Project Biotechnology 3

Department
  • Master's Program Biotechnology
Course unit code
  • BT_MA16_3_11
Number of ECTS credits allocated
  • 4.0
Name of lecturer(s)
  • Dipl.-Ing. Dr. Hirschl-Neuhauser Sonja, Mag. Ralser Claudia, Bakk. biol., Kaiser Christiane, BSc, Dr. Trockenbacher Alexander
Mode of delivery
  • face-to-face
Recommended optional program components
  • none
Recommended or required reading
  • Sambrook J., Rusell D., Maniatis T.: Molecular cloning: A laboratory manual, 3rd Edition, Cold Spring Harbor Laboratory Press, 2001
    Surzycki, S.: Basic Techniques in Molecular Biology, Springer 2000
    Mülhardt, C.: Der Experimentator: Molekularbiologie / Genomics, Spektrum Akad. Verlag, 2008
    Brown T.A.: Essential molecular biology: a practical approach Vol.1+2 - 2nd Edition, Oxford University Press, 2000
    Dyson M, Durocher Y.: Expression systems, Scion Publishing, 2007
    McEntyre J., Ostell J., : The NCBI Handbook, National Center for Biotech-nology Information, 2002
Assessment methods and criteria
  • Course immanent examination
Level of course unit
  • Master
Year of study
  • Fall 2025
Semester when the course unit is delivered
  • 3
Language of instruction
  • English
Learning outcomes of the course unit
  • Participants in this course are able to plan and perform the induced expression of recombinant proteins in Pichia pastoris in a fermentor. They implement the necessary prearrangements for running the fermentor and are able to perform a batch as well as a fed-batch fermentation.
    Graduates of the course are qualified to prepare relevant reports and provide suggestions for optimization.
Course contents
  • This course is a continuation to the practical course "Project Biotechnology 2". The recombinant Pichia pastoris strains established in the previous project parts will be fermented in a large scale during this course. This includes:
    • planning the fermentation
    • preparation of media and solutions
    • prearrangement of fermenter: calibrations, filling, sterilization
    • preparation of preculture and culture
    • fermentation: inoculation, sterile sample taking, data logging, induction of protein expression, batch and fed-batch fermentation
    • analytics
    • evaluation of results:
    comparison of growth behavior of native and recombinant strain
    comparison of growth behavior in shaking flasks and fermentor
    • functional assay for the expressed proteins
Planned learning activities and teaching methods
  • The practical course comprises an interactive mix of discussions and individual and group work.
Work placement(s)
  • none

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