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PMID: 6768721 Published · ppublish English Journal Article

Methylenetetrahydrofolate-dependent biosynthesis of ribothymidine in transfer RNA of Streptococcus faecalis. Evidence for reduction of the 1-carbon unit by FADH2.

The Journal of biological chemistry ·Vol. 255 ·No. 10 ·1980-05-25 ·Pages 4387-90

Delk AS, Nagle DP, Rabinowitz JC

Abstract

The methyl carbon of ribothymidine in Loop IV of the tRNA of Streptococcus faecalis, Bacillus subtilis, and some other microorganisms is derived directly from 5,10-methylenetetrahydrofolate, not S-adenosylmethionine. The pure enzyme from S. faecalis also requires FADH2. We have obtained evidence that tetrahydrofolate is a product of the reaction and demonstrated that label from [5-3H]5-deazaFMNH2 is incorporated into the methyl moiety of ribothymidine. These data indicate that the enzyme uses methylenetetrahydrofolate solely as a 1-carbon donor and employs FADH2 as a reducing agent in vitro according to the following reaction: tRNA(U psi C) + CH2 = THF + FADH2 leads to tRNA(T psi C) + THF + FAD.

MeSH Terms
Enterococcus faecalis/drug effects,metabolism Flavin-Adenine Dinucleotide/metabolism Methylation Methyltransferases/metabolism Oxidation-Reduction RNA, Transfer/biosynthesis Ribonucleosides/analysis Species Specificity Tetrahydrofolates/pharmacology Uridine/analogs & derivatives,biosynthesis
Chemicals
Ribonucleosides Tetrahydrofolates 5,10-methylenetetrahydrofolic acid Flavin-Adenine Dinucleotide ribothymidine RNA, Transfer Methyltransferases ribothymidyl synthase Uridine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Delk A S
Nagle D P
Rabinowitz J C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1980-05-25
Pages
4387-90
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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