“…An adapted diffusion method using 10 μL of hydro-alcoholic extract (50:50; 100 mg/mL) was performed on Potato Dextrose Agar medium inoculated with standard fungal cell suspensions (1 McFarland) belonging to A. niger , A. flavus , A. pseudoglaucus , A. nidulans , A. flavus oryzae , A. versicolor , A. montevidensis , A. clavatus , P. chrysogenum , P. corylophylum , P. expansum , P. digitatum , P. brevicompactum , P. namylowskii , Rhizopus oryzae , A. alternata , F. proliferatum , M. circinelloides , P. lilacinum and on Mueller Hinton (MH) for the bacterial strains, (0.5 McFarland) belonging to B. subtilis , B. megaterium , B. thuringiensis , B. cereus , B. pumilus , B. atrophaeus , A. aurascens , A. globiformis , and P. koreensis, previously isolated from the cultural heritage churches and museum collections of three different geographic locations in Romania [ 19 , 20 , 21 ]. After 5–7 days of incubation at room temperature/24 h at 37 °C the growth inhibition diameters were measured and converted in arbitrary units as previously described [ 21 ].…”