Effects of synthetic lysophosphatidylcholines on suspension cultures of the Chinese hamster ovary DG44 cells in protein-free media
- Authors
- Kim, In-Kyoung; Lim, Dong-Jin; Park, Hong-Woo
- Issue Date
- Jul-2008
- Publisher
- 한국생물공학회
- Keywords
- Chinese hamster ovary cells; lysophosphatidylcholines; protein-free medium; suspension culture
- Citation
- Biotechnology and Bioprocess Engineering, v.13, no.4, pp 396 - 400
- Pages
- 5
- Indexed
- SCIE
SCOPUS
KCI
- Journal Title
- Biotechnology and Bioprocess Engineering
- Volume
- 13
- Number
- 4
- Start Page
- 396
- End Page
- 400
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/171981
- DOI
- 10.1007/s12257-008-0148-7
- ISSN
- 1226-8372
1976-3816
- Abstract
- This study described the effects of synthetic lysophosphatidylcholines on the growth of recombinant CHO-DG44 cells in suspension. Overall, cell growth characteristics were improved when cultivated in suspension in a protein-free medium supplemented with natural soybean lysophosphatidylcholines. To substitute synthetic lysophosphatidylcholines for the naturally occurring lysophosphatidylcholines, we implemented a systematic approach in which twelve synthetic lysophosphatidylcholines were grouped into three lipid mixtures according to the length of their acyl chains. We found that synthetic lysophosphatidylcholines with medium acyl chain lengths (C14-C18), including oleoyl lysophosphatidylcholine (618:1) could increase cell growth in the protein-free media. The fortified protein-free medium with medium acyl chain length lysophosphatidylcholines (C14-C18) maintained growth of CHO-DG44 cells over five consecutive passages, whereas the cell growth in a CHO protein-free medium was decreased gradually after four passages. We also observed that the restorative effect of oleoyl lysophosphatidylcholine was comparable to that of natural lysophosphatidylcholine in batch and long-term cultivation. These results show that synthetic lysophosphatidylcholines can be used as lipid supplements in either protein-free media or chemically defined media for CHO cell suspension cultures.
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