Reactions of Essential Sulfhydryl Residues of Dehydrogenases with Nicotinamide-(S-Methylmercury-Thioinosine) Dinucleotide

  • Sulfhydryl Groups, Methylmercury Containing Inactivator, Coenzyme Analogue Nicotinamide-(S-methylmercury-thioinosine) dinucleotide was formed by reaction of nicotin­ amide-(6-thiopurine) dinucleotide with methylmercury chloride. The compound exhibits coenzyme properties in the test with LDH (Km=1.5 × 10-4 м , Vmax=12500) and LADH (Km=1.7 × 10-4 м, Vmax=27) and inactivates YADH and GAPDH. From incubations with LDH and LADH the mercury containing coenzyme could be regained by column chromatography. The compound seems to be qualified for the X-ray structure analysis of the coenzyme-enzyme complex for some dehyrogenases based on the proportion of the heavy metal.

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Metadaten
Author:Christoph Woenckhaus, Helmut Duchmann
URN:urn:nbn:de:hebis:30:3-721082
DOI:https://doi.org/10.1515/znc-1975-9-1002
ISSN:0939-5075
ISSN:1865-7125
Parent Title (German):Zeitschrift für Naturforschung, C
Publisher:Verlag der Zeitschrift für Naturforschung
Place of publication:Tübingen
Document Type:Article
Language:English
Date of Publication (online):2014/06/02
Year of first Publication:1975
Publishing Institution:Universitätsbibliothek Johann Christian Senckenberg
Release Date:2024/01/30
Tag:Coenzyme Analogue; Methylmercury Containing Inactivator; Sulfhydryl Groups
Volume:30.1975
Issue:9-10
Page Number:3
First Page:562
Last Page:564
Institutes:Medizin
Biochemie, Chemie und Pharmazie / Biochemie und Chemie
Dewey Decimal Classification:5 Naturwissenschaften und Mathematik / 54 Chemie / 540 Chemie und zugeordnete Wissenschaften
5 Naturwissenschaften und Mathematik / 57 Biowissenschaften; Biologie / 570 Biowissenschaften; Biologie
Sammlungen:Universitätspublikationen
Licence (German):License LogoCreative Commons - Namensnennung-Nicht kommerziell-Keine Bearbeitung 3.0