TY - JOUR
T1 - Engineering bacterium for biofilm formation and L-lysine production in continuous fermentation
AU - Peng, Xiwei
AU - Zhang, Di
AU - Yuan, Jingyi
AU - Yang, Hongdan
AU - Li, Mengting
AU - Zhang, Huifang
AU - Niu, Huanqing
AU - Zhu, Chenjie
AU - Chen, Yong
AU - Zhao, Chunguang
AU - Guo, Ting
AU - Wang, Zhenyu
AU - Liu, Dong
AU - Ying, Hanjie
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/12
Y1 - 2024/12
N2 - Microbial biofilms provide advantages in fermentation processes. However, Corynebacterium glutamicum (C. glutamicum) usually exhibits relatively poor biofilm formation compared to other industrial strains. To develop a biofilm-enhanced fermentation process for C. glutamicum, seven genes potentially related to biofilm formation in C. glutamicum were systematically investigated, which include ppk2B, glgC, virB11, cslA, NCgl2909, NCgl0350 and exeR. Deletion of the NCgl0350, NCgl2909 genes and heterologous expression of the cslA gene were found to increase biofilm amounts by 16.9%, 21.2% and 135%, respectively, compared to the wild-type strain. Meanwhile, the production of L-lysine by engineered strains was assessed in biofilm-based continuous fermentation. The most notable result was observed for the cslA-expressing strain, which produced an average of 26.1% higher L-lysine compared with that of wild-type strain in 6-L bioreactors. In conclusion, this study offers valuable insights into the biofilm formation in C. glutamicum and its application in continuous fermentation processes.
AB - Microbial biofilms provide advantages in fermentation processes. However, Corynebacterium glutamicum (C. glutamicum) usually exhibits relatively poor biofilm formation compared to other industrial strains. To develop a biofilm-enhanced fermentation process for C. glutamicum, seven genes potentially related to biofilm formation in C. glutamicum were systematically investigated, which include ppk2B, glgC, virB11, cslA, NCgl2909, NCgl0350 and exeR. Deletion of the NCgl0350, NCgl2909 genes and heterologous expression of the cslA gene were found to increase biofilm amounts by 16.9%, 21.2% and 135%, respectively, compared to the wild-type strain. Meanwhile, the production of L-lysine by engineered strains was assessed in biofilm-based continuous fermentation. The most notable result was observed for the cslA-expressing strain, which produced an average of 26.1% higher L-lysine compared with that of wild-type strain in 6-L bioreactors. In conclusion, this study offers valuable insights into the biofilm formation in C. glutamicum and its application in continuous fermentation processes.
KW - Biofilm-enhanced fermentation
KW - C. glutamicum
KW - Gene deletion and expression
KW - Microbial biofilms
UR - http://www.scopus.com/inward/record.url?scp=85206237855&partnerID=8YFLogxK
U2 - 10.1016/j.biortech.2024.131567
DO - 10.1016/j.biortech.2024.131567
M3 - 文章
C2 - 39393651
AN - SCOPUS:85206237855
SN - 0960-8524
VL - 414
JO - Bioresource Technology
JF - Bioresource Technology
M1 - 131567
ER -