Betts Jonathan I, Doig Steven D, Baganz Frank
The Advanced Centre for Biochemical Engineering, Department of Biochemical Engineering, University College London, Torrington Place, London WC1E 7JE, UK.
Biotechnol Prog. 2006 May-Jun;22(3):681-8. doi: 10.1021/bp050369y.
The aim of this study was to characterize the engineering environment of an instrumented 10 mL miniature stirred-tank bioreactor and evaluate its potential as a scale-down device for microbial fermentation processes. Miniature bioreactors such as the one detailed in this work have been developed by several research groups and companies and seek to address the current bottleneck at the screening stage of bioprocess development. The miniature bioreactor was characterized in terms of overall volumetric oxygen transfer coefficient and mixing time over a wide range of impeller speeds. Power input to the miniature bioreactor was directly measured, and from this the power number of each impeller was calculated and specific power input estimated, allowing the performance of the miniature bioreactor to be directly compared with that of a conventional 7 L bioreactor. The capability of the miniature bioreactor to carry out microbial fermentations was also investigated. Replicate batch fermentations of Escherichia coli DH5alpha producing plasmid DNA were performed at equal specific power input, under fully aerobic and oxygen-limiting conditions. The results showed a high degree of equivalence between the two scales with regard to growth and product kinetics. This was underlined by the equal maximum specific growth rate and equal specific DNA product yield on biomass obtained at the two scales of operation, demonstrating the feasibility of scaling down to 10 mL on the basis of equivalent specific power input.
本研究的目的是表征一个配备仪器的10 mL微型搅拌罐生物反应器的工程环境,并评估其作为微生物发酵过程的缩小装置的潜力。几个研究小组和公司已经开发出了如本文详细介绍的这种微型生物反应器,旨在解决生物工艺开发筛选阶段当前的瓶颈问题。在很宽的叶轮转速范围内,对微型生物反应器的总体积氧传递系数和混合时间进行了表征。直接测量了输入到微型生物反应器的功率,并据此计算了每个叶轮的功率数,估算了比功率输入,从而能够将微型生物反应器的性能与传统的7 L生物反应器的性能直接进行比较。还研究了微型生物反应器进行微生物发酵的能力。在完全好氧和限氧条件下,以相等的比功率输入对产质粒DNA的大肠杆菌DH5α进行了重复分批发酵。结果表明,在生长和产物动力学方面,两种规模具有高度的等效性。两种操作规模下获得的最大比生长速率相等以及基于生物量的比DNA产物产量相等,突出了这一点,证明了在等效比功率输入的基础上缩小至10 mL的可行性。