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细菌对草甘膦的抗性由大肠杆菌膜外排转运蛋白的过表达赋予。

Bacterial glyphosate resistance conferred by overexpression of an E. coli membrane efflux transporter.

机构信息

Monsanto Company, 700 Chesterfield Parkway North, St. Louis, MO 63017, USA.

出版信息

J Ind Microbiol Biotechnol. 2012 Apr;39(4):641-7. doi: 10.1007/s10295-011-1057-x. Epub 2011 Nov 17.

Abstract

Glyphosate herbicide-resistant crop plants, introduced commercially in 1994, now represent approximately 85% of the land area devoted to transgenic crops. Herbicide resistance in commercial glyphosate-resistant crops is due to expression of a variant form of a bacterial 5-enolpyruvylshikimate-3-phosphate synthase with a significantly decreased binding affinity for glyphosate at the target site of the enzyme. As a result of widespread and recurrent glyphosate use, often as the only herbicide used for weed management, increasing numbers of weedy species have evolved resistance to glyphosate. Weed resistance is most often due to changes in herbicide translocation patterns, presumed to be through the activity of an as yet unidentified membrane transporter in plants. To provide insight into glyphosate resistance mechanisms and identify a potential glyphosate transporter, we screened Escherichia coli genomic DNA for alternate sources of glyphosate resistance genes. Our search identified a single non-target gene that, when overexpressed in E. coli and Pseudomonas, confers high-level glyphosate resistance. The gene, yhhS, encodes a predicted membrane transporter of the major facilitator superfamily involved in drug efflux. We report here that an alternative mode of glyphosate resistance in E. coli is due to reduced accumulation of glyphosate in cells that overexpress this membrane transporter and discuss the implications for potential alternative resistance mechanisms in other organisms such as plants.

摘要

1994 年商业化推出的抗草甘膦除草剂作物植物,现在约占转基因作物种植面积的 85%。商业上使用的抗草甘膦作物的除草剂抗性是由于表达了一种细菌 5-烯醇丙酮酰莽草酸-3-磷酸合酶的变体形式,该变体与酶的靶位上的草甘膦的结合亲和力显著降低。由于草甘膦的广泛和反复使用,通常作为唯一用于杂草管理的除草剂,越来越多的杂草物种已经对草甘膦产生了抗性。杂草抗性最常见的原因是除草剂转运模式的变化,据推测是通过植物中尚未鉴定的膜转运蛋白的活性。为了深入了解草甘膦抗性机制并鉴定潜在的草甘膦转运蛋白,我们从大肠杆菌基因组 DNA 中筛选了抗草甘膦基因的替代来源。我们的搜索确定了一个单一的非靶基因,当在大肠杆菌和铜绿假单胞菌中过表达时,赋予高水平的草甘膦抗性。该基因 yhhS 编码一种预测的膜转运蛋白,属于主要易化因子超家族,参与药物外排。我们在这里报告,大肠杆菌中另一种草甘膦抗性模式是由于过表达这种膜转运蛋白的细胞中草甘膦积累减少所致,并讨论了在其他生物体(如植物)中潜在的替代抗性机制的意义。

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