Advanced Biomass R&D Center, Yuseong-gu, Daejeon, Republic of Korea.
Department of Chemical and Biomolecular Engineering, KAIST, Yuseong-gu, Daejeon, Republic of Korea.
Biotechnol Bioeng. 2019 Mar;116(3):555-568. doi: 10.1002/bit.26894. Epub 2019 Jan 3.
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 ), 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 day . 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.
微藻是有前途的生物材料可持续和环保生产的原料,可以通过基因工程进行改良。还需要优化从工程微藻生产生物材料的工艺。我们之前报道过,通过过表达碱性螺旋-环-螺旋转录因子(NsbHLH2)来遗传改良工业微藻盐藻(Nannochloropsis salina)。这些转化体在分批培养的早期阶段表现出更好的生长和脂质生产能力。然而,它们对营养物质的吸收更快,导致在后期更早出现饥饿和生长减少。我们试图通过在连续培养中以可变稀释率和进料氮浓度来生长其中一个转化体来优化生长和脂质生产。与野生型相比,NsbHLH2 转化体在高稀释率(0.5 天)下消耗更多的硝酸盐,并产生更多的生物量。随后,连续培养中的氮限制导致脂肪酸甲酯的产量增加了 83.6 mg l day。为了阐明遗传机制,我们鉴定了含有 E 盒的基因,E 盒是碱性螺旋-环-螺旋转录因子的结合位点。在这些基因中,我们选择了 18 个与生长和脂质代谢有关的基因,并通过实时定量聚合酶链反应揭示了它们对表型的积极贡献。这些结果证明 NsbHLH2 可用于生产生物量和脂质。