Viscosity reduction of cassava for very high gravity ethanol fermentation using cell wall degrading enzymes from Aspergillus aculeatus

被引:34
作者
Poonsrisawat, Aphisit [1 ]
Wanlapatit, Sittichoke [2 ]
Paemanee, Atchara [3 ]
Eurwilaichitr, Lily [1 ]
Piyachomkwan, Kuakoon [2 ]
Champreda, Verawat [1 ]
机构
[1] Natl Ctr Genet Engn & Biotechnol, Enzyme Technol Lab, Klongluang 12120, Pathum Thani, Thailand
[2] Kasetsart Univ, Natl Ctr Genet Engn & Biotechnol, Cassava & Starch Technol Res Unit, Bangkok 10900, Thailand
[3] Natl Ctr Genet Engn & Biotechnol, Genome Inst, Klongluang 12120, Pathum Thani, Thailand
关键词
Aspergillus aculeatus; Bioethanol; Cell wall degrading enzyme; Very high gravity fermentation; Viscosity; FUEL ALCOHOL; SACCHAROMYCES-CEREVISIAE; SWEET-POTATO; SACCHARIFICATION; STARCH; GRAIN; BIOLOGY;
D O I
10.1016/j.procbio.2014.07.016
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cassava is an important feedstock for bioethanol production; however, its use in very high gravity (VHG) fermentation is limited by the high viscosity of mash due to the presence of plant cell wall derived polysaccharides. In this study, viscosity reduction of cassava root mash, chips, and pulp was achieved using a mixture of cell wall degrading enzymes prepared from solid state fermentation of Aspergillus aculeatus BCC17849. Proteomic analysis showed the mixture contained endo- and exo-acting cellulases, hemicellulases, and pectinases from various glycosyl hydrolase families. Enzymatic pretreatment of cassava substrates with the enzyme mixture containing endoglucanase, FPase, xylanase, polygalacturonase, beta-glucanase, and mannanase activities at 45 degrees C, pH 5.0 for 2 h reduced viscosity to the operating level of <500 mPa s, equivalent to the final viscosity of 3.0-51.3% of the initial levels. Simultaneous saccharification and fermentation of the pretreated root mash (32% initial solid) by Saccharomyces cerevisiae with a conventional high-temperature liquefaction process and an uncooked process using a raw starch degrading amylase at 32 degrees C for 96 h led to a final ethanol concentration of 19.65 and 17.54% (v/v), respectively. The results demonstrated potential of the enzyme for improving process efficiency and economics in VHG bioethanol production. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1950 / 1957
页数:8
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