Core oligosaccharide
Core oligosaccharide (or Core-OS) is a short chain of sugar residues within Gram-negative lipopolysaccharide (LPS). Core-OS are highly diverse among bacterial species and even within strains of species [1]
Structure
[edit]
The core domain always contains an oligosaccharide component which attaches directly to lipid A and commonly contains sugars such as heptose and 3-deoxy-D-mannooctulosonic acid (also known as KDO or keto-deoxyoctulosonate).[2] The LPS Cores of many bacteria also contain non-carbohydrate components, such as phosphate, amino acids, and ethanolamine substituents.
Many core structures have been described in the literature, this description is based on the traditional general structure (as found in enteric bacteria and Pseudomonas). See the figure above for an overview of the structure found in E. coli R1.
Inner core
[edit]The "base" of the inner core is 1–3 KDO residues. The last KDO is often modified with a phosphate or ethanolamine group. From the KDOs, there are attached 2–3 heptoses (i.e. L-glycero-D-mannoheptulose) that are usually phosphorylated. These KDO and heptoses comprise the "inner core". The ketosidic bond between KDO and lipid A (α2→6) is especially susceptible to acid cleavage. LPS researchers use a weak acid treatment to separate the lipid and polysaccharide portions of LPS.
An LPS molecule that includes only a lipid A and an inner core (or less. See example) is referred to as "deep-rough LPS".
Outer core
[edit]The outer core is made of hexose residues that are attached to the last heptose residue in the inner core. Hexoses often found in the outer core include: D-glucose, D-mannose, D-galactose, etc.. There are usually at least three hexoses bound β1→3, with the O antigen being ligated to the third hexose. Other hexose are often found attached to the outer core, branching from the main oligomer.
LPS that include lipid A and a complete core oligosaccharide (inner and outer) is referred to as "rough LPS."
Biosynthesis
[edit]The enzymes involved in core oligosaccharide synthesis are conserved among Escherichia coli and Salmonella. Pseudomonas aeruginosa has some unique enzymes.[3]: 273
Function
[edit]The mechanism whereby the core oligosaccharide of lipopolysaccharide affect the membrane behavior is not well understood.
See also
[edit]References
[edit]- ^ a b Heinrichs DE, Yethon JA, Whitfield C (October 1998). "Molecular basis for structural diversity in the core regions of the lipopolysaccharides of Escherichia coli and Salmonella enterica". Molecular Microbiology. 30 (2): 221–32. doi:10.1046/j.1365-2958.1998.01063.x. PMID 9791168.
- ^ Hershberger C, Binkley SB (April 1968). "Chemistry and metabolism of 3-deoxy-D-mannooctulosonic acid. I. Stereochemical determination". The Journal of Biological Chemistry. 243 (7): 1578–84. PMID 4296687.[permanent dead link]
- ^ King JD, Kocíncová D, Westman EL, Lam JS (October 2009). "Review: Lipopolysaccharide biosynthesis in Pseudomonas aeruginosa". Innate Immunity. 15 (5): 261–312. doi:10.1177/1753425909106436. PMID 19710102.