Cited by 78Bacterial Genetics and BiotechnologyLipid Membrane Structure and BehaviorMicrobial Metabolic Engineering and Bioproduction

Growth rate-dependent changes in Escherichia coli membrane structure and protein leakage

Shokri, A. Sandén, G. Larss, A.·2002·Applied Microbiology and Biotechnology

Abstract

The phospholipid and fatty acid content of the Escherichia coli membrane were investigated during continuous cultivation. At low growth rates, there was an increase in cardiolipin produced at the expense of phosphatidylethanolamine. Phosphatidylglycerol had a maximum at a growth rate of 0.3 h(-1). The amount of cyclic fatty acids was markedly increased at lower growth rates, while there was an evident minimum at 0.3 h(-1). This was also the case for saturated fatty acids. At this point, the unsaturated fatty acids had a maximum depending mainly on changes in cis-vaccenic acid. The mechanical strength towards sonication and osmotic shock/enzymatic treatment showed that the cells were more rigid at low dilution rates. However, this was accompanied by a higher cell lysis, a reduced capacity for total and specific protein production and a lower yield of cells. The amount of lipid A in the medium (endotoxin) was constant and negligible at all growth rates. The leakage of periplasmic protein to the medium had an optimum at 0.3 h(-1), resulting in a transport of 20% of the total recombinant product. It is argued that this constitutes the point of highest membrane fluidity and thus an increase possibility for protein transport.

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Crossref · 10.1007/s00253-001-0889-0

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  • Metabolic stress leads to high accumulation of antibody fragments in the periplasm, saturating the secretory machinery and generating a more permeable membrane structure that allows higher diffusive leakage of periplasm proteins outside the cells.

    “The metabolic stress leads to a high accumulation of antibody fragments in the periplasm saturating the secretory machinery. This event generates a more permeable membrane structure that, after sufficient product accumulation in the periplasm, allows a higher diffusive leakage of the periplasm proteins outside the cells [86,144].”

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Authors
Shokri, A. S.
Corresponding author
Shokri, A. Sandén, G. Larss, A.
Venue
Applied Microbiology and Biotechnology
Published
2002-03-01
Volume
58
Issue
3
Pages
386-392
ISSN
  • 0175-7598 (ISSN-L)
  • 1432-0614
OpenAlex
W2017366960
Cited by
78
References
0
Citations by year
2026: 4 · 2025: 1 · 2024: 2 · 2023: 3 · 2021: 3 · 2020: 5 · 2018: 6 · 2017: 3 · 2016: 4 · 2015: 3 · 2014: 2 · 2013: 7 · 2012: 4
FWCI
1.77
Type
journal article
Language
en
Open access
closed
Locations
  • Applied Microbiology and Biotechnology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Bacterial Genetics and Biotechnology
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
Keywords
Escherichia coli, membrane structure, growth rate, cardiolipin, phosphatidylethanolamine, phosphatidylglycerol, cyclic fatty acids, cis-vaccenic acid, membrane fluidity, cell lysis, protein leakage, lipid A, continuous cropping, dilution rate, recombinant protein expression
MeSH terms
beta-Lactamases, Cell Membrane, Cells, Cultured, Culture Media, Escherichia coli, Fatty Acids, Kinetics, Membrane Potentials, Phospholipids, Sonication, Protein Transport, Escherichia coli Proteins

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