Multifaceted characterization of cell wall decomposition products formed during ammonia fiber expansion (AFEX) and dilute acid based pretreatments

被引:209
作者
Chundawat, Shishir P. S. [1 ,5 ]
Vismeh, Ramin [2 ]
Sharma, Lekh N. [4 ]
Humpula, James F. [1 ,5 ]
Sousa, Leonardo da Costa [1 ]
Chambliss, C. Kevin [4 ]
Jones, A. Daniel [2 ,3 ]
Balan, Venkatesh [1 ,5 ]
Dale, Bruce E. [1 ,5 ]
机构
[1] Michigan State Univ, Biomass Convers Res Lab, Lansing, MI 48910 USA
[2] Michigan State Univ, Dept Chem, E Lansing, MI 48824 USA
[3] Michigan State Univ, Dept Biochem & Mol Biol, E Lansing, MI 48824 USA
[4] Baylor Univ, Dept Chem & Biochem, Waco, TX 76798 USA
[5] Michigan State Univ, DOE Great Lakes Bioenergy Res Ctr GLBRC, E Lansing, MI 48824 USA
基金
美国食品与农业研究所;
关键词
AFEX; Ammonolysis; Degradation products; Lignocellulosic corn stover; Dilute-acid pretreatment; DEGRADATION-PRODUCTS; CORN STOVER; SACCHAROMYCES-CEREVISIAE; ENZYMATIC-HYDROLYSIS; IDENTIFICATION; FERMENTATION; INHIBITION; CONVERSION; BIOMASS; YEAST;
D O I
10.1016/j.biortech.2010.06.027
中图分类号
S2 [农业工程];
学科分类号
0828 ;
摘要
Decomposition products formed/released during ammonia fiber expansion (AFEX) and dilute acid (DA) pretreatment of corn stover (CS) were quantified using robust mass spectrometry based analytical platforms. Ammonolytic cleavage of cell wall ester linkages during AFEX resulted in the formation of acetamide (25 mg/g AFEX CS) and various phenolic amides (15 mg/g AFEX CS) that are effective nutrients for downstream fermentation. After ammonolysis, Maillard reactions with carbonyl-containing intermediates represent the second largest sink for ammonia during AFEX. On the other hand, several carboxylic acids were formed (e.g. 35 mg acetic acid/g DA CS) during DA pretreatment. Formation of furans was 36-fold lower for AFEX compared to DA treatment; while carboxylic acids (e.g. lactic and succinic acids) yield was 100-1000-fold lower during AFEX compared to previous reports using sodium hydroxide as pretreatment reagent. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:8429 / 8438
页数:10
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