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The heterotrimeric Gα protein Pga1 regulates biosynthesis of penicillin, chrysogenin and roquefortine in Penicillium chrysogenum

机译:异映酰基Gα蛋白PGA1调节青霉素,Chrysogenin和Chrysogenum中青霉素和Roquefortine的生物合成

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We have studied the role of the pga1 gene of Penicillium chrysogenum, encoding the alpha subunit of a heterotrimeric G protein, in secondary metabolite production. The dominant activating pga1G42Rmutation caused an increase in the production of the three secondary metabolites penicillin, the yellow pigment chrysogenin and the mycotoxin roquefortine, whereas the dominant inactivating pga1G203Rallele and the deletion of the pga1 gene resulted in a decrease of the amount of produced penicillin and roquefortine. Chrysogenin is produced in solid medium as a yellow pigment, and its biosynthesis is clearly enhanced by the presence of the dominant activating pga1G42Rallele. Roquefortine is produced associated with mycelium during the first 3?days in submerged cultures, and is released to the medium afterwards; dominant activating and inactivating pga1 mutations result in upregulation and downregulation of roquefortine biosynthesis recpectively. Pga1 regulates penicillin biosynthesis by controlling expression of the penicillin biosynthetic genes; the three genes pcbAB, pcbC and penDE showed elevated transcript levels in transformants expressing the pga1G42Rallele, whereas in transformants with the inactivating pga1G203Rallele and in the pga1-deleted mutant their transcript levels were lower than those in the parental strains. Increase of intracellular cAMP levels had no effect on penicillin production. In summary, the dominant activating pga1G42Rallele upregulates the biosynthesis of three secondary metabolites in Penicillium chrysogenum to a different extent.
机译:我们已经研究了青霉甲基替昔甙的PGA1基因的作用,在次生脱钛矿生产中编码异映上的G蛋白的α亚基。显性激活PGA1G42和培养的三次代谢物青霉素,黄色颜料Chrysogenin和霉菌毒素罗奇亚弗(霉菌毒素)增加,而灭活PGA1G203RallelE和PGA1基因的缺失导致产生的青霉素和罗氏量减少。 Chrysogenin以固体培养基生产为黄色颜料,通过存在显性活化PGA1G42Rallele明确提高其生物合成。在浸没式培养物中的前3天内与菌丝体相关联的羊貂鱼,然后之后释放到介质;显性激活和失活的PGA1突变导致康菲塔内生物合成的上调和下调。 PGA1通过控制青霉素生物合成基因的表达来调节青霉素生物合成;三个基因PCBAB,PCBC和PENDE在表达PGA1G42RALLE的转化体中显示出升高的转录物水平,而在与灭活PGA1G203RALLE的转化体中,在PGA1缺失的突变体中,它们的转录水平低于父母株中的转录物水平。细胞内阵营水平的增加对青霉素产生没有影响。总之,显性激活PGA1G42Rallele将Penicillium Chrysogenum中的三次代谢产物的生物合成升高到不同程度。

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