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PMID: 8608153 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Metabolic role of cytoplasmic isozymes of 5,10-methylenetetrahydrofolate dehydrogenase in Saccharomyces cerevisiae.

Biochemistry ·Vol. 35 ·No. 9 ·1996-03-05 ·Pages 3122-32

West MG, Horne DW, Appling DR

Abstract

Saccharomyces cerevisiae possesses two cytosolic 5,10-methylenetetrahydrofolate (CH2-THF) dehydrogenases that differ in their redox cofactor specificity: an NAD-dependent dehydrogenase encoded by the MTD1 gene and an NADP-dependent activity as part of the trifunctional C1-THF synthase encoded by the ADE3 gene. The experiments described here were designed to define the metabolic roles of the NAD- and NADP-dependent CH2-THF dehydrogenases in one-carbon interconversions and de novo purine biosynthesis. Growth studies showed that the NAD-dependent CH2-THF dehydrogenase is interchangeable with the NADP-dependent CH2-THF dehydrogenase when flow of one-carbon units is in the oxidative direction but that it does not participate significantly when flux is in the reductive direction. 13C NMR experiments with [2-13C]glycine and unlabeled formate confirmed the latter conclusion. Direct measurements of cellular folate coenzyme levels revealed substantial levels of 10-formyl-THF (CHO-THF), the one-carbon donor used in purine synthesis, in the purine-requiring ade3 deletion strain. Thus, CHO-THF is necessary but not sufficient for de novo purine synthesis in yeast. Disruption of the MTD1 gene in this strain resulted in undetectable CHO-THF, indicating that the NAD-dependent CH2-THF dehydrogenase was responsible for CHO-THF production in the ade3 deletion strain. Finally, we examined the ability of wild-type and catalytically-inactive domains of the cytoplasmic C1-THF synthase to complement the adenine auxotrophy of the ade3 deletion strain. Both the dehydrogenase/cyclohydrolase (D/C) domain and the synthetase domain could functionally replace the full-length protein, but, at least for the D/C domain, complementation was not dependent on catalytic activity. These results reveal a catalytic role for the NAD-dependent CH2-THF dehydrogenase in the oxidation of cytoplasmic one-carbon units and indicate that the cytoplasmic C1-THF synthase plays both catalytic and noncatalytic roles in de novo purine biosynthesis in yeast.

MeSH Terms
Animals CHO Cells Cricetinae Cytosol/enzymology Genotype Glycine/metabolism Isoenzymes/biosynthesis,chemistry,metabolism Kinetics Liver/enzymology Magnetic Resonance Spectroscopy Methylenetetrahydrofolate Dehydrogenase (NADP)/biosynthesis,chemistry,metabolism Models, Biological NAD/metabolism NADP/metabolism Phenotype Plasmids Rats Recombinant Proteins/biosynthesis,chemistry,metabolism Saccharomyces cerevisiae/enzymology,genetics,growth & development Species Specificity
Chemicals
Isoenzymes Recombinant Proteins NAD NADP Methylenetetrahydrofolate Dehydrogenase (NADP) Glycine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
West M G
Department of Chemistry and Biochemistry and The Biochemical Institute, The University of Texas, Austin, 78712, USA.
Horne D W
Appling D R
Article Info
Journal
Biochemistry
Abbr.
Biochemistry
ISSN
0006-2960
Published
1996-03-05
Pages
3122-32
Language
English
Region
United States
NLM ID
0370623
Subset
IM
Grants
NIDDK NIH HHS · DK32189 · United States
NCRR NIH HHS · RR09276 · United States
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