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An enzymatic cyclopentyl[b]indole formation involved in scytonemin biosynthesis.

Journal of the American Chemical Society (2009-09-29)
Emily P Balskus, Christopher T Walsh
RÉSUMÉ

Previous studies of the biosynthetic enzymes involved in the assembly of scytonemin (1), a cyanobacterial sunscreen, have identified beta-ketoacid 2 as an important intermediate that is produced by ThDP-dependent enzyme ScyA. We now report that ScyC, previously annotated as a hypothetical protein, catalyzes cyclization and decarboxylation of 2 to generate ketone 5. Assembly of the cyclopentyl[b]indole structure in this manner has little precedent in the chemical literature. Additional mechanistic experiments have revealed that cyclization likely precedes decarboxylation and that the latter event may provide a driving force for cyclopentane formation.

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L-Leucine Dehydrogenase from Bacillus cereus, lyophilized powder, ≥60 units/mg protein