High cell density in microbial cell cultivation is about 10 times to a normal density that can be obtained without extraordinary efforts in a batch culture. For instance, if a 5~10g/L of E.coli cell density is considered a normal cell density, 50~100g/L would be called a high cell density. In animal cell culture 106~107/ml cell density would be a high cell density if 105~106 cells/ml. An immobilized cell matrix can have a cell density of 108cells/ml, but the cell density in the reactor can be lower or much lower than that in the matrix. Extra efforts mean fed-batch, continuous culture, membrane cell recycle for high cell density culture and use of pure oxygen. Several HCDC systems developed at biochemical engineering laboratory of KAIST during the last 30 years will be introduced with a theoretical simulation showing the equivalence of MSC-HCDC with similar titer to fed-batch but with much higher productivities in lactic acid and monoclonal antibody production. Especially depth filter perfusion system (DFPS) for monoclonal antibody production appears to be suitable for MSCHCDC pilot test because of its simplicity in immobilization and no need in separation of cells from the product stream. MSC-HCDC: multi-stage continuous high cell density culture
저자
Ho Nam Chang [ Department of Chemical and Biomolecular Engineering, KAIST ]
한국생물공학회 [The Korean Society for Biotechnology and Bioengineering]
설립연도
1984
분야
공학>생물공학
소개
이 법인은 생물 공학의 발전과 보급에 이바지하고, 회원 상호 간의 연구 협력과 친목을 도모함을 목적으로 한다
1. 생물공학 분야의 발전을 위한 연구 협력
2. 생물공학의 실용화를 촉진시키기 위한 산학 협동
3. 학술연구 발표회, 강연회, 연수회 등 학술활동의 개최
4. 국,영문 학술지,소식지,학술회의 Proceedings 및 학술도서의 발간
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