Wu Cindy H, Le David, Mulchandani Ashok, Chen Wilfred
Dept. of Chemical and Environmental Engineering, University of California, Riverside, CA 92521, USA.
Biotechnol Prog. 2009 May-Jun;25(3):898-903. doi: 10.1002/btpr.203.
This work demonstrates improvement of a whole-cell cadmium detection sensor through construction of a gene circuit. A cadmium (II) specific regulatory promoter, P(cadR,) from Psuedomonas putida 06909, is used in the assembly of a toggle circuit. The circuit contains the cadR promoter fused to lacIq and gfp, and a divergently transcribed tac promoter and cadR. The toggle sensor exhibits lower background fluorescence, and a 20-fold lower detection limit in comparison to a nontoggle gene circuit. The detection limit of the toggle sensor is 0.01 microM (1.12 ppb) cadmium chloride, and tunable with the addition of isopropyl-b-D-thiogalactopyranoside (IPTG). The toggle sensor is highly specific to cadmium (II), and no response is elicited from zinc, lead, manganese, nickel, copper, and mercury.
这项工作通过构建基因回路展示了全细胞镉检测传感器的改进。来自恶臭假单胞菌06909的镉(II)特异性调控启动子P(cadR)用于构建一个双稳电路。该电路包含与lacIq和gfp融合的cadR启动子,以及一个反向转录的tac启动子和cadR。与非双稳基因回路相比,双稳传感器具有更低的背景荧光和低20倍的检测限。双稳传感器的氯化镉检测限为0.01微摩尔(1.12 ppb),并可通过添加异丙基-β-D-硫代半乳糖苷(IPTG)进行调节。双稳传感器对镉(II)具有高度特异性,对锌、铅、锰、镍、铜和汞无响应。