Pilot scale fed-batch fermentation in a closed loop mixed reactor for the biotransformation of crude glycerol into ethanol and hydrogen by Escherichia coli MG1655

2016 ◽  
Vol 91 ◽  
pp. 37-47 ◽  
Author(s):  
O. Cofré ◽  
M. Ramírez ◽  
J.M. Gómez ◽  
D. Cantero
2019 ◽  
Vol 12 (1) ◽  
Author(s):  
Yao-De Wang ◽  
Jin-Yi Liao ◽  
Chung-Jen Chiang ◽  
Yun-Peng Chao

Abstract Background Fed-batch fermentation has been conventionally implemented for the production of lactic acid with a high titer and high productivity. However, its operation needs a complicated control which increases the production cost. Results This issue was addressed by simplifying the production scheme. Escherichia coli was manipulated for its glycerol dissimilation and d-lactate synthesis pathways and then subjected to adaptive evolution under high crude glycerol. Batch fermentation in the two-stage mode was performed by controlling the dissolved oxygen (DO), and the evolved strain deprived of poxB enabled production of 100 g/L d-lactate with productivity of 1.85 g/L/h. To increase productivity, the producer strain was further evolved to improve its growth rate on crude glycerol. The fermentation was performed to undergo the aerobic growth with low substrate, followed by the anaerobic production with high substrate. Moreover, the intracellular redox of the strain was balanced by fulfillment of the anaerobic respiratory chain with nitrate reduction. Without controlling the DO, the microbial fermentation resulted in the homofermentative production of d-lactate (ca. 0.97 g/g) with a titer of 115 g/L and productivity of 3.29 g/L/h. Conclusions The proposed fermentation strategy achieves the highest yield based on crude glycerol and a comparable titer and productivity as compared to the approach by fed-batch fermentation. It holds a promise to sustain the continued development of the crude glycerol-based biorefinery.


2014 ◽  
Vol 989-994 ◽  
pp. 997-1002 ◽  
Author(s):  
Jian Wang ◽  
Jia Kai Sun ◽  
Qing Yang Xu

Metabolic engineering ofCorynebacterium glutamicumhas sought to divert carbon into L-isoleucine. However, the fermentation period of this strain is long. TheC.glutamicumYILW strain (LeuL, AHVr, SGr, Leu-MEr) was previously derived by repeated compound mutagenesis which could accumulate 20.2 g/L L-isoleucine in a 5-L jar fermentor. Overexpression of the threonine dehydratase gene (ilvA) fromCorynebacterium glutamicumYILW and coexpression of threonine dehydratase and acetolactate synthase (ilvBN) from it were employed to divert carbon flux toward L-isoleucine. The strainE. coliTRFC with the expression ofilvA could accumulate L-isoleucine of 6.8 g/L without accumulation of any L-threonine by fed-batch fermentation in a 5-L jar fermentor. However, the production of L-isoleucine by the strainE.coliTRFC with the co-expression ofilvA andilvBN was decreased by 19.1%, and the production of L-valine was increased by 40% compared with that ofE. coliTRFC with the expression ofilvA.


2004 ◽  
Vol 26 (19) ◽  
pp. 1533-1539 ◽  
Author(s):  
Heléne Sundström ◽  
Fredrik Wållberg ◽  
Erika Ledung ◽  
Bo Norrman ◽  
Christopher J. Hewitt ◽  
...  

2018 ◽  
Vol 41 (10) ◽  
pp. 1509-1518 ◽  
Author(s):  
Yuewen Su ◽  
Qun-qun Guo ◽  
Sen Wang ◽  
Xin Zhang ◽  
Jian Wang

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