AI Article Synopsis

  • * The research focuses on using lignocellulolytic enzymes to convert palm oil mill effluent (POME) into reducing sugars, with enzyme assays showing high productivity for several enzymes, including endoglucanase and β-glucosidase.
  • * Optimized conditions (15 hours incubation, 10% enzyme loading, pH 4.8) yielded 3.75 g/l of reducing sugar and a biohydrogen gas production of 302.78 ml H.L POME, demonstrating the potential

Article Abstract

Mushroom cultivation along with the palm oil industry in Malaysia have contributed to large volumes of accumulated lignocellulosic residues that cause serious environmental pollution when these agroresidues are burned. In this study, we illustrated the utilization of lignocellulolytic enzymes from the spent mushroom substrate of for the hydrolysis of palm oil mill effluent (POME). The hydrolysate was used for the production of biohydrogen gas and enzyme assays were carried out to determine the productivities/activities of lignin peroxidase, laccase, xylanase, endoglucanase and β-glucosidase in spent mushroom substrate. Further, the enzyme cocktails were concentrated for the hydrolysis of POME. Central composite design of response surface methodology was performed to examine the effects of enzyme loading, incubation time and pH on the reducing sugar yield. Productivities of the enzymes for xylanase, laccase, endoglucanase, lignin peroxidase and β-glucosidase were 2.3, 4.1, 14.6, 214.1, and 915.4 U g, respectively. A maximum of 3.75 g/l of reducing sugar was obtained under optimized conditions of 15 h incubation time with 10% enzyme loading (v/v) at a pH of 4.8, which was consistent with the predicted reducing sugar concentration (3.76 g/l). The biohydrogen cumulative volume (302.78 ml H.L POME) and 83.52% biohydrogen gas were recorded using batch fermentation which indicated that the enzymes of spent mushroom substrate can be utilized for hydrolysis of POME.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9705832PMC
http://dx.doi.org/10.4014/jmb.2103.03020DOI Listing

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