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Cloning and functional analysis of the second geranylgeranyl diphosphate synthase gene influencing helvolic acid biosynthesis in Metarhizium anisopliae

机译:影响香附子异戊酸生物合成的第二个香叶基香叶基二磷酸香叶酯合酶基因的克隆和功能分析

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A gene (ggs2) having high similarity to the geranylgeranyl diphosphate synthase (GGPP synthase) gene was cloned from Metarhizium anisopliae NAFF635007. The ggs2 gene (1,239-bp open reading frame with no intron) encoded a protein of 412 amino acids, and the transcription occurred only after late log-phase during the growth. Gene disruption of ggs2, performed to clarify the function in M. anisopliae, resulted in decreased GGPP synthase activity together with a slight delay of sporulation. An high performance liquid chromatography (HPLC) comparison of compound profiles between the wild-type strain and the disruptant revealed that a compound was abolished by the ggs2 disruption. Purification and structural elucidation by 1H-NMR and mass spectrometry analyses revealed that the lost compound is helvolic acid. Furthermore, the pathogenic- ity assay against two species of insect larvae revealed that the ggs2-disruptant possessed much weaker toxicity than the wild-type strain. Based on these results, it was concluded that ggs2 encodes the GGPP synthase influencing the biosynthesis of secondary metabolites in various species, including helvolic acid in M. anisopliae. To the best of our knowledge, this is the first report to identify a GGPP synthase gene related to secondary metabolism in entomopathogenic fungi.
机译:从棉兰分枝杆菌NAFF635007克隆了与香叶基香叶基二磷酸合酶(GGPP合酶)基因具有高度相似性的基因(ggs2)。 ggs2基因(没有内含子的1,239 bp开放阅读框)编码412个氨基酸的蛋白质,并且转录仅在生长过程中的对数后期才发生。 ggs2的基因破坏是为了澄清沙门氏菌的功能,导致GGPP合酶活性降低,孢子形成略有延迟。高效液相色谱(HPLC)比较野生型菌株和破坏剂之间的化合物概况,发现化合物因ggs2破坏而被废除。通过1 H-NMR和质谱分析的纯化和结构解析表明,丢失的化合物为羟乙酸。此外,针对两种昆虫幼虫的致病性分析表明,ggs2破坏剂的毒性比野生型菌株弱得多。根据这些结果,可以得出结论,ggs2编码GGPP合酶,影响各种物种中次生代谢产物的生物合成,包括分枝杆菌中的羟乙酸。据我们所知,这是鉴定与致病性真菌次级代谢相关的GGPP合酶基因的第一份报告。

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