4.7 Article

Photoprotection mechanisms against ultraviolet radiation in Heterocapsa sp (Dinophyceae) are influenced by nitrogen availability: Mycosporine-like amino acids vs. xanthophyll cycle

Journal

LIMNOLOGY AND OCEANOGRAPHY
Volume 55, Issue 2, Pages 899-908

Publisher

WILEY
DOI: 10.4319/lo.2009.55.2.0899

Keywords

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Funding

  1. Ministry of Science and Innovation of Spain [CGL2008 05407-C03-01]
  2. Junta de Andalucia research group Photobiology and Biotechnology of Marine Organisms'' [RNM-295]

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The photoprotective and acclimation capacity against ultraviolet radiation (UVR) was assessed for the dinoflagellate Heterocapsa sp. We examined the effect of UVR and N availability on photosynthetic activity and on the accumulation of photoprotective substances such as mycosporine-like amino acids (MAAs) and xanthophyll cycle pigments. Cells were cultivated under two different light treatments, photosynthetically active radiation (PAR) and PAR + UVR, and at two NaNO3 concentrations, mid nitrogen (MN, 0.1 mmol L-1) and high nitrogen (HN, 1 mmol L-1) for 6 d. MAA and photosynthetic pigment contents as well as maximum quantum yield of fluorescence (F-v:F-m) and electron transport rate were analyzed at the initial time and after 3 and 6 d of experimentation. F-v:F-m decreased because of UVR and N limitation. N enrichment reduced the deleterious effect of UVR on photosynthesis. The content of photosynthetic pigments and MAAs was higher at HN than at MN supply and a positive effect of UVR on MAA and pigment accumulation was observed, suggesting that under HN conditions the deleterious UVR effect is counteracted by MAAs. Under N limitation thermal energy dissipation takes place by the xanthophyll cycle, i.e., an increase of the de-epoxidation degree was observed under these culture conditions. However, UVR seems to favor diadinoxanthin accumulation; thus, no photoprotection through the xanthophyll cycle seems available in cells exposed to PAR + UVR and MN. We conclude that not only MAA accumulation but also N availability is very important to determine the photoprotective capacity against UVR of Heterocapsa sp.

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