Cloning, expression, process analytical technology (PAT) enabled monitoring and control of glycoengineered pichia pastoris cultivation for human interferon α2b production

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dc.contributor.authorSrikanth, Katla
dc.date.accessioned2020-08-03T06:32:06Z
dc.date.accessioned2023-10-19T11:05:23Z
dc.date.available2020-08-03T06:32:06Z
dc.date.available2023-10-19T11:05:23Z
dc.date.issued2019
dc.descriptionSupervisor: Senthilkumar Sivaprakasamen_US
dc.description.abstractRecombinant huIFNα2b has been expressed on various platforms, which includes bacteria, yeast, insect cell lines, mammalian cell lines and plants. Expression of recombinant huIFNα2b in E. coli yielded high huIFNα2b titer but the expressed protein forms inclusion bodies and loses the activity during renaturation process. Also, the expressed protein lacks post-translational modifications and exhibited very less plasma life. The plasma life of huIFNα2b expressed by E. coli increased to certain extent through pegylation but could affect the patient’s quality life on long-term use. To achieve the post translational modifications of the recombinant huIFNα2b insect cell lines and mammalian cell lines were considered as viable platform. But, the expressed huIFNα2b yield is low and the protein is partially glycosylated. Mammalian cell lines were used to express rightly processed glycosylated huIFNα2b but it is limited by low yield, high cost, challenges of scale-up, and the problems associated with purification. Few literature reports are available for the expression of recombinant huIFNα2b in P. pastoris but failed to report the extent of post translational modifications of the expressed protein and the maximum protein yield reported was 600 mg/L. The present thesis work is aimed to address the gaps pertaining to reported literature. In this work a glycoengineered P. pastoris clone expressing homogenous human-like N-glycosylated huIFNα2b was achieved using N-Glycoengineering approach. Medium optimization and Process Analytical Technology (PAT) based real-time monitoring and control studies (Dielectric Spectroscopy) resulted in enhanced expression of recombinant huIFNα2b (1.48 g/L). Finally an optimum mixed feed strategy (Methanol + sorbitol) was deduced using Biocalorimetry as PAT tool for real-time monitoring. This strategy resulted in reduced biomass heat yield coefficient (YQ/X), Oxycalorific value (YQ/O2) and enhanced expression. The purified glycosylated huIFNα2b of the present thesis work was biologically active exhibiting antiviral and antiproliferative properties and also with increased pharmacokinetic property (plasma half-life).en_US
dc.identifier.otherROLL NO.126106006
dc.identifier.urihttps://gyan.iitg.ac.in/handle/123456789/1457
dc.language.isoenen_US
dc.relation.ispartofseriesTH-2123;
dc.subjectBIOSCIENCES AND BIOENGINEERINGen_US
dc.titleCloning, expression, process analytical technology (PAT) enabled monitoring and control of glycoengineered pichia pastoris cultivation for human interferon α2b productionen_US
dc.typeThesisen_US
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