Department of Chemical Engineering, The University of Adelaide, Adelaide, Australia.
Biotechnol Bioeng. 1991 Aug 5;38(4):363-70. doi: 10.1002/bit.260380406.
The high-pressure homogenization of Escherichia coli, strain JM101, containing inclusion bodies of recombinant porcine somatotropin was investigated. A novel technique employing an analytical disc centrifuge was used to monitor the disruption. This a direct technique which measures cell disintegration rather than soluble protein release. The technique is particularly suited to measurements where the disruption approaches 100%. The disk centrifuge provides a size distribution of the homogenate, and furnishes evidence for the preferential disruption of larger cells. For E. coli containing inclusion bodies, and increase in the cell feed concentration from 145 g/L (wet weight) to 330 g/L resulted is poorer homogenization. Poorer disruption was also obtained by lowering the feed temperature from 20 degrees C to 5 degrees C. Only slight variations in performance were obtained by increasing the feed pH from 7.5 to 9.0 or by storing the feed at 4 degrees C for 24 h prior to disruption. Comparison with uninduced E. coli strain JM101, showed that the disruption obtained is higher for bacteria containing a recombinant inclusion body.
用高压匀浆法破碎含重组猪生长激素包涵体的大肠杆菌 JM101 细胞。采用分析碟片式离心机的新技术来监测细胞破碎过程。该技术是一种直接的测量方法,可用于测定细胞破碎程度,而非测定可溶性蛋白的释放量。这种技术特别适合于接近 100%破碎的测量。碟片式离心机可提供匀浆的粒度分布,并提供证据证明较大的细胞优先破碎。对于含包涵体的大肠杆菌,将细胞进料浓度从 145g/L(湿重)增加到 330g/L 会导致匀浆效果变差。从 20°C 降低到 5°C 也会导致较差的破碎。将进料 pH 值从 7.5 增加到 9.0 或在破碎前将进料在 4°C 下储存 24 小时,仅会对性能产生轻微影响。与未诱导的大肠杆菌 JM101 相比,含重组包涵体的细菌获得的破碎程度更高。