Novel, unnatural benzo-1,2,3-thiadiazole-7-carboxylate elicitors of taxoid biosynthesis

被引:34
|
作者
Xu, Yufang
Zhao, Zhengjiang
Qian, Xuhong
Qian, Zhigang
Tian, Wenhong
Zhong, Jianjiang
机构
[1] E China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Sch Pharm, Shanghai 200237, Peoples R China
[2] E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Shanghai 200237, Peoples R China
关键词
benzo-1,2,3-thiadiazole-7-carboxylate derivatives; chemically synthesized elicitors; plant defense; plant cell culture; taxoid induction; secondary metabolites; CELL-SUSPENSION CULTURES; PHENYLALANINE AMMONIA-LYASE; METHYL JASMONATE; OXIDATIVE BURST; TAXUS-CHINENSIS; SALICYLIC-ACID; REPEATED ELICITATION; PHASEOLUS-LUNATUS; PLANT DEFENSE; BACCATIN III;
D O I
10.1021/jf0618574
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
In order to establish the chemical biological technology for production of valuable secondary metabolites, a novel family of unnatural elicitors derived from the plant activator benzo-1,2,3-thiadiazole-7-carboxylic acid were designed and synthesized. New synthetic elicitors that showed powerful eliciting activities upon taxoid biosynthesis by Taxus chinensis suspension cells were obtained. For example, benzo-1,2,3-thiadiazole-7-carboxylic acid 2-(2-hydroxybenzoxyl) ethyl ester was more effective and resulted in nearly 40% increase in taxuyunnanine C content and production in comparison with methyl jasmonate, which was previously reported as the most powerful chemical elicitor for taxoid biosynthesis. The novel class of elicitors was found to induce plant defense responses, including promotion of H2O2 levels originating from oxidative burst and activation of phenylalanine ammonia lyase. Interestingly the plant defense responses induced corresponded well to the superior stimulating activity in T. chinensis cell cultures. The work indicates that the newly synthesized benzothiadiazoles can act as a new family of elicitors for taxoid biosynthesis in plant cells.
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页码:8793 / 8798
页数:6
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