Abstract
AbstractMelanins are a class of darkly pigmented biopolymers which are widely distributed among living organisms. The molecular and cellular mechanisms adopted by bacteria, fungi and animals to synthesize melanin, have been well described, but less is known regarding their production in plants. Here, a pair of barley near isogenic lines, bred to differ with respect to the pigmentation of the spike, was compared in order to understand the tissue and cellular location of melanin deposition. The melanic nature of the pigments purified from black spikes was confirmed by a series of solubility tests and Fourier transform infrared spectroscopy. An analysis of grains harvested at various stages of their development revealed that intracellular pigmented structures first appeared in the pericarp and the husk of black spike plants at early dough stage. The co-localization of these structures with red autofluorescence suggested that they form in chloroplast-derived plastids, here designated “melanoplasts”. Differences in dynamics of plastid internal structure during grain ripening were detected between the lines by transmission electron microscopy. Both lines accumulated plastoglobuli inside plastids, which persisted in black grain pericarp tissue up to the hard dough stage, while neither plastoglobuli nor any plastids were observed in grain of the control line at this stage. The role of plastoglobuli in melanin synthesis is discussed.
Publisher
Springer Science and Business Media LLC
Reference47 articles.
1. Nicolaus, R. A., Piattelli, M. & Fattorusso, E. The structure of melanins and melanogenesis-IV. On some nature of melanins. Tetrahedron. 20, 1163–1172 (1964).
2. Britton, G. 1983. Biohimija prirodnyh pigmentov [The biochemistry of natural pigments, Cambridge university press, translated from English] (russ. ed. Zaprometov, M.N.) 259-279 (Mir, 1986).
3. Solano, F. Melanins: skin pigments and much more – types, structural, models, biological functions, and formation routes. New J. Sci. 2014, 498276 (2014).
4. Gerdemann, C., Eicken, C. & Krebs, B. The crystal structure of catechol oxidase: new insight into the function of type-3 copper proteins. Acc. Chem. Res. 35, 183–191 (2002).
5. Langfelder, K., Streibel, M., Jahn, B., Haase, G. & Brakhage, A. A. Biosynthesis of fungal melanins and their importance for human pathogenic fungi. Fungal Genet. Biol. 38, 143–158 (2003).
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