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首页> 外文期刊>Pest Management Science >Persistence and translocation of a benzothizdiazole derivative in tomato plants in relation to systemic acquired resistance against Pseudomonas syringae pv tomato
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Persistence and translocation of a benzothizdiazole derivative in tomato plants in relation to systemic acquired resistance against Pseudomonas syringae pv tomato

机译:番茄植物中苯并噻唑二唑衍生物的持久性和易位性与对丁香假单胞菌光伏番茄的系统获得性抗性相关

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摘要

A reproducible and accurate procedure, based on HPLC analysis, has been developed to determine simultaneously acibenzolar-S-methyl (CGA 245 704) and its acid derivative (CGA 210 007) in tomato leaves. The limit of detection and quantification of the method are 0.015 and 0.15mg litre~1 for CGA 245 704 and 0.030 and 0.30mg litre1 for CGA 210 007. In tomato plants treated with 250 IXM CGA 245 704, it was found that the inducer rapidly translocates from treated leaves (cotyledons, 1st and 2nd) to untreated leaves (3rd to 5th), with the maximum translocation (40% of the total quantity found) occurring ~h after the treatment. CGA 245 704 residues decreased as time elapsed in both treated and untreated tomato leaves, reaching negligible values 72 h after treatment. The acid derivative, CGA 210 007, was formed in tomato plants as early as 2 h after CGA 245 704 treatment, albeit only in the treated leaves. CGA 210 007 residues decreased in treated tomato leaves with a trend similar to that observed for CGA 245 794· Treatment of tomato plants with CGA 245 704 or CGA 210 007 at 250 IXM systemically protected the plants against Pseudomonas syringae pv tomato attacks, the causal agent of bacterial speak disease. Evidence of this were reductions in the degree of infection, the bacterial lesion diameter and the bacterial growth in planta. Since neither CGA 245 704 nor CGA 210 007 inhibited bacterial growth in vitro and the protection against bacterial speak of tomato was observed when the two compounds were completely degraded, the protection must be due to the activation of the plant’s defence mechanisms.
机译:已经开发了一种基于HPLC分析的可重复且准确的方法,可同时测定番茄叶片中的苯并噻吩-S-甲基(CGA 245 704)及其酸衍生物(CGA 210 007)。该方法的检测和定量限分别为CGA 245 704为0.015和0.15mg升〜1,CGA 210 007为0.030和0.30mg升〜1。在用250 IXM CGA 245 704处理的番茄植株中,发现诱导剂迅速从处理过的叶片(子叶,第一和第二叶)转移到未处理的叶片(第三到第五叶),最大移位(占发现总量的40%)发生在处理后约h。在处理和未处理的番茄叶片中,随着时间的流逝,CGA 245704残留量均减少,处理后72小时达到可忽略不计的值。尽管仅在处理过的叶片中,酸衍生物CGA 210 007早在CGA 245 704处理后2小时就在番茄植株中形成。处理过的番茄叶片中的CGA 210007残留量减少,其趋势与CGA 245794观察到的趋势相似。在250 IXM下用CGA 245704或CGA 210007处理番茄植株可系统性地保护植物免受丁香假单胞菌(Pseudomonas syringae)pv番茄的侵害。细菌说疾病。有证据表明,感染程度,细菌病灶直径减小以及植物中细菌的生长减少。由于CGA 245 704和CGA 210 007均未抑制体外细菌生长,并且当两种化合物完全降解时未观察到对番茄的细菌保护作用,因此保护作用必须归因于植物防御机制的激活。

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