Endoglucanase and β-glycosidase activities in an evergreen oak litter: annual variation and regulating factors

This paper represents the third part of a larger study about the processes involved in litter biodegradation in an oak copse in France. It concerns the variations in activities of endoglucanases and of β-glycosidases over 13 months in forest litter. Evergreen oak (Quercus ilex L.) litter was taken as a model because Q. ilex is the most abundant tree species in forests of the French Mediterranean area. The activities of several endoglucanases and β-glycosidases, and the concentrations of the proteins and reducing sugars were measured in the evergreen oak litter between October 1997 and October 1998. Several biotic and abiotic factors, potentially involved in the regulation of the activities of these hydrolyzing enzymes, were also measured: culturable heterotrophic bacteria, cellulolytic bacteria and cellulolytic fungi, moisture, temperature and pH of the litter. Under this Mediterranean climate, the moisture of the litter was strongly correlated with many factors and is likely to be important in regulating the temporal dynamics of various biological parameters. A multiple regression analysis showed that the annual dynamic of the culturable heterotrophic bacteria was primarily influenced by moisture but also by variations in concentration of reducing sugars in the litter. Moreover, these bacteria were correlated with the activities of several β-glycosidases, and specifically with the N-acetyl-glucosaminidases (r=0.93). No relationships were established between the number of cellulolytic microorganisms (bacteria and fungi) and the activities of endoglucanases (i.e. cellulases and hemicellulases). The seasonal trends of certain biotic processes, and the influence of pH and of temperature on these processes are also discussed. Electrophoretic analyses were used to estimate the number of cellulase and xylanase isoenzymes in the litter, and to study their fluctuations over one year. The prevailing cellulase isoenzyme had a Rf of 0.64, and there was no relationship between the abundance of cellulolytic microorganisms and the electrophoretic profiles of the cellulases. In the case of the xylanases, the electrophoretic profiles were homogenous throughout the year, and the prevailing xylanase had a Rf of 0.75.