Marine Drugs (Nov 2018)

Carotenoid Profiling of a Red Seaweed <i>Pyropia yezoensis</i>: Insights into Biosynthetic Pathways in the Order Bangiales

  • Jiro Koizumi,
  • Naoki Takatani,
  • Noritoki Kobayashi,
  • Koji Mikami,
  • Kazuo Miyashita,
  • Yumiko Yamano,
  • Akimori Wada,
  • Takashi Maoka,
  • Masashi Hosokawa

DOI
https://doi.org/10.3390/md16110426
Journal volume & issue
Vol. 16, no. 11
p. 426

Abstract

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Carotenoids are natural pigments that contribute to light harvesting and photo-protection in photosynthetic organisms. In this study, we analyzed the carotenoid profiles, including mono-hydroxy and epoxy-carotenoids, in the economically valuable red seaweed Pyropia yezoensis, to clarify the detailed biosynthetic and metabolic pathways in the order Bangiales. P. yezoensis contained lutein, zeaxanthin, α-carotene, and β-carotene, as major carotenoids in both the thallus and conchocelis stages. Monohydroxy intermediate carotenoids for the synthesis of lutein with an ε-ring from α-carotene, α-cryptoxanthin (β,ε-caroten-3’-ol), and zeinoxanthin (β,ε-caroten-3-ol) were identified. In addition, β-cryptoxanthin, an intermediate in zeaxanthin synthesis from β-carotene, was also detected. We also identified lutein-5,6-epoxide and antheraxanthin, which are metabolic products of epoxy conversion from lutein and zeaxanthin, respectively, by LC-MS and 1H-NMR. This is the first report of monohydroxy-carotenoids with an ε-ring and 5,6-epoxy-carotenoids in Bangiales. These results provide new insights into the biosynthetic and metabolic pathways of carotenoids in red seaweeds.

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