Disentangling the regulatory response of Agrobacterium tumefaciens CHLDO to glyphosate for engineering whole-cell phosphonate biosensors

Fiorella Masotti, Nicolas Krink, Nicolas Lencina, Natalia Gottig, Jorgelina Ottado, Pablo Ivan Nikel
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Abstract

Phosphonates (PHTs), organic compounds with a stable C-P bond, are widely distributed in nature. Glyphosate (GP), a synthetic PHT, is extensively used in agriculture and has been linked to various human health issues and environmental damage. Given the prevalence of GP, developing cost-effective, on-site methods for GP detection is key for assessing pollution and reducing exposure risks. We adopted Agrobacterium tumefaciens CHLDO, a natural GP degrader, as the source of genetic parts for constructing PHT biosensors. In this species, the phn gene cluster, encoding the C-P lyase pathway, is regulated by the PhnF transcriptional repressor and is part of the Pho regulon. We selected the phnG promoter, which displays a dose-dependent response to GP, to build a set of whole-cell biosensors. Through stepwise optimization of the transcriptional cascade, we created a biosensor capable of detecting GP in the 0.25-50 uM range in various samples, including soil and water.
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厘清农杆菌 CHLDO 对草甘膦的调控响应以设计全细胞膦酸盐生物传感器
膦酸盐(PHTs)是一种具有稳定 C-P 键的有机化合物,在自然界中广泛分布。草甘膦(GP)是一种人工合成的 PHT,广泛用于农业,与各种人类健康问题和环境破坏有关。鉴于 GP 的普遍存在,开发具有成本效益的现场 GP 检测方法是评估污染和降低暴露风险的关键。我们采用农杆菌 CHLDO(一种天然 GP 降解菌)作为构建 PHT 生物传感器的基因部件来源。在该物种中,编码 C-P 裂解酶途径的 phn 基因簇受 PhnF 转录抑制因子调控,是 Pho 调节子的一部分。我们选择了phnG启动子来构建全细胞生物传感器。通过逐步优化转录级联,我们创建了一种生物传感器,能够检测各种样品(包括土壤和水)中 0.25-50 uM 范围内的 GP。
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