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Recombinant multi-functional cellulase activity in submerged fermentation of lignocellulosic wastes

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  • Yang, Peizhou
  • Guo, Liqiong
  • Cheng, Shujie
  • Lou, Nannan
  • Lin, Junfang

Abstract

The expression of the multi-functional cellulase gene mfc in Coprinopsis cinerea is modulated using glyceraldehyde-3-phosphate dehydrogenase (gpd) promoter fragments from Agaricus bisporus, Flammulina velutipes, and Lentinula edodes. In submerged fermentation, with banana peels as the growth substrate, highest activities of endo-β-1,4-glucanase (0.48 U/ml), total cellulase (0.26 U/ml) and endo-β-1,4-xylanase (38.10 U/ml) were noted in the culture liquid Cabm44, which uses a 275 bp gpd fragment from A. bisporus. The lignocellulolytic enzymatic activities were increased nearly twofold in comparison with the wild-type strain.

Suggested Citation

  • Yang, Peizhou & Guo, Liqiong & Cheng, Shujie & Lou, Nannan & Lin, Junfang, 2011. "Recombinant multi-functional cellulase activity in submerged fermentation of lignocellulosic wastes," Renewable Energy, Elsevier, vol. 36(12), pages 3268-3272.
    • Handle: RePEc:eee:renene:v:36:y:2011:i:12:p:3268-3272
    DOI: 10.1016/j.renene.2011.04.019
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    References listed on IDEAS

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    1. Kosugi, Akihiko & Kondo, Akihiko & Ueda, Mitsuyoshi & Murata, Yoshinori & Vaithanomsat, Pilanee & Thanapase, Warunee & Arai, Takamitsu & Mori, Yutaka, 2009. "Production of ethanol from cassava pulp via fermentation with a surface-engineered yeast strain displaying glucoamylase," Renewable Energy, Elsevier, vol. 34(5), pages 1354-1358.
    2. Ge, Leilei & Wang, Peng & Mou, Haijin, 2011. "Study on saccharification techniques of seaweed wastes for the transformation of ethanol," Renewable Energy, Elsevier, vol. 36(1), pages 84-89.
    3. Sukumaran, Rajeev K. & Singhania, Reeta Rani & Mathew, Gincy Marina & Pandey, Ashok, 2009. "Cellulase production using biomass feed stock and its application in lignocellulose saccharification for bio-ethanol production," Renewable Energy, Elsevier, vol. 34(2), pages 421-424.
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