A Type I/Type III PKS Hybrid Generates Cinnamomycin A-D

3,5-Dihydroxybenzoic acid (3,5-DHBA), biosynthe-sized by type III PKS and tailoring enzymes, is an unconventional starter unit for bacterial type I PKS. Genome mining of 3,5-DHBA-specific biosynthetic gene clusters could lead to discovering new type I/type III PKS hybrids. Herein, we report the discovery and characterization of atypical compounds, namely cinnamomycin A- D, exhibiting selective antiproliferative activity. The biosynthetic pathway of cinnamomycins was proposed based on genetic manipulation, enzymatic reaction, and precursor feeding.

Automated summary

Through genome mining, the discovery and characterization of atypical compounds, cinnamomycin A-D, with selective antiproliferative activity. The biosynthetic pathway of cinnamomycins was proposed based on genetic manipulation, enzymatic reaction, and precursor feeding.