4.8 Article

Sequential saccharification of corn fiber and ethanol production by the brown rot fungus Gloeophyllum trabeum

期刊

BIORESOURCE TECHNOLOGY
卷 101, 期 10, 页码 3526-3533

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.biortech.2009.12.115

关键词

Ethanol; Corn fiber; Lignocellulosic biomass; Fungus; Saccharification

资金

  1. Iowa Energy Center (IEC), Ames, IA [0404]
  2. Cooperative State Research, Education, and Extension Service, US Department of Agriculture [2004-34188-15067]

向作者/读者索取更多资源

Degradation of lignocellulosic biomass to sugars through a purely biological process is a key to sustainable biofuel production. Hydrolysis of the corn wet-milling co-product-corn fiber-to simple sugars by the brown rot fungus Gloeophyllum trabeum was studied in suspended-culture and solid-state fermentations. Suspended-culture experiments were not effective in producing harvestable sugars from the corn fiber. The fungus consumed sugars released by fungal extracellular enzymes. Solid-state fermentation demonstrated up to 40% fiber degradation within 9 days. Enzyme activity assays on solid-state fermentation filtrates confirmed the involvement of starch- and cellulose-degrading enzymes. To reduce fungal consumption of sugars and to accelerate enzyme activity, 2- and 3-d solid-state fermentation biomasses (fiber and fungus) were submerged in buffer and incubated at 37 degrees C without shaking. This anaerobic incubation converted up to almost 11% of the corn fiber into harvestable reducing sugars. Sugars released by G. trabeum were fermented to a maximum yield of 3.3 g ethanol/100 g fiber. This is the first report, to our knowledge, of G, trabeum fermenting sugar to ethanol. The addition of Saccharomyces cerevisiae as a coculture led to more rapid fermentation to a maximum yield of 4.0 g ethanol/100 g fiber. The findings demonstrate the potential for this simple fungal process, requiring no pretreatment of the corn fiber, to produce more ethanol by hydrolyzing and fermenting carbohydrates in this lignocellulosic co-product. (c) 2010 Elsevier Ltd. All rights reserved.

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