Azaphilones, Fungal secondary metabolites of the pyranequinone structure, r
eact with ammonia yielding vinylogous 4-pyridones. The pigments also react
with amines, such as proteins, amino acids and nucleic acids, to form water
-soluble pigments. Their most remarkable and valuable properties include th
e natural origin, yellow-red spectra, thermostability (in comparison with o
ther natural red pigments), and easy derivatization. So far, they have been
identified in a variety of fungal sources. Of the microorganisms tested, o
nly genera Monascus, Penicillium and Chaetomium are good producers of azaph
ilone pigments. However, similar structures were also identified in Aspergi
llus ustus, Cochliobolus lunata, Talaromyces sp. and Emericella falconensis
. The microorganisms could be a promising source of the new group of natura
l pigments for food and cosmetic industry.