Shen Jingjing, Li Yongfeng, Huang Xing, Yu Xinyan, He Jian, Li Shunpeng
Key Laboratory of Microbiological Engineering of Agricultural Environment, Ministry of Agriculture, Microbiology Department, College of Life Science, Nanjing Agricultural University, Nanjing 210095, China.
Sheng Wu Gong Cheng Xue Bao. 2009 Jul;25(7):1007-13.
Acetohydroxyacid synthase (AHAS) catalyses the first reaction in the pathway for synthesis of the branched-chain amino acids. AHAS is the target for sulfonylurea, imidazolinone and other AHAS-inhibitor herbicides. Herbicides-resistant AHAS genes have potential application in plant transgenetic engineering and development of new generation herbicide. The AHAS isozyme genes ilvBN, ilvGM and ilvIH were cloned from metsulfuron-methyl resistant strain Klebsiella sp. HR11 and metsulfuron-methyl sensitive strain Klebsiella pneumoniae MGH 78578. Homologous sequences comparison indicated that the differences in AHAS isozyme genes at amino acid levels between strain HR11 and strain MGH 78578 were mainly on the large subunits of ilvBN and ilvGM. The three AHAS isozyme genes from HR11 and MGH 78578 were ligated into the expression vector pET29a(+) and expressed in Escherichia coli BL21, respectively. The results of enzyme inhibition assay showed that only ilvBN and ilvGM from strain HR11 showed strong resistance to AHAS-inhibitor herbicides, while ilvIH from strain HR11 and ilvBN, ilvGM and ilvIH from strain MGH78578 were sensitive to AHAS-inhibitor herbicides.
乙酰羟酸合酶(AHAS)催化支链氨基酸合成途径中的第一步反应。AHAS是磺酰脲类、咪唑啉酮类及其他AHAS抑制剂类除草剂的作用靶点。抗除草剂AHAS基因在植物转基因工程及新一代除草剂开发中具有潜在应用价值。从耐甲磺隆菌株克雷伯氏菌HR11和对甲磺隆敏感的肺炎克雷伯氏菌MGH 78578中克隆了AHAS同工酶基因ilvBN、ilvGM和ilvIH。同源序列比较表明,HR11菌株和MGH 78578菌株之间AHAS同工酶基因在氨基酸水平上的差异主要存在于ilvBN和ilvGM的大亚基上。将来自HR11和MGH 78578的三个AHAS同工酶基因分别连接到表达载体pET29a(+)中,并在大肠杆菌BL21中表达。酶抑制试验结果表明,只有HR11菌株的ilvBN和ilvGM对AHAS抑制剂类除草剂表现出强抗性,而HR11菌株的ilvIH以及MGH78578菌株的ilvBN、ilvGM和ilvIH对AHAS抑制剂类除草剂敏感。