Optimization of Cellulase Production by Aspergillus niger ITV 02 from Sweet Sorghum Bagasse in Submerged Culture Using a Box-Behnken Design

被引:21
作者
Infanzon-Rodriguez, M. I. [1 ]
Ragazzo-Sanchez, J. A. [1 ]
del Moral, S. [2 ]
Calderon-Santoyo, M. [1 ]
Gutierrez-Rivera, B. [3 ]
Aguilar-Uscanga, M. G. [2 ]
机构
[1] Inst Tecnol Tepic, Tecnol Nacl Mexico, Integral Food Res Lab, Tepic 63175, Nayarit, Mexico
[2] Inst Tecnol Veracruz, Tecnol Nacl Mexico, Czda MA de Quevedo 2779, Veracruz 91860, Veracruz, Mexico
[3] Inst Tecnol Super Tierra Blanca, Tecnol Nacl Mexico, Ave Veracruz S-N Col PEMEX, Tierra Blanca 95180, Veracruz, Mexico
关键词
Aspergillus niger; Cellulase; Nitrogen; Carbon source; Sweet sorghum bagasse; PURIFICATION; POLYSACCHARIDES; HYDROLYSIS; DIVERSITY; XYLANASE;
D O I
10.1007/s12355-019-00765-2
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
The objective of this study was to evaluate the effects of nitrogen and carbon source on cellulase activity of Aspergillus niger ITV 02. The results obtained showed that nitrogen had an influence on the increase in cellulase activity by A. niger ITV 02 during submerged fermentation. Optimal concentrations obtained from nitrogen sources, using a Box-Behnken design were 0.9 g/L urea, 2.4 g/L ammonium sulfate and 1.5 g/L yeast extract, obtaining endoglucanase and beta-glucosidase specific activities of 24.63 U/mg and 72.66 U/mg, respectively, at 50 h of fermentation. Subsequently, the effect of three carbon sources was evaluated: carboxymethylcellulose, delignified sweet sorghum bagasse (DSSB) and sweet sorghum bagasse cellulose (SSBC). Maximum cellulase specific activity was obtained when using DSSB, increasing endoglucanase activity fivefold and beta-glucosidase activity 1.25-fold (126.72 and 85 U/mg) respectively. SSBC hydrolysis using enzymatic extract produced 18 g/L reducing sugars, equivalent to a 25% residue conversion. These results showed that it is possible to obtain an extract with cellulase activity from A. niger ITV 02 to be used in SSBC hydrolysis using low-cost substrates such as DSSB, which would contribute to a reduction in second-generation ethanol process production costs and an increase in the availability of enzymes for this use.
引用
收藏
页码:266 / 273
页数:8
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