Biosynthetic studies have shown the incorporation of DL-[2,3,3-H-2(3)]
-tyrosine into the chromophore of pseudobactin, a siderophore produced
by Pseudomonas fluorescens B 10. A subsequent feeding using DL-[2',5'
,6'- H-2(3)]-3,4-dihydroxyphenylalanine showed no incorporation of the
label, suggesting that oxidation of the aryl ring occurs after the in
corporation of tyrosine. The C-13 NMR assignments of pseudobactin are
also reported herein.