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Methylenetetrahydrofolate-dependent biosynthesis of ribothymidine in transfer RNA of Streptococcus faecalis. Evidence for reduction of the 1-carbon unit by FADH2.
- Source :
-
The Journal of biological chemistry [J Biol Chem] 1980 May 25; Vol. 255 (10), pp. 4387-90. - Publication Year :
- 1980
-
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.
- Subjects :
- Enterococcus faecalis drug effects
Methylation
Methyltransferases metabolism
Oxidation-Reduction
Ribonucleosides analysis
Species Specificity
Uridine biosynthesis
Enterococcus faecalis metabolism
Flavin-Adenine Dinucleotide metabolism
RNA, Transfer biosynthesis
Tetrahydrofolates pharmacology
Uridine analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 0021-9258
- Volume :
- 255
- Issue :
- 10
- Database :
- MEDLINE
- Journal :
- The Journal of biological chemistry
- Publication Type :
- Academic Journal
- Accession number :
- 6768721