Table 4.
Metabolic composition of red exudate produced by two novel Penicillium species on MEA and PDA after 7 days of cultivation at 25 °C, as identified by LC–MS (El-Elimat et al., 2013, Paguigan et al., 2017).
Compound Name a | Molecular Formula |
P. krskae | P. silybi | ||
---|---|---|---|---|---|
PDA | MEA | PDA | MEA | ||
2-hydroxyemodic acid | C15H8O8 | − | − | + | − |
(+)-2’S-Isorhodoptilometrin | C17H14O6 | + | + | + | + |
1’-Hydroxy-2’-ketoisorhodoptilometrin | C17H12O7 | + | − | + | + |
7-Chloro-1’-hydroxyisorhodoptilometrin | C17H13O7Cl | + b | + | − | + |
1’-Hydroxyisorhodoptilometrin | C17H14O7 | + b | + | + | + |
2-Chloroemodic acid | C15H7ClO7 | + b | + | + | + |
2-Chloro-isorhodoptilometrin * | C17H13O6Cl | + b | + | − | + |
2-Chloro-desmethyl dermoquinone * | C17H11O6Cl | + b | + | − | + |
7-Chlorocitreosein | C15H9ClO6 | + b | + | − | + |
O-Demethyldermoquinone | C17H12O6 | + | + | + | + |
Emodic acid | C15H8O7 | + | + | + | + |
Emodin | C15H10O5 | + | − | + | + |
ω-Hydroxyemodin (citreorosein) | C15H10O6 | + b | + | + | + |
a In alphabetical order; * newly discovered compound; b elucidated also by nuclear magnetic resonance (NMR).