Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity

This study was aimed to establish a method to produce in-house recombinant human DNA topoisomerase. The DNA topoisomerase I (Topo I) and DNA topoisomerase II (Topo II) coding regions were amplified from the cDNA of breast cancer cells, MDA-MB-231. Topo I and Topo II coding region were ligated int...

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Main Author: Chan, Mooi Kwai
Format: Thesis
Language:English
Published: 2017
Subjects:
Online Access:http://eprints.usm.my/47831/
http://eprints.usm.my/47831/1/EXPRESSION%20OF%20RECOMBINANT%20HUMAN%20DNA.pdf%20cut.pdf
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author Chan, Mooi Kwai
author_facet Chan, Mooi Kwai
author_sort Chan, Mooi Kwai
building USM Institutional Repository
collection Online Access
description This study was aimed to establish a method to produce in-house recombinant human DNA topoisomerase. The DNA topoisomerase I (Topo I) and DNA topoisomerase II (Topo II) coding regions were amplified from the cDNA of breast cancer cells, MDA-MB-231. Topo I and Topo II coding region were ligated into expression vector, pPICZ--A and pPICZ--C, respectively. Subsequently, the constructed recombinant vectors were transformed into four types of Pichia pastoris strain, X-33, GS115, SMD1168H and KM71H. PCR screening for recombinant clones was performed and followed by selection of multicopy clones using agar plates containing increasing concentrations of Zeocin. The selected multicopy clones were then induced for enzymes expression in a shake flask system. Topo I was expressed relatively higher in GS115 than other Pichia strains.
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institution Universiti Sains Malaysia
institution_category Local University
language English
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publishDate 2017
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spelling usm-478312020-10-28T09:23:17Z http://eprints.usm.my/47831/ Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity Chan, Mooi Kwai QP Physiology This study was aimed to establish a method to produce in-house recombinant human DNA topoisomerase. The DNA topoisomerase I (Topo I) and DNA topoisomerase II (Topo II) coding regions were amplified from the cDNA of breast cancer cells, MDA-MB-231. Topo I and Topo II coding region were ligated into expression vector, pPICZ--A and pPICZ--C, respectively. Subsequently, the constructed recombinant vectors were transformed into four types of Pichia pastoris strain, X-33, GS115, SMD1168H and KM71H. PCR screening for recombinant clones was performed and followed by selection of multicopy clones using agar plates containing increasing concentrations of Zeocin. The selected multicopy clones were then induced for enzymes expression in a shake flask system. Topo I was expressed relatively higher in GS115 than other Pichia strains. 2017-11 Thesis NonPeerReviewed application/pdf en http://eprints.usm.my/47831/1/EXPRESSION%20OF%20RECOMBINANT%20HUMAN%20DNA.pdf%20cut.pdf Chan, Mooi Kwai (2017) Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity. PhD thesis, Universiti Sains Malaysia.
spellingShingle QP Physiology
Chan, Mooi Kwai
Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity
title Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity
title_full Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity
title_fullStr Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity
title_full_unstemmed Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity
title_short Expression Of Recombinant Human Dna Topoisomerase In Pichia Pastoris And Analysis Of Its Activity
title_sort expression of recombinant human dna topoisomerase in pichia pastoris and analysis of its activity
topic QP Physiology
url http://eprints.usm.my/47831/
http://eprints.usm.my/47831/1/EXPRESSION%20OF%20RECOMBINANT%20HUMAN%20DNA.pdf%20cut.pdf