详细信息

Analysis of biodegradation performance of furfural and 5-hydroxymethylfurfural by Amorphotheca resinae ZN1  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Analysis of biodegradation performance of furfural and 5-hydroxymethylfurfural by Amorphotheca resinae ZN1

作者:Ran, Hong[1];Zhang, Jian[1];Gao, Qiuqiang[1];Lin, Zhanglin[2];Bao, Jie[1]

机构:[1]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China;[2]Tsinghua Univ, Dept Chem Engn, Beijing 100084, Peoples R China

年份:2014

卷号:7

期号:1

外文期刊名:BIOTECHNOLOGY FOR BIOFUELS

收录:;EI(收录号:20141617593613);WOS:【SCI-EXPANDED(收录号:WOS:000334634200001)】;

基金:This research was supported by the National Basic Research Program of China (2013CB733902/2011CB707406), the Natural Science Foundation of China (21306048/31300070), the National High-Tech Program of China (2012AA022301/2014AA021901), and the Fundamental Research Funds for the Central Universities of China (WF1214025/1314036).

语种:英文

外文关键词:Biodegradation; furfural; 5-hydroxymethylfurfural; Amorphotheca resinae ZN1; lignocellulose; pretreatment; oxygen supply; substrate priority

摘要:Background: Furfural and 5-hydroxymethylfurfural (HMF) are the degradation products of lignocellulose during pretreatment operations and significantly inhibit the consequent enzymatic hydrolysis and fermentation processes. The biodetoxification fungus Amorphotheca resinae ZN1 had demonstrated its excellent capacity on degrading lignocellulose derived inhibitors and helped the fermentation processes to achieve high yield of ethanol and biochemicals. Analysis of the biological degradation performance of furfural and HMF by A. resinae ZN1 will provide essential information for their fast and complete removal from the pretreated lignocellulose materials and facilitate the consequent ethanol fermentation. Results: The degradation performance of furfural and HMF by A. resinae ZN1 was investigated by capturing intermediate metabolic products at various culture conditions. A. resinae ZN1 converts furfural/HMF into furfuryl/HMF alcohols and furoic/HMF acids simultaneously at aerobic condition, and only the corresponding furfuryl/HMF alcohols are obtained at anaerobic condition. The existence of glucose accelerates the degradation rate of furfural and HMF by A. resinae ZN1 and the cell mass growth rate aerobically. Remarkably, glucose is not consumed before furfural or HMF is degraded to a low threshold concentration. The finding suggests that furfural or HMF has a substrate priority of utilization by A. resinae ZN1 than glucose. This property may help the detoxification of furfural and HMF to be operated without consuming glucose. Conclusions: The biological degradation performance of furfural and HMF by A. resinae ZN1 was investigated experimentally. Oxygen supply is important on the complete biodegradation of furfural and HMF by A. resinae ZN1. Furfural or HMF has the priority of substrate utilization than glucose by A. resinae ZN1. This study provided important information for detoxification enhancement and strain modification.

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