High throughput automated microbial bioreactor system used for clone selection and rapid scale-down process optimization

被引:37
作者
Velez-Suberbie, M. Lourdes [1 ]
Betts, John P. J. [2 ]
Walker, Kelly L. [3 ]
Robinson, Colin [3 ]
Zoro, Barney [2 ]
Keshavarz-Moore, Eli [1 ]
机构
[1] UCL, Dept Biochem Engn, Adv Ctr Biochem Engn, Gower St,Bernard Katz Bldg, London WC1E 6BT, England
[2] Sartorius Stedim Biotech, York Way, Royston SG8 5WY, Herts, England
[3] Univ Kent, Sch Biosci, Ctr Mol Proc, Canterbury CT2 7NJ, Kent, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
E; coli; single use microbioreactor; high throughput; scale-down; ambr; 15; fermentation; CULTURE PROCESS-DEVELOPMENT; ESCHERICHIA-COLI; CELL-CULTURE; MINIATURE BIOREACTOR; E; COLI; ANTIBODY FRAGMENTS; PROTEIN-PRODUCTION; PATHWAY; IMPACT; GROWTH;
D O I
10.1002/btpr.2534
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
High throughput automated fermentation systems have become a useful tool in early bioprocess development. In this study, we investigated a 24 x 15 mL single use microbioreactor system, ambr 15f, designed for microbial culture. We compared the fed-batch growth and production capabilities of this system for two Escherichia coli strains, BL21 (DE3) and MC4100, and two industrially relevant molecules, hGH and scFv. In addition, different carbon sources were tested using bolus, linear or exponential feeding strategies, showing the capacity of the ambr 15f system to handle automated feeding. We used power per unit volume (P/V) as a scale criterion to compare the ambr 15f with 1 L stirred bioreactors which were previously scaled-up to 20 L with a different biological system, thus showing a potential 1,300 fold scale comparability in terms of both growth and product yield. By exposing the cells grown in the ambr 15f system to a level of shear expected in an industrial centrifuge, we determined that the cells are as robust as those from a bench scale bioreactor. These results provide evidence that the ambr 15f system is an efficient high throughput microbial system that can be used for strain and molecule selection as well as rapid scale-up. (c) 2017 The Authors Biotechnology Progress published by Wiley Periodicals, Inc. on behalf of American Institute of Chemical Engineers Biotechnol. Prog., 34:58-68, 2018
引用
收藏
页码:58 / 68
页数:11
相关论文
共 42 条
[21]   Application of High-Throughput Mini-Bioreactor System for Systematic Scale-Down Modeling, Process Characterization, and Control Strategy Development [J].
Janakiraman, Vijay ;
Kwiatkowski, Chris ;
Kshirsagar, Rashmi ;
Ryll, Thomas ;
Huang, Yao-Ming .
BIOTECHNOLOGY PROGRESS, 2015, 31 (06) :1623-1632
[22]   Validation of a high-throughput fermentation system based on online monitoring of biomass and fluorescence in continuously shaken microtiter plates [J].
Kensy, Frank ;
Zang, Emerson ;
Faulhammer, Christian ;
Tan, Rung-Kai ;
Buechs, Jochen .
MICROBIAL CELL FACTORIES, 2009, 8
[23]   Robotic Platform for Parallelized Cultivation and Monitoring of Microbial Growth Parameters in Microwell Plates [J].
Knepper, Andreas ;
Heiser, Michael ;
Glauche, Florian ;
Neubauer, Peter .
JALA, 2014, 19 (06) :593-601
[24]   Design of a prototype miniature bioreactor for high throughput automated bioprocessing [J].
Lamping, SR ;
Zhang, H ;
Allen, B ;
Shamlou, PA .
CHEMICAL ENGINEERING SCIENCE, 2003, 58 (3-6) :747-758
[25]   High cell-density culture of Escherichia coli [J].
Lee, SY .
TRENDS IN BIOTECHNOLOGY, 1996, 14 (03) :98-105
[26]   HIGH CELL-DENSITY CULTIVATION OF ESCHERICHIA-COLI-W USING SUCROSE AS A CARBON SOURCE [J].
LEE, SY ;
CHANG, HN .
BIOTECHNOLOGY LETTERS, 1993, 15 (09) :971-974
[27]   High-yield export of a native heterologous protein to the periplasm by the tat translocation pathway in Escherichia coli [J].
Matos, Cristina F. R. O. ;
Branston, Steven D. ;
Albiniak, Anna ;
Dhanoya, Arjun ;
Freedman, Robert B. ;
Keshavarz-Moore, Eli ;
Robinson, Colin .
BIOTECHNOLOGY AND BIOENGINEERING, 2012, 109 (10) :2533-2542
[28]  
Moses S., 2012, Adv. Biosci. ., V2012, P918, DOI DOI 10.4236/ABB.2012.37113
[29]   Consistent development of bioprocesses from microliter cultures to the industrial scale [J].
Neubauer, Peter ;
Cruz, Nicolas ;
Glauche, Florian ;
Junne, Stefan ;
Knepper, Andreas ;
Raven, Michael .
ENGINEERING IN LIFE SCIENCES, 2013, 13 (03) :224-238
[30]   The physical characterisation of a microscale parallel bioreactor platform with an industrial CHO cell line expressing an IgG4 [J].
Nienow, Alvin W. ;
Rielly, Christopher D. ;
Brosnan, Kathryn ;
Bargh, Neil ;
Lee, Kenneth ;
Coopman, Karen ;
Hewitt, Christopher J. .
BIOCHEMICAL ENGINEERING JOURNAL, 2013, 76 :25-36