Abstract

BackgroundThe therapeutic and health promoting role of highly unsaturated fatty acids (HUFAs) from fish, i.e. eicosapentaenoic acid (EPA, 20:5n-3) and docosahexaenoic acid (DHA, 22:6n-3) are well known. These same benefits may however be shared by some of their precursors, the polyunsaturated fatty acids (PUFAs), such as stearidonic acid (SDA, 18:4 n-3). In order to obtain alternative sources for the large-scale production of PUFAs, new searches are being conducted focusing on higher plants oils which can contain these n-3 and n-6 C18 precursors, i.e. SDA and GLA (18:3n-6, γ-linolenic acid).ResultsThe establishment of the novel Echium acanthocarpum hairy root cultures represents a powerful tool in order to research the accumulation and metabolism of fatty acids (FAs) in a plant particularly rich in GLA and SDA. Furthermore, this study constitutes the first example of a Boraginaceae species hairy root induction and establishment for FA studies and production. The dominant PUFAs, 18:2n-6 (LA, linoleic acid) and 18:3n-6 (GLA), accounted for about 50% of total FAs obtained, while the n-3 PUFAs, 18:3n-3 (ALA, α-linolenic acid) and 18:4n-3 (SDA), represented approximately 5% of the total. Production of FAs did not parallel hairy root growth, and the optimal productivity was always associated with the highest biomass density during the culture period. Assuming a compromise between FA production and hairy root biomass, it was determined that sampling times 4 and 5 gave the most useful FA yields. Total lipid amounts were in general comparable between the different hairy root lines (29.75 and 60.95 mg/g DW), with the major lipid classes being triacylglycerols. The FAs were chiefly stored in the hairy roots with very minute amounts being released into the liquid nutrient medium.ConclusionsThe novel results presented here show the utility and high potential of E. acanthocarpum hairy roots. They are capable of biosynthesizing and accumulating a large range of polyunsaturated FAs, including the target GLA and SDA fatty acids in appreciable quantities.

Highlights

  • The therapeutic and health promoting role of highly unsaturated fatty acids (HUFAs) from fish, i.e. eicosapentaenoic acid (EPA, 20:5n-3) and docosahexaenoic acid (DHA, 22:6n-3) are well known

  • Line HR E1.5 grew faster and reached its maximum fresh weight (FW) after 30 days (1.51 g), statistical differences were not detected from day 20 onwards (Figure 1)

  • We focused on the production of polyunsaturated fatty acids (PUFAs) due to their known health benefits with a particular emphasis on omega-3 stearidonic acid (SDA), a precursor of valued HUFAs, such as EPA and DHA, and n-6 GLA, a known modulator of eicosanoids derived from ARA

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Summary

Introduction

The therapeutic and health promoting role of highly unsaturated fatty acids (HUFAs) from fish, i.e. eicosapentaenoic acid (EPA, 20:5n-3) and docosahexaenoic acid (DHA, 22:6n-3) are well known These same benefits may be shared by some of their precursors, the polyunsaturated fatty acids (PUFAs), such as stearidonic acid (SDA, 18:4 n-3). Stearidonic acid (SDA, 18:4n-3) and gammalinolenic acid (GLA, 18:3n-6) are scarce polyunsaturated fatty acids (PUFAs) They act as precursors for a range of physiologically essential highly unsaturated fatty acids (HUFAs), including eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA) and arachidonic acid (ARA, 20:4n-6). It is known that organisms able to synthesize HUFAs follow two different pathways; the more common aerobic pathway utilizes desaturase and elongase enzymes, while the anaerobic pathway is catalyzed by polyketide synthases [8] The former consists of consecutive elongation and desaturation cycles of the carbon chain. This route is characterized by a lack of desaturation reaction at Δ4-position, but successive Δ5 and Δ6-desaturations of a-linolenic acid (ALA, 18:3n-3), generating a six double bond C24 intermediate which is shortened by peroxisomal b-oxidation eventually forming DHA [9]

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