Chemistry:N-Acetylglucosamine

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Short description: Biological molecule


N-Acetylglucosamine
N-Acetylglucosamine.svg
Haworth projection of N-Acetylglucosamine.svg
Names
IUPAC name
β-D-(Acetylamino)-2-deoxy-glucopyranose
Other names
N-Acetyl-D-glucosamine
GlcNAc
NAG
Identifiers
3D model (JSmol)
1247660
ChEBI
ChEMBL
ChemSpider
EC Number
  • 231-368-2
721281
KEGG
UNII
Properties
C8H15NO6
Molar mass 221.21
Melting point 211
Related compounds
Related Monosaccharides
N-Acetylgalactosamine
Related compounds
Glucosamine
Glucose
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N-Acetylglucosamine molecule

N-Acetylglucosamine (GlcNAc) is an amide derivative of the monosaccharide glucose. It is a secondary amide between glucosamine and acetic acid. It is significant in several biological systems.

It is part of a biopolymer in the bacterial cell wall, which is built from alternating units of GlcNAc and N-acetylmuramic acid (MurNAc), cross-linked with oligopeptides at the lactic acid residue of MurNAc. This layered structure is called peptidoglycan (formerly called murein).

GlcNAc is the monomeric unit of the polymer chitin, which forms the exoskeletons of arthropods like insects and crustaceans. It is the main component of the radulas of mollusks, the beaks of cephalopods, and a major component of the cell walls of most fungi.

Polymerized with glucuronic acid, it forms hyaluronan.

GlcNAc has been reported to be an inhibitor of elastase release from human polymorphonuclear leukocytes (range 8–17% inhibition), however this is much weaker than the inhibition seen with N-acetylgalactosamine (range 92–100%).[1]

Medical uses

It has been proposed as a treatment for autoimmune diseases and recent tests have claimed some success.[2][3]

O-GlcNAcylation

Main page: Biology:O-GlcNAc

O-GlcNAcylation is the process of adding a single N-acetylglucosamine sugar to the serine or threonine of a protein.[4] Comparable to phosphorylation, addition or removal of N-acetylglucosamine is a means of activating or deactivating enzymes or transcription factors.[4] In fact, O-GlcNAcylation and phosphorylation often compete for the same serine/threonine sites.[4] O-GlcNAcylation most often occurs on chromatin proteins, and is often seen as a response to stress.[4]

Hyperglycemia increases O-GlcNAcylation, leading to insulin resistance.[5] Increased O-GlcNAcylation due to hyperglycemia is evidently a dysfunctional form of O-GlcNAcylation. O-GlcNAcylation decline in the brain with age is associated with cognitive decline. When O-GlcNAcylation was increased in the hippocampus of aged mice, spatial learning and memory improved.[6]

See also

References

  1. "Inhibition of elastase enzyme release from human polymorphonuclear leukocytes by N-acetyl-galactosamine and N-acetyl-glucosamine". Clinical and Experimental Rheumatology 9 (1): 17–21. 1991. PMID 2054963. 
  2. "N-acetylglucosamine inhibits T-helper 1 (Th1)/T-helper 17 (Th17) cell responses and treats experimental autoimmune encephalomyelitis". The Journal of Biological Chemistry 286 (46): 40133–40141. November 2011. doi:10.1074/jbc.M111.277814. PMID 21965673. 
  3. "N-acetylglucosamine inhibits inflammation and neurodegeneration markers in multiple sclerosis: a mechanistic trial". Journal of Neuroinflammation 20 (1): 209. September 2023. doi:10.1186/s12974-023-02893-9. PMID 37705084. 
  4. 4.0 4.1 4.2 4.3 "Cross talk between O-GlcNAcylation and phosphorylation: roles in signaling, transcription, and chronic disease". Annual Review of Biochemistry 80: 825–858. 2011. doi:10.1146/annurev-biochem-060608-102511. PMID 21391816. 
  5. "Protein O-GlcNAcylation in diabetes and diabetic complications". Expert Review of Proteomics 10 (4): 365–380. August 2013. doi:10.1586/14789450.2013.820536. PMID 23992419. 
  6. "Neuronal O-GlcNAcylation Improves Cognitive Function in the Aged Mouse Brain". Current Biology 29 (20): 3359–3369.e4. October 2019. doi:10.1016/j.cub.2019.08.003. PMID 31588002. 

External links