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一种快速筛选方法,用于检测丙酮酸正磷酸双激酶的特异性抑制剂,作为C4植物选择性除草剂的先导化合物。

A rapid screening method to detect specific inhibitors of pyruvate orthophosphate dikinase as leads for C4 plant-selective herbicides.

作者信息

Doyle Jason R, Burnell James N, Haines Dianne S, Llewellyn Lyndon E, Motti Cherie A, Tapiolas Dianne M

机构信息

Australian Institute of Marine Science, Townsville, Queensland, Australia.

出版信息

J Biomol Screen. 2005 Feb;10(1):67-75. doi: 10.1177/1087057104269978.

Abstract

Plants using the C(4) photosynthetic pathway are highly represented among the world's worst weeds, with only 4 C(4) species being agriculturally productive (maize, sorghum, millet, and sugar cane). With the C(4) acid cycle operating as a biochemical appendage of C(3) photosynthesis, the additional enzymes involved in C(4) photosynthesis represent an attractive target for the development of weed-specific herbicides. The rate-limiting enzyme of this metabolic pathway is pyruvate orthophosphate dikinase (PPDK). PPDK, coupled with phosphoenolpyruvate carboxylase and nicotinamide adenine dinucleotide-malate dehydrogenase, was used to develop a microplate-based assay to detect inhibitors of enzymes of the C(4) acid cycle. The resulting assay had a Z' factor of 0.61, making it a high-quality assay able to reliably identify active test samples. Organic extracts of 6679 marine macroscopic organisms were tested within the assay, and 343 were identified that inhibited the 3 enzyme-coupled reaction. A high confirmation rate was achieved, with 95% of these hit extracts proving active again upon retesting. Sequential addition of phosphoenolpyruvate and oxaloacetate to the assay facilitated identification of 83 extracts that specifically inhibited PPDK.

摘要

采用C(4)光合途径的植物在世界上最有害的杂草中占比很高,只有4种C(4)植物具有农业生产价值(玉米、高粱、小米和甘蔗)。由于C(4)酸循环作为C(3)光合作用的生化附属过程运行,参与C(4)光合作用的额外酶成为开发杂草专用除草剂的一个有吸引力的靶点。该代谢途径的限速酶是丙酮酸磷酸双激酶(PPDK)。PPDK与磷酸烯醇式丙酮酸羧化酶和烟酰胺腺嘌呤二核苷酸 - 苹果酸脱氢酶一起,被用于开发一种基于微孔板的检测方法,以检测C(4)酸循环中酶的抑制剂。所得检测方法的Z'因子为0.61,使其成为一种能够可靠识别活性测试样品的高质量检测方法。在该检测方法中对6679种海洋大型生物的有机提取物进行了测试,鉴定出343种能够抑制三酶偶联反应的提取物。确认率很高,这些有活性的提取物在重新测试时有95%再次证明具有活性。在检测方法中依次加入磷酸烯醇式丙酮酸和草酰乙酸有助于鉴定出83种特异性抑制PPDK的提取物。

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