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Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum

[Image: see text] 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...

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Autores principales: Lei, Ming, Peng, Xiwei, Sun, Wenjun, Zhang, Di, Wang, Zhenyu, Yang, Zhengjiao, Zhang, Chong, Yu, Bin, Niu, Huanqing, Ying, Hanjie, Ouyang, Pingkai, Liu, Dong, Chen, Yong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153679/
https://www.ncbi.nlm.nih.gov/pubmed/34056170
http://dx.doi.org/10.1021/acsomega.1c00226
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author Lei, Ming
Peng, Xiwei
Sun, Wenjun
Zhang, Di
Wang, Zhenyu
Yang, Zhengjiao
Zhang, Chong
Yu, Bin
Niu, Huanqing
Ying, Hanjie
Ouyang, Pingkai
Liu, Dong
Chen, Yong
author_facet Lei, Ming
Peng, Xiwei
Sun, Wenjun
Zhang, Di
Wang, Zhenyu
Yang, Zhengjiao
Zhang, Chong
Yu, Bin
Niu, Huanqing
Ying, Hanjie
Ouyang, Pingkai
Liu, Dong
Chen, Yong
author_sort Lei, Ming
collection PubMed
description [Image: see text] 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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spelling pubmed-81536792021-05-27 Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum Lei, Ming Peng, Xiwei Sun, Wenjun Zhang, Di Wang, Zhenyu Yang, Zhengjiao Zhang, Chong Yu, Bin Niu, Huanqing Ying, Hanjie Ouyang, Pingkai Liu, Dong Chen, Yong ACS Omega [Image: see text] 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. American Chemical Society 2021-04-07 /pmc/articles/PMC8153679/ /pubmed/34056170 http://dx.doi.org/10.1021/acsomega.1c00226 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Lei, Ming
Peng, Xiwei
Sun, Wenjun
Zhang, Di
Wang, Zhenyu
Yang, Zhengjiao
Zhang, Chong
Yu, Bin
Niu, Huanqing
Ying, Hanjie
Ouyang, Pingkai
Liu, Dong
Chen, Yong
Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
title Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
title_full Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
title_fullStr Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
title_full_unstemmed Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
title_short Nonsterile l-Lysine Fermentation Using Engineered Phosphite-Grown Corynebacterium glutamicum
title_sort nonsterile l-lysine fermentation using engineered phosphite-grown corynebacterium glutamicum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8153679/
https://www.ncbi.nlm.nih.gov/pubmed/34056170
http://dx.doi.org/10.1021/acsomega.1c00226
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