4.5 Article

Direct cellobiose production from cellulose using sextuple beta-glucosidase gene deletion Neurospora crassa mutants

Journal

ENZYME AND MICROBIAL TECHNOLOGY
Volume 52, Issue 3, Pages 184-189

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.enzmictec.2012.12.010

Keywords

Neurospora crassa; Beta-glucosidase; Cellulase; Cellobiose

Funding

  1. Agriculture and Food Research Initiative from the USDA National Institute of Food and Agriculture [2011-67009-20060]
  2. California Energy Commission [55779A/08-03]
  3. NIFA [2011-67009-20060, 579889] Funding Source: Federal RePORTER

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Direct cellobiose production from cellulose by a genetically modified fungus-Neurospora crassa, was explored in this study. A library of N. crassa sextuple beta-glucosidase (bgl) gene deletion strains was constructed. Various concentrations of cellobiose were detected in the culture broth of the N. crassa sextuple beta-glucosidase (bgl) gene deletion strains when grown on Avicel without exogenous cellulase addition. The sextuple bgl deletion strains expressing one of the three basally transcribed bgl genes are the best cellobiose producers. For most sextuple strains, the multiple bgl gene deletion has no negative effect on the production of other cellulases. The induction of major endoglucanases and exoglucanases on Avicel in most of the sextuple bgl deletions strains was as fast as or faster than that of the wild type, except for strain F4. The best cellobiose producing strain, F5, produced 7.7 g/L of cellobiose from 20 g/L of Avicel in four days and utilized the Avicel as fast as did the wild type (even in the presence of high cellobiose concentration). The cellobiose yield from cellulose was about 48.3%. (c) 2013 Elsevier Inc. All rights reserved.

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