Sunflower (Helianthus annuus) long-chain acyl-coenzyme A synthetases expressed at high levels in developing seeds

Long chain fatty acid synthetases (LACSs) activate the fatty acid chains produced by plastidial de novo biosynthesis to generate acyl‐CoA derivatives, important intermediates in lipid metabolism. Oilseeds, like sunflower, accumulate high levels of triacylglycerols (TAGs) in their seeds to nourish th...

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Published inPhysiologia plantarum Vol. 150; no. 3; pp. 363 - 373
Main Authors Aznar-Moreno, Jose A., Venegas Calerón, Mónica, Martínez-Force, Enrique, Garcés, Rafael, Mullen, Robert, Gidda, Satinder K., Salas, Joaquín J.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.03.2014
Wiley Subscription Services, Inc
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ISSN0031-9317
1399-3054
1399-3054
DOI10.1111/ppl.12107

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Summary:Long chain fatty acid synthetases (LACSs) activate the fatty acid chains produced by plastidial de novo biosynthesis to generate acyl‐CoA derivatives, important intermediates in lipid metabolism. Oilseeds, like sunflower, accumulate high levels of triacylglycerols (TAGs) in their seeds to nourish the embryo during germination. This requires that sunflower seed endosperm supports very active glycerolipid synthesis during development. Sunflower seed plastids produce large amounts of fatty acids, which must be activated through the action of LACSs, in order to be incorporated into TAGs. We cloned two different LACS genes from developing sunflower endosperm, HaLACS1 and HaLACS2, which displayed sequence homology with Arabidopsis LACS9 and LACS8 genes, respectively. These genes were expressed at high levels in developing seeds and exhibited distinct subcellular distributions. We generated constructs in which these proteins were fused to green fluorescent protein and performed transient expression experiments in tobacco cells. The HaLACS1 protein associated with the external envelope of tobacco chloroplasts, whereas HaLACS2 was strongly bound to the endoplasmic reticulum. Finally, both proteins were overexpressed in Escherichia coli and recovered as active enzymes in the bacterial membranes. Both enzymes displayed similar substrate specificities, with a very high preference for oleic acid and weaker activity toward stearic acid. On the basis of our findings, we discuss the role of these enzymes in sunflower oil synthesis.
Bibliography:ark:/67375/WNG-SKCFRKF4-5
Ministerio de Economia y Competitividad
istex:21AC126EB68DF07D00D987D109569904C7F3DF86
ArticleID:PPL12107
Natural Sciences and Engineering Research Council of Canada (NSERC)
FEDER - No. AGL2011-23187
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:0031-9317
1399-3054
1399-3054
DOI:10.1111/ppl.12107