4.4 Article

Production of Cellulase from Kraft Paper Mill Sludge by Trichoderma Reesei Rut C-30

Journal

APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
Volume 161, Issue 1-8, Pages 382-394

Publisher

HUMANA PRESS INC
DOI: 10.1007/s12010-009-8863-x

Keywords

Cellulase production; Lignocellulosic substrates; Paper mill sludge; Ethanol production

Funding

  1. Masada Oxynol
  2. LLC
  3. Alabama Center for Pulp and Bioresource Engineering, Laboratory of Biofuels and Biomaterials
  4. Auburn University

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Paper mill sludge is a solid waste material generated from pulping and papermaking operations. Because of high glucan content and its well-dispersed structure, paper mill sludges are well suited for bioconversion into value-added products. It also has high ash content originated from inorganic additives used in papermaking, which causes hindrance to bioconversion. In this study, paper mill sludges from Kraft process were de-ashed by a centrifugal cleaner and successive treatment by sulfuric acid and sodium hydroxide, and used as a substrate for cellulase production. The treated sludge was the only carbon source for cellulase production, and predominantly inorganic nutrients were used as the nitrogen source for this bioprocess. The cellulase enzyme produced from the de-ashed sludge exhibited cellulase activity of 8 filter paper unit (FPU)/mL, close to that obtainable from pure cellulosic substrates. The yield of cellulase enzyme was 307 FPU/g glucan of de-ashed sludge. Specific activity was 8.0 FPU/mg protein. In activity tests conducted against the corn stover and alpha-cellulose, the xylanse activity was found to be higher than that of a commercial cellulase. Relatively high xylan content in the sludge appears to have induced high xylanase production. Simultaneous saccharification and fermentation (SSF) was performed using partially de-ashed sludge as the feedstock for ethanol production using Sacharomyces cerevisiae and the cellulase produced in-house from the sludge. With 6% (w/v) glucan feed, ethanol yield of 72% of theoretical maximum and 24.4 g/L ethanol concentration were achieved. These results were identical to those of the SSF using commercial cellulases.

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