毕赤酵母
稀释
生物反应器
体积热力学
几丁质酶
稳态(化学)
重组DNA
色谱法
化学
连续搅拌釜式反应器
喷射
生物化学
酶
热力学
有机化学
物理
基因
物理化学
作者
B. M. Schilling,Jason C. Goodrick,Nan Chi Wan
摘要
The feasibility of large-scale production of recombinant human chitinase using a constitutive Pichia pastoris expression system was demonstrated in a 21-L continuous stirred tank reactor. A steady-state recombinant protein concentration of 250 mg/L in the supernatant was sustained for 1 month at a dilution rate of 0.042 h−1 (equivalent to one volume exchange per day), enabling a volumetric productivity of 144 mg/L d (240 U/L d). The steady-state dry cell weight concentration in this high cell density culture reached 110 g/L. Considering safety and economical aspects, all large-scale cultivations were conducted without molecular oxygen supplementation. Conventional air sparging was used instead. The oxygen demand of the process was determined by off-gas analysis (OUR = 4.8 g O2 L−1 h−1 with kLa = 846 h−1) and evaluated with regard to further reactor scale-up.
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