Abstract

Ricinoleic acid (RA), a hydroxyl fatty acid, is suitable for medical and industrial uses and is produced in high-oil-accumulating organisms such as castor bean and the ergot fungus Claviceps. We report here the efficient production of RA in a transgenic diatom Chaetoceros gracilis expressing the fatty acid hydroxylase gene (CpFAH) from Claviceps purpurea. In transgenic C. gracilis, RA content increased at low temperatures, reaching 2.2 pg/cell when cultured for 7 d at 15 °C, without affecting cell growth, and was enhanced (3.3 pg/cell) by the co-expression of a palmitic acid-specific elongase gene. Most of the accumulated RA was linked with monoestolide triacylglycerol (ME TAG), in which one RA molecule was esterified to the α position of the glycerol backbone and was further esterified at its hydroxy group with a fatty acid or second RA moiety, or 1-OH TAG, in which RA was esterified to the glycerol backbone. Overall, 80% of RA was accumulated as ME TAGs. Furthermore, exogenous RA-methyl ester suppressed the growth of wild-type diatoms in a dose-dependent manner and was rapidly converted to ME TAG. These results suggest that C. gracilis masks the hydroxyl group and accumulates RA as the less-toxic ME TAG.

Highlights

  • Levels of ricinoleic acid (RA) than RcFAH-expressing lines[14]; the expression of CpFAH and the resulting RA production was shown to markedly suppress cell growth in fission yeast[12]

  • We report that a CpFAH-expressing transgenic C. gracilis produced RA in photoautotrophic conditions, without any negative effects on cell growth, and that increased RA levels were achieved by co-expressing a palmitic acid (16:0)-specific fatty acid elongase, Mortierella alpina long chain fatty acid elongase[1] (MALCE1)

  • Most of the synthesised RA accumulated as monoestolide triacylglycerols (ME TAGs), in which the RA hydroxyl group was masked by other fatty acids, which might explain its reduced cellular toxicity

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Summary

Introduction

Levels of RA than RcFAH-expressing lines[14]; the expression of CpFAH and the resulting RA production was shown to markedly suppress cell growth in fission yeast[12] This cellular toxicity was probably caused by the incorporation of RA into phospholipid fractions, which could affect membrane properties[12]. Holic et al.[12] improved RA production and prevented its cellular toxicity, and Yazawa et al.[5] reported that the co-expression of CpFAH and a phospholipase gene suppressed RA toxicity as well These authors demonstrated that phospholipase-expressing fission yeast lines secreted RA into the culture medium[15,16]. Most of the synthesised RA accumulated as monoestolide triacylglycerols (ME TAGs), in which the RA hydroxyl group was masked by other fatty acids, which might explain its reduced cellular toxicity

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