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Orthologous promoters from related methylotrophic yeasts surpass expression of endogenous promoters of Pichia pastoris

机译:来自相关甲型繁殖酵母的直向性启动子超越<斜视> Pichia Pastoris的内源性启动子的表达

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Methylotrophic yeasts such as Komagataella phaffii (syn. Pichia pastoris , Pp ), Hansenula polymorpha ( Hp ), Candida boidinii ( Cb ) and Pichia methanolica ( Pm ) are widely used protein production platforms. Typically, strong, tightly regulated promoters of genes coding for their methanol utilization (MUT) pathways are used to drive heterologous gene expression. Despite highly similar open reading frames in the MUT pathways of the four yeasts, the regulation of the respective promoters varies strongly between species. While most endogenous Pp MUT promoters remain tightly repressed after depletion of a repressing carbon, Hp , Cb and Pm MUT promoters are derepressed to up to 70% of methanol induced levels, enabling methanol free production processes in their respective host background. Here, we have tested a series of orthologous promoters from Hp , Cb and Pm in Pp . Unexpectedly, when induced with methanol, the promoter of the HpMOX gene reached very similar expression levels as the strong methanol, inducible, and most frequently used promoter of the Pp alcohol oxidase 1 gene ( P _( PpAOX1 )). The HpFMD promoter even surpassed P _( PpAOX1 ) up to three-fold, when induced with methanol, and reached under methanol-free/derepressed conditions similar expression as the methanol induced P _( PpAOX1 ). These results demonstrate that orthologous promoters from related yeast species can give access to otherwise unobtainable regulatory profiles and may even considerably surpass endogenous promoters in P. pastoris .
机译:Komagataella phaffii(Syn。Pichia Pastoris,PP),Hansenula多肽(HP),念珠菌Boidinii(CB)和Pichia Methanolica(PM)是广泛使用的蛋白质生产平台。通常,编码其甲醇使用(mut)途径的基因的强烈紧密调节的启动子用于驱动异源基因表达。尽管在四酵母的MUT途径中具有高度相似的开放阅读框架,但各自的启动子的调节在物种之间强烈变化。虽然大多数内源性PP mut启动子在抑制碳的耗尽后保持紧密抑制,但是HP,CB和PM mut启动子对高达70%的甲醇诱导的水平进行大量,使得在其各自的宿主背景中能够提供甲醇的生产过程。在这里,我们已经测试了PP中的HP,CB和PM的一系列原理启动子。出乎意料的是,当用甲醇诱导时,HPMOX基因的启动子达到了PP醇氧化酶1基因的强甲醇,诱导和最常用的促进剂非常相似的表达水平(P _(PPAOX1))。当用甲醇诱导时,HPFMD启动子甚至超过P _(PPAOX1)至三倍,并且在无甲醇/ DERE甲基条件下达到与甲醇诱导的P _(PPAOX1)相似的表达。这些结果表明,相关酵母物种的直言不讳的启动子可以进入否则无法获得的调节型材,并且甚至可能在P. Pastoris中显着超过内源性启动子。

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