首页> 外文期刊>Veterinary Immunology and Immunopathology >Evaluation of new Cu(II) complexes as a novel class of inhibitors against plant carbonic anhydrase, glutathione reductase, and photosynthetic activity in photosystem II
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Evaluation of new Cu(II) complexes as a novel class of inhibitors against plant carbonic anhydrase, glutathione reductase, and photosynthetic activity in photosystem II

机译:新型铜(II)复合物作为一种针对植物碳酸酐酶,谷胱甘肽还原酶和照相中的光合活性的新型抑制剂

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摘要

Increasing inefficiency of production of important agricultural plants raises one of the biggest problems in the modern world. Herbicide application is still the best method of weed management. Traditional herbicides blocking only one of the plant metabolic pathways is ineffective due to the rapid growth of herbicide-resistant weeds. The synthesis of novel compounds effectively suppressing several metabolic processes, and therefore achieving the synergism effect would serve as the alternative approach to weed problem. For this reason, recently, we synthesized a series of nine novel Cu(II) complexes and four ligands, characterized them with different analyses techniques, and carried out their primary evaluation as inhibitors of photosynthetic electron transfer in spinach thylakoids (design, synthesis, and evaluation of a series of Cu(II) based metal-organic complexes as possible inhibitors of photosynthesis, J Photochem Photobiol B, submitted). Here, we evaluated in vitro inhibitory potency of these agents against: photochemistry and carbonic anhydrase activity of photosystem II (PSII); alpha-carbonic anhydrase from bovine erythrocytes; as well as glutathione reductase from chloroplast and baker's yeast. Our results show that all Cu(II) complexes excellently inhibit glutathione reductase and PSII carbonic anhydrase activity. Some of them also decently inhibit PSII photosynthetic activity.
机译:增加重要农业植物的产量效率低下提出了现代世界的最大问题之一。除草剂应用仍然是杂草管理的最佳方法。由于除草剂抗性杂草的快速生长,传统除草剂仅阻断其中一种植物代谢途径是无效的。新型化合物的合成有效抑制了几种代谢过程,因此实现了协同作用将作为杂草问题的替代方法。由于这个原因,我们合成了一系列九种新型Cu(II)络合物和四种配体,其用不同的分析技术表征,并进行其作为菠菜紫曲面上光合电子转移的抑制剂的主要评价(设计,合成和评估一系列基于Cu(II)的金属 - 有机络合物,作为光合作用的可能抑制剂,JIPCHEM Photobiol B,提交)。在这里,我们评估了这些药剂的体外抑制效力,反对:光化学和光学系统II(PSII)的碳酸酐酶活性;来自牛红细胞的α-碳酸酐酶;以及来自叶绿体和面包酵母的谷胱甘肽还原酶。我们的研究结果表明,所有Cu(II)复合体都很好地抑制谷胱甘肽还原酶和PSII碳酸酐酶活性。其中一些也体面抑制了Psii光合活动。

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