Literature DB >> 6776984

Influence of lipids with branched-chain fatty acids on the physical, morphological and functional properties of Escherichia coli cytoplasmic membrane.

S Legendre, L Letellier, E Shechter.   

Abstract

Escherichia coli cells (unsaturated fatty acid auxotroph) have been adapted to grow on branched-chain fatty acids. Membrane vesicles were isolated from cells grown on a mixture of branched-chain fatty acids isolated from the lipids of Bacillus subtilis (E. coli (B. subtilis) membranes) and on a pure synthetic anti-isononadecanoic acid (E. coli (aC19) membranes). We have shown, using wide-angle X-ray diffraction and differential scanning calorimetry, that the ordered state of the lipids is perturbed in the case of E. coli (B. subtilis) membranes but is unperturbed in the case of E. coli (aC19) membranes. The perturbation leads to the presence of a large wide-angle X-ray diffraction at 4.25--4.3 A, as opposed to the presence of a sharp 4.2 A reflection in unperturbed systems. We have shown, using freeze-fracture electron microscopy, that a protein segregation exists in the case of E. coli (aC19) membranes (at low temperature the integral membrane proteins aggregate in the membrane domains containing the disordered lipids); we do not observe such segregation in the case of E. coli (B. subtilis) membranes. We conclude that in cases where the branching of the fatty acids introduces a perturbation of the lipid order, the integral membrane proteins can still be accommodated in membrane domains containing the 'perturbed' ordered lipids. Finally, we have determined the rate of beta-galactoside transport in E. coli (aC19) and E. coli (B. subtilis) membranes as a function of temperature. We have shown that, in both cases, the Arrhenius representations display an increased slope in the region of the disorder-to-order transition. We conclude that such an increased slope may have different origins. In the case of E. coli (aC19) membranes, it is the result of the aggregation of the beta-galactoside carriers together with other integral membrane proteins which may lead to the inactivation of the carriers; in the case of E. coli (B. subtilis) membranes, it is the result of the partial immobilisation of the carriers embedded in a lipid environment, of which the fluidity, despite the perturbation of its lipid order, is still much less than that associated with lipids in a totally disordered state.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 6776984     DOI: 10.1016/0005-2736(80)90328-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  10 in total

1.  Critical role of anteiso-C15:0 fatty acid in the growth of Listeria monocytogenes at low temperatures.

Authors:  B A Annous; L A Becker; D O Bayles; D P Labeda; B J Wilkinson
Journal:  Appl Environ Microbiol       Date:  1997-10       Impact factor: 4.792

Review 2.  Uncoupler-resistant mutants of bacteria.

Authors:  T A Krulwich; P G Quirk; A A Guffanti
Journal:  Microbiol Rev       Date:  1990-03

3.  Identification of a developmental chemoattractant in Myxococcus xanthus through metabolic engineering.

Authors:  D B Kearns; A Venot; P J Bonner; B Stevens; G J Boons; L J Shimkets
Journal:  Proc Natl Acad Sci U S A       Date:  2001-11-20       Impact factor: 11.205

4.  Global and Targeted Lipid Analysis of Gemmata obscuriglobus Reveals the Presence of Lipopolysaccharide, a Signature of the Classical Gram-Negative Outer Membrane.

Authors:  Rajendra Mahat; Corrine Seebart; Franco Basile; Naomi L Ward
Journal:  J Bacteriol       Date:  2015-10-19       Impact factor: 3.490

5.  Propionyl coenzyme A carboxylase is required for development of Myxococcus xanthus.

Authors:  Y Kimura; R Sato; K Mimura; M Sato
Journal:  J Bacteriol       Date:  1997-11       Impact factor: 3.490

Review 6.  Iso- and anteiso-fatty acids in bacteria: biosynthesis, function, and taxonomic significance.

Authors:  T Kaneda
Journal:  Microbiol Rev       Date:  1991-06

7.  Influence of fatty acid precursors, including food preservatives, on the growth and fatty acid composition of Listeria monocytogenes at 37 and 10degreesC.

Authors:  Mudcharee Julotok; Atul K Singh; Craig Gatto; Brian J Wilkinson
Journal:  Appl Environ Microbiol       Date:  2010-01-04       Impact factor: 4.792

8.  Staphylococcus aureus FabI: inhibition, substrate recognition, and potential implications for in vivo essentiality.

Authors:  Johannes Schiebel; Andrew Chang; Hao Lu; Michael V Baxter; Peter J Tonge; Caroline Kisker
Journal:  Structure       Date:  2012-05-09       Impact factor: 5.006

9.  Growth-Environment Dependent Modulation of Staphylococcus aureus Branched-Chain to Straight-Chain Fatty Acid Ratio and Incorporation of Unsaturated Fatty Acids.

Authors:  Suranjana Sen; Sirisha Sirobhushanam; Seth R Johnson; Yang Song; Ryan Tefft; Craig Gatto; Brian J Wilkinson
Journal:  PLoS One       Date:  2016-10-27       Impact factor: 3.240

10.  Interrelationships between Fatty Acid Composition, Staphyloxanthin Content, Fluidity, and Carbon Flow in the Staphylococcus aureus Membrane.

Authors:  Kiran B Tiwari; Craig Gatto; Brian J Wilkinson
Journal:  Molecules       Date:  2018-05-17       Impact factor: 4.411

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.