Team:CCU Taiwan/Safety

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Filtering system

Heating system

SAFETY

  The escaping of genetically modified organisms from labs is a serious problem since it will bring up unpredictable impacts to our ecosystem. We take biosafety very seriously when we design every parts of our experiment and the design of our production line. Our design of our production line insure that there's no genetically modified yeasts (also non-genetically modified yeasts) could survived and pass the whole production line and leak into the environment or residue on our products. We also dealt cautiously with wastes produced from the experiment and participated in safety training, to minimum the chance of causing biohazard pollution, or simply hurt ourselves.

Filtering system

  The average size of the P. pastoris is about 4–6 μm (Gmeiner, C. et al. 2015), the filter we use is 33 kDa, which is equivalent to the size of tens of nanometers (Bacher, G. ey al. 2001), enough to block all the yeasts form leaking out the fermentation tank.

Heating system

  According to the literature (Martínez, D. et al. 2015), heating at 70 °C for 1 day, and incubate at 30 °C for 48 hr. Under this temperature, it is sufficient to kill any yeasts that escape from the Filtering system. The minimum operating temperature of Extrusion Granulation will be over 110 °C. Therefore, no yeast will escape from the production line we designed.

Following were our heating test:

Figure1: P. pastoris heated at 30 °C for 1 day , and incubate at 30 °C for 48 hr.
(left: 0.005, right: 0.05)

Figure2: P. pastoris heated at 50 °C for 1 day , and incubate at 30 °C for 48 hr.

Figure3: P. pastoris heated at 70 °C for 1 day , and incubate at 30 °C for 48 hr.

  We found that our P. pastoris not survival after were heated at 50 °C for 30 minutes. Thus, our production line heat process would kill P. pastoris passing through the filter.

Reference

Gmeiner, C., Saadati, A., Maresch, D., Krasteva, S., Frank, M., Altmann, F., … Spadiut, O. (2015). Development of a fed-batch process for a recombinant Pichia pastoris Δoch1 strain expressing a plant peroxidase. Microbial Cell Factories, 14(1). doi:10.1186/s12934-014-0183-3

Bacher, G., Szymanski, W. W., Kaufman, S. L., Zöllner, P., Blaas, D., & Allmaier, G. (2001). Charge-reduced nano electrospray ionization combined with differential mobility analysis of peptides, proteins, glycoproteins, noncovalent protein complexes and viruses. Journal of Mass Spectrometry, 36(9), 1038–1052.doi:10.1002/jms.208

3. Martínez, D., Menéndez, C., Echemendia, F. M., Hernández, L., Sobrino, A., & Trujillo, L. E. (2015). Kinetics of sucrose hydrolysis by immobilized recombinant Pichia pastoris cells in a batch reactors. J Microb Biochem Technol, 7, 294-6.