Previous small-scale methods for plasmid DNA (pDNA) purification fail to meet theindustry’s demand for sufficient quantities. Greater volumes of bacterial lysates are a consequence of larger volumetric fermentations and traditional large-scale down-stream purification processes have some disadvantages and limitations. The market is believed to continue to expand, hence the need for efficient, cost-effective, andscalable purification processes becomes apparent. A crucial trade-off exists between pDNA yield and purity, necessitating careful consideration in chromatographic pu-rification steps. Each step enhances purity while likely sacrificing yield. In order to achieve a higher degree of pDNA yield, optimal purification entails a single chro-matographic step, specifically anion-exchange chromatography (AEX) in combina-tion with filtration. Alternatively, a two-step purification approach involving AEX followed by hydrophobic interaction chromatography (HIC) is recommended to elim-inate complementary impurities and achieve a high level of purity. Furthermore, the utilization of monolithic chromatographic supports is suggested to facilitate the sug-gested purification strategies. This is due to monoliths promoting higher binding capacities, ensuring robust and consistent results even at high flow rates.
Identifer | oai:union.ndltd.org:UPSALLA1/oai:DiVA.org:uu-502905 |
Date | January 2023 |
Creators | Eriksson, Matilda, Wells, Alva, Frey, Maria, Johansson, Lisa, Pettersson, Gabriel, Sjöberg, David |
Publisher | Uppsala universitet, Institutionen för biologisk grundutbildning |
Source Sets | DiVA Archive at Upsalla University |
Language | English |
Detected Language | English |
Type | Student thesis, info:eu-repo/semantics/bachelorThesis, text |
Format | application/pdf |
Rights | info:eu-repo/semantics/openAccess |
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