The
asexually produced spores (i.e.,
conidia) of
P. commune are smooth and spherical, ranging from 3.5 to 5.0 μm in diameter, borne in disordered chains on
conidiophores with rough-walled
stipes. The conidium-bearing stalks are either produced singularly or in bundled groups known as
fascicles. The stalk lengths are usually 200 to 400 μm. Conidia are dull grey green or grey turquoise in colour.
Penicillium commune can be distinguished by its fast growth on creatine sucrose neutral agar (CSN) while showing a slow growth rate on
malt extract agar (MEA) and restricted growth on
Czapek medium (CZA) and
Czapek yeast extract agar (CYA). The appearance of colonies on MEA ranges from soft, velvety and grown in unison to granular and barely grown together. The underside of colonies produced on MEA are pale-yellow coloured and sun-yellow coloured. Colonies on CZA and CYA range from soft and velvety to slightly fluffy with
exudate present that can be clear to brown coloured. In addition, the underside of the colonies grown on CZA and CYA are creamy/ dull yellow to brown-yellow in colour. The production of purple pigment has also been observed. No sexual stage has been described. However, genetic analysis indicate that none of the
P. commune (in the "lumper" sense,
sensu lato) genomes sequenced include loss-of-function mutations related to sexual reproduction.
P. fuscoglaucum is likely sexual as there is a 1:1 balance between the MAT1-1 and MAT1-2 mating types and obvious recombination signatures.
P. biforme shows a distortion in the ratio favoring MAT1-2 as well as signatures, consistent with early human clonal intervention in open-air environments where sexual reproduction occurs in a limited fashion.
P. camemberti is fully clonal, being all MAT1-2 and showing no signs of recombination. ==Physiology==