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PMID: 8395705 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Synthesis and degradation of cyclic ADP-ribose by NAD glycohydrolases.

Science (New York, N.Y.) ·Vol. 261 ·No. 5126 ·1993-09-03 ·Pages 1330-3

Kim H, Jacobson EL, Jacobson MK

Abstract

Cyclic adenosine diphosphoribose (cADPR), a recently discovered metabolite of nicotinamide adenine dinucleotide (NAD), is a potent calcium-releasing agent postulated to be a new second messenger. An enzyme that catalyzes the synthesis of cADPR from NAD and the hydrolysis of cADPR to ADP-ribose (ADPR) was purified to homogeneity from canine spleen microsomes. The net conversion of NAD to ADPR categorizes this enzyme as an NAD glycohydrolase. NAD glycohydrolases are ubiquitous membrane-bound enzymes that have been known for many years but whose function has not been identified. The results presented here suggest that these enzymes may function in the regulation of calcium homeostasis by the ability to synthesize and degrade cADPR.

MeSH Terms
Adenosine Diphosphate Ribose/analogs & derivatives,biosynthesis,metabolism Animals Calcium/metabolism Cyclic ADP-Ribose Dogs Hydrolysis Kinetics NAD/metabolism NAD+ Nucleosidase/isolation & purification,metabolism Spleen/enzymology
Chemicals
NAD Cyclic ADP-Ribose Adenosine Diphosphate Ribose NAD+ Nucleosidase Calcium
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kim H
Department of Biochemistry and Molecular Biology, University of North Texas Health Science Center at Fort Worth 76107.
Jacobson E L
Jacobson M K
Article Info
Journal
Science (New York, N.Y.)
Abbr.
Science
ISSN
0036-8075
Published
1993-09-03
Pages
1330-3
Language
English
Region
United States
NLM ID
0404511
Subset
IM
Grants
NCI NIH HHS · CA43894 · United States
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