Productivity enhancement in L-lysine fermentation using oxygen-enhanced bioreactor and oxygen vector

Introduction: L-lysine is a bulk product. In industrial production using high-biomass fermentation, the high density of bacteria and the intensity of production require sufficient cellular respiratory metabolism for support. Conventional bioreactors often have difficulty meeting the oxygen supply co...

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Bibliographic Details
Main Authors: Sun, P. (Author), Wang, J. (Author), Wang, S. (Author), Xu, Q. (Author), Zhang, Z. (Author), Zhao, S. (Author)
Format: Article
Language:English
Published: Frontiers Media S.A. 2023
Subjects:
Online Access:View Fulltext in Publisher
LEADER 04270nam a2200457Ia 4500
001 10.3389-fbioe.2023.1181963
008 230526s2023 CNT 000 0 und d
020 |a 22964185 (ISSN) 
245 1 0 |a Productivity enhancement in L-lysine fermentation using oxygen-enhanced bioreactor and oxygen vector 
260 0 |b Frontiers Media S.A.  |c 2023 
856 |z View Fulltext in Publisher  |u https://doi.org/10.3389/fbioe.2023.1181963 
520 3 |a Introduction: L-lysine is a bulk product. In industrial production using high-biomass fermentation, the high density of bacteria and the intensity of production require sufficient cellular respiratory metabolism for support. Conventional bioreactors often have difficulty meeting the oxygen supply conditions for this fermentation process, which is not conducive to improving the sugar-amino acid conversion rate. In this study, we designed and developed an oxygen-enhanced bioreactor to address this problem. Methods: This bioreactor optimizes the aeration mix using an internal liquid flow guide and multiple propellers. Results: Compared with a conventional bioreactor, it improved the kLa from 367.57 to 875.64 h-1, an increase of 238.22%. The results show that the oxygen supply capacity of the oxygen-enhanced bioreactor is better than that of the conventional bioreactor. Its oxygenating effect increased the dissolved oxygen in the middle and late stages of fermentation by an average of 20%. The increased viability of Corynebacterium glutamicum LS260 in the mid to late stages of growth resulted in a yield of 185.3 g/L of L-lysine, 74.57% conversion of lysine from glucose, and productivity of 2.57 g/L/h, an increase of 11.0%, 6.01%, and 8.2%, respectively, over a conventional bioreactor. Oxygen vectors can further improve the production performance of lysine strains by increasing the oxygen uptake capacity of microorganisms. We compared the effects of different oxygen vectors on the production of L-lysine from LS260 fermentation and concluded that n-dodecane was the most suitable. Bacterial growth was smoother under these conditions, with a 2.78% increase in bacterial volume, a 6.53% increase in lysine production, and a 5.83% increase in conversion. The different addition times of the oxygen vectors also affected the final yield and conversion, with the addition of oxygen vectors at 0 h, 8 h, 16 h, and 24 h of fermentation increasing the yield by 6.31%, 12.44%, 9.93%, and 7.39%, respectively, compared to fermentation without the addition of oxygen vectors. The conversion rates increased by 5.83%, 8.73%, 7.13%, and 6.13%, respectively. The best results were achieved by adding oxygen vehicles at the 8th hour of fermentation, with a lysine yield of 208.36 g/L and a conversion rate of 83.3%. In addition, n-dodecane significantly reduced the amount of foam produced during fermentation, which is beneficial for fermentation control and equipment. Conclusion: The new oxygen-enhanced bioreactor improves oxygen transfer efficiency, and oxygen vectors enhance the ability of cells to take up oxygen, which effectively solves the problem of insufficient oxygen supply during lysine fermentation. This study provides a new bioreactor and production solution for lysine fermentation. Copyright © 2023 Wang, Wang, Zhao, Sun, Zhang and Xu. 
650 0 4 |a Amino acids 
650 0 4 |a Bacteria 
650 0 4 |a Bioconversion 
650 0 4 |a Bioreactors 
650 0 4 |a Conversion rates 
650 0 4 |a Dissolved oxygen 
650 0 4 |a Fermentation 
650 0 4 |a fermentation engineering 
650 0 4 |a Fermentation engineering 
650 0 4 |a Late stage 
650 0 4 |a L-lysine 
650 0 4 |a Lysine fermentation 
650 0 4 |a metabolic flux 
650 0 4 |a Metabolic flux 
650 0 4 |a N -dodecane 
650 0 4 |a Oxygen supply 
650 0 4 |a Oxygen vector 
650 0 4 |a oxygen vectors 
650 0 4 |a oxygen-enhanced bioreactor 
650 0 4 |a Oxygen-enhanced bioreactor 
650 0 4 |a Productivity enhancement 
650 0 4 |a Vectors 
700 1 0 |a Sun, P.  |e author 
700 1 0 |a Wang, J.  |e author 
700 1 0 |a Wang, S.  |e author 
700 1 0 |a Xu, Q.  |e author 
700 1 0 |a Zhang, Z.  |e author 
700 1 0 |a Zhao, S.  |e author 
773 |t Frontiers in Bioengineering and Biotechnology  |x 22964185 (ISSN)  |g 11