Engineering Gluconbacter oxydans with efficient co-utilization of glucose and sorbitol for one-step biosynthesis of 2-keto-L-gulonic

被引:0
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作者
Li G. [1 ,2 ,3 ,4 ]
Wang X. [1 ,2 ,3 ,4 ]
Zeng W. [1 ,2 ]
Qin Z. [1 ,2 ]
Li J. [1 ,2 ]
Chen J. [1 ,2 ]
Zhou J. [1 ,2 ,3 ,4 ]
机构
[1] Engineering Research Center of Ministry of Education on Food Synthetic Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, 214122, Jiangsu
[2] Science Center for Future Foods, Jiangnan University, Wuxi
[3] Key Laboratory of Industrial Biotechnology, Ministry of Education and School of Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, 214122, Jiangsu
[4] Jiangsu Province Engineering Research Center of Food Synthetic Biotechnology, Jiangnan University, 1800 Lihu Road, Wuxi, 214122, Jiangsu
关键词
2,5-diketo-D-glucose; 2-KLG; 4-keto-D-arabate synthase; Browning; Promoter; Vitamin C;
D O I
10.1016/j.biortech.2024.131098
中图分类号
学科分类号
摘要
As the highest-demand vitamin, the development of a one-step vitamin C synthesis process has been slow for a long time. In previous research, a Gluconobacter oxydans strain (GKLG9) was constructed that can directly synthesize 2-keto-L-gulonic acid (2-KLG) from glucose, but carbon source utilization remained low. Therefore, this study first identified the gene 4kas (4-keto-D-arabate synthase) to reduce the loss of extracellular carbon and inhibit the browning of fermentation broth. Then, promoter engineering was conducted to enhance the intracellular glucose transport pathway and concentrate intracellular glucose metabolism on the pentose phosphate pathway to provide more reducing power. Finally, by introducing the D-sorbitol pathway, the titer of 2-KLG was increased to 38.6 g/L within 60 h in a 5-L bioreactor, with a glucose-to-2-KLG conversion rate of about 46 %. This study is an important step in the development of single-bacterial one-step fermentation to produce 2-KLG. © 2024 Elsevier Ltd
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