Abstract

Porphyra dioica is a commercial seaweed consumed all over the world, mostly in the shape of nori sheets used for “sushi” preparation. It is a well-known part of the Asian diet with health benefits, which have been associated, among others, to the high levels of n-3 and n-6 fatty acids in this red alga. However, other highly valued lipids of Porphyra are polar lipids that remain largely undescribed and can have both nutritional value and bioactivity, thus could contribute to the valorization of this seaweed. In this context, the present work aims to identify the lipidome of two life cycle stages of the Atlantic species Porphyra dioica: the early life stage conchocelis produced in an indoor-nursery, and young blades produced outdoors using an integrated multitrophic aquaculture (IMTA) framework. Both the blades (gametophyte) and conchocelis (sporophyte) are commercialized in the food and cosmetics sectors. Liquid chromatography coupled to Q–Exactive high resolution-mass spectrometry (MS) platform was used to gain insight into the lipidome of these species. Our results allowed the identification of 110 and 100 lipid molecular species in the lipidome of the blade and conchocelis, respectively. These lipid molecular species were distributed as follows (blade/conchocelis): 14/15 glycolipids (GLs), 93/79 phospholipids (PLs), and 3/6 betaine lipids. Both life stages displayed a similar profile of GLs and comprised 20:4(n-6) and 20:5(n-3) fatty acids that contribute to n-3 and n-6 fatty acid pool recorded and rank among the molecular species with higher potential bioactivity. PLs’ profile was different between the two life stages surveyed, mainly due to the number and relative abundance of molecular species. This finding suggests that differences between both life stages were more likely related with shifts in the lipids of extraplastidial membranes rather than in plastidial membranes. PLs contained n-6 and n-3 precursors and in both life stages of Porphyra dioica the n-6/n-3 ratio recorded was less than 2, highlighting the potential benefits of using these life stages in human diet to prevent chronic diseases. Atherogenic and thrombogenic indexes of blades (0.85 and 0.49, respectively) and conchocelis (0.34 and 0.30, respectively) are much lower than those reported for other Rhodophyta, which highlights their potential application as food or as functional ingredients. Overall, MS-based platforms represent a powerful tool to characterize lipid metabolism and target lipids along different life stages of algal species displaying complex life cycles (such as Porphyra dioica), contributing to their biotechnological application.

Highlights

  • Porphyra spp. (Bangiales, Rhodophyta) is among the most important commercial seaweeds, Porphyra produced spp. (Bangiales, Rhodophyta) is among the most important seaweeds, being massively and traditionally consumed in Asia for nutrition andcommercial with recognized human being massively produced and traditionally consumed inAsia for nutrition and with recognized health benefits [1,2]

  • The lipid extracts of the two life stages of Porphyra dioica analyzed in the present study accounted for about 8600 ± 120 mg kg−1 dry biomass of blade and 10,800 ± 90 mg kg−1 dry biomass of conchocelis

  • This work reports for the first time the full characterization of the lipidome of Porphyra dioica blade and conchocelis life stages

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Summary

Introduction

Porphyra spp. (Bangiales, Rhodophyta) is among the most important commercial seaweeds, Porphyra produced spp. (Bangiales, Rhodophyta) is among the most important seaweeds, being massively and traditionally consumed in Asia for nutrition andcommercial with recognized human being massively produced and traditionally consumed in. The lack of knowledge on the lipidome of Porphyra species, at a molecular level, has encouraged us to identify and characterize the polar lipid profile of the conchocelis phase (indoor nursery) and young blades (outdoor cultures) of Porphyra dioica cultivated on a land-based integrated multitrophic aquaculture (IMTA) system. To achieve this characterization, we have used hydrophilic interaction chromatography coupled to Q–Exactive high resolution-mass spectrometry instrument (LC–MS) and gas chromatography coupled to mass spectrometry (GC–MS). Overall, the results obtained foster the valorization of Porphyra dioica for its traditional use as food and as a source of high value compounds for biotechnological applications

Results and Discussion
Fatty Acids Profile from Porphyra Dioica
Polar Lipids from Porphyra dioica
Betaine Lipids
Number
Total Lipid Extraction
Nutritional Values
Conclusions
Full Text
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