Efficient Autoinducible Expression of Recombinant Proteins via the DegSU Quorum Sensing System in a Robust Bacillus subtilis

被引:0
|
作者
Zong, Hong [1 ,2 ,3 ]
Zhang, Liya [1 ,2 ,3 ]
Cheng, Yiwen [1 ,2 ,3 ]
Sheng, Zhiying [1 ,2 ,3 ]
Bin, Zhuge [1 ,2 ,3 ]
Lu, Xinyao [1 ,2 ,3 ]
机构
[1] Jiangnan Univ, Sch Biotechnol, Minist Educ, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Key Lab Ind Biotechnol, Minist Educ, Wuxi 214122, Peoples R China
[3] Jiangnan Univ, Sch Biotechnol, Lab Ind Microorganism & Res & Design Ctr Polyols, Wuxi 214122, Peoples R China
来源
ACS SYNTHETIC BIOLOGY | 2025年 / 14卷 / 01期
关键词
<italic>Bacillus subtilis</italic>; autoinducible; quorum sensing (QS); recombinant protein; DegU-P; transcription efficiency; RESPONSE REGULATOR DEGU; TRANSCRIPTION FACTOR DEGU; PROTEASE PRODUCTION; MUTATIONAL ANALYSIS; ACETOIN PRODUCTION; GENE; PHOSPHORYLATION; PROMOTER; PROGRESS; BINDING;
D O I
10.1021/acssynbio.4c00798
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
DegSU quorum sensing (QS) system enables autoinducible expression of recombinant proteins in Bacillus subtilis . However, insufficient promoter strength and a complex regulatory circuit limit its practical application. Here, the QS-responsive promoter P aprE was modified by core region mutation, upstream truncation, and addition of activating binding sites, yielding PE742 with a 118.3% increase in strength. A mathematical model was developed to accurately quantify the regulatory process from a comprehensive perspective. Guided by this model, the DegSU QS system was further optimized in a robust B. subtilis by knocking out competitive target genes sacB and amyE, operons pgs and srfA, introducing variants degU L113F and degQ36Hy, and increasing regulatory strength by 84.0%. A 52.5% increase in acetoin titer and a 65.9% increase in extracellular carboxypeptidase activity validated the industrial value of this study. Overall, this study addresses the limitations of the DegSU QS system in practical application and demonstrates its potential for high-level recombinant protein production.
引用
收藏
页码:273 / 284
页数:12
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