School of Environmental Science and Engineering, Shandong University, 27 Shanda Nanlu, Jinan, 250100, P.R. China.
Department of Civil and Environmental Engineering, University of Illinois at Urbana-Champaign, 205 North Mathews Ave, Urbana, IL, 61801, United States.
Sci Rep. 2018 Feb 13;8(1):2906. doi: 10.1038/s41598-018-21350-9.
Synthetic biology enables infinite possibilities in biotechnology via employing genetic modules. However, not many researches have explored the potentials of synthetic biology in environmental bioprocesses. In this study, we introduced a genetic module harboring the codon-optimized tetracycline degrading gene, tetX.co, into the model host, Escherichia coli, and generated a prototypal whole-cell biodevice for the degradation of a target antibiotic. Our results suggested that E. coli with the tetX.co-module driven by either the P or P promoters conferred resistance up to 50 μg/mL of tetracycline and degrades over 95% of tetracycline within 24 h. The detoxification ability of tetX was further verified in conditioned media by typical E. coli K-12 and B strains as well as Shewanella oneidensis. Our strategy demonstrated the feasibility of introducing genetic modules into model hosts to enable environmental functions, and this work will inspire more environmental innovations through synthetic biological devices.
合成生物学通过采用遗传模块,在生物技术方面实现了无限可能。然而,在环境生物工艺中,合成生物学的潜力还没有得到很多研究的探索。在这项研究中,我们将一个含有密码子优化的四环素降解基因 tetX.co 的遗传模块引入模型宿主大肠杆菌中,并生成了一个用于降解目标抗生素的原型全细胞生物降解设备。我们的结果表明,由 P 或 P 启动子驱动的 tetX.co 模块的大肠杆菌赋予了高达 50μg/ml 的四环素抗性,并在 24 小时内降解了超过 95%的四环素。tetX 的解毒能力在条件培养基中也被典型的大肠杆菌 K-12 和 B 菌株以及希瓦氏菌 oneidensis 进一步验证。我们的策略展示了将遗传模块引入模型宿主以实现环境功能的可行性,这项工作将通过合成生物器件激发更多的环境创新。