A disposable picolitre bioreactor for cultivation and investigation of industrially relevant bacteria on the single cell level.

TitleA disposable picolitre bioreactor for cultivation and investigation of industrially relevant bacteria on the single cell level.
Publication TypeJournal Article
Year of Publication2012
AuthorsGrünberger, A, Paczia, N, Probst, C, Schendzielorz, G, Eggeling, L, Noack, S, Wiechert, W, Kohlheyer, D
JournalLab Chip
Volume12
Issue11
Pagination2060-8
Date Published2012 May 8
ISSN1473-0189
KeywordsBioreactors, Corynebacterium glutamicum, Dimethylpolysiloxanes, Escherichia coli, Lysine, Microfluidic Analytical Techniques, Microscopy
Abstract

In the continuously growing field of industrial biotechnology the scale-up from lab to industrial scale is still a major hurdle to develop competitive bioprocesses. During scale-up the productivity of single cells might be affected by bioreactor inhomogeneity and population heterogeneity. Currently, these complex interactions are difficult to investigate. In this report, design, fabrication and operation of a disposable picolitre cultivation system is described, in which environmental conditions can be well controlled on a short time scale and bacterial microcolony growth experiments can be observed by time-lapse microscopy. Three exemplary investigations will be discussed emphasizing the applicability and versatility of the device. Growth and analysis of industrially relevant bacteria with single cell resolution (in particular Escherichia coli and Corynebacterium glutamicum) starting from one single mother cell to densely packed cultures is demonstrated. Applying the picolitre bioreactor, 1.5-fold increased growth rates of C. glutamicum wild type cells were observed compared to typical 1 litre lab-scale batch cultivation. Moreover, the device was used to analyse and quantify the morphological changes of an industrially relevant l-lysine producer C. glutamicum after artificially inducing starvation conditions. Instead of a one week lab-scale experiment, only 1 h was sufficient to reveal the same information. Furthermore, time lapse microscopy during 24 h picolitre cultivation of an arginine producing strain containing a genetically encoded fluorescence sensor disclosed time dependent single cell productivity and growth, which was not possible with conventional methods.

DOI10.1039/c2lc40156h
Alternate JournalLab Chip