Integration Stability of sHBsAg-Multi Expression Cassettes in Pichia pastoris GS115 during Methanol Induction

Hepatitis B is the major health problem worldwide including in Indonesia. Vaccination is the best prevention strategy for the disease. For the purpose of vaccine development and to decrease drug import, production of Hepatitis B Virus (HBV) small surface antigen (sHBsAg) from Indonesian HBV subtype...

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Main Authors: Naully, Patricia Gita (Author), Nurainy, Neni (Author), Restiawaty, Elvi (Author), Natalia, Dessy (Author), Retnoningrum, Debbie Soefie (Author), Niloperbowo, Wardono (Author), Giri-Rachman, Ernawati Arifin (Author)
Format: EJournal Article
Published: Bogor Agricultural University, Indonesia, 2020-10-01.
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001 HAYATI_33952_20893
042 |a dc 
100 1 0 |a Naully, Patricia Gita   |e author 
700 1 0 |a Nurainy, Neni   |e author 
700 1 0 |a Restiawaty, Elvi   |e author 
700 1 0 |a Natalia, Dessy   |e author 
700 1 0 |a Retnoningrum, Debbie Soefie   |e author 
700 1 0 |a Niloperbowo, Wardono   |e author 
700 1 0 |a Giri-Rachman, Ernawati Arifin   |e author 
245 0 0 |a Integration Stability of sHBsAg-Multi Expression Cassettes in Pichia pastoris GS115 during Methanol Induction 
260 |b Bogor Agricultural University, Indonesia,   |c 2020-10-01. 
500 |a https://journal.ipb.ac.id/index.php/hayati/article/view/33952 
520 |a Hepatitis B is the major health problem worldwide including in Indonesia. Vaccination is the best prevention strategy for the disease. For the purpose of vaccine development and to decrease drug import, production of Hepatitis B Virus (HBV) small surface antigen (sHBsAg) from Indonesian HBV subtype is needed. The recombinant protein production can be conducted by integrating multi expression cassettes of sHBsAg gene in Pichia pastoris chromosome using gene replacement method. Such integration method turns out to allow loss of foreign gene from chromosome by excisional recombination-mediated looping out. This research was aimed to determine integration stability of four copies of sHBsAg expression cassette in P. pastoris GS115 chromosome inducted with 2% methanol in FM22 medium. The methanol induction was conducted twice at 63-h and 75-h. Integration stability determination was conducted qualitatively using PCR and quantitatively using qPCR absolute quantification. A band of 208 bp with similar intensity was observed after amplification of genomic DNA. All samples generated the same Ct value of around 22 with four copies of sHBsAg gene per genome. The result from this experiment shows that integration of four copies of sHBsAg expression cassette in P. pastoris GS115 chromosome is stable during methanol induction. 
546 |a eng 
655 7 |a info:eu-repo/semantics/article  |2 local 
655 7 |a info:eu-repo/semantics/publishedVersion  |2 local 
655 7 |a Peer-reviewed Article  |2 local 
786 0 |n HAYATI Journal of Biosciences; Vol. 27 No. 4 (2020): October 2020; 283 
786 0 |n 2086-4094 
786 0 |n 1978-3019 
787 0 |n https://journal.ipb.ac.id/index.php/hayati/article/view/33952/20893 
856 4 1 |u https://journal.ipb.ac.id/index.php/hayati/article/view/33952/20893  |z Get fulltext