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. 2014 Aug 21;15(8):14610–14631. doi: 10.3390/ijms150814610

Table 1.

Exemplary selection of NRPS (nonribosomal peptide synthetases) pathways generating cyclic dipeptide (CDP)-containing natural products. Shown are the different modification enzymes found inside those gene clusters, their putative function as well as the substrate CDP-scaffold used by those enymes.

Biosynthetic Pathway Modification Enzymes Putative Function CDP Substrate
Thaxtomin [24,69,70]
(Streptomyces scabies)
TxtC Hydroxylation cWY
Brevianamide [71]
(Aspergillus fumigatus)
Afu8g00240 Oxidative cyclization cWP
Afu8g00230 Oxidative cyclization
Afu8g00220 Hydroxylation
Afu8g00200 O-methylation
Afu8g00190 Hydroxylation
Ergotamine [72]
(Claviceps purpurae)
CpP4501 Hydroxylation cFP
CpCAT2 Hydroperoxidation
CpOX3 Oxidative cyclization
Meleagrin [73]
(Penicillium chrysogenum)
Pc21g15430 C3-reverse-prenylation cWH
Pc21g15440 O-methylation
Pc21g15450 Oxidative cyclization
Pc21g15460 N-hydroxylation
Pc21g15470 α,β-dehydrogenatioin
Acetylazonalenin [74]
(Neosartorya fischeri)
AnaPT C3-reverse-prenylation cWF
AnaAT N-acetylation
Gliotoxin [75]
(Aspergillus fumigatus)
GliC Oxidation cFS
GliF Oxidation
GliG Sulfurization
GliI Cyclopropane-formation
GliM O-methylation
GliN N-methylation