A high-resolution method for the localization of proanthocyanidins in plant tissues

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Abstract

Background: Histochemical staining of plant tissues with 4-dimethylaminocinnamaldehyde (DMACA) or vanillin-HCl is widely used to characterize spatial patterns of proanthocyanidin accumulation in plant tissues. These methods are limited in their ability to allow high-resolution imaging of proanthocyanidin deposits.Results: Tissue embedding techniques were used in combination with DMACA staining to analyze the accumulation of proanthocyanidins in Lotus corniculatus (L.) and Trifolium repens (L.) tissues. Embedding of plant tissues in LR White or paraffin matrices, with or without DMACA staining, preserved the physical integrity of the plant tissues, allowing high-resolution imaging that facilitated cell-specific localization of proanthocyanidins. A brown coloration was seen in proanthocyanidin-producing cells when plant tissues were embedded without DMACA staining and this was likely to have been due to non-enzymatic oxidation of proanthocyanidins and the formation of colored semiquinones and quinones.Conclusions: This paper presents a simple, high-resolution method for analysis of proanthocyanidin accumulation in organs, tissues and cells of two plant species with different patterns of proanthocyanidin accumulation, namely Lotus corniculatus (birdsfoot trefoil) and Trifolium repens (white clover). This technique was used to characterize cell type-specific patterns of proanthocyanidin accumulation in white clover flowers at different stages of development. © 2011 Abeynayake et al; licensee BioMed Central Ltd.

Figures

  • Figure 1 Proanthocyanidin accumulation in white clover tissues. An immature inflorescence before (A) and after (B) DMACA staining. A mature flower after DMACA staining (C). Immature inflorescences at early (D) and late (E) stages of development and a mature flower (F) after DMACA staining and embedding in LR White resin. Bars represent 2 mm.
  • Figure 2 Proanthocyanidin accumulation in Lotus corniculatus leaves. A L. corniculatus leaf stained with DMACA (A-B). A L. corniculatus leaf stained with DMACA and embedded in LR White resin (C-D). A L. corniculatus leaf embedded in LR White resin without DMACA staining (E). Transverse section of a L. corniculatus leaf after DMACA staining and embedding in LR White resin (F-G). In Panel G, the cell walls have been stained with Toluidine Blue after sectioning of the samples shown in panel F. Transverse section of an unstained L. corniculatus leaf embedded in LR White resin without DMACA staining (H). cu-cuticle; sm-spongy mesophyll cells; va-vacuole; vb-vascular bundle. Bars represent 200 μm (A-E) and 50 μm (F-H).
  • Figure 3 Cell-specific localization of proanthocyanidins in white clover floral organs. Corolla of a white clover flower (A). Transverse sections through petals at different stages of development after DMACA staining and embedding in LR White resin (B-C). Longitudinal section through an immature white clover flower (D). Longitudinal section through an immature white clover flower (E). Longitudinal section through a trichome (F). All tissues were stained with DMACA and embedded in LR White resin. ab-abaxial surface of organ; ad-adaxial surface of organ; cacarpel; kp-keel petals; ov-ovule; se-sepals; sf-stamen filament; sp-standard petal; wp-wing petal; tr-trichomes; va-vacuole. Bars represent 1 mm (A), 50 μm (B-E) and 5 μm (F).
  • Figure 4 Accumulation of a colored metabolite in epidermal cells of white clover floral organs. Longitudinal section through an immature white clover flower (A), and developing seeds in a mature flower (B, C) after embedding of tissues in paraffin. ab-abaxial surface of organ; ad-adaxial surface of organ; ca-carpel; sc-seed coat; se-sepal; sf-stamen filament; sp-standard petal; va-vacuole. Bars represent 100 μm (A-B) and 10 μm (C).

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APA

Abeynayake, S. W., Panter, S., Mouradov, A., & Spangenberg, G. (2011). A high-resolution method for the localization of proanthocyanidins in plant tissues. Plant Methods, 7(1). https://doi.org/10.1186/1746-4811-7-13

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