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Direct mapping of hydrangea blue-complex in sepal tissues of Hydrangea macrophylla

机译:绣球花植物萼片中绣球花蓝色复合物的直接映射

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The original sepal color of Hydrangea macrophylla is blue, although it is well known that sepal color easily changes from blue through purple to red. All the colors are due to a unique anthocyanin, 3-O-glucosyldelphinidin, and both aluminum ion (Al3+) and copigments, 5-O-caffeoyl and/or 5-O-p-coumaroylquinic acid are essential for blue coloration. A mixture of 3-O-glucosyldelphinidin, 5-O-acylquinic acid, and Al3+ in a buffer solution at pH 4 produces a stable blue solution with visible absorption and circular dichroism spectra identical to those of the sepals, then, we named this blue pigment as ‘hydrangea blue-complex’. The hydrangea blue-complex consists of 3-O-glucosyldelphinidin, Al3+, and 5-O-acylquinic acid in a ratio 1:1:1 as determined by the electrospray ionization time-of-flight mass spectrometry and nuclear magnetic resonance spectra. To map the distribution of hydrangea blue-complex in sepal tissues, we carried out cryo-time-of-flight secondary ion mass spectrometry analysis. The spectrum of the reproduced hydrangea blue-complex with negative mode-detection gave a molecular ion at m/z?=?841, which was consistent with the results of ESI-TOF MS. The same molecular ion peak at m/z?=?841 was detected in freeze-fixed blue sepal-tissue. In sepal tissues, the blue cells were located in the second layer and the mass spectrometry imaging of the ion attributable to hydrangea blue-complex overlapped with the same area of the blue cells. In colorless epidermal cells, atomic ion of Al3+ was hardly detected and potassium adduct ion of 5-O-caffeoyl and/or 3-O-acylquinic acid were found. This is the first report about the distribution of aluminum, potassium, hydrangea blue-complex, and copigment in sepal tissues and the first evidence that aluminum and hydrangea blue-complex exist in blue sepal cells and are involved in blue coloration.
机译:绣球花的原始萼片是蓝色的,尽管众所周知,萼片颜色容易从蓝色变为红色。所有颜色都是由于独特的花青素,3-O-葡糖糖氰基氨苄蛋白和铝离子(Al3 +)和Copigments,5-O-咖啡酰基和/或5-O-P-香豆酰基喹啉对蓝色着色至必要。在pH4的缓冲溶液中,3 o-葡糖苷蛋白蛋白,5-α-酰上型酸和Al3 +的混合物产生稳定的蓝溶液,其具有与萼片的可见吸收和圆形二色性谱,然后,我们命名为此蓝色颜料作为'绣球花蓝色复合物'。绣球花蓝色复合物由3-O-葡萄糖氧化胺蛋白,Al3 +和5-O-酰基醌类以1:1:1的比例组成,如电喷雾电离飞行时间质谱和核磁共振谱确定。为了在萼片组织中映射绣球花蓝色复合物的分布,我们进行了低温 - 飞行时间的二级离子质谱分析。具有负模式检测的再生绣球花的光谱在m / zα=Δ=Δ=α841中得到分子离子,其与ESI-TOF MS的结果一致。在冻结固定的蓝色萼片组中检测到m /z≤=α= 841的相同分子离子峰。在萼片组织中,蓝细胞位于第二层中,并且可归因于与蓝色细胞的相同面积重叠的绣球基蓝色复合物的离子的质谱成像。在无色表皮细胞中,几乎没有检测到Al3 +的原子离子,并发现5-O-咖啡酰基和/或3-O-酰基型酸的钾加合离子。这是一份关于铝,钾,绣球花的分布和萼片组织中分布的第一个报告,以及铝和绣球花蓝色复合物中存在蓝色萼片细胞的第一种证据,并且参与蓝色着色。

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