Abstract
We studied the origin of the N-1 atom of the pyrimidine moiety of thiamin in a eucaryote, Saccharomyces cerevisiae. The competitive effects of 14N-compounds on the incorporation of 15N-NH4Cl into the pyrimidine moiety were examined. Amino acids, the bases of nucleic acids and glucosamine did not decrease 15N incorporation, but pyridoxine did. We conclude that the N-atom of pyridoxine is the origin of the N-1 atom of the pyrimidine of thiamin synthesized by S. cerevisiae. We also suggest that the N-atom of pyridoxine is derived from glutamine.
MeSH terms
-
Amino Acids / metabolism
-
Amino Acids / pharmacology
-
Ammonium Chloride / metabolism
-
Gas Chromatography-Mass Spectrometry
-
Glucosamine / metabolism
-
Glucosamine / pharmacology
-
Purines / metabolism
-
Purines / pharmacology
-
Pyridoxine / chemistry
-
Pyridoxine / metabolism*
-
Pyrimidines / metabolism
-
Pyrimidines / pharmacology
-
Saccharomyces cerevisiae / growth & development
-
Saccharomyces cerevisiae / metabolism*
-
Thiamine / biosynthesis*
-
Thiamine / chemistry
Substances
-
Amino Acids
-
Purines
-
Pyrimidines
-
Ammonium Chloride
-
Pyridoxine
-
Glucosamine
-
Thiamine