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首页> 外文期刊>Molecular Plant-Microbe Interactions >Expression Pattern of Genes Encoding Farnesyl Diphosphate Synthase and Sesquiterpene Cyclase in Cotton Suspension-Cultured Cells Treated with Fungal Elicitors
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Expression Pattern of Genes Encoding Farnesyl Diphosphate Synthase and Sesquiterpene Cyclase in Cotton Suspension-Cultured Cells Treated with Fungal Elicitors

机译:真菌诱导剂处理棉花悬浮培养细胞中法呢基二磷酸合酶和倍半萜烯环化酶编码基因的表达模式

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摘要

Cotton plants accumulate sesquiterpene aldehydes in pigment glands. The two enzymes farnesyl diphosphate synthase (FPS) and (+)-δ-cadinene synthase (CAD), a sesquiterpene cyclase, are involved in the biosynthesis of these secondary metabolites. A full-length cDNA ( garfps ) encoding FPS was isolated from Gossypium arboreum and identified by in vitro enzymatic assay of the garfps protein heterologously expressed in Escherichia coli . Treatment of G. arboreum suspension-cultured cells with an elicitor preparation obtained from the phytopathogenic fungus Verticillium dahliae dramatically induced transcription of both FPS and CAD, paralleling the accumulation of the sesquiterpene aldehydes in these cells. For G. australe, a wild species from Australia, the V. dahliae elicitor preparation also caused an induction of FPS but only a low rate of induction of CAD, apparently because of a constitutive expression of the sesquiterpene cyclase gene in suspension-cultured cells. Two transcripts and proteins of FPS were detected in the elicited G. australe cells; the smaller FPS seemed to be de novo synthesized after elicitation. Furthermore, G. australe -cultured cells accumulated the cadinene, instead of sesquiterpene aldehydes, indicating that the biosynthetic pathway leading to sesquiterpene aldehydes was absent or blocked after FPP cyclization.
机译:棉花植物在色素腺体中积累倍半萜醛。法呢基二磷酸合酶(FPS)和倍半萜烯环化酶(+)-δ-卡丹烯合酶(CAD)这两种酶参与了这些次生代谢产物的生物合成。从棉铃兰中分离到编码FPS的全长cDNA(garfps),并通过体外酶法鉴定了在大肠杆菌中异源表达的garfps蛋白。用得自植物病原性真菌黄萎病菌的激发剂制剂处理植物假单胞菌悬浮培养的细胞,可显着诱导FPS和CAD的转录,与倍半萜烯醛在这些细胞中的积累平行。对于来自澳大利亚的野生种G. australe,V。dahliae激发子制剂也引起了FPS的诱导,但CAD的诱导率却很低,这显然是由于倍半萜环化酶基因在悬浮培养细胞中的组成型表达。在诱发的G. australe细胞中检测到FPS的两个转录本和蛋白质。较小的FPS似乎是在激发后重新合成的。此外,在GPP的培养下,细胞积累了卡丁烯,而不是倍半萜醛,这表明在FPP环化后,没有导致倍半萜醛的生物合成途径。

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