Hui Chang-Ye, Guo Yan, Liu Lisa, Zhang Nai-Xing, Gao Chao-Xian, Yang Xue-Qin, Yi Juan
Department of Pathology & Toxicology, Shenzhen Prevention and Treatment Center for Occupational Diseases Shenzhen China
National Key Clinical Specialty of Occupational Diseases, Shenzhen Prevention and Treatment Center for Occupational Diseases Shenzhen China.
RSC Adv. 2020 Jul 28;10(47):28106-28113. doi: 10.1039/d0ra04815a. eCollection 2020 Jul 27.
Environmental risks continue to grow due to heavy metal contamination caused by anthropogenic activities. Accumulation of harmful quantities of lead poses a threat to aquatic organisms, plants, and human beings. Whole-cell biosensors, which can proliferate independently, can detect the bioavailable fraction to assess the effect of target heavy metal on the environmental ecosystem. In this study, the biosynthesis pathway of violacein was heterogeneously constructed under the control of the T7 lac promoter in . A dose-response relationship existed between the inducer and the production of violacein. The biosynthesis pathway of violacein was finally engineered under the regulation of Pb(ii)-dependent metalloregulator PbrR to assemble Pb(ii)-inducible whole-cell biosensor. It permitted specific biosensing of Pb(ii) with extraordinary selectivity, and could resist the interferences from various metal ions. Color change by the intracellular accumulation of violacein could be recognized with the naked eye directly with high concentration of lead exposure, and quantified by determining the absorbance at 490 nm after butanol extraction. A good linear range for Pb(ii) concentrations of 0.1875-1.5 μM was obtained. The novel pigment-based whole-cell biosensor could detect concentrations as low as 0.1875 μM Pb(ii) based on quantification of violacein extracted by butanol, which is significantly lower than reported fluorescent protein-based PbrR-regulated biosensors based on direct measurement of whole cell fluorescence. These results indicate that genetically controlled violacein biosynthesis can enable a sensitive, visual, and qualitative biosensor for monitoring the presence of bioavailable Pb(ii) in lead-contaminated water.
由于人为活动导致的重金属污染,环境风险持续增加。有害量铅的积累对水生生物、植物和人类构成威胁。能够独立增殖的全细胞生物传感器可以检测生物可利用部分,以评估目标重金属对环境生态系统的影响。在本研究中,在T7 lac启动子的控制下,在大肠杆菌中异源构建了紫罗碱的生物合成途径。诱导剂与紫罗碱的产生之间存在剂量反应关系。最终在依赖Pb(II)的金属调节蛋白PbrR的调控下对紫罗碱的生物合成途径进行工程改造,以组装Pb(II)诱导型全细胞生物传感器。它允许对Pb(II)进行具有非凡选择性的特异性生物传感,并能抵抗各种金属离子的干扰。在高浓度铅暴露下,通过肉眼可以直接识别紫罗碱在细胞内积累引起的颜色变化,并在丁醇提取后通过测定490nm处的吸光度进行定量。获得了Pb(II)浓度为0.1875 - 1.5μM的良好线性范围。基于丁醇提取的紫罗碱定量,这种新型色素基全细胞生物传感器可以检测低至0.1875μM Pb(II)的浓度,这明显低于基于直接测量全细胞荧光的已报道的基于荧光蛋白的PbrR调控生物传感器。这些结果表明,基因控制的紫罗碱生物合成可以实现一种灵敏、可视化和定性的生物传感器,用于监测铅污染水中生物可利用的Pb(II)的存在。