期刊文献+

农药靶标抗性研究在大学化学生物学综合实验中的实践 被引量:1

Application of Study of Pesticide Target Resistance in University Comprehensive Experiment of Chemical Biology
原文传递
导出
摘要 乙酰羟酸合成酶是目前国际上备受关注的几类超高效商品化除草剂的作用靶标酶,其关键位点的突变是除草剂抗性形成的根源。选择其中2个单点突变体,从分子克隆、突变、蛋白的表达、纯化,到酶学检测等方面,全方位研究了乙酰羟酸合成酶野生型和2个突变体的性质和功能。整套实验包括了多种基本单元操作以及一些具有挑战性的设计性实验,涉及化学生物学的理论与操作较为全面。本实验教学可以使学生从原理上理解农药使用的必要性、农药造成的抗药性以及如何从分子结构的角度设计开发新型绿色农药。 Acetohydroxyacid synthase(AHAS) is the target enzyme of several types of super-efficient commercial herbicides attracting great international attention. The mutation of key residues of AHAS is the source of herbicide resistance formation. The nature and function of wild type and two single-site mutants of AHAS were studied thoroughly from gene cloning and mutation, protein expression and purification, to enzyme assay. Many basic manipulation and several challenging design experiments were included in the whole experiment process, in which the comprehensive theory and operation of chemical biology were involved. The course will help the students in principle to understand the necessity of pesticide application, the cause of pesticide resistance, design and development of new green pesticides from the perspective of molecular structure.
作者 欧阳砥 牛聪伟 席真 OU-YANG Di;NIU Cong-Wei;XI Zhen(College of Chemistry,Nankai University,Tianjin 300071,China)
出处 《化学教育(中英文)》 CAS 北大核心 2021年第18期113-120,共8页 Chinese Journal of Chemical Education
关键词 农药靶标的化学生物学 乙酰羟酸合成酶 除草剂 农药抗性 chemical biology of pesticide target resistance acetohydroxyacid synthase herbicide pesticide resistance
  • 相关文献

参考文献2

二级参考文献20

  • 1席真,牛聪伟,李庆霞,欧阳砥,班树荣.除草剂靶酶—AHAS酶及基因突变体与除草剂设计(I)·野生型和突变型E.coliAHAS II酶动力学性质的系统研究[J].农药学学报,2005,7(3):215-220. 被引量:12
  • 2Duggleby R G, Pang S S. Acetohydroxyacid synthase[J]. J Biochem Mol Biol, 2000, 33:1-36.
  • 3Ibdah M, Bar-Ilan A, Livnah O, et al. Homology modeling of the structure of bacterial acetohydroxy acid synthase and examination of the active site by site-directed mutagenesis[J]. Biochemistry, 1996, 35:16282-16291.
  • 4Brons-Poulsen J, Petersen N E, Horder M, et al. An improved PCR-based method for site directed mutagenesis using megaprimers[J]. Mol Cell Probes, 1998, 12:345-348.
  • 5Engel S, Vyazmensky M, Vinogradov M, et al. Role of a conserved arginine in the mechanism of acetohydroxyacid synthase[J]. J Biol Chem, 2004, 279:24803-24812.
  • 6Bradford M M. Rapid and sensitive method for quantitation of microgram quantities of protein utilizing principle of protein-dye binding[J]. Anal Biochem, 1976, 72:248-254.
  • 7Westerfeld W W. A colorimetric determination of blood acetoin[J]. J Biol Chem, 1945, 161:495-502.
  • 8Singh B K, Stidham M A, Shaner D L. Assay of acetohydroxyacid synthase[J]. Anal Biochem, 1988, 171:173-179.
  • 9Le D T, Yoon M Y, Kim Y T, et al. Roles of conserved methionine residues in tobacco acetolactate synthase[J]. Biochem Biophys Res Commun, 2003, 306:1075-7082.
  • 10Schloss J V. Chemistry and Plant Production: Herbicides Inhibiting Branched Chain Amino Acid Biosynthesis-Recent Developments (Setter J, Ed. ) [ A in M ]. Springer-Verlag,Berlin, 1994. 3-14.

共引文献12

同被引文献9

引证文献1

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部