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

  • Yufang Xu
  • , Zhengjiang Zhao
  • , Xuhong Qian*
  • , Zhigang Qian
  • , Wenhong Tian
  • , Jianjiang Zhong
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

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.

Original languageEnglish
Pages (from-to)8793-8798
Number of pages6
JournalJournal of Agricultural and Food Chemistry
Volume54
Issue number23
DOIs
StatePublished - 15 Nov 2006
Externally publishedYes

Keywords

  • Benzo-1,2,3-thiadiazole-7-carboxylate derivatives
  • Chemically synthesized elicitors
  • Plant cell culture
  • Plant defense
  • Secondary metabolites
  • Taxoid induction

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