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

机译:新型,非天然的紫杉烷生物合成苯并1,2,3-噻二唑-7-羧酸酯引发剂

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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.
机译:为了建立用于生产有价值的次级代谢产物的化学生物学技术,设计并合成了衍生自植物活化剂苯并-1,2,3-噻二唑-7-羧酸的新的非天然引发剂家族。获得了新的合成激发子,其在由南方红豆杉悬浮细胞生物合成紫杉烷后显示出强大的激发活性。例如,与茉莉酸甲酯相比,苯并-1,2,3-噻二唑-7-羧酸2-(2-羟基苯甲酰基)乙酯更有效,并且紫杉烷氨酸C含量和产量提高了近40%。以前被报道为紫杉类生物合成中最强大的化学激发剂。发现了新颖的引发剂类,其诱导植物防御反应,包括促进源自氧化爆发和苯丙氨酸氨裂合酶活化的H 2 O 2水平。有趣的是,诱导的植物防御反应与中华三叶草细胞培养物中的优异刺激活性很好地对应。这项工作表明,新合成的苯并噻二唑可作为植物细胞中紫杉烷类生物合成的新引发剂家族。

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