大肠杆菌
降级(电信)
1,2-二氯乙烷
代谢工程
化学
环境化学
微生物学
环境科学
生物化学
生物
工程类
酶
电信
基因
催化作用
作者
Yongdong Deng,Wenhui Zhang,Zhihao Zuo,Hao Zhang,Jing Xu,Jianjie Gao,Xiaogang Wang,Zhenjun Li,Xiao-Yan Fu,Xiaogang Wang,Xiaogang Wang,Yong‐Sheng Tian,Ri‐He Peng,Quan-Hong Yao
标识
DOI:10.1016/j.jhazmat.2024.134476
摘要
1,2-Dichloroethane (1,2-DCA), a widely utilized chemical intermediate and organic solvent in industry, frequently enters the environment due to accidental leaks and mishandling during application processes. Thus, the in-situ remediation of contaminated sites has become increasingly urgent. However, traditional remediation methods are inefficient and costly, while bioremediation presents a green, efficient, and non-secondary polluting alternative. In this study, an engineered strain capable of completely degrading 1,2-DCA was constructed. We introduced six exogenous genes of the 1,2-DCA degradation pathway into E. coli and confirmed their normal transcription and efficient expression in this engineered strain through qRT-PCR and proteomics. The degradation experiments showed that the strain completely degraded 2 mM 1,2-DCA within 12 h. Furthermore, the results of isotope tracing verified that the final degradation product, malic acid, entered the tricarboxylic acid cycle (TCA) of E. coli and was ultimately fully metabolized. Also, morphological changes in the engineered strain and control strain exposed to 1,2-DCA were observed under SEM, and the results revealed that the engineered strain is more tolerant to 1,2-DCA than the control strain. In conclusion, this study paved a new way for humanity to deal with the increasingly complex environmental challenges.
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