2007
DOI: 10.1007/s12010-007-9058-y
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Production of cellulolytic and hemicellulolytic enzymes from Aureobasidium pulluans on solid state fermentation

Abstract: This article investigates a strain of the yeast Aureobasidium pullulans for cellulase and hemicellulase production in solid state fermentation. Among the substrates analyzed, the wheat bran culture presented the highest enzymatic production (1.05 U/mL endoglucanase, 1.3 U/mL beta-glucosidase, and 5.0 U/mL xylanase). Avicelase activity was not detected. The optimum pH and temperature for xylanase, endoglucanase and beta-glucosidase were 5.0 and 50, 4.5 and 60, 4.0 and 75 degrees C, respectively. These enzymes r… Show more

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Cited by 20 publications
(9 citation statements)
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References 32 publications
(38 reference statements)
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“…This inhibition halo evidenced the diffusion of metabolites. We hypothesized that the secretion of metabolites and enzymes like cellulolytic and hemicellulolytic enzymes (Leite et al 2007) and the capacity of this fungus to form biofilms (Metzger et al 2006) could have contributed to the success of the endophyte controlling R. solani. In future, the microscopic characterization of the hyphal interactions should be performed to further characterize the fungal interactions.…”
Section: Discussionmentioning
confidence: 99%
“…This inhibition halo evidenced the diffusion of metabolites. We hypothesized that the secretion of metabolites and enzymes like cellulolytic and hemicellulolytic enzymes (Leite et al 2007) and the capacity of this fungus to form biofilms (Metzger et al 2006) could have contributed to the success of the endophyte controlling R. solani. In future, the microscopic characterization of the hyphal interactions should be performed to further characterize the fungal interactions.…”
Section: Discussionmentioning
confidence: 99%
“…They were then paper filtered (Whatman, no. 1) and centrifuged at 1232.6 × g for 5 min (ITR, Brazil), yielding the crude enzyme extract from the supernatant to be used for the determination of enzyme activity [21].…”
Section: Aqueous Enzymatic Extractionmentioning
confidence: 99%
“…The microorganisms were placed on an orbital shaker (Marconi, Brazil) (130 rpm, 35ºC, 30 min), paper filtered (Whatman, no. 1), and then centrifuged (ITR, Brazil) (3000 rpm, 5 min), yielding the crude enzyme extract for the determination of enzyme activity (adapted from Leite et al 2007). The supernatant crude enzyme extract was used for determination of enzyme activities.…”
Section: Aqueous Enzymatic Extractionmentioning
confidence: 99%
“…The enzymatic reaction was stopped with 2 mL of sodium carbonate 2 M (Impex), and the resulting product was quantified spectrophotometrically (Bioespectro, Brazil) at 410 nm (Leite et al 2007). One unit of enzyme activity was defined as the amount of enzyme able to release 1 μmol of nitrophenol per minute of reaction.…”
Section: Amylase Cmcase and Xylanase Activitiesmentioning
confidence: 99%