Abstract

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.

Highlights

  • The plant species Hydrangea macrophylla originates from Japan and East Asia

  • A combination of electrospray ionization time-of-flight mass spectrometry (ESI-TOF-MS)14 and nuclear magnetic resonance15 revealed that the molecular structure of the blue metal-complex pigment in hydrangea is composed of 1 and 2 and/or 3 with Al3+ in the ratio 1:1:1; we named this complex “hydrangea blue-complex” (Fig. 1C)14,15

  • The most promising technique for in planta visualization of such water-soluble chemicals contained in vacuoles is the cryo-time-of-flight secondary ion mass spectrometry of freeze-fixed samples16–20

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Summary

Introduction

The plant species Hydrangea macrophylla originates from Japan and East Asia. The original color of its sepals is blue (Fig. 1A, the left), but thanks to extensive breeding efforts, hydrangeas with various colors, from red (Fig. 1A, the right), to white and green are available nowadays. Before conducting the cryo-TOF-SIMS of the sepal tissue, we analyzed the reproduced hydrangea blue-complex and other standard solutions by cryo-TOF-SIMS to test whether this method can be applied to analyze the complex and give the same molecular ions as detected with ESI-TOF MS analysis14. The molecular ion peaks at m/z = 841 and m/z = 843 were detected with the negative and positive mode, respectively, confirming that the complex composed of 1, 2, and Al3+ in the ratio of 1:1:1 existed in the solution14.

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