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. 2009 Mar 6;75(9):2869–2878. doi: 10.1128/AEM.02326-08

FIG. 6.

FIG. 6.

Proposed pathway for the biosynthesis of the 4-propenyl-2,3-dihydropyrrole-2-carboxylic acid moiety in sibiromycin, which is the suggested substrate for the NRPS enzymes catalyzing diazepine ring formation. The branching points for the anthramycin, tomaymycin, and lincomycin A biosyntheses are indicated.