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. 2016 Apr 21;55(23):6784–6788. doi: 10.1002/anie.201511882

Figure 3.

Figure 3

HPLC (DAD, 210–600 nm) chromatograms. A) Extract from WT B. fulva; B) extract from B. fulva Δpks1; C) extract from untransformed A. oryzae NSAR1; D) extract from A. oryzae transformant BF‐PMCH; E) extract from A. oryzae transformant BF‐PMCH+KIs; F) extract from A. oryzae transformant BF‐PMCH+KIs+PEBPs; G) Purified agnestadride A (8); H) Purified byssochlamic acid (1). Compounds 12, 12′, and 13 are cometabolites of 1 and have been previously identified and characterized.10