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首页> 外文期刊>植物環境工学 >Effect of red light and blue light on the anthocyanin accumulation and expression of anthocyanin biosynthesis genes in red-leaf lettuce.
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Effect of red light and blue light on the anthocyanin accumulation and expression of anthocyanin biosynthesis genes in red-leaf lettuce.

机译:红光和蓝光对红叶莴苣中花青素生物合成基因的花青素累积和表达的影响。

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摘要

Since anthocyanin accumulation would become insufficient if protected culture of the red leaf lettuce is carried out, the method for improving the quality of lettuce is required. Our previous study showed that the combined irradiation of blue light and UV-B at night resulted in notable promotion of anthocyanin synthesis. In this research, we investigated whether the blue light intensity of a light period would influence anthocyanin accumulation. When the blue light intensity of the light period was increased, anthocyanin accumulation was promoted, but it was restricted to a temporary effect. To the next, we investigated the anthocyanin accumulation of the red leaf lettuce under low photosynthesis photon flux density condition using red and blue LED. As a result, anthocyanin content was the highest in 100 micro mol m-2 s-1 blue light or simultaneous irradiation with 20 micro mol m-2 s-1 red and 80 micro mol m-2 s-1 blue light. The second was simultaneous irradiation with 50 micro mol m-2 s-1 red and 50 micro mol m-2 s-1 blue light, the 3rd was simultaneous irradiation with 80 micro mol m-2 s-1 red and 20 micro mol m-2 s-1 blue light, and 100 micro mol m-2 s-1 red light was the lowest. To clarify the molecular regulation of the anthocyanin biosynthesis by light quality, we isolated five anthocyanin biosynthetic genes, CHS, F3H, DFR, ANS and UFGT from the red-leaf lettuce. Gene expression analysis from treatment to 48 hours was conducted by the real-time PCR method. The expression of the genes which involve in anthocyanin biosynthesis were not able to be observed in 100 micro mol m-2 s-1 red light. On the other hand, in the case of 100 micro mol m-2 s-1 blue light and simultaneous irradiation with 50 micro mol m-2 s-1 red and 50 micro mol m-2 s-1 blue light, up to 24 hours after the light quality treatments, the enhanced expression of CHS, F3H, DFR, ANS, and UFGT were observed. Moreover, although the expression of F3H, DFR, and ANS were high level in simultaneous irradiation with 80 micro mol m-2 s-1 red and 20 micro mol m-2 s-1 blue light, the expression of CHS and UFGT was not so high. Therefore, it became clear to the biosynthetic mechanism of anthocyanin of red leaf lettuce that the ratio of red light and blue light is closely related.
机译:由于在进行了红叶莴苣的受保护培养的情况下,花青素积累将变得不足,因此需要提高生菜质量的方法。我们之前的研究表明,蓝光和UV-B的结合照射在晚上导致花青素合成的显着促进。在这项研究中,我们研究了光周期的蓝光强度是否会影响花青素积累。当光周期的蓝光强度增加时,促进了花青素积累,但局限于临时效果。到接下来,我们使用红色和蓝色LED研究了在低光合光子光子磁通密度条件下红叶莴苣的花青素积累。结果,花青素含量在100微米M -2℃ s -1 -1 / sup>蓝光或用20微mol m -2 -2的同时照射Sup> S -1 红色和80微mol m -2 s -1 蓝光。第二种是用50微mol m -2℃的同时照射-2℃ s -1 -1 / sup>红色和50微mol m -2 s -1 蓝光,第3次,用80微mol m -2 -2 -2 / s -1 -1 -1 / sup>红色和20微mol m -2 S -1 蓝光,100微米m m -2 s -1 红光是最低的。以阐明轻质质量的花青素生物合成的分子调节,我们分离出五种花青素生物合成基因, CHS , DFR,来自红叶莴苣的ANS 和 UFGT 。通过实时PCR方法进行治疗的基因表达分析至48小时。在100微米M -2 / SOP> -1 -1 -1 / SOP>红光中不能观察到涉及花青素生物合成的基因的表达。另一方面,在100微米m mol m -2 / st -1 -1 / sup>蓝光和用50微mol m -2 S -1 红色和50微米M -2 s -1 -1 蓝光,在轻质质量处理后长达24小时,观察到增强的 chs , f3h , ans, ans和 UFGT 的表达。此外,尽管 F3h , DFR-i>和 ans的表达在同时照射80微mol m -2 < / sup> s -1 红色和20微mol m -2 s -1 蓝光,表达 chs UFGT 并不那么高。因此,对于红叶生菜的半硅藻的生物合成机制变得清楚,红光和蓝光的比例密切相关。

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