» Articles » PMID: 2556992

Detection of CMP-N-acetylneuraminic Acid Hydroxylase Activity in Fractionated Mouse Liver

Overview
Journal Biochem J
Specialty Biochemistry
Date 1989 Oct 15
PMID 2556992
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The finding that N-glycoloylneuraminic acid (Neu5Gc) in pig submandibular gland is synthesized by hydroxylation of the sugar nucleotide CMP-Neu5Ac [Shaw & Schauer (1988) Biol. Chem. Hoppe-Seyler 369, 477-486] prompted us to investigate further the biosynthesis of this sialic acid in mouse liver. Free [14C]Neu5Ac, CMP-[14C]Neu5Ac and [14C]Neu5Ac glycosidically bound by Gal alpha 2-3- and Gal alpha 2-6-GlcNAc beta 1-4 linkages to fetuin were employed as potential substrates in experiments with fractionated mouse liver homogenates. The only substrate to be hydroxylated was the CMP-Neu5Ac glycoside. The product of the reaction was identified by chemical and enzymic methods as CMP-Neu5Gc. All of the CMP-Neu5Ac hydroxylase activity was detected in the high-speed supernatant fraction. The hydroxylase required a reduced nicotinamide nucleotide [NAD(P)H] coenzyme and molecular oxygen for activity. Furthermore, the activity of this enzyme was enhanced by exogenously added Fe2+ or Fe3+ ions, all other metal salts tested having a negligible or inhibitory influence. This hydroxylase is therefore tentatively classified as a monooxygenase. The cofactor requirement and CMP-Neu5Ac substrate specificity are identical to those of the enzyme in high-speed supernatants of pig submandibular gland, suggesting that this is a common route of Neu5Gc biosynthesis. The relevance of these results to the regulation of Neu5Gc expression in sialoglycoconjugates is discussed.

Citing Articles

Intestine specific regulation of pig cytidine-5'-monophospho-N-acetylneuraminic acid hydroxylase gene for N-glycolylneuraminic acid biosynthesis.

Song K, Kwak C, Chung T, Ha S, Park J, Ha K Sci Rep. 2019; 9(1):4292.

PMID: 30862964 PMC: 6414617. DOI: 10.1038/s41598-019-40522-9.


Exploration of the Sialic Acid World.

Schauer R, Kamerling J Adv Carbohydr Chem Biochem. 2018; 75:1-213.

PMID: 30509400 PMC: 7112061. DOI: 10.1016/bs.accb.2018.09.001.


Poor Patient and Graft Outcome After Induction Treatment by Antithymocyte Globulin in Recipients of a Kidney Graft After Nonrenal Organ Transplantation.

Mai H, Treilhaud M, Leviatan Ben-Arye S, Yu H, Perreault H, Ang E Transplant Direct. 2018; 4(4):e357.

PMID: 29707628 PMC: 5908458. DOI: 10.1097/TXD.0000000000000772.


-glycolyl groups of nonhuman chondroitin sulfates survive in ancient fossils.

Bergfeld A, Lawrence R, Diaz S, Pearce O, Ghaderi D, Gagneux P Proc Natl Acad Sci U S A. 2017; 114(39):E8155-E8164.

PMID: 28893995 PMC: 5625913. DOI: 10.1073/pnas.1706306114.


Streptococcus pneumoniae Senses a Human-like Sialic Acid Profile via the Response Regulator CiaR.

Hentrich K, Lofling J, Pathak A, Nizet V, Varki A, Henriques-Normark B Cell Host Microbe. 2016; 20(3):307-317.

PMID: 27593514 PMC: 5025396. DOI: 10.1016/j.chom.2016.07.019.


References
1.
Schauer R . [Biosynthesis of N-glycoloylneuraminic acid by an ascorbic acid- or NADP-dependent N-acetyl hydroxylating "N-acetylneuraminate: O2-oxidoreductase" in homogenates of porcine submaxillary gland]. Hoppe Seylers Z Physiol Chem. 1970; 351(7):783-91. View

2.
Bohm P, DAUBER S, BAUMEISTER L . [Occurrence and determination of neuraminic acid in the blood]. Klin Wochenschr. 1954; 32(13-14):289-92. DOI: 10.1007/BF01467396. View

3.
Cardinale G, UDENFRIEND S . Prolyl hydroxylase. Adv Enzymol Relat Areas Mol Biol. 1974; 41(0):245-300. DOI: 10.1002/9780470122860.ch6. View

4.
Schauer R, Schoop H, FAILLARD H . [On biosynthesis of the glycolyl groups of N-glycolylneuraminic acid. Oxidative conversion of N-acetyl groups to glycolyl groups]. Hoppe Seylers Z Physiol Chem. 1968; 349(5):645-52. View

5.
Schoop H, Schauer R, FAILLARD H . [On the biosynthesis of N-glycolyneuraminic acid. Oxidative formation of N-glycolylneuraminic acid from N-acetylneuraminic acid]. Hoppe Seylers Z Physiol Chem. 1969; 350(2):155-62. View