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PMID: 7041113 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Osmotic regulation and the biosynthesis of membrane-derived oligosaccharides in Escherichia coli.

Kennedy EP

Abstract

The membrane-derived oligosaccharides (MDO) of Escherichia coli are periplasmic constituents containing 8-10 glucose units in a highly branched structure, linked by beta 1-2 and beta 1-6 bonds [Schneider, J. E. Reinhold, V., Rumley, M. K. & Kennedy, E. P. (1979) J. Biol. Chem. 254, 10135-10138]. The MDO are multiply substituted with sn-1-phosphoglycerol residues (derived from membrane phosphatidylglycerol) and with O-succinyl ester residues and, thus, are high anionic. Experiments in this paper offer evidence that the biosynthesis of MDO is an important aspects of osmoregulation in E. coli. Cells grown in medium of low osmolarity (ca. 50 mosM) synthesize 16 times more MDO than those grown in the same medium with 0.4 M NaCl. In cells grown in medium of low osmolarity, it appears that MDO is the principal source of fixed anion in the periplasmic space and, thus, acts to maintain the high osmotic pressure and Donnan membrane potential of the periplasmic compartment Regulation of MDO synthesis in response to changes in osmolarity of the medium appears to occur at the genetic level because the synthesis of new protein is needed to permit the production of MDO at high rates after shift of cells to medium of low osmolarity.

MeSH Terms
Bacterial Proteins/biosynthesis Cell Membrane/metabolism Culture Media Escherichia coli/metabolism Oligosaccharides/biosynthesis Osmolar Concentration
Chemicals
Bacterial Proteins Culture Media Oligosaccharides
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Kennedy E P
References (13)
13 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1982-02-00
Pages
1092-5
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC345906
Subset
IM
Grants
NIGMS NIH HHS · GM 22057 · United States
NIGMS NIH HHS · GM19822 · United States
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