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PMID: 7093223 Published · ppublish English Comparative Study Journal Article

Synthesis and characterization of diastereomers of guanosine 5'-O-(1-thiotriphosphate) and guanosine 5'-O-(2-thiotriphosphate).

Biochemistry ·Vol. 21 ·No. 9 ·1982-04-27 ·Pages 1983-9

Connolly BA, Romaniuk PJ, Eckstein F

Abstract

The synthesis and characterization of guanosine 5'-O-(1-thiotriphosphate) (GTP alpha S) and guanosine 5'-O-(2-thiotriphosphate) (GTP beta S) using chemical and enzymatic methods are described. GTP alpha S A (SP diastereomer) can be prepared enzymatically from a chemically synthesized mixture of the diastereomers of guanosine 5'-O-(1-thiodiphosphate) (GDP alpha S) with phosphoglycerate kinase. GTP alpha S B (RP diastereomer) can be similarly synthesized with succinyl-CoA synthetase and by back-digesting the small amounts of GTP alpha S A formed with phosphoglycerate kinase. Guanosine 5'-O-(2-thiodiphosphate) (GDP beta S) serves as the precursor for both GTP beta S A (SP diastereomer), prepared with pyruvate kinase and by back-digesting with glycerol kinase, and GTP beta S B (RP diastereomer), obtained with acetate kinase and by back-digesting with myosin. These analogues can be gamma-32P labeled by 32Pi exchange with either phosphoglycerate kinase-phosphoglyceraldehyde dehydrogenase or succinyl-CoA synthetase. Finally, the interaction of these four nucleotides with acetate kinase, RNA polymerase, and succinyl-CoA synthetase is described.

MeSH Terms
Acetate Kinase/metabolism DNA-Directed RNA Polymerases/metabolism Guanosine 5'-O-(3-Thiotriphosphate)/analogs & derivatives Guanosine Triphosphate/analogs & derivatives,chemical synthesis In Vitro Techniques Kinetics Methods Stereoisomerism Substrate Specificity Succinate-CoA Ligases/metabolism Thionucleotides/chemical synthesis
Chemicals
Thionucleotides guanosine 5'-O-(1-thiotriphosphate) guanosine 5'-O-(2-thiotriphosphate) Guanosine 5'-O-(3-Thiotriphosphate) Guanosine Triphosphate Acetate Kinase DNA-Directed RNA Polymerases Succinate-CoA Ligases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Connolly B A
Romaniuk P J
Eckstein F
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1982-04-27
Pages
1983-9
Language
English
Region
United States
NLM ID
0370623
Subset
IM
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