Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"

KatG is the gene in Mycobacterium tuberculosis which responsible for encoding of catalase peroxidase enzyme to enable its survival in host macrophage. KatG also reported to play an important role in enabling the killing effect of the antituberculous pro-drug, isoniazid (IN H). The mutation of thi...

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Main Author: Mohd Hamzah, Mohd Nasir
Format: Monograph
Language:English
Published: Universiti Sains Malaysia 2006
Subjects:
Online Access:http://eprints.usm.my/48619/1/Mohd%20Hamzah%20Bin%20Mohd%20Nasir%20-%2024%20pages.pdf
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author Mohd Hamzah, Mohd Nasir
author_facet Mohd Hamzah, Mohd Nasir
author_sort Mohd Hamzah, Mohd Nasir
collection USM
description KatG is the gene in Mycobacterium tuberculosis which responsible for encoding of catalase peroxidase enzyme to enable its survival in host macrophage. KatG also reported to play an important role in enabling the killing effect of the antituberculous pro-drug, isoniazid (IN H). The mutation of this gene has been reported to create resistancy of Mycobacterium tuberculosis toward INH treatment. Since the killing effect of the drug has a significant relation with this gene, the structure and properties of KatG should be study for further information. EcoRI restriction enzyme was found to produce 2252 bp of DNA product. The gene was then sliced out from pCR®2.1-TOPO by using EcoRI restriction enzyme and ligated into a high-level protein expression vector, pRSET for expression assay. The recombinant sequenced has been confirmed by EcoRIPvull restriction analysis. The gene has also been sequenced by cycle sequencing and the primers are M13F, M13R, KG3 and KGS.
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spelling usm.eprints-486192021-03-16T04:44:20Z http://eprints.usm.my/48619/ Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system" Mohd Hamzah, Mohd Nasir R Medicine (General) KatG is the gene in Mycobacterium tuberculosis which responsible for encoding of catalase peroxidase enzyme to enable its survival in host macrophage. KatG also reported to play an important role in enabling the killing effect of the antituberculous pro-drug, isoniazid (IN H). The mutation of this gene has been reported to create resistancy of Mycobacterium tuberculosis toward INH treatment. Since the killing effect of the drug has a significant relation with this gene, the structure and properties of KatG should be study for further information. EcoRI restriction enzyme was found to produce 2252 bp of DNA product. The gene was then sliced out from pCR®2.1-TOPO by using EcoRI restriction enzyme and ligated into a high-level protein expression vector, pRSET for expression assay. The recombinant sequenced has been confirmed by EcoRIPvull restriction analysis. The gene has also been sequenced by cycle sequencing and the primers are M13F, M13R, KG3 and KGS. Universiti Sains Malaysia 2006 Monograph NonPeerReviewed application/pdf en http://eprints.usm.my/48619/1/Mohd%20Hamzah%20Bin%20Mohd%20Nasir%20-%2024%20pages.pdf Mohd Hamzah, Mohd Nasir (2006) Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system". Other. Universiti Sains Malaysia. (Submitted)
spellingShingle R Medicine (General)
Mohd Hamzah, Mohd Nasir
Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"
title Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"
title_full Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"
title_fullStr Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"
title_full_unstemmed Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"
title_short Subcloning of Mycobacterium tuberculosis KatG gene in bacterial expression system"
title_sort subcloning of mycobacterium tuberculosis katg gene in bacterial expression system
topic R Medicine (General)
url http://eprints.usm.my/48619/1/Mohd%20Hamzah%20Bin%20Mohd%20Nasir%20-%2024%20pages.pdf
work_keys_str_mv AT mohdhamzahmohdnasir subcloningofmycobacteriumtuberculosiskatggeneinbacterialexpressionsystem