NAD hydrolysis: chemical and enzymatic mechanisms.

Abstract:

:The pyridine nucleotides have important non-redox activities as cellular effectors and metabolic regulators [1-3]. The enzyme-catalyzed cleavage of the nicotinamide-ribosyl bond of NAD+ and the attendant delivery of the ADPRibosyl moiety to acceptors is central to these many diverse biological activities. Included are the medically important NAD-dependent toxins associated with cholera, diphtheria, pertussis, and related diseases [4]; the reversible ADPRibosylation-mediated biological regulatory systems [5,6]; the synthesis of poly(ADPRibose) in response to DNA damage or cellular division [7]; and the synthesis of cyclic ADPRibose as part of an independent, calcium-mediated regulatory system [8]. As will be presented in this chapter, all evidence points to both the chemical and enzyme-catalyzed cleavage of the nicotinamide-ribosyl bond being dissociative in character via an oxocarbenium intermediate.

journal_name

Mol Cell Biochem

authors

Oppenheimer NJ

doi

10.1007/BF00928468

subject

Has Abstract

pub_date

1994-09-01 00:00:00

pages

245-51

issue

1-2

eissn

0300-8177

issn

1573-4919

journal_volume

138

pub_type

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