The enzyme also shows a mo derate activity to wards starch that may be indicates be side hydrolyzes a -(1,6)-glycosidic linkage in starch, it also hydrolyzes a -(1,4)- glycosidi c simi lar to a -amylase. Unfortunately the enzyme from wild-type bacteria is in lower yield an d in this studies, we intend to clone and sequence the pullulanase gene and also expressed the gene in a high expression system to be able to produce in a high yield before characterizing expressed protein.
format Monograph
id my.utm.eprints-2754
institution Universiti Teknologi Malaysia
language en
publishDate 2006
publisher Universiti Teknologi Malaysia
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spelling my.utm.eprints-27542017-10-11T04:29:44Z http://eprints.utm.my/2754/ Cloning and expression of pullulanase gene from locally isolated bacillus SP Nik Mahmood, Nik Azmi Md. Illias, Rosli Md. Salleh, Madihah Hassan, Osman Kamaruddin, Kamarulzaman Shahab, Neelam Q Science (General) Bacterial pullulanase represents one of th e starch-degrading enzymes that are widely used in the starch processing indu stry along with amylases. Amylases hydrolyze a -(1,4 )-glycosidic linkage in starch to produce a mixture of glucose , maltooligo sacchari de and limited a-dextrin. All the remaining a -(1,6)-glycosid ic branches in the products are hydrolyzed by p ullulanase. This is an advantage t o improve glucose production by coupling pullulanase and amylase in the p rocess. As such, many pullulana e enzyme has been isolated and one has been showing optimum pH of 10-10.5 which is suitable for use in dishwasher detergent additive in removal of star ch stain. We have recently iso lated a few bacterias that have shown potentially pullulanase producers by the holo-zone in pullulan-plate assay. One of them, we named Bacillus –1 sho ws a bigger holo-zone among others, Bacillus- 1 is highly active in pH more than 7. The enzyme also shows a mo derate activity to wards starch that may be indicates be side hydrolyzes a -(1,6)-glycosidic linkage in starch, it also hydrolyzes a -(1,4)- glycosidi c simi lar to a -amylase. Unfortunately the enzyme from wild-type bacteria is in lower yield an d in this studies, we intend to clone and sequence the pullulanase gene and also expressed the gene in a high expression system to be able to produce in a high yield before characterizing expressed protein. Universiti Teknologi Malaysia 2006-03-31 Monograph NonPeerReviewed application/pdf en http://eprints.utm.my/2754/1/74189.pdf Nik Mahmood, Nik Azmi and Md. Illias, Rosli and Md. Salleh, Madihah and Hassan, Osman and Kamaruddin, Kamarulzaman and Shahab, Neelam (2006) Cloning and expression of pullulanase gene from locally isolated bacillus SP. Project Report. Universiti Teknologi Malaysia. (Unpublished) https://www.researchgate.net/publication/254655826_Cloning_and_Expression_of_Pullulanase_a_Gene_from_Locally_Isolated_Bacillus
spellingShingle Q Science (General)
Nik Mahmood, Nik Azmi
Md. Illias, Rosli
Md. Salleh, Madihah
Hassan, Osman
Kamaruddin, Kamarulzaman
Shahab, Neelam
Cloning and expression of pullulanase gene from locally isolated bacillus SP
title Cloning and expression of pullulanase gene from locally isolated bacillus SP
title_full Cloning and expression of pullulanase gene from locally isolated bacillus SP
title_fullStr Cloning and expression of pullulanase gene from locally isolated bacillus SP
title_full_unstemmed Cloning and expression of pullulanase gene from locally isolated bacillus SP
title_short Cloning and expression of pullulanase gene from locally isolated bacillus SP
title_sort cloning and expression of pullulanase gene from locally isolated bacillus sp
topic Q Science (General)
url http://eprints.utm.my/2754/1/74189.pdf
http://eprints.utm.my/2754/
https://www.researchgate.net/publication/254655826_Cloning_and_Expression_of_Pullulanase_a_Gene_from_Locally_Isolated_Bacillus
url_provider http://eprints.utm.my/