Engineering of probiotic Saccharomyces boulardii as a host for living therapeutic applications

buir.advisorŞeker, Urartu Özgür Şafak
dc.contributor.authorKurt, Orhan Nedim
dc.date.accessioned2022-09-16T12:31:06Z
dc.date.available2022-09-16T12:31:06Z
dc.date.copyright2022-09
dc.date.issued2022-09
dc.date.submitted2022-09-14
dc.descriptionCataloged from PDF version of article.en_US
dc.descriptionThesis (Master's): Bilkent University, Graduate Program in Materials Science and Nanotechnology, İhsan Doğramacı Bilkent University, 2022.en_US
dc.descriptionIncludes bibliographical references (leaves 39-41).en_US
dc.description.abstractTherapeutic molecules or biologically active agents used in the treatments of disorders have been manufactured employing chemical synthesis methods with high costs and limited accessibility. Even though this approach to producing therapeutic molecules has enabled life-changing substances to be produced, there are still countless diseases waiting for a cure. Therefore, it would not be possible to meet the treatment needs via just conventional manufacturing approaches. Living therapeutics are programmed cells for the production and direct delivery of therapeutic molecules to the human body. Indeed, biologically engineered cells have been used for a long time to manufacture biomolecules in industrial settings. Also, there have been many studies that designed and programmed living organisms to cure diseases such as cancer, diabetes, inflammatory bowel syndrome, ulcer, and colitis. accharomyces boulardii CNCM I-745 is a yeast strain used as a probiotic for a very long time in humans. S. boulardii is the first and the only yeast strain approved to be used in human medicine so far. It has been shown that S.boulardii has many benefits to its host, including restoring the microbiome and competing with pathogens. Also, S.boulardii is a promising organism to be engineered and programmed as a living therapeutic factory due to its great compatibility with the human body and its metabolic features enabling us to manufacture complex molecules. Aiming for this, we created a TRP1 auxotroph S.boulardii strain using synthetic biology tools to eliminate the use of antibiotic resistance genes in the further steps since it would be problematic for the spread of antibiotic resistance. To do that, we employed the CRISPR CAS-9 system and a donor DNA harboring a stop codon to be inserted into the target gene (TRP1). After verifying the construction of the TRP1 auxotroph strain, we designed an episomal expression vector comprising a strong, constitutive promoter, extracellular signal sequence (Alpha sequence), and a terminator (CYC1). Next, we inserted the Intrinsic Factor protein (the key protein responsible for vitamin B12 absorption) sequence into the vector to recombinantly produce it and secrete it into the gut. However, according to our preliminary data, we could not observe an expression of the protein of interest, suggesting that the system needs further optimization and investigation to work properly. Considering the lack of auxotrophic yeast strains available to be engineered for therapeutic purposes, our engineered S.boulardii strain can be employed in yeast-based living therapeutics applications against different disorders waiting for their treatment.en_US
dc.description.provenanceSubmitted by Betül Özen (ozen@bilkent.edu.tr) on 2022-09-16T12:31:06Z No. of bitstreams: 1 B161299.pdf: 2295210 bytes, checksum: fdeabd157d563929ab7488808d375f04 (MD5)en
dc.description.provenanceMade available in DSpace on 2022-09-16T12:31:06Z (GMT). No. of bitstreams: 1 B161299.pdf: 2295210 bytes, checksum: fdeabd157d563929ab7488808d375f04 (MD5) Previous issue date: 2022-09en
dc.description.statementofresponsibilityby Orhan Nedim Kurten_US
dc.embargo.release2023-03-09
dc.format.extentxi, 84 leaves : illustrations ; 30 cm.en_US
dc.identifier.itemidB161299
dc.identifier.urihttp://hdl.handle.net/11693/110526
dc.language.isoEnglishen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectLiving therapeuticsen_US
dc.subjectSynthetic biologyen_US
dc.subjectSaccharomyces boulardiien_US
dc.subjectCRISPR Cas-9en_US
dc.subjectB12 deficiencyen_US
dc.subjectIntrinsic factoren_US
dc.titleEngineering of probiotic Saccharomyces boulardii as a host for living therapeutic applicationsen_US
dc.title.alternativeProbiyotik Saccharomyces boulardii’nin yaşayan terapötik uygulamalarında konak olarak kullanılmak üzere geliştirilmesien_US
dc.typeThesisen_US
thesis.degree.disciplineMaterials Science and Nanotechnology
thesis.degree.grantorBilkent University
thesis.degree.levelMaster's
thesis.degree.nameMS (Master of Science)

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