BSc Biological Chemistry state exams and defences - September 2026

BSc Biological Chemistry state exams

16. 9. 2026

9:15-12:45

• C3: Biology of Microorganisms
• C4: Molecular Biology and Genetics
• C5: Biochemistry

18. 9. 2026

8:30 - 15:00

• C3: Biomedicine + Biology of Animals
• C4: Molecular Biology and Genetics
• C5: Biochemistry

BSc Biological Chemistry defences

16. 9. 2026, C5

• 13:00-13:45: De novo DNA methylation establishment in oocytes of nonmodel
  Cricetidae rodents.
• 13:45-14:30: Purification of MICOS complex in Trypanosoma Brucei.
• 14:30-15:15: Temperature dependence of spectroscopic properties of carotenoids.
• 15:15-16:00: Bioaugmentation of psychrophilic bacteria from permafrost soil.
• 16:00 16:45: Optimization of a wet digestion protocol for digestibility marker analysis
  in aquaculture.

17. 9. 2026, C5

• 8:00-8:45: Dissecting +4 mRNA context effect on near-cognate UAA stop codon
  readthrough.
• 8:45-9:30: Bioinformatics identification and characterisation of Wolbachia prevalence in
  a tropical skipper butterfly taxon (Hesperiidae: Eudaminae) using Whole-Genome Sequencing data.
• 9:30-10:15: Encapsulation of electron transport proteins into viral capsids: engineering of
  ferredoxin, ferredoxin-NADP+ reductase, and P22 virus-like particle components.
• 10:15-11:00: Cloning and recombinant production of Lucillia sericata enzyme
  with therapeutic potential.
• 11:00-11:45: Evolutionary conservation of PRC2 catalytic subunit in the green lineage.
• 12:45-13:30: Cloning and Expression of Selected Antigenic Proteins from Borrelia duttoni.
• 13:30-14:15: The effect of nutrient availability on the chemical composition and
  litter decomposition of Phalaris arundinacea.
• 14:15-15:00: Determination of meropenem in medicinal products using HPLC with UV
  detection.
• 15:00-15:45: AFM-based Elucidation of the Impact of Surfaces on the Self-Assembly
  of Two Adamantyl-Substituted, Conjugated Systems.
• 15:45-16:30: Optimization of Silane-based molecularly imprinted polymers for the
  detection of 2,4-dichlorophenoxyacetic acid.