Abstract
A C-methyltransferase that catalyses the transfer of a methyl group from S-adenosylmethionine to C-3 of tryptophan, resulting in beta-methyltryptophan, has been identified in cell-free extracts of streptonigrin-producing Streptomyces flocculus. The absolute configuration of the product was shown to be (2S,3R)-beta-methyltryptophan by high-pressure liquid chromatography and reactivity with D- and L-amino acid oxidases. In shake culture, maximum specific activity occurs after S. flocculus enters stationary phase, but before significant streptonigrin accumulates.
Original language | English (US) |
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Pages (from-to) | 309-313 |
Number of pages | 5 |
Journal | The Biochemical journal |
Volume | 220 |
Issue number | 1 |
DOIs | |
State | Published - May 15 1984 |