Mucor circinelloides LU M40 produced 12.2 mU ml(-1) of linamarase activity
when grown in a 3 1 fermenter in the following optimized medium (g l(-1) de
ionized water): pectin, 10.0; (NH4)(2)SO4, 1.0; KH2PO4, 2.0; Na2HPO4, 0.7;
MgSO4. 7H(2)O, 0.5; yeast extract, 1.0; Tween-80, 1.0, added after 48 h of
fermentation. The purified linamarase was a dimeric protein with a molecula
r mass of 210 Kda; the enzyme showed optimum catalytic activity at pH 5.5 a
nd 40 degrees C and had a wide range (3.0-7.0) of pH stability. The enzyme
substrate specificity on plant cyanogenic glycosides was wied; the K-m valu
e for linamarin was 2.93 mmol l(-1). The addition, before processing, of th
e fungal crude enzyme to cassava roots facilitated and shortened detoxifica
tion; after 24 h of fermentation, all cyanogenic glycosides were hydrolysed
.