TY - JOUR
T1 - Modular Design of a Copper Ion Biosensor Based on the MAPK Signaling Pathway in Saccharomyces cerevisiae
AU - Wang, Tao
AU - Ding, Shuwen
AU - Xu, Jiao
AU - Cai, Guohao
AU - Zhang, Yiqing
AU - Qi, Yingxuan
AU - Jiang, Yujia
AU - Zhang, Ping
AU - Wang, Tianjing
AU - Xin, Fengxue
AU - Shen, Tao
AU - Liu, Guannan
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025
Y1 - 2025
N2 - 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.
AB - 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.
KW - Copper ion biosensor
KW - CRISPR-Cas9
KW - MAPK signaling
KW - Quorum sensing
KW - S. cerevisiae
UR - http://www.scopus.com/inward/record.url?scp=105009130622&partnerID=8YFLogxK
U2 - 10.1021/acssynbio.5c00276
DO - 10.1021/acssynbio.5c00276
M3 - 文章
AN - SCOPUS:105009130622
SN - 2161-5063
JO - ACS Synthetic Biology
JF - ACS Synthetic Biology
ER -