in bean the 9.5 cellulase appears to function in the shedding of various organs such as fruits, flowers, and leaves. The acid cellulases function in loosening the cellulose fibrils of the cell wall to allow expansion and growth
the enzyme shows multisubstrate specificity, showing significantly higher activity with lichenan and beta-glucan and lower activity with laminarin, hydroxyethylcellulose, and steam exploded bagasse
the enzyme shows multisubstrate specificity, showing significantly higher activity with lichenan and beta-glucan and lower activity with laminarin, hydroxyethylcellulose, and steam exploded bagasse
Bgl7A can effectively hydrolyze beta-1,4 bonds and some beta-1,3 linkages in beta-glucan. Belonging to the group of non-specific endoglucanase, Bgl7A can hydrolyze not only beta-glucan and cellulose but also laminarin and oat spelt xylan
EBI-244 is active on a range of high molecular weight carbohydrate substrates containing beta-1,4-linked glucose, including carboxymethyl cellulose, Avicel, and filter paper, it is active toward 4-nitrophenyl-cellobioside but inactive toward 4-nitrophenyl-glucoside
beta-1,4-endoglucanases show activities of the cleavage of the cellulose backbone due to an endocleavage. Oligosaccharides of different lengths as well as cellobiose and glucose are formed
possible role of the enzyme in the softening of pericarp tissue and in the liquefaction of locules that takes place during ripening. Cel1 EGase responds to pathogen infection and supports a relationship between EGases, plant defense responses and fruit ripening. mRNA abundance is down-regulated in response to fungal infection. It is rapidly reduced 1 day after pathagen infection and completely suppressed 4 days after infection
possible role of the enzyme in the softening of pericarp tissue and in the liquefaction of locules that takes place during ripening. Cel1 EGase responds to pathogen infection and supports a relationship between EGases, plant defense responses and fruit ripening. mRNA abundance is down-regulated in response to fungal infection. It is rapidly reduced 1 day after pathagen infection and completely suppressed 4 days after infection
among the processings of medicinal and aromatic plants, distillation waste of Cymbopogon winterianus, and bioprocessings of Artemisia annua (an industrial pharmaceutically important plant and source of artemisnin, an antimalarial compound) are selected on the basis of their capability to support higher levels of production of total cellulases, whereas garden waste, primarily consisting of Cynodon dactylon, is considered as the control, representing other lignocellulosic waste. Marc of Artemisia annua, a waste produced in huge amounts after the processing of the Artemisia annua herb, is found to be the suitable substrate for this fungus for maximizing the production of all three constituents of cellulase
among the processings of medicinal and aromatic plants, distillation waste of Cymbopogon winterianus, and bioprocessings of Artemisia annua (an industrial pharmaceutically important plant and source of artemisnin, an antimalarial compound) are selected on the basis of their capability to support higher levels of production of total cellulases, whereas garden waste, primarily consisting of Cynodon dactylon, is considered as the control, representing other lignocellulosic waste. Marc of Artemisia annua, a waste produced in huge amounts after the processing of the Artemisia annua herb, is found to be the suitable substrate for this fungus for maximizing the production of all three constituents of cellulase
among the processings of medicinal and aromatic plants, distillation waste of Cymbopogon winterianus, and bioprocessings of Artemisia annua (an industrial pharmaceutically important plant and source of artemisnin, an antimalarial compound) are selected on the basis of their capability to support higher levels of production of total cellulases, whereas garden waste, primarily consisting of Cynodon dactylon, is considered as the control, representing other lignocellulosic waste. Marc of Artemisia annua, a waste produced in huge amounts after the processing of the Artemisia annua herb, is found to be the suitable substrate for this fungus for maximizing the production of all three constituents of cellulase
among the processings of medicinal and aromatic plants, distillation waste of Cymbopogon winterianus, and bioprocessings of Artemisia annua (an industrial pharmaceutically important plant and source of artemisnin, an antimalarial compound) are selected on the basis of their capability to support higher levels of production of total cellulases, whereas garden waste, primarily consisting of Cynodon dactylon, is considered as the control, representing other lignocellulosic waste. Marc of Artemisia annua, a waste produced in huge amounts after the processing of the Artemisia annua herb, is found to be the suitable substrate for this fungus for maximizing the production of all three constituents of cellulase
among the processings of medicinal and aromatic plants, distillation waste of Cymbopogon winterianus, and bioprocessings of Artemisia annua (an industrial pharmaceutically important plant and source of artemisnin, an antimalarial compound) are selected on the basis of their capability to support higher levels of production of total cellulases, whereas garden waste, primarily consisting of Cynodon dactylon, is considered as the control, representing other lignocellulosic waste. Marc of Artemisia annua, a waste produced in huge amounts after the processing of the Artemisia annua herb, is found to be the suitable substrate for this fungus for maximizing the production of all three constituents of cellulase