Abiotic stress modifies the synthesis of alpha‐tocopherol and beta‐carotene in phytoplankton species

We performed laboratory experiments to investi‐gate whether the synthesis of the antioxidants α‐tocopherol (vitamin E) and β‐carotene in phytoplankton depends on changes in abiotic factors. Cultures of Nodularia spumigena, Phaeodactylum tricornutum, Skeletonema costatum, Dunaliella tertiolecta, Pror...

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Published inJournal of phycology Vol. 50; no. 4; pp. 753 - 759
Main Authors Häubner, Norbert, Sylvander, Peter, Vuori, Kristiina, Snoeijs, Pauline, Wood, M
Format Journal Article
LanguageEnglish
Published United States Blackwell Pub 01.08.2014
Blackwell Publishing Ltd
Wiley Subscription Services, Inc
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Summary:We performed laboratory experiments to investi‐gate whether the synthesis of the antioxidants α‐tocopherol (vitamin E) and β‐carotene in phytoplankton depends on changes in abiotic factors. Cultures of Nodularia spumigena, Phaeodactylum tricornutum, Skeletonema costatum, Dunaliella tertiolecta, Prorocentrum cordatum, and Rhodomonas salina were incubated at different tempe‐ratures, photon flux densities and salinities for 48 h. We found that abiotic stress, within natural ecological ranges, affects the synthesis of the two antioxidants in different ways in different species. In most cases antioxidant production was stimulated by increased abiotic stress. In P. tricornutum KAC 37 and D. tertiolecta SCCAP K‐0591, both good producers of this compound, α‐tocopherol accumulation was negatively affected by environmentally induced higher photosystem II efficiency (Fᵥ/Fₘ). On the other hand, β‐carotene accumulation was positively affected by higher Fᵥ/Fₘ in N. spumigena KAC 7, P. tricornutum KAC 37, D. tertiolecta SCCAP K‐0591 and R. salina SCCAP K‐0294. These different patterns in the synthesis of the two compounds may be explained by their different locations and functions in the cell. While α‐tocopherol is heavily involved in the protection of prevention of lipid peroxidation in membranes, β‐carotene performs immediate photo‐oxidative protection in the antennae complex of photosystem II. Overall, our results suggest a high variability in the antioxidant pool of natural aquatic ecosystems, which can be subject to short‐term temperature, photon flux density and salinity fluctuations. The antioxidant levels in natural phytoplankton communities depend on species composition, the physiological condition of the species, and their respective strategies to deal with reactive oxygen species. Since α‐tocopherol and β‐carotene, as well as many other nonenzymatic antioxidants, are exclusively produced by photo‐synthetic organisms, and are required by higher trophic levels through dietary intake, regime shifts in the phytoplankton as a result of large‐scale environmental changes, such as climate change, may have serious consequences for aquatic food webs.
Bibliography:http://dx.doi.org/10.1111/jpy.12198
Table S1. Summary of the six phytoplankton species used in the experiments, showing phylogeny, strains and culture salinity. SSCAP = Scandinavian Culture Collection of Algae & Protozoa, University of Copenhagen, Denmark; KAC = Kalmar Algae collection, Linnaeus University, Kalmar, Sweden. Table S2. Summary of analytical procedures for the quantification of tocopherols in phytoplankton cells on Whatman™ GF/F glass fiber filters frozen at −80°C. This method was adapted after Häubner (). Table S3. Summary of analytical procedures for the quantification of fat-soluble pigments (chlorophylls and carotenoids) in phytoplankton cells on Whatman™ GF/F glass fiber filters frozen at −80°C. This method was adapted after Wright and Jeffrey (). Table S4. Initial PSII efficiency, biomass, and concentrations of α-tocopherol and β-carotene of the six phytoplankton species at t = 0 of the two experiments, expressed as mean ± standard deviation (N = 3). Table S5. Results of two-way factorial ANOVA analyses with experiment (Exp1 and Exp2) and species (all species except for R. salina, which was used only in Exp1) as predictor variables and PSII efficiency (Fv/Fm), biomass (mg C · L−1) and concentrations of α-tocopherol and β-carotene as response variables. Table S6. Results of two-way factorial ANOVA analyses for Exp1 (data in Fig. ) with temperature (5°C, 15°C and 25°C) and light (photon flux density 50 and 240 μmol photons · m−2 · s−1) as predictor variables and PSII efficiency (Fv/Fm), growth rate (mg C · L−1 · d−1), and concentrations of α-tocopherol and β-carotene as response variables. Table S7. Results of two-way factorial ANOVA analyses for Exp2 (data in Fig. ) with temperature (5°C, 15°C and 25°C) and salinity (−50% and +50%) as predictor variables and PSII efficiency (Fv/Fm), growth rate (mg C · L−1 · d−1) and concentrations of α-tocopherol and β-carotene as response variables.
ArticleID:JPY12198
istex:7F19696DD35F5B344AF054E6412A718182A058ED
ark:/67375/WNG-4JD11WGR-5
EU Strukturstöd FiV Dnr - No. 231-0692-04
Formas - No. 21.9/2003-1033; No. 21.0/2004-0313
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
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ISSN:0022-3646
1529-8817
1529-8817
DOI:10.1111/jpy.12198