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Functional overexpression and characterization of lipogenesis-related genes in the oleaginous yeast Yarrowia lipolytica

机译:产油酵母解脂耶氏酵母中脂肪生成相关基因的功能性过表达和表征

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Single cell oil (SCO) is an attractive energy source due to scalability, utilization of low-cost renewable feed-stocks, and type of product(s) made. Engineering strains capable of producing high lipid titers and yields is crucial to the economic viability of these processes. However, lipid synthesis in cells is a complex phenomenon subject to multiple layers of regulation, making gene target identification a challenging task. In this study, we aimed to identify genes in the oleaginous yeast Yarrowia lipolytica whose overexpression enhances lipid production by this organism. To this end, we examined the effect of the overexpression of a set of 44 native genes on lipid production in Y. lipolytica, including those involved in glycerolipid synthesis, fatty acid synthesis, central carbon metabolism, NADPH generation, regulation, and metabolite transport and characterized each resulting strain's ability to produce lipids growing on both glucose and acetate as a sole carbon source. Our results suggest that a diverse subset of genes was effective at individually influencing lipid production in Y. lipolytica, sometimes in a substrate-dependent manner. The most productive strain on glucose overexpressed the diacylglycerol acyltransferase DGA2 gene, increasing lipid titer, cellular content, and yield by 236, 165, and 246 %, respectively, over our control strain. On acetate, our most productive strain overexpressed the acylglycerol-phosphate acyltransferase SLC1 gene, with a lipid titer, cellular content, and yield increase of 99, 91, and 151 %, respectively, over the control strain. Aside from genes encoding enzymes that directly catalyze the reactions of lipid synthesis, other ways by which lipogenesis was increased in these cells include over-expressing the glycerol-3-phosphate dehydrogenase (GPD1) gene to increase production of glycerol head groups and over-expressing the 6-phosphogluconolactonase (SOL3) gene from the oxidative pentose phosphate pathway to increase NADPH availability for fatty acid synthesis. Taken together, our study demonstrates that the overall kinetics of microbial lipid synthesis is sensitive to a wide variety of factors. Fully optimizing a strain for single cell oil processes could involve manipulating and balancing many of these factors, and, due to mechanistic differences by which each gene product investigated here impacts lipid synthesis, there is a high likelihood that many of these genes will work synergistically to further increase lipid production when simultaneously overexpressed.
机译:由于可扩展性,低成本可再生原料的利用以及所生产产品的类型,单细胞油(SCO)是一种有吸引力的能源。能够产生高脂质滴度和高产量的工程菌株对于这些方法的经济可行性至关重要。然而,细胞中脂质的合成是一个复杂的现象,需要进行多层调节,使基因靶标的鉴定成为一项艰巨的任务。在这项研究中,我们旨在鉴定含油酵母解脂耶氏酵母中的基因,该基因的过表达增强了该生物体的脂质生产。为此,我们研究了一组44个天然基因过表达对解脂耶氏酵母中脂质产生的影响,包括参与甘油脂合成,脂肪酸合成,中心碳代谢,NADPH生成,调节和代谢物转运以及表征了每种菌株产生的能力,即它们在葡萄糖和乙酸盐上作为唯一碳源生长的脂质。我们的结果表明,不同的基因子集可以有效地单独影响解脂耶氏酵母中的脂质产生,有时以底物依赖性方式有效。最高产的葡萄糖菌株过表达二酰基甘油酰基转移酶DGA2基因,与我们的对照菌株相比,脂质滴度,细胞含量和产率分别提高了236%,165%和246%。在乙酸盐上,我们最有生产力的菌株过表达了酰基甘油-磷酸酯酰基转移酶SLC1基因,与对照菌株相比,脂质滴度,细胞含量和产率分别提高了99%,91%和151%。除了编码直接催化脂质合成反应的酶的基因外,在这些细胞中增加脂肪生成的其他方法包括过表达甘油3磷酸脱氢酶(GPD1)基因以增加甘油头基的产生和过表达氧化戊糖磷酸途径中的6-磷酸葡萄糖酸内酯酶(SOL3)基因可增加NADPH在脂肪酸合成中的利用率。综上所述,我们的研究表明微生物脂质合成的整体动力学对多种因素敏感。为单细胞油过程完全优化菌株可能涉及操纵和平衡许多这些因素,并且由于本文研究的每种基因产物影响脂质合成的机制差异,这些基因中的许多极有可能协同作用同时过量表达时,进一步增加脂质的产生。

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