Construction of an Engineered Escherichia coli with Efficient Chemotactic and Metabolizing Ability toward Tetrathionate

被引:1
|
作者
Wang, Xin-Ge [1 ]
Zou, Zhen-Ping [1 ]
Du, Yue [1 ]
Ye, Bang-Ce [1 ]
Zhou, Ying [1 ]
机构
[1] East China Univ Sci & Technol, Lab Biosyst & Microanal, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
来源
ACS SYNTHETIC BIOLOGY | 2023年 / 12卷 / 11期
基金
中国国家自然科学基金;
关键词
directional migration; tetrathionate reductase genecluster; inflammatory bowel disease; engineeredbacteria; TtrSR two-component system; INFLAMMATORY-BOWEL-DISEASE; ELECTRON-ACCEPTOR; SALMONELLA; BACTERIA; ETHANOLAMINE; KINETICS; MUTANTS; CROHNS;
D O I
10.1021/acssynbio.3c00445
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The emergence of genetically engineered bacteria has provided a new means for the diagnosis and treatment of diseases. However, in vivo applications of these engineered bacteria are hindered by their inefficient accumulation in areas of inflammation. In this study, we constructed an engineered Escherichia coli (E. coli) for directional migration toward tetrathionate (a biomarker of gut inflammation), which is regulated by the TtrSR two-component system (TCS) from Shewanella baltica OS195 (S. baltica). Specifically, we removed endogenous cheZ to control the motility of E. coli. Moreover, we introduced the reductase gene cluster (ttrBCA) from Salmonella enterica serotype typhimurium (S. typhimurium), a major pathogen causing gut inflammation, into E. coli to metabolize tetrathionate. The resulting strain was tested for its motility along the gradients of tetrathionate; the engineered strain exhibits tropism to tetrathionate compared with the original strain. Furthermore, the engineered E. coli could only restore its smooth swimming ability when tetrathionate existed. With these modifications enabling tetrathionate-mediated chemotactic and metabolizing activity, this strategy with therapeutic elements will provide a great potential opportunity for target treatment of various diseases by swapping the corresponding genetic circuits.
引用
收藏
页码:3414 / 3423
页数:10
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