A new screening method for simultaneous detection of endo-beta-1,4-man
nanase and endo-beta-1,4-xylanase producing microorganisms is describe
d. Two differently dyed substrates Ostazin Brilliant Red-galactomannan
and Remazol Brilliant Blue-xylan were incorporated into the same agar
media. Decolorizing of one or both substrates around the cell colonie
s indicates secretion of the corresponding enzyme(s). The method was u
sed to screen 449 yeasts and yeast-like microorganisms belonging to 68
different genera. The secretion of endo-beta-1,4-mannanases and/or en
do-beta-1,4-xylanases was found within 10 genera (42 positive strains
out of 261 tested). A low frequency of occurrence of endo-beta-1,4-man
nanase was observed within the genera Cryptococcus (1 positive strain
out of 15 tested), Geotrichum (1 of 6) and Pichia (1 of 35). The highe
st frequency of occurrence of endo-beta-1,4-mannanases was found withi
n the genera Stephanoascus (2 of 2) and Aureobasidium (14 of 14). Stra
ins hydrolyzing Ostazin Brilliant Red-galactomannan were cultivated in
liquid media containing 1% locust bean gum. The best producers of ext
racellular endo-beta-1,4-mannanases were found to be the strains of Au
reobasidium pullulans.