Nonsterile l -Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
Author(s) -
Ming Lei,
Xiwei Peng,
Wenjun Sun,
Di Zhang,
Zhenyu Wang,
Zhengjiao Yang,
Chong Zhang,
Bin Yu,
Huanqing Niu,
Hanjie Ying,
Pingkai Ouyang,
Dong Liu,
Yong Chen
Publication year - 2021
Publication title -
acs omega
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.779
H-Index - 40
ISSN - 2470-1343
DOI - 10.1021/acsomega.1c00226
Subject(s) - corynebacterium glutamicum , fermentation , lysine , biochemistry , strain (injury) , amino acid , bacteria , chemistry , food science , biology , gene , genetics , anatomy
Fermentation using Corynebacterium glutamicum is an important method for the industrial production of amino acids. However, conventional fermentation processes using C. glutamicum are susceptible to microbial contamination and therefore require equipment sterilization or antibiotic dosing. To establish a more robust fermentation process, l-lysine-producing C. glutamicum was engineered to efficiently utilize xenobiotic phosphite (Pt) by optimizing the expression of Pt dehydrogenase in the exeR genome locus. This ability provided C. glutamicum with a competitive advantage over common contaminating microbes when grown on media containing Pt as a phosphorus source instead of phosphate. As a result, the engineered strain could produce 41.00 g/L l-lysine under nonsterile conditions during batch fermentation for 60 h, whereas the original strain required 72 h to produce 40.78 g/L l-lysine under sterile conditions. Therefore, the recombinant strain can efficiently produce l-lysine under nonsterilized conditions with unaffected production efficiency. Although this anticontamination strategy has been previously reported for other species, this is the first time it has been demonstrated in C. glutamicum ; these findings should aid in the further development of cost-efficient amino acid fermentation processes.
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