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首页> 外文期刊>Photosynthesis Research: An International Journal >Binding site of novel 2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine herbicides in the D1 protein of Photosystem II
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Binding site of novel 2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine herbicides in the D1 protein of Photosystem II

机译:新型2-苄氨基-4-甲基-6-三氟甲基-1,3,5-三嗪除草剂在光系统II的D1蛋白中的结合位点

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A series of replacement experiments of [C-14]-triazines, [C-14]-atrazine and [7-C-14]-2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine, bound to thylakoids isolated from wild-type and atrazine-resistant Chenopodium album (lambsquarters) were conducted. Replacement experiments of [C-14]-triazines bound to wild-type Chenopodium thylakoids with non-labeled atrazine and 2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine were carried out, to elucidate whether benzylamino-1,3,5-triazines use the same binding niche as atrazine. [C-14]-Atrazine and [7-C-14]-2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine bound to wild-type thylakoids were replaced by non-labeled 2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine and non-labeled atrazine, respectively. The above two replacements showed mutual competition. To clarify further whether benzylamino-1,3,5-triazines bind at the D1-protein to amino acid residue( s) different from atrazine or not, experiments to replace [7-C-14]-2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazines bound to atrazine-resistant Chenopodium thylakoids by non-labeled atrazine, 2-(4-bromobenzylamino)-4-methyl-6-trifluoromethyl-1,3,5-triazine, DCMU and DNOC were carried out. Although the bound [7-C-14]-2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine was difficult to be replaced even with high concentrations of atrazine, [C-14]-labeled 1,3,5-triazine was competitively replaced by non-labeled 2-(4-bromobenzylamino)-4-methyl-6-trifluoromethyl-1,3,5-triazine, DCMU or DNOC. Thus, 2-benzylamino-4-methyl-6-trifluoromethyl-1,3,5-triazine herbicides are considered to bind to the same niche at the D1 protein as atrazine, but use amino acid residue(s) different from those involved with atrazine binding.
机译:[C-14]-三嗪,[C-14] -at去津和[7-C-14] -2-苄基氨基-4-甲基-6-三氟甲基-1,3,5-三嗪的一系列替代实验,绑定到类囊体分离自野生型和耐阿特拉津的藜属专辑(羔羊)。进行了未标记的azine去津和2-苄基氨基-4-甲基-6-三氟甲基-1,3,5-三嗪与野生型藜衣藻类固醇结合的[C-14]-三嗪的替代实验,以阐明是否苄基氨基-1,3,5-三嗪使用与阿特拉津相同的结合位。与野生型类囊体结合的[C-14]-阿特拉津和[7-C-14] -2-苄基氨基-4-甲基-6-三氟甲基-1,3,5-三嗪被未标记的2-苄基氨基取代-4-甲基-6-三氟甲基-1,3,5-三嗪和未标记的阿特拉津。以上两个替代品显示出相互竞争。为了进一步阐明苄基氨基-1,3,5-三嗪是否在D1蛋白上结合到不同于阿特拉津的氨基酸残基上,请尝试替换[7-C-14] -2-苄基氨基-4-甲基-6-三氟甲基-1,3,5-三嗪通过未标记的阿特拉津,2-(4-溴苄基氨基)-4-甲基-6-三氟甲基-1,3,5-三嗪,DCMU与耐阿特拉津的类扁豆类固醇结合和DNOC进行。尽管即使用高浓度的阿特拉津也很难取代结合的[7-C-14] -2-苄基氨基-4-甲基-6-三氟甲基-1,3,5-三嗪,但[C-14]标记为1 1,3,5-三嗪被未标记的2-(4-溴苄氨基)-4-甲基-6-三氟甲基-1,3,5-三嗪,DCMU或DNOC取代。因此,人们认为2-苄基氨基-4-甲基-6-三氟甲基-1,3,5-三嗪除草剂在D1蛋白上与阿特拉津具有相同的利基结合能力,但使用的氨基酸残基不同于与阿特拉津有关的残基。阿特拉津结合。

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