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Differential expression of anthocyanin biosynthesis genes in Daucus carota callus culture in response to ammonium and potassium nitrate ratio in the culture medium

机译:培养基中硝酸铵和硝酸钾比值对胡萝卜胡萝卜愈伤组织花色苷生物合成基因的差异表达

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摘要

Anthocyanins are major water-soluble and dynamic colouring plant pigment present in plant tissues with the high antioxidant properties. The role of ammonium and potassium nitrate in the culture medium on anthocyanin augmentation is probed thoroughly, but the mechanism of its biosynthesis continues to be unclear. Hence, the present study was undertaken to optimise nitrate ratio in the culture medium for anthocyanin augmentation and examination of its biosynthesis pathway in callus culture of Daucus carota. MS basal medium fortified with various ratio of NH4NO3:KNO3 was employed to find their impact on biomass, anthocyanin augmentation and the expression profile of anthocyanin biosynthesis genes in the callus culture. The data indicated that the highest anthocyanin content (9.30 ± 0.25 mg/100 g FW) was seen in callus grown on the medium supplemented with 20.0 mM NH4NO3:37.6 mM KNO3 and the least was seen in the medium which contained 40.0 mM NH4NO3:18.8 mM KNO3 (2.74 ± 0.27 mg/100 g FW). This indicates an optimal concentration of NH4NO3:KNO3 ratio is essential to produce a higher amount of anthocyanin in in vitro culture. Meanwhile, anthocyanin biosynthesis genes were differentially expressed as confirmed by qRT-PCR in the time interval of 5, 10, 15, 20 and 25 days. The transcript levels of nine anthocyanin biosynthesis genes were increased in the response of varying NH4NO3:KNO3 ratio in the medium. The transcript level of early genes PAL, 4CL, CHS and CHI increased by 19.5, 21.0, 16.2 and 9.98-fold, respectively, compared with control. In addition, late biosynthesis genes LDOX and UFGT resulted in the transcript level of 11.3 and 13.6-fold, respectively.
机译:花青素是存在于植物组织中的主要水溶性和动态着色植物色素,具有很高的抗氧化性能。氨水和硝酸钾在培养基中对花青素增加的作用已被彻底探究,但其生物合成的机制仍不清楚。因此,进行本研究以优化培养基中的硝酸盐比率以增加花色苷,并检查其在胡萝卜茎愈伤组织培养中的生物合成途径。使用以各种比例的NH4NO3:KNO3强化的MS基础培养基,研究其对愈伤组织培养物中生物量,花色苷增加和花色苷生物合成基因表达谱的影响。数据表明,在添加20.0 mM NH4NO3:37.6 mM KNO3的培养基上生长的愈伤组织中,花青素含量最高(9.30±±0.25 mg / 100 g FW),而在包含40.0 mM NH4NO3:18.8的培养基中观察到的花青素含量最高mM KNO3(2.74±0.27 mg / 100 g FW)。这表明最佳浓度的NH4NO3:KNO3比值对于在体外培养中产生更高量的花色苷至关重要。同时,如通过qRT-PCR证实的,在5、10、15、20和25天的时间间隔中花色苷生物合成基因差异表达。在培养基中变化的NH4NO3:KNO3比值的响应中,九个花色苷生物合成基因的转录水平增加了。与对照相比,早期基因PAL,4CL,CHS和CHI的转录水平分别增加了19.5、21.0、16.2和9.98倍。此外,后期生物合成基因LDOX和UFGT的转录水平分别为11.3和13.6倍。

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