TY - JOUR
T1 - Biofilm engineering to improve succinic acid production in Escherichia coli by enhancing extracellular polysaccharide synthesis
AU - Pan, Runze
AU - Yuan, Yicheng
AU - Xu, Anming
AU - Jiang, Wankui
AU - Zhang, Wenming
AU - Barriuso, Jorge
AU - Jiang, Yujia
AU - Xin, Fengxue
AU - Jiang, Min
N1 - Publisher Copyright:
© 2025
PY - 2025/9
Y1 - 2025/9
N2 - Biofilms play crucial roles in enhancing microbial tolerance to environmental stress. Biofilm engineering in industrial microorganisms has been a promising and efficient approach to improve the production of metabolites. In this study, the psl gene cluster from Pseudomonas aeruginosa, for extracellular polysaccharide synthesis, was first introduced in a succinic acid (SA) producing Escherichia coli strain to enhance the biofilm formation ability. The engineered strain Suc260 (pslA-J) showed the improved tolerance to harsh environments and improved SA synthesis capability. Compared to the control, strain Suc260 (pslA-J) produced 70.54 g/L of SA from glucose in a 5 L bioreactor, representing an increase of 13.41 %. To further enhance the synthesis efficiency of SA, a cell immobilization fermentation system based on biofilms on alginate beads was designed. Finally, 62.66 g/L of SA with a yield of 0.76 g/g was produced from wheat straw hydrolysate in a 5 L bioreactor at the optimal pH of 6.8. When the pH was adjusted to a lower value (pH 6.0), the SA production and yield still reached 57.67 g/L and 0.75 g/g, respectively, representing 28.96 % and 42.15 % higher than those of the control strain. This study provides an efficient platform technology for the production of bio-based SA in large scale.
AB - Biofilms play crucial roles in enhancing microbial tolerance to environmental stress. Biofilm engineering in industrial microorganisms has been a promising and efficient approach to improve the production of metabolites. In this study, the psl gene cluster from Pseudomonas aeruginosa, for extracellular polysaccharide synthesis, was first introduced in a succinic acid (SA) producing Escherichia coli strain to enhance the biofilm formation ability. The engineered strain Suc260 (pslA-J) showed the improved tolerance to harsh environments and improved SA synthesis capability. Compared to the control, strain Suc260 (pslA-J) produced 70.54 g/L of SA from glucose in a 5 L bioreactor, representing an increase of 13.41 %. To further enhance the synthesis efficiency of SA, a cell immobilization fermentation system based on biofilms on alginate beads was designed. Finally, 62.66 g/L of SA with a yield of 0.76 g/g was produced from wheat straw hydrolysate in a 5 L bioreactor at the optimal pH of 6.8. When the pH was adjusted to a lower value (pH 6.0), the SA production and yield still reached 57.67 g/L and 0.75 g/g, respectively, representing 28.96 % and 42.15 % higher than those of the control strain. This study provides an efficient platform technology for the production of bio-based SA in large scale.
KW - Biofilm
KW - E. coli
KW - Immobilization
KW - Succinic acid
KW - Wheat straw hydrolysate
UR - http://www.scopus.com/inward/record.url?scp=105004232875&partnerID=8YFLogxK
U2 - 10.1016/j.biortech.2025.132627
DO - 10.1016/j.biortech.2025.132627
M3 - 文章
AN - SCOPUS:105004232875
SN - 0960-8524
VL - 431
JO - Bioresource Technology
JF - Bioresource Technology
M1 - 132627
ER -