KDN (deaminated neuraminic acid): dreamful past and exciting future of the newest member of the sialic acid family
- PMID: 16897172
- DOI: 10.1007/s10719-006-6484-y
KDN (deaminated neuraminic acid): dreamful past and exciting future of the newest member of the sialic acid family
Abstract
KDN is an abbreviation for 2-keto-3-deoxy-D-glycero-D-galacto-nononic acid, and its natural occurrence was revealed in 1986 by a research group including the present authors. Since sialic acid was used as a synonym for N-acylneuraminic acid at that time, there was an argument if this deaminated neuraminic acid belongs to the family of sialic acids. In this review, we describe the 20 years history of studies on KDN (KDNology), through which KDN has established its position as a distinct member of the sialic acid family. These studies have clarified that: (1) KDN occurs widely among vertebrates and bacteria similar to the occurrence of the more common sialic acid, N-acetylneuraminic acid (Neu5Ac), but its abundant occurrence in animals is limited to lower vertebrates. (2) KDN is found in almost all types of glycoconjugates, including glycolipids, glycoproteins and capsular polysaccharides. (3) KDN residues are linked to almost all glycan structures in place of Neu5Ac. All linkage types known for Neu5Ac; alpha2,3-, alpha2,4-, alpha2,6-, and alpha2,8- are also found for KDN. (4) KDN is biosynthesized de novo using mannose as a precursor sugar, which is activated to CMP-KDN and transferred to acceptor sugar residues. These reactions are catalyzed by enzymes, some of which preferably recognize KDN, but many others prefer Neu5Ac to KDN. In addition to these basic findings, elevated expression of KDN was found in fetal human red blood cells compared with adult red blood cells, and ovarian tumor tissues compared with normal controls. KDNase, an enzyme which specifically cleaves KDN-linkages, was discovered in a bacterium and monoclonal antibodies that specifically recognize KDN residues in KDNalpha2,3-Gal- and KDNalpha2,8-KDN-linkages have been developed. These have been used for identification of KDN-containing molecules. Based on past basic studies and variety of findings, future perspective of KDNology is presented.
Similar articles
-
2-Keto-3-deoxy-D-glycero-D-galacto-nononic acid (KDN)- and N-acetylneuraminic acid-cleaving sialidase (KDN-sialidase) and KDN-cleaving hydrolase (KDNase) from the hepatopancreas of oyster, Crassostrea virginica.J Biol Chem. 1999 Nov 5;274(45):31974-80. doi: 10.1074/jbc.274.45.31974. J Biol Chem. 1999. PMID: 10542227
-
Occurrence of free deaminoneuraminic acid (KDN)-containing complex-type N-glycans in human prostate cancers.Glycobiology. 2013 Jun;23(6):634-42. doi: 10.1093/glycob/cws132. Epub 2012 Sep 12. Glycobiology. 2013. PMID: 22975979
-
Identification of KDN-Gangliosides.Methods Mol Biol. 2018;1804:429-435. doi: 10.1007/978-1-4939-8552-4_22. Methods Mol Biol. 2018. PMID: 29926423
-
[Recent advances in glycobiology on KDN-containing glycoconjugates].Seikagaku. 1997 Jan;69(1):44-51. Seikagaku. 1997. PMID: 9038402 Review. Japanese. No abstract available.
-
Polysialic acids.Int J Biochem. 1993 Nov;25(11):1517-27. doi: 10.1016/0020-711x(93)90507-b. Int J Biochem. 1993. PMID: 8288019 Review.
Cited by
-
Antibodies Against Unusual Forms of Sialylated Glycans.Acta Naturae. 2022 Apr-Jun;14(2):85-92. doi: 10.32607/actanaturae.11631. Acta Naturae. 2022. PMID: 35923565 Free PMC article.
-
Sialylation in protostomes: a perspective from Drosophila genetics and biochemistry.Glycoconj J. 2009 Apr;26(3):313-24. doi: 10.1007/s10719-008-9154-4. Epub 2008 Jun 21. Glycoconj J. 2009. PMID: 18568399 Review.
-
Human symbiont Bacteroides thetaiotaomicron synthesizes 2-keto-3-deoxy-D-glycero-D- galacto-nononic acid (KDN).Chem Biol. 2008 Sep 22;15(9):893-7. doi: 10.1016/j.chembiol.2008.08.005. Chem Biol. 2008. PMID: 18804026 Free PMC article.
-
Host Sialic Acids: A Delicacy for the Pathogen with Discerning Taste.Microbiol Spectr. 2015 Aug;3(4):10.1128/microbiolspec.MBP-0005-2014. doi: 10.1128/microbiolspec.MBP-0005-2014. Microbiol Spectr. 2015. PMID: 26350327 Free PMC article. Review.
-
Hypoxia Alters Epigenetic and N-Glycosylation Profiles of Ovarian and Breast Cancer Cell Lines in-vitro.Front Oncol. 2020 Jul 29;10:1218. doi: 10.3389/fonc.2020.01218. eCollection 2020. Front Oncol. 2020. PMID: 32850359 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
Miscellaneous