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Unraveling the regulation of sophorolipid biosynthesis in Starmerella bombicola

机译:解开Starmerella Bomicola中Sophorlipid生物合成的调节

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Starmerella bombicola very efficiently produces the secondary metabolites sophorolipids (SLs). Their biosynthesis is not-growth associated and highly upregulated in the stationary phase. Despite high industrial and academic interest, the underlying regulation of SL biosynthesis remains unknown. In this paper, potential regulation of SL biosynthesis through the telomere positioning effect (TPE) was investigated, as the SL gene cluster is located adjacent to a telomere. An additional copy of this gene cluster was introduced elsewhere in the genome to investigate if this results in a decoy of regulation. Indeed, for the new strain, the onset of SL production was shifted to the exponential phase. This result was confirmed by RT-qPCR analysis. The TPE effect was further investigated by developing and applying a suitable reporter system for this non-conventional yeast, enabling non-biased comparison of gene expression between the subtelomeric CYP52M1- and the URA3 locus. This was done with a constitutive endogenous promotor (pGAPD) and one of the endogenous promotors of the SL biosynthetic gene cluster (pCYP52M1). A clear positioning effect was observed for both promotors with significantly higher GFP expression levels at the URA3 locus. No clear GFP upregulation was observed in the stationary phase for any of the new strains.
机译:Starmerella Bombicola非常有效地产生次级代谢物槐胶(SLS)。它们的生物合成在固定阶段有关和高度上调的不良增长。尽管工业高等,但SL生物合成的潜在调节仍然未知。在本文中,研究了通过端粒定位效果(TPE)对SL生物合成的潜在调节,因为SL基因簇位于端粒附近。在基因组的其他地方引入了该基因簇的另一种拷贝,以研究这是否导致调节的诱饵。实际上,对于新菌株,SL生产的发作转移到指数阶段。通过RT-QPCR分析证实了该结果。通过对该非常规酵母进行合适的报告系统进一步研究TPE效应,从而能够在子细胞计CYP52M1-和URA3基因座之间的基因表达的非偏见比较。这是用组成型内源性启动子(PGAPD)和SL生物合成基因簇(PCYP52M1)的内源引导者进行的。对于ura3基因座的GFP表达水平显着较高的推广剂,观察到明确的定位效果。对于任何新菌株的固定相,未观察到明确的GFP上调。

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