RelA1 gene control of Escherichia coli lipid structure and cell performance during glucose limited fed-batch conditions

被引:0
作者
Atefeh Shokri
Andres Veide
Gen Larsson
机构
[1] AlbaNova University Center,The Swedish Centre for Bioprocess Technology
来源
Applied Microbiology and Biotechnology | 2006年 / 73卷
关键词
Phosphatidyl Ethanolamine; Stringent Response; Amino Acid Starvation; Glucose Limitation; Cyclic Fatty Acid;
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学科分类号
摘要
At increasing glucose limitation, typical for fed-batch cultivation performance, cultivation of Escherichia coli (relA1) results in development of a lipid structure that radically differs from the wild type and is characterised by accumulation of neutral phospholipids and saturated fatty acids. The mutant can, furthermore, not change the level of cardiolipin, which is generally the hallmark of changes to severe glucose limitation. The result suggests an increased negative control in the mutant with respect to the flux to phosphatidyl glycerol and cardolipin as well as to unsaturated fatty acids. Opposite to the wild type, the cardiolipin-depleted membrane is more fragile with respect to sonication and osmotic chock, at severe limitation, and results in extensive foaming during the process. Protein leakage and cell lysis is, however, lower in the mutant most likely due to the increased amounts of saturated fatty acids, which might be a possible strategy to overcome the reduced amounts of membrane-strengthening cardiolipin. The membrane potential of the outer surface is negative, however less negative for the mutant. This was supported by aqueous two-phase extraction experiments which, furthermore indicated a difference in outer surface hydrofobicity. These findings suggest that the relA1 gene has a defined, but ppGpp-independent, role in cells with a slowly decreasing metabolism of glucose to control the membrane morphology.
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页码:464 / 473
页数:9
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  • [1] Albertsson P-Å(1962)Counter-current distribution of cells Exp Cell Res 28 296-322
  • [2] Baird GD(1976)A rapid and sensitive method for the quantitation of microgram quantities of protein utilising the principle of protein dye binding Anal Biochem 72 248-254
  • [3] Bradford MM(1999)Scale down of recombinant protein production: a comparative study of scaling performance Bioprocess Eng 20 377-389
  • [4] Bylund F(1998)The fats of Mol Microbiol 27 1-8
  • [5] Guillard F(1971) during infancy and old age: regulation by global regulators, alarmones and lipid intermediates J Biol Chem 246 4371-4373
  • [6] Enfors S-O(1998)Synthesis of guanosine 5′-diphosphate, 2′-(or 3′-) diphosphate and related nucleotides in a variety of physiological conditions Bioprocess Eng 18 135-142
  • [7] Trägårdh C(1988)Comparison of the Baker’s yeast process performance in laboratory and production scale Biotechnol Bioeng 32 741-748
  • [8] Larsson G(1996)Release of periplasmic enzymes and other physiological effects of β-lactamase overproduction in Microbiol Res 151 337-342
  • [9] DiRusso CC(1995)Influence of phospholipid composition on excretion of β-lactamase from a stringent/relaxed Appl Microbiol Biotechnol 43 89-92
  • [10] Nyström T(1974) K12 strain pair Acta Chem Scand B 28 873-882