Park Yun-Ji, Han Jong-Eun, Lee Hyoshin, Jung Yu-Jin, Murthy Hosakatte Niranjana, Park So-Young
Department of Horticulture, Division of Animal, Horticultural and Food Sciences, Chungbuk National University, Cheongju, 28644, Republic of Korea.
Department of Forest Genetic Resources, National Institute of Forest Science, 39 Onjeong-ro, Suwon, 16631, Republic of Korea.
AMB Express. 2020 Aug 13;10(1):140. doi: 10.1186/s13568-020-01079-3.
Miraculin, derived from the miracle fruit (Synsepalum dulcificum), is a taste-regulating protein that interacts with human sweet-taste receptors and transforms sourness into sweet taste. Since miracle fruit is cultivated in West Africa, mass production of miraculin is limited by regional and seasonal constraints. Here, we investigated mass production of recombinant miraculin in carrot (Daucus carota L.) callus cultures using an air-lift bioreactor. To increase miraculin expression, the oxidative stress-inducible SWPA2 promoter was used to drive the expression of miraculin gene under various stress treatments. An 8 h treatment of hydrogen peroxide (HO) and salt (NaCl) increased the expression of miraculin gene by fivefold compared with the untreated control. On the other hand, abscisic acid, salicylic acid, and methyl jasmonate treatments showed no significant impact on miraculin gene expression compared with the control. This shows that since HO and NaCl treatments induce oxidative stress, they activate the SWPA2 promoter and consequently up-regulate miraculin gene expression. Thus, the results of this study provide a foundation for industrial-scale production of recombinant miraculin protein using transgenic carrot cells as a heterologous host.
奇异果甜蛋白是从神秘果(Synsepalum dulcificum)中提取的一种味觉调节蛋白,它与人的甜味受体相互作用,能将酸味转化为甜味。由于神秘果生长于西非,奇异果甜蛋白的大规模生产受到地域和季节的限制。在此,我们研究了利用气升式生物反应器在胡萝卜(Daucus carota L.)愈伤组织培养物中大规模生产重组奇异果甜蛋白的方法。为提高奇异果甜蛋白的表达量,在各种胁迫处理下,利用氧化应激诱导型SWPA2启动子驱动奇异果甜蛋白基因的表达。与未处理的对照相比,用双氧水(HO)和盐(NaCl)处理8小时可使奇异果甜蛋白基因的表达量提高五倍。另一方面,与对照相比,脱落酸、水杨酸和茉莉酸甲酯处理对奇异果甜蛋白基因的表达没有显著影响。这表明,由于HO和NaCl处理可诱导氧化应激,它们激活了SWPA2启动子,从而上调了奇异果甜蛋白基因的表达。因此,本研究结果为利用转基因胡萝卜细胞作为异源宿主进行重组奇异果甜蛋白的工业化生产奠定了基础。