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首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >The modification of phytosterol profiles and in vitro photosynthetic electron transport of Galium aparine L. (cleavers) treated with the fungicide, epoxiconazole.
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The modification of phytosterol profiles and in vitro photosynthetic electron transport of Galium aparine L. (cleavers) treated with the fungicide, epoxiconazole.

机译:杀菌剂环氧环唑处理的镓天冬氨酸L.(切割刀)的植物甾醇谱的修饰和体外光合电子传递。

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摘要

Foliar application of the triazole fungicide, epoxiconazole, retarded the growth of Galium aparine (cleavers). GC-MS and GC analysis clearly indicated that phytosterol biosynthesis in stem and leaflet tissue was significantly affected by this treatment. For example, in leaflet tissues, 125 g ai ha-1 (field rate) caused reductions in campesterol and sitosterol of 81 and 75%, respectively. C14-methyl phytosterol such as 14alpha-methylergost-8-enol, obtusifoliol and dihydroobtusifoliol were detected in treated tissues, indicating that epoxiconazole inhibits the cytochrome P-450 dependent obtusifoliol 14alpha-demethylase. In addition, ratios of campesterol to sitosterol were reduced. Stigmasterol was not detected in control or treated tissues. Preliminary determination of photosynthetic characteristics of isolated thylakoids from treated plants indicated that electron transport and oxygen evolution were impaired by epoxiconazole, and that these effects were dose-related. Ten days after treatment, oxygen evolution from thylakoids (determined as electron flow from water to ferricyanide) isolated from control plants was 24.2 鎚ol mg-1 chl h-1, whilst treatment with 125 g and 250 g ai ha-1 reduced this rate to 15.2 鎚ol and 8.2 鎚ol mg-1 chl h-1, an inhibition of 37 and 67% respectively. These results suggest that epoxiconazole influences thylakoid integrity and function in addition to phytosterol biosynthesis in G. aparine.
机译:叶面喷洒三唑类杀真菌剂环磷唑,可抑制猪a素(切割刀)的生长。 GC-MS和GC分析清楚地表明,这种处理显着影响茎和小叶组织中植物甾醇的生物合成。例如,在小叶组织中,125 g ai ha-1(田间速率)导致菜油甾醇和谷固醇减少分别为81%和75%。在处理过的组织中检测到C14-甲基植物甾醇,例如14α-甲基麦角8-烯醇,奥托西佛利醇和二氢奥托西佛利醇,表明环氧康唑可抑制细胞色素P-450依赖性奥托西佛利醇14α-脱甲基酶。另外,菜油甾醇与谷甾醇的比例降低。在对照或经处理的组织中未检测到Stigmasterol。初步确定从处理过的植物中分离的类囊体的光合特性表明,环氧环唑会损害电子传输和氧气的释放,并且这些效应与剂量有关。处理十天后,从对照植物中分离出的类囊体中的氧释放量(确定为从水到铁氰化物的电子流)为24.2锤酚mg-1 chl h-1,而用125 g和250 g ai ha-1处理降低了该速率抑制15.2锤醇和8.2锤醇mg-1 chl h-1,分别抑制37%和67%。这些结果表明,环磷唑除了影响G.aparine中植物甾醇的生物合成外,还影响类囊体的完整性和功能。

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