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Increased biomass and lipid production by continuous cultivation of Nannochloropsis salina transformant overexpressing a bHLH transcription factor

机译:通过连续培养Nannochloropsis Salina转化体的过表达BHLH转录因子,增加生物量和脂质生产

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摘要

Microalgae are promising feedstocks for sustainable and eco-friendly production of biomaterials, which can be improved by genetic engineering. It is also necessary to optimize the processes to produce biomaterials from engineered microalgae. We previously reported that genetic improvements of an industrial microalga Nannochloropsis salina by overexpressing a basic helix-loop-helix transcription factor (NsbHLH2). These transformants showed an improved growth and lipid production particularly during the early phase of culture under batch culture. However, they had faster uptake of nutrients, resulting in earlier starvation and reduced growth during the later stages. We attempted to optimize the growth and lipid production by growing one of the transformants in continuous culture with variable dilution rate and feed nitrogen concentration. Relative to wild-type, NsbHLH2 transformant consumed more nitrate at a high dilution rate (0.5 day(-1)), and had greater biomass production. Subsequently, nitrogen limitation at continuous cultivation led to an increased fatty acid methyl ester production by 83.6 mg l(-1) day(-1). To elucidate genetic mechanisms, we identified the genes containing E-boxes, known as binding sites for bHLH transcription factors. Among these, we selected 18 genes involved in the growth and lipid metabolism, and revealed their positive contribution to the phenotypes via quantitative real-time polymerase chain reaction. These results provide proof-of-concept that NsbHLH2 can be used to produce biomass and lipids.
机译:微藻是可持续和环保生物材料生产的前途原料,可以通过基因工程来改善。还有必要优化从工程化微藻生产生物材料的过程。我们之前报道了通过过表达碱性螺旋环 - 螺旋转录因子(NSBHLH2)来遗传改善工业微藻Nannochloropsis Salina。这些转化体尤其显示出改善的生长和脂质生产,特别是在分批培养下培养的早期阶段。然而,它们具有更快的营养素吸收,导致早期的饥饿和后期阶段的增长降低。我们试图通过使用可变稀释率和饲料氮浓度的连续培养物中的一种转化体来优化生长和脂质生产。相对于野生型,NSBHLH2转化体以高稀释率(0.5天(-1))消耗更多的硝酸盐,并具有更大的生物质产生。随后,连续培养时的氮气限制导致增加脂肪酸甲酯产生83.6mg L(-1)天(-1)。为了阐明遗传机制,我们鉴定了含有E箱的基因,称为BHLH转录因子的结合位点。其中,我们选择了参与生长和脂质代谢的18个基因,并通过定量实时聚合酶链反应揭示了对表型的积极贡献。这些结果提供了概念的证据,即NSBHLH2可用于产生生物质和脂质。

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