Lactose autoinduction with enzymatic glucose release: Characterization of the cultivation system in bioreactor

被引:17
作者
Mayer, Sonja [1 ]
Junne, Stefan [2 ]
Ukkonen, Kaisa [1 ,3 ]
Glazyrina, Julia [2 ]
Glauche, Florian [2 ]
Neubauer, Peter [2 ]
Vasala, Antti [1 ]
机构
[1] BioSilta Oy, FI-90014 Oulu, Finland
[2] Tech Univ Berlin, Dept Biotechnol, Chair Bioproc Engn, D-13355 Berlin, Germany
[3] Univ Oulu, Dept Proc & Environm Engn, Bioproc Engn Lab, FI-90014 Oulu, Finland
关键词
Lactose autoinduction; Enzymatic glucose delivery; Fed-batch; Bioreactor; HIGH-CELL-DENSITY; ESCHERICHIA-COLI; LAC REPRESSOR; RECOMBINANT PROTEINS; BETA-GALACTOSIDASE; RNA-POLYMERASE; EXPRESSION; CULTURES; IMPROVES; INDUCER;
D O I
10.1016/j.pep.2013.10.024
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The lactose autoinduction system for recombinant protein production was combined with enzymatic glucose release as a method to provide a constant feed of glucose instead of using glycerol as a carbon substrate. Bioreactor cultivation confirmed that the slow glucose feed does not prevent the induction by lactose. HPLC studies showed that with successful recombinant protein production only a very low amount of lactose was metabolized during glucose-limited fed-batch conditions by the Escherichia coli strain BL21(DE3)pLysS in well-aerated conditions, which are problematic for glycerol-based autoinduction systems. We propose that slow enzymatic glucose feed does not cause a full activation of the lactose operon. However recombinant PDI-A protein (A-domain of human disulfide isomerase) was steadily produced until the end of the cultivation. The results of the cultivations confirmed our earlier observations with shaken cultures showing that lactose autoinduction cultures based on enzymatic glucose feed have good scalability, and that this system can be applied also to bioreactor cultivations. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:67 / 72
页数:6
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