Literature DB >> 6330111

Regulation of the synthesis of membrane-derived oligosaccharides in Escherichia coli. Assay of phosphoglycerol transferase I in vivo.

J P Bohin, E P Kennedy.   

Abstract

Membrane-derived oligosaccharides are periplasmic constituents of Escherchia coli and other Gram-negative bacteria. Oligosaccharides in this family may be variously substituted with O-succinyl ester residues, and with sn-1-phosphoglycerol and phosphoethanolamine residues derived from membrane phospholipids. Membrane-derived oligosaccharides appear to be important in osmoregulation, because their synthesis is under strict control (Kennedy, E.P. (1982) Proc. Natl. Acad. Sci. U.S.A. 79, 1092-1095). Maximum rate of synthesis is at very low osmolarity of the medium. Phosphoglycerol residues are transferred from phosphatidylglycerol to membrane-derived oligosaccharides, or to certain beta-glucoside acceptors, in a reaction catalyzed by phosphoglycerol transferase I, an enzyme of the inner membrane (Jackson, B. J., and Kennedy, E.P. (1983) J. Biol. Chem. 258, 2394-2398). We now report that this enzyme catalyzes the transfer of phosphoglycerol residues to arbutin (p-hydroxyphenyl-beta-D-glucoside) added to the medium with Km similar to that observed with the cell-free enzyme. The active site of the enzyme must therefore be on the periplasmic face of the inner membrane. We assayed phosphoglycerol transferase I in vivo and found that it is present and completely active even in cells growing in medium of very high osmolarity, in which the synthesis of membrane-derived oligosaccharides is severely reduced. We conclude that osmotic regulation must occur at the stage of the synthesis of oligosaccharide chains. A study of the kinetics of transfer of phosphoglycerol residues to membrane-derived oligosaccharides in vivo revealed that synthesis of the polyglucose chains must stop abruptly upon transfer of cells from medium of low to high osmolarity, inconsistent with a model postulating simple dilution of some rate-limiting enzyme during growth at the higher osmolarity.

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Year:  1984        PMID: 6330111

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  11 in total

1.  Isolation and characterization of Escherichia coli mutants blocked in production of membrane-derived oligosaccharides.

Authors:  A C Weissborn; M K Rumley; E P Kennedy
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

2.  The Brucella abortus cyclic beta-1,2-glucan virulence factor is substituted with O-ester-linked succinyl residues.

Authors:  Mara S Roset; Andrés E Ciocchini; Rodolfo A Ugalde; Nora Iñón de Iannino
Journal:  J Bacteriol       Date:  2006-07       Impact factor: 3.490

3.  Biochemical characterization of avirulent Agrobacterium tumefaciens chvA mutants: synthesis and excretion of beta-(1-2)glucan.

Authors:  N I de Iannino; R A Ugalde
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

4.  An atypical lipoteichoic acid from Clostridium perfringens elicits a broadly cross-reactive and protective immune response.

Authors:  Cory Q Wenzel; Dominic C Mills; Justyna M Dobruchowska; Jiri Vlach; Harald Nothaft; Patrick Nation; Parastoo Azadi; Stephen B Melville; Russell W Carlson; Mario F Feldman; Christine M Szymanski
Journal:  J Biol Chem       Date:  2020-05-18       Impact factor: 5.157

5.  Physical map location of the Escherichia coli gene encoding phosphoglycerol transferase I.

Authors:  E Lanfroy; J P Bohin
Journal:  J Bacteriol       Date:  1993-09       Impact factor: 3.490

6.  UDP-glucose is a potential intracellular signal molecule in the control of expression of sigma S and sigma S-dependent genes in Escherichia coli.

Authors:  J Böhringer; D Fischer; G Mosler; R Hengge-Aronis
Journal:  J Bacteriol       Date:  1995-01       Impact factor: 3.490

7.  The mdoC gene of Escherichia coli encodes a membrane protein that is required for succinylation of osmoregulated periplasmic glucans.

Authors:  J M Lacroix; E Lanfroy; V Cogez; Y Lequette; A Bohin; J P Bohin
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

8.  A novel cyclic beta-1,2-glucan mutant of Rhizobium meliloti.

Authors:  M W Breedveld; J A Hadley; K J Miller
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

9.  Transfer of phosphoethanolamine residues from phosphatidylethanolamine to the membrane-derived oligosaccharides of Escherichia coli.

Authors:  K J Miller; E P Kennedy
Journal:  J Bacteriol       Date:  1987-02       Impact factor: 3.490

10.  Biosynthesis of membrane-derived oligosaccharides: characterization of mdoB mutants defective in phosphoglycerol transferase I activity.

Authors:  B J Jackson; J P Bohin; E P Kennedy
Journal:  J Bacteriol       Date:  1984-12       Impact factor: 3.490

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