Lu Wei, Li Liang, Chen Ming, Zhou Zhengfu, Zhang Wei, Ping Shuzhen, Yan Yongliang, Wang Jin, Lin Min
Biotechnology Research Institute, Chinese Academy of Agricultural Sciences/Key Laboratory of Crop Biotechnology, Ministry of Agriculture, Beijing 100081, China.
Mol Biosyst. 2013 Mar;9(3):522-30. doi: 10.1039/c2mb25374g. Epub 2012 Dec 18.
The shikimate pathway enzymes offer attractive targets for the development of antimetabolites. Glyphosate is an effective antimetabolite that inhibits 5-enolpyruvylshikimate-3-phosphate (EPSP) synthase in the shikimate pathway, thereby resulting in a shortage of the chorismate-derived essential aromatic amino acids. However, little is known about the genome-wide transcriptional responses of bacteria to glyphosate shock. In the current study, a transcriptome analysis of Escherichia coli (E. coli) exposed to glyphosate identified the differential expression of 1040 genes, which represent 23.2% of the genome. The differentially expressed genes are primarily involved in amino acid metabolism, cell motility, and central carbon metabolism, indicating that the impact of glyphosate on the shikimate pathway also extends to other metabolic pathways. Expectedly, almost all genes encoding the proteins for the shikimate and specific aromatic amino acid pathways were downregulated after the addition of glyphosate. Furthermore, the expression of many energy- and metabolism-related genes was repressed. In contrast, glyphosate treatment induced the coordinated upregulation of at least 50 genes related to cell motility and chemotaxis. The reverse transcription-quantitative real-time PCR (RT-qPCR) data showed that the expression profiles of selected genes from the referred pathways were found to be consistent with the microarray data. The results suggest that the presence of glyphosate during growth induces metabolic starvation, an energy drain and other non-target effects.
莽草酸途径的酶为抗代谢物的开发提供了有吸引力的靶点。草甘膦是一种有效的抗代谢物,它抑制莽草酸途径中的5-烯醇丙酮酸莽草酸-3-磷酸(EPSP)合酶,从而导致分支酸衍生的必需芳香族氨基酸短缺。然而,关于细菌对草甘膦冲击的全基因组转录反应知之甚少。在当前的研究中,对暴露于草甘膦的大肠杆菌进行转录组分析,确定了1040个基因的差异表达,这些基因占基因组的23.2%。差异表达的基因主要参与氨基酸代谢、细胞运动和中心碳代谢,这表明草甘膦对莽草酸途径的影响也扩展到其他代谢途径。不出所料,添加草甘膦后,几乎所有编码莽草酸和特定芳香族氨基酸途径蛋白质的基因都被下调。此外,许多与能量和代谢相关的基因的表达也受到抑制。相反,草甘膦处理诱导了至少50个与细胞运动和趋化性相关的基因的协同上调。逆转录定量实时PCR(RT-qPCR)数据表明,从上述途径中选择的基因的表达谱与微阵列数据一致。结果表明,生长过程中草甘膦的存在会诱导代谢饥饿、能量消耗和其他非靶向效应。