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E. coli filament formation induced by heterologous S-layer expression.
- Source :
-
Bioengineered bugs [Bioeng Bugs] 2011 May-Jun; Vol. 2 (3), pp. 178-81. Date of Electronic Publication: 2011 May 01. - Publication Year :
- 2011
-
Abstract
- Escherichia coli is a rod-shaped intestinal bacterium which has a size of 1.1-1.5 µm x 2.0-6.0 µm. The fast cell division process and the uncomplicated living conditions have turned E. coli into a widely used host in genetic engineering and into one of the best studied microorganisms of all. We used E. coli BL21(DE3) as host for heterologous expression of S-layer proteins of Lysinibacillus sphaericus JG-A12 in order to enable a fast and high efficient protein production. The S-layer expression induced in E. coli an unusual elongation of the cells, thus producing filaments of > 100 µm in length. In the stationary growth phase, E. coli filaments develop tube-like structures that contain E. coli single cells. Fluorescence microscopic analyses of S-layer expressing E. coli cells that were stained with membrane stain FM (®) 5-95 verify the membrane origin of the tubes. Analyses of DAPI stained GFP-S-layer expressing E. coli support the assumption of a disordered cell division that is induced by the huge amount of recombinant S-layer proteins. However, the underlying mechanism is still not characterized in detail. These results describe the occurrence of a novel stable cell form of E. coli as a result of a disordered cell division process.
- Subjects :
- Bacillaceae genetics
Bacterial Proteins metabolism
Escherichia coli metabolism
Fimbriae, Bacterial genetics
Membrane Glycoproteins metabolism
Bacterial Proteins genetics
Escherichia coli genetics
Escherichia coli growth & development
Fimbriae, Bacterial metabolism
Gene Expression
Membrane Glycoproteins genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1949-1026
- Volume :
- 2
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Bioengineered bugs
- Publication Type :
- Academic Journal
- Accession number :
- 21637007
- Full Text :
- https://doi.org/10.4161/bbug.2.3.15418