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pubmed-article:1512712pubmed:abstractTextExperiments on the incorporation of D- and L-[alanine-3-13C,2-15N]tryptophan into the antibiotic pyrrolnitrin in Pseudomonas aureofaciens confirmed earlier conclusions about the conversion of L-tryptophan into pyrrolnitrin. They also demonstrated that a fraction of the D isomer is incorporated without breakage of the 15N-carbon bond, consistent with the operation of a second pathway from D-tryptophan to pyrrolnitrin. Cell-free experiments confirmed the conversion of 3-(o-aminophenyl)pyrrole into aminopyrrolnitrin but failed to detect enzymatic oxidation of the latter to pyrrolnitrin.lld:pubmed
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pubmed-article:1512712pubmed:articleTitleBiosynthesis of pyrrolnitrin. Incorporation of 13C, 15N double-labelled D- and L-tryptophan.lld:pubmed
pubmed-article:1512712pubmed:affiliationDepartment of Chemistry, University of Washington, Seattle 91895.lld:pubmed
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pubmed-article:1512712pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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