Heterologous Expression Of Xylanase Gene From Klebsiella Pneumoniae In E. Coli Bl21 (De3) For Potential Use In Green Technology

Mohd Hasnain, Hussain and Suhaila, Bt Zainol and Chong, Nikson Fatt Ming and Awang Ahmad Sallehin, Awang Husaini (2013) Heterologous Expression Of Xylanase Gene From Klebsiella Pneumoniae In E. Coli Bl21 (De3) For Potential Use In Green Technology. In: Conference ICGAI, November 12-14, 2013, Yogyakarta, INDONESIA.

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Abstract

A xylanolytic bacterium was isolated from sago plantation humus. Isolation and characterization of xylanase DNA sequence showed a total length of 642 bp. The full length xylanase gene was cloned in pSTAG vector and expressed in E. coli BL21 (DE3). In silico characterization determines the recombinant xylanase has a molecular weight of 23.9 kDa. The activity of crude recombinant xylanase was 2.015 U/mL, which was higher than the crude native xylanase activity that was only 0.642 U/mL at maximum. Staining of the birchwood xylan agar plate with Congo red showed a clearing zone around E. coli BL21 (DE3) that has positive recombinant xylanase even without the addition of IPTG, implying leaky expression had occurred. Further analysis showed the existence of two forms of the xylanase. These xylanases were enzymes with the size of 25kDa that accumulates in the cell, and the other as a 20kDa mature extracellular xylanase.

Item Type: Proceeding (Paper)
Uncontrolled Keywords: Klebsiella pneumoniae, heterologous expression, cloning, recombinant xylanase, unimas, university, universiti, Borneo, Malaysia, Sarawak, Kuching, Samarahan, ipta, education, research, Universiti Malaysia Sarawak
Subjects: G Geography. Anthropology. Recreation > GE Environmental Sciences
Q Science > QR Microbiology
Divisions: Academic Faculties, Institutes and Centres > Faculty of Resource Science and Technology
Faculties, Institutes, Centres > Faculty of Resource Science and Technology
Depositing User: Karen Kornalius
Date Deposited: 30 Nov 2015 00:53
Last Modified: 04 Jan 2022 04:06
URI: http://ir.unimas.my/id/eprint/9820

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