Modular Design of a Copper Ion Biosensor Based on the MAPK Signaling Pathway in Saccharomyces cerevisiae

酿酒酵母 模块化设计 生物传感器 铜 MAPK/ERK通路 化学 计算生物学 合成生物学 信号转导 生物化学 计算机科学 细胞生物学 生物 酵母 程序设计语言 有机化学
作者
Tao Wang,Ding Shuwen,Jiao Xu,Guohao Cai,Yiqing Zhang,Yongfen Qi,Yujia Jiang,Ping Zhang,Tianjing Wang,Fengxue Xin,Tao Shen,Guannan Liu
出处
期刊:ACS Synthetic Biology [American Chemical Society]
卷期号:14 (7): 2854-2864 被引量:1
标识
DOI:10.1021/acssynbio.5c00276
摘要

Copper ion poses serious threats to both the environment and human health. To develop a yeast biosensor with reduced background noise and enhanced detection sensitivity, we constructed a quorum-sensing module with amplified positive feedback. This biosensor employs a copper ion-pheromone communication system, which allows haploid a-type yeast (MATa) to express the α-pheromone gene (mfα2) under the control of the copper ion-inducible promoter pCUP1. The α-pheromone activates the mitogen-activated protein kinase (MAPK) signaling pathway, which in turn induces the expression of the green fluorescent protein (GFP) gene via the pheromone-inducible promoter pprm1. To improve the performance of the biosensor, we optimized the prm1 promoter and constructed the Ste5ΔN-CTM chassis. Specifically, the promoter intensity was improved by converting the three nonconsensus Pheromone Response Elements (PRE) in pprm1 into consensus PRE sequences, resulting in the prm1 Pro promoter. The Ste5ΔN-CTM strain continuously activates the MAPK signaling pathway. Next, to offset the loss of sensitivity and dynamic response range caused by endogenous pheromone degradation, we knocked out the pheromone degradation gene bar1 using CRISPR-Cas9 gene editing technology. Additionally, we established a functional model relating the copper ion concentration to the GFP signal output. In conclusion, this study designed a modular copper ion biosensor system by integrating sensing, amplification, and signal-reporting components, laying a foundation for the development of biosensors for other heavy metals.
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