Recombinant Peptide Production Softens Escherichia coli Cells and Increases Their Size during C-Limited Fed-Batch Cultivation

被引:3
|
作者
Weber, Andreas [1 ,2 ]
Gibisch, Martin [1 ]
Tyrakowski, Daniel [2 ]
Cserjan-Puschmann, Monika [1 ]
Toca-Herrera, Jose L. [2 ]
Striedner, Gerald [1 ]
机构
[1] Univ Nat Resources & Life Sci, Inst Bioproc Sci & Engn, Dept Biotechnol, Christian Doppler Lab Prod Next Level Biopharmaceu, Muthgasse 18, A-1190 Vienna, Austria
[2] Univ Nat Resources & Life Sci, Inst Biophys, Dept Bionanosci, Muthgasse 11, A-1190 Vienna, Austria
基金
奥地利科学基金会;
关键词
bacteria; peptide expression; membrane properties; periplasmic space; viscoelasticity; atomic force microscopy; TURGOR PRESSURE; GROWTH-RATE; SURFACE; MODELS; SHAPE; WALL;
D O I
10.3390/ijms24032641
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stress-associated changes in the mechanical properties at the single-cell level of Escherichia coli (E. coli) cultures in bioreactors are still poorly investigated. In our study, we compared peptide-producing and non-producing BL21(DE3) cells in a fed-batch cultivation with tightly controlled process parameters. The cell growth, peptide content, and cell lysis were analysed, and changes in the mechanical properties were investigated using atomic force microscopy. Recombinant-tagged somatostatin-28 was expressed as soluble up to 197 +/- 11 mg g(-1). The length of both cultivated strains increased throughout the cultivation by up to 17.6%, with nearly constant diameters. The peptide-producing cells were significantly softer than the non-producers throughout the cultivation, and respective Young's moduli decreased by up to 57% over time. A minimum Young's modulus of 1.6 MPa was observed after 23 h of the fed-batch. Furthermore, an analysis of the viscoelastic properties revealed that peptide-producing BL21(DE3) appeared more fluid-like and softer than the non-producing reference. For the first time, we provide evidence that the physical properties (i.e., the mechanical properties) on the single-cell level are significantly influenced by the metabolic burden imposed by the recombinant peptide expression and C-limitation in bioreactors.
引用
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页数:15
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