• Title of article

    Methenyltetrahydrofolate Cyclohydrolase Catalyzes the Synthesis of (6S)-5-Formyltetrahydrofolate

  • Author/Authors

    Pelletier، نويسنده , , Joelle N. and MacKenzie، نويسنده , , Robert E.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 1996
  • Pages
    9
  • From page
    220
  • To page
    228
  • Abstract
    The methenyltetrahydrofolate cyclohydrolase activity of the bifunctional methylenetetrahydrofolate dehydrogenase/cyclohydrolase domain catalyzes the conversion of 5,10-methenyltetrahydrofolate to 10-formyltetrahydrofolate. We have observed that in the presence of this domain, 10-formyltetrahydrofolate is converted to 5-formyltetrahydrofolate. The effects of nucleotide analogs on the initial rates of this reaction were found to be similar to their effects on the cyclohydrolase activity, establishing that 5-formyltetrahydrofolate production is dependent on the cyclohydrolase. The specific activity of 5-formyltetrahydrofolate production is approximately 7 × 104-fold lower than that of the cyclohydrolase activity but can be used to obtain quantitative conversion of 10-formylH4folate to 5-formyltetrahydrofolate, in mg amounts. This “side-reaction” may contribute to thein vivoproduction of (6S)-5-formyltetrahydrofolate.
  • Journal title
    Bioorganic Chemistry: an International Journal
  • Serial Year
    1996
  • Journal title
    Bioorganic Chemistry: an International Journal
  • Record number

    1385191