TRIGGERING OF CELLULASE BIOSYNTHESIS BY CELLULOSE IN TRICHODERMA-REESEI - INVOLVEMENT OF A CONSTITUTIVE, SOPHOROSE-INDUCIBLE, GLUCOSE-INHIBITED BETA-DIGLUCOSIDE PERMEASE
Cp. Kubicek et al., TRIGGERING OF CELLULASE BIOSYNTHESIS BY CELLULOSE IN TRICHODERMA-REESEI - INVOLVEMENT OF A CONSTITUTIVE, SOPHOROSE-INDUCIBLE, GLUCOSE-INHIBITED BETA-DIGLUCOSIDE PERMEASE, The Journal of biological chemistry, 268(26), 1993, pp. 19364-19368
We prepared [U-C-14]cellobiose by cultivating Acetobacter pasteurianus
in the presence of [U-C-14]glucose and hydrolyzing the [U-C-14]cellul
ose formed with beta-glucosidase-free cellulase from Trichoderma reese
i. This C-14-labeled cellobiose was used to investigate the presence o
f an uptake system for cellobiose in T. reesei. Evidence was obtained
for the presence of a high affinity (K(m) for cellobiose 0.3 muM) but
low activity (2.5 milliunits/mg fungal dry weight) cellobiose permease
. The permease is formed constitutively, but higher levels are formed
after addition of sophorose (glucosyl-beta-1,2-diglucoside), a reputed
cellulase inducer. The permease appears to be specific for beta-diglu
cosides, as the uptake of [U-C-14]cellobiose is inhibited by sophorose
, gentiobiose (glucosyl-,beta-1,3-glucoside), and cellobiose. Under th
ese conditions, cellooligodextrines (n, 4-7; final concentration, 1 mM
) are not inhibitors. Glucose, but no other monosaccharides, inhibits
the permease. The hypersecretory mutant T. reesei RUT C-30 exhibits el
evated permease activities, whereas in T. reesei QM 9979, a mutant str
ain defective in the induction of cellulases by cellulose or sophorose
, strongly reduced permease activities were demonstrated. The results
stress a hitherto not recognized point of control in the induction of
cellulases by T. reesei at the level of uptake of cellulose oligosacch
arides.