详细信息
Tolerance and transcriptional analysis of Corynebacterium glutamicum on biotransformation of toxic furaldehyde and benzaldehyde inhibitory compounds ( SCI-EXPANDED收录 EI收录)
文献类型:期刊文献
英文题名:Tolerance and transcriptional analysis of Corynebacterium glutamicum on biotransformation of toxic furaldehyde and benzaldehyde inhibitory compounds
作者:Zhou, Pingping[1];Khushk, Imrana[1];Gao, Qiuqiang[1];Bao, Jie[1]
机构:[1]East China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
年份:2019
卷号:46
期号:7
起止页码:951
外文期刊名:JOURNAL OF INDUSTRIAL MICROBIOLOGY & BIOTECHNOLOGY
收录:;EI(收录号:20242616368981);WOS:【SCI-EXPANDED(收录号:WOS:000474432800006)】;
基金:This research was supported by the National Natural Science Foundation of China (31961133006/31300070) and the National Key Research and Development Program of China (2017YFB0309302).
语种:英文
外文关键词:Corynebacterium glutamicum S9114; Furaldehydes; Benzaldehydes; Biotransformation; Transcriptional response
摘要:Furaldehydes and benzaldehydes are among the most toxic inhibitors from lignocellulose pretreatment on microbial growth and metabolism. The bioconversion of aldehyde inhibitors into less toxic alcohols or acids (biotransformation) is the prerequisite condition for efficient biorefinery fermentations. This study found that Corynebacterium glutamicum S9114 demonstrated excellent tolerance and biotransformation capacity to five typical aldehyde inhibitors including two furaldehydes: 2-furaldehyde (furfural), 5-(hydroxymethyl)-2-furaldehyde, and three benzaldehydes: 4-hydroxybenzaldehyde, 4-hydroxy-3-methoxybenzaldehyde (vanillin), and 4-hydroxy-3,5-dimethoxybenzaldehyde (syringaldehyde). Transcription levels of 93 genes hypothesized to be responsible for five aldehydes biotransformation were examined by qRT-PCR. Multiple genes showed significantly up-regulated expression against furaldehydes or benzaldehydes. Overexpression of CGS9114_RS01115 in C. glutamicum resulted in the increased conversion of all five aldehyde inhibitors. The significant oxidoreductase genes responsible for each or multiple inhibitors biotransformation identified in this study will serve as a component of key gene device library for robust biorefinery fermentation strains development in the future biorefinery applications.
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