Metabolic engineering of Corynebacterium glutamicum for efficient production of succinate from lignocellulosic hydrolysate

被引:47
作者
Mao, Yufeng [1 ]
Li, Guiying [1 ]
Chang, Zhishuai [1 ]
Tao, Ran [1 ]
Cui, Zhenzhen [1 ]
Wang, Zhiwen [1 ]
Tang, Ya-jie [2 ]
Chen, Tao [1 ]
Zhao, Xueming [1 ]
机构
[1] Tianjin Univ, Sch Chem Engn & Technol, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Key Lab Syst Bioengn,Minist Educ,SynBio Res Platf, Tianjin 300072, Peoples R China
[2] Hubei Univ Technol, Key Lab Fermentat Engn, Minist Educ, Wuhan 430068, Hubei, Peoples R China
来源
BIOTECHNOLOGY FOR BIOFUELS | 2018年 / 11卷
基金
中国国家自然科学基金;
关键词
Corynebacterium glutamicum; Succinate; Xylose; Lignocellulosic hydrolysate; RECOMBINANT SACCHAROMYCES-CEREVISIAE; PENTOSE-PHOSPHATE PATHWAY; ACID PRODUCTION; ACTINOBACILLUS-SUCCINOGENES; XYLOSE UTILIZATION; ESCHERICHIA-COLI; CORN STALK; ETHANOL-PRODUCTION; SUGARCANE BAGASSE; BACILLUS-SUBTILIS;
D O I
10.1186/s13068-018-1094-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Succinate has been recognized as one of the most important bio-based building block chemicals due to its numerous potential applications. However, efficient methods for the production of succinate from lignocellulosic feedstock were rarely reported. Nevertheless, Corynebacterium glutamicum was engineered to efficiently produce succinate from glucose in our previous study. Results: In this work, C. glutamicum was engineered for efficient succinate production from lignocellulosic hydrolysate. First, xylose utilization of C. glutamicum was optimized by heterologous expression of xylA and xylB genes from different sources. Next, xylA and xylB from Xanthomonas campestris were selected among four candidates to accelerate xylose consumption and cell growth. Subsequently, the optimal xylA and xylB were co-expressed in C. glutamicum strain SAZ3 (Delta ldhA Delta pta Delta pqo Delta catP(sod)-ppcP(sod)-pyc) along with genes encoding pyruvate carboxylase, citrate synthase, and a succinate exporter to achieve succinate production from xylose in a two-stage fermentation process. Xylose utilization and succinate production were further improved by overexpressing the endogenous tkt and tal genes and introducing araE from Bacillus subtilis. The final strain C. glutamicum CGS5 showed an excellent ability to produce succinate in two-stage fermentations by co-utilizing a glucose-xylose mixture under anaerobic conditions. A succinate titer of 98.6 g L-1 was produced from corn stalk hydrolysate with a yield of 0.87 g/g total substrates and a productivity of 4.29 g L-1 h(-1) during the anaerobic stage. Conclusion: This work introduces an efficient process for the bioconversion of biomass into succinate using a thoroughly engineered strain of C. glutamicum. To the best of our knowledge, this is the highest titer of succinate produced from non-food lignocellulosic feedstock, which highlights that the biosafety level 1 microorganism C. glutamicum is a promising platform for the envisioned lignocellulosic biorefinery.
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页数:17
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