Literature DB >> 19416651

The lipopolysaccharide transport system of Gram-negative bacteria.

Paola Sperandeo1, Gianni Dehò, Alessandra Polissi.   

Abstract

The cell envelope of Gram-negative bacteria consists of two distinct membranes, the inner (IM) and the outer membrane (OM) separated by the periplasm. The OM contains in the outer leaflet the lipopolysaccharide (LPS), a complex lipid with important biological activities. In the host it elicits the innate immune response whereas in the bacterium it is responsible for the peculiar permeability barrier properties exhibited by the OM. The chemical structure of LPS and its biosynthetic pathways have been fully elucidated. By contrast only recently details of the transport and assembly of LPS into the OM have emerged. LPS is synthesized in the cytoplasm and at the inner leaflet of the IM and needs to cross two different compartments, the IM and the periplasm, to reach its final destination at the OM. This review focuses on recent studies that led to our present understanding of the protein machine implicated in LPS transport and in assembly at the cell surface.

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Year:  2009        PMID: 19416651     DOI: 10.1016/j.bbalip.2009.01.011

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


  66 in total

1.  Regulated assembly of the transenvelope protein complex required for lipopolysaccharide export.

Authors:  Elizaveta Freinkman; Suguru Okuda; Natividad Ruiz; Daniel Kahne
Journal:  Biochemistry       Date:  2012-06-08       Impact factor: 3.162

2.  Concentration-dependent oligomerization and oligomeric arrangement of LptA.

Authors:  Jacqueline A Merten; Kathryn M Schultz; Candice S Klug
Journal:  Protein Sci       Date:  2011-12-21       Impact factor: 6.725

3.  Mutational analysis of the Shigella flexneri O-antigen polymerase Wzy: identification of Wzz-dependent Wzy mutants.

Authors:  Pratiti Nath; Elizabeth Ngoc Hoa Tran; Renato Morona
Journal:  J Bacteriol       Date:  2014-10-13       Impact factor: 3.490

4.  Membrane topology and identification of critical amino acid residues in the Wzx O-antigen translocase from Escherichia coli O157:H4.

Authors:  Cristina L Marolda; Bo Li; Michael Lung; Mei Yang; Anna Hanuszkiewicz; Amanda Roa Rosales; Miguel A Valvano
Journal:  J Bacteriol       Date:  2010-09-24       Impact factor: 3.490

5.  Disruption of LptA oligomerization and affinity of the LptA-LptC interaction.

Authors:  Kathryn M Schultz; Jimmy B Feix; Candice S Klug
Journal:  Protein Sci       Date:  2013-11       Impact factor: 6.725

6.  Structure-guided investigation of lipopolysaccharide O-antigen chain length regulators reveals regions critical for modal length control.

Authors:  Sergei Kalynych; Xiang Ruan; Miguel A Valvano; Miroslaw Cygler
Journal:  J Bacteriol       Date:  2011-06-03       Impact factor: 3.490

7.  Overexpression of LolCDE allows deletion of the Escherichia coli gene encoding apolipoprotein N-acyltransferase.

Authors:  Shin-ichiro Narita; Hajime Tokuda
Journal:  J Bacteriol       Date:  2011-07-08       Impact factor: 3.490

8.  Roles of predicted glycosyltransferases in the biosynthesis of the Rhizobium etli CE3 O antigen.

Authors:  Kristylea J Ojeda; Laurie Simonds; K Dale Noel
Journal:  J Bacteriol       Date:  2013-02-22       Impact factor: 3.490

9.  Regulation of cell size in response to nutrient availability by fatty acid biosynthesis in Escherichia coli.

Authors:  Zhizhong Yao; Rebecca M Davis; Roy Kishony; Daniel Kahne; Natividad Ruiz
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-20       Impact factor: 11.205

10.  Helicobacter pylori lipopolysaccharide modification, Lewis antigen expression, and gastric colonization are cholesterol-dependent.

Authors:  Ellen Hildebrandt; David J McGee
Journal:  BMC Microbiol       Date:  2009-12-14       Impact factor: 3.605

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