4.5 Article

Fungal secretomes enhance sugar beet pulp hydrolysis

期刊

BIOTECHNOLOGY JOURNAL
卷 9, 期 4, 页码 483-492

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/biot.201300214

关键词

Cellulases; Hemicellulases; Neurospora crassa; Sclerotium rolfsii; Trametes multicolor

资金

  1. doctoral program BioTop - Biomolecular Technology of Proteins of the Austrian Science Fund FWF [FWF W1224]
  2. European Commission [BIOENERGY FP7-PEOPLE-2013-ITN-607793]
  3. Austrian Agency for International Mobility, OEAD (bilateral scientific project Austria-Croatia) [13-2010]
  4. Ministry of Science, Education and Sport Republic of Croatia [058-0581990-1997, 058-0581990-2004]

向作者/读者索取更多资源

The recalcitrance of lignocellulose makes enzymatic hydrolysis of plant biomass for the production of second generation biofuels a major challenge. This work investigates an efficient and economic approach for the enzymatic hydrolysis of sugar beet pulp (SBP), which is a difficult to degrade, hemicellulose-rich by-product of the table sugar industry. Three fungal strains were grown on different substrates and the production of various extracellular hydrolytic and oxidative enzymes involved in pectin, hemicellulose, and cellulose breakdown were monitored. In a second step, the ability of the culture supernatants to hydrolyze thermally pretreated SBP was tested in batch experiments. The supernatant of Sclerotium rolfsii, a soil-borne facultative plant pathogen, was found to have the highest hydrolytic activity on SBP and was selected for further hydrolyzation experiments. A low enzyme load of 0.2 mg g(-1) protein from the culture supernatant was sufficient to hydrolyze a large fraction of the pectin and hemicelluloses present in SBP. The addition of Trichoderma reesei cellulase (1-17.5 mg g(-1) SBP) resulted in almost complete hydrolyzation of cellulose. It was found that the combination of pectinolytic, hemicellulolytic, and cellulolytic activities works synergistically on the complex SBP composite, and a combination of these hydrolytic enzymes is required to achieve a high degree of enzymatic SBP hydrolysis with a low enzyme load.

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