Revealing novel protein interaction partners of glyphosate in Escherichia coli

被引:0
|
作者
Aldehoff, Alix Sarah [1 ]
Tuerkowsky, Dominique [1 ]
Lohmann, Patrick [1 ]
Homsi, Masun Nabhan [1 ]
Rolle-Kampczyk, Ulrike [1 ]
Ueberham, Elke [2 ]
Lehmann, Joerg [2 ,3 ]
von Bergen, Martin [1 ,4 ,5 ]
Jehmlich, Nico [1 ]
Haange, Sven-Bastiaan [1 ]
机构
[1] Helmholtz Ctr Environm Res GmbH UFZ, Dept Mol Toxicol, Leipzig, Germany
[2] Fraunhofer Inst Cell Therapy & Immunol IZI, Dept Preclin Dev & Validat, Leipzig, Germany
[3] Fraunhofer Cluster Excellence Immune Mediated Dis, Hannover, Germany
[4] Univ Leipzig, Inst Biochem, Fac Biosci Pharm & Psychol, Leipzig, Germany
[5] German Ctr Integrat Biodivers Res iDiv, Leipzig, Germany
关键词
Glyphosate; Escherichia coli; Acute and chronic exposure; Thermal proteome profiling; Protein interaction partner; SHIKIMIC ACID; LUMAZINE SYNTHASE; POTENT INHIBITOR; BIOSYNTHESIS; RIBOFLAVIN; PATHWAY; GENOME; WATER; AMPA;
D O I
10.1016/j.envint.2024.109243
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Despite all debates about its safe use, glyphosate remains the most widely applied active ingredient in herbicide products, with renewed approval in the European Union until 2033. Non-target organisms are commonly exposed to glyphosate as a matter of its mode of application, with its broader environmental and biological impacts remaining under investigation. Glyphosate displays structural similarity to phosphoenolpyruvate (PEP), thereby competitively inhibiting the 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS), crucial for the synthesis of aromatic amino acids in plants, fungi, bacteria, and archaea. Most microbes, including the gut bacterium Escherichia coli (E. coli), possess a glyphosate-sensitive class I EPSPS, making them vulnerable to glyphosate's effects. Yet, little is known about glyphosate's interactions with other bacterial proteins or its broader modes of action at the proteome level. Here, we employed a quantitative proteomics and thermal proteome profiling (TPP) approach to identify novel protein binding partners of glyphosate in the E. coli proteome. Glyphosate exposure significantly altered amino acid synthesizing pathways. The abundance of shikimate pathway proteins was increased, suggesting a compensatory mechanism. Extracellular riboflavin concentrations were elevated upon glyphosate exposure, while intracellular levels remained stable. Beyond the target enzyme EPSPS, thermal proteome profiling indicated an effect of glyphosate on the thermal stability of certain proteins, including AroH and ProA, indicating interactions. Similar to the competitive binding between PEP and glyphosate at EPSPS, one reason for the interaction of AroH and ProA with the herbicide could be a high structural similarity between their substrates and glyphosate. Overall, glyphosate induced metabolic disturbances in E. coli, extending beyond its primary target, thereby providing new insights into glyphosate's broader impact on microbial systems.
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页数:13
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