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Trasformation of chitinase gene in yeast pichia pastrosis X33

The discovery of methylotrophic yeast Pichia pastoris has led to efforts in making it a versatile system for the heterologous protein production correspond with the increasing demand for recombinant protein and bioproducts, Chitinase is a group of enzyme that capable to degrade chitin into its low...

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Main Author: Sakinah, Binti Ibrahim.
Format: Final Year Project Report
Language:English
Published: Universiti Malaysia Sarawak (UNIMAS) 2015
Subjects:
Q Science (General)
QR Microbiology
Online Access:http://ir.unimas.my/id/eprint/26831/2/Sakinah%20Binti%20Ibrahim%20%28fulltext%29.pdf
http://ir.unimas.my/id/eprint/26831/
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spelling my.unimas.ir.268312024-01-31T07:49:34Z http://ir.unimas.my/id/eprint/26831/ Trasformation of chitinase gene in yeast pichia pastrosis X33 Sakinah, Binti Ibrahim. Q Science (General) QR Microbiology The discovery of methylotrophic yeast Pichia pastoris has led to efforts in making it a versatile system for the heterologous protein production correspond with the increasing demand for recombinant protein and bioproducts, Chitinase is a group of enzyme that capable to degrade chitin into its low molecular product chitooligomers, Chitinase bas attracted attention due to its potential in industrial processes such as in biocontrol of plant pathogenic fungi and insect, and production of chitooligosaccharides, that involve in the plant's defense mechanism, However. in biotechnology chitinaso still not commercially used due to high production cost, therefore it is a challenge for scientists to formulate a reliable method to produce chitinase at lower cost In this study, the chitinase gene that was isolated from tbe Metroxylon sagu was constructed under the plasmid pPICZuC in the previous study. The plasmid pPICZuC/chilinase was extracted from the cellular cell, Escherichia coli XLI-Blue, then transformed into P. pastoris X33 by using the EasYCompTM kit Finally, direct PCR screening was done to check the integmtion of chitinase gene into the yeast, and Mut phenotype analysis was done to evaluate the methanol utilization type of the recombinant clones, Based on this study, the tmnsformation was proven its success by the direct PCR screening as the chitinase gene was integrated into the yeast genome. The production of recombinant protein cbitinase "ill assist a means to study the biological functions and activities of this protein especially in plant M. sagu, Universiti Malaysia Sarawak (UNIMAS) 2015 Final Year Project Report NonPeerReviewed text en http://ir.unimas.my/id/eprint/26831/2/Sakinah%20Binti%20Ibrahim%20%28fulltext%29.pdf Sakinah, Binti Ibrahim. (2015) Trasformation of chitinase gene in yeast pichia pastrosis X33. [Final Year Project Report] (Unpublished)
institution Universiti Malaysia Sarawak
building Centre for Academic Information Services (CAIS)
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Malaysia Sarawak
content_source UNIMAS Institutional Repository
url_provider http://ir.unimas.my/
language English
topic Q Science (General)
QR Microbiology
spellingShingle Q Science (General)
QR Microbiology
Sakinah, Binti Ibrahim.
Trasformation of chitinase gene in yeast pichia pastrosis X33
description The discovery of methylotrophic yeast Pichia pastoris has led to efforts in making it a versatile system for the heterologous protein production correspond with the increasing demand for recombinant protein and bioproducts, Chitinase is a group of enzyme that capable to degrade chitin into its low molecular product chitooligomers, Chitinase bas attracted attention due to its potential in industrial processes such as in biocontrol of plant pathogenic fungi and insect, and production of chitooligosaccharides, that involve in the plant's defense mechanism, However. in biotechnology chitinaso still not commercially used due to high production cost, therefore it is a challenge for scientists to formulate a reliable method to produce chitinase at lower cost In this study, the chitinase gene that was isolated from tbe Metroxylon sagu was constructed under the plasmid pPICZuC in the previous study. The plasmid pPICZuC/chilinase was extracted from the cellular cell, Escherichia coli XLI-Blue, then transformed into P. pastoris X33 by using the EasYCompTM kit Finally, direct PCR screening was done to check the integmtion of chitinase gene into the yeast, and Mut phenotype analysis was done to evaluate the methanol utilization type of the recombinant clones, Based on this study, the tmnsformation was proven its success by the direct PCR screening as the chitinase gene was integrated into the yeast genome. The production of recombinant protein cbitinase "ill assist a means to study the biological functions and activities of this protein especially in plant M. sagu,
format Final Year Project Report
author Sakinah, Binti Ibrahim.
author_facet Sakinah, Binti Ibrahim.
author_sort Sakinah, Binti Ibrahim.
title Trasformation of chitinase gene in yeast pichia pastrosis X33
title_short Trasformation of chitinase gene in yeast pichia pastrosis X33
title_full Trasformation of chitinase gene in yeast pichia pastrosis X33
title_fullStr Trasformation of chitinase gene in yeast pichia pastrosis X33
title_full_unstemmed Trasformation of chitinase gene in yeast pichia pastrosis X33
title_sort trasformation of chitinase gene in yeast pichia pastrosis x33
publisher Universiti Malaysia Sarawak (UNIMAS)
publishDate 2015
url http://ir.unimas.my/id/eprint/26831/2/Sakinah%20Binti%20Ibrahim%20%28fulltext%29.pdf
http://ir.unimas.my/id/eprint/26831/
_version_ 1789945459624640512
score 13.211869

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