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Biosynthesis of triacylglycerols containing ricinoleate in castor microsomes using 1‐acyl‐2‐oleoyl‐ sn ‐glycero‐3‐phosphocholine as the substrate of oleoyl‐12‐hydroxylase
Author(s) -
Lin JiannTsyh,
Woodruff Carol L.,
Lagouche Olivier J.,
McKeon Thomas A.,
Stafford Allan E.,
GoodrichTanrikulu Marta,
Singleton John A.,
Haney Carol A.
Publication year - 1998
Publication title -
lipids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 120
eISSN - 1558-9307
pISSN - 0024-4201
DOI - 10.1007/s11745-998-0180-3
Subject(s) - chemistry , phosphocholine , metabolite , glyceride , glycerol , phosphatidylcholine , biochemistry , substrate (aquarium) , microsome , chromatography , biosynthesis , fatty acid , phospholipid , stereochemistry , enzyme , biology , membrane , ecology
We have examined the biosynthetic pathway of triacylglycerols containing ricinoleate to determine the steps in the pathway that lead to the high levels of ricinoleate incorporation in castor oil. The biosynthetic pathway was studied by analysis of products resulting from castor microsomal incubation of 1‐palmitoyl‐2‐[ 14 C]oleoyl‐ sn ‐glycero‐3‐phosphocholine, the substrate of oleoyl‐12‐hydroxylase, using high‐performance liquid chromatography, gas chromatography, mass spectrometry, and/or thin‐layer chromatography. In addition to formation of the immediate and major metabolite, 1‐palmitoyl‐2‐[ 14 C]rici‐noleoyl‐ sn ‐glycero‐3‐phosphocholine, 14 C‐labeled 2‐linoleoyl‐phosphatidylcholine (PC), and 14 C‐labeled phosphatidylethanolamine were also identified as the metabolites. In addition, the four triacylglycerols that constitute castor oil, triricinolein, 1,2‐diricinoleoyl‐3‐oleoyl‐ sn ‐glycerol, 1,2‐diricinoleoyl‐3‐linoleoyl‐ sn ‐glycerol, 1,2‐diricinoleoyl‐3‐linolenoyl‐ sn ‐glycerol, were also identified as labeled metabolites in the incubation along with labeled fatty acids: ricinoleate, oleate, and linoleate. The conversion of PC to free fatty acids by phospholipase A 2 strongly favored ricinoleate among the fatty acids on the sn ‐2 position of PC. A major metabolite, 1‐palmitoyl‐2‐oleoyl‐ sn ‐glycerol, was identified as the phospholipase C hydrolyte of the substrate; however, its conversion to triacylglycerols was blocked. In the separate incubations of 2‐[ 14 C]ricinoleoyl‐PC and [ 14 C]ricinoleate plus CoA, the metabolites were free ricinoleate and the same triacylglycerols that result from incubation with 2‐oleoyl‐PC. Our results demonstrate the proposed pathway: 2‐oleoyl‐PC. Out results demonstrate the proposed pathway: 2‐oleoyl‐PC→2‐ricinoleoyl‐PC→ricinoleate →triacylglycerols. The first two steps as well as the step of diacylglycerol acyltransferase show preference for producing ricinoleate and incorporating it in triacylglycerols over oleate and linoleate. Thus, the productions of these triacylglycerols in this relatively short incubation (30 min), as well as the availability of 2‐oleoyl‐PC in vivo , reflect the in vivo drive to produce triricinolein in castor bean.