Seeds of 40 oilseed species from 23 different plant families (Brassicaceae, Cucurbitaceae, Fabaceae, Sapindaceae, Malvaceae, Gnetaceae, Clusiaceae, Bruseraceae, Ranunculaceae, Convolvulaceae, Amaranthaceae, Tiliaceae, Basellaceae, Solanaceae, Umbelliferae, Labiatae, Compositae, Theaceae, Euphorbiaceae, Caesalpiniaceae, Sapotaceae, Anacardiaceae, and Connaraceae) grown in Vietnam were analyzed for oilseed oil content, FA, and vitamin E. The seed oil content varied between 0.2 g/100 g for Mangifera indica and 75.7 g/100 g for Calophyllum inophyllum, whereas only nine seeds contained more than 40% oil. The tocopherol content ranged from 26 (Sapindus mukorossi) to 9361 mg/kg (Litchi chinensis). In nine seed oils unusual FA such as conjugated, cyclopropenoic, or epoxy FA were found.The oleochemical industry is increasingly interested in custommade and novel oils with specific FA compositions for applications in the oil and pharmaceutical industries (1). Such oils can be used for the synthesis of high-quality products without expensive purification of raw materials. In addition, oilseed breeders are searching for species to produce beneficial new genotypes (1). A recent example is rapeseed oil with 40 to 60% lauric acid, which normally contains little or none of this FA (2).Plant seeds contain tocopherols and tocotrienols, which are used as natural antioxidants and vitamin E (3-5). In nature four different derivatives of tocopherols and tocotrienols (α-, β-, γ-, and δ) can be found, which differ in the methylation of the chroman ring. The antioxidant activity increases for tocopherols and tocotrienols in the order α to δ, whereas the biological activity is inversely proportional to the antioxidant activity (6,7). Plastochromanol-8 (P-8) is a related compound that is more effective against oxidation than α-tocopherol (8).A large part of the genetic resources of the world is located in the southern hemisphere. These can be considered as potential sources of raw material for the development of future medicines and food, as well as renewable resources with interesting FA and associated enzyme systems. Unfortunately, very little information about this genetic potential is available and many species are disappearing. Therefore, identifying commercially valuable lipid-bearing plants is a timely issue.Vietnam is very rich in plants, most of which have not been investigated with respect to their FA and tocopherol compositions. Some information about the FA composition of oilseeds is available in the Seed Oil Fatty Acid (SOFA) database (9), but to our knowledge this database contains only very limited data about seed oils from plants grown in Vietnam. Therefore, the aim of this work was to determine the FA and tocopherol compositions of native North Vietnamese seeds. Correlations between the content of PUFA and the tocopherol/tocotrienol composition were objects of special interest. MATERIALS AND METHODSPlant material. Seeds from 40 plant species grown in Vietnam were obtained from a typical Vietnamese market and used for the in...

Sixteen scleractinian species of six coral families (Acroporidae, Pocilloporidae, Poritidae, Faviidae, Pectiniidae, and Fungiidae) from Vietnam were analyzed for fatty acid (FA) composition. Except for the Poritidae species, total lipids of the corals had the same set of FAs, about 50% of them being unsaturated acids. Some coral families had high levels of characteristic FAs: 20:3(n-6), 20:4(n-3), and 22:6(n-3) in Pocilloporidae; 18:1(n-9) and 22:6(n-3) in Poritidae; and 18:3(n-6) and 22:5(n-3) in Faviidae. For the first time in hexacorals, unsaturated C(24) FAs (24:1(n-9), 24:2(n-6), 24:2(5,9), 24:3(5,9,17), and 24:4(n-3)) were discovered in the Poritidae species. The highest level of 18:1(n-7), odd-chain and branched FAs (7.5% in total) was detected in Sandalolitha robusta. The data obtained on the contents of ten principal C(18)-C(22) polyunsaturated FAs (PUFAs) for the 16 specimens were combined with data on the 19 reef-building coral specimens investigated previously and subjected to multidimensional scale analysis (MSA). The representative coral families (Acroporidae, Pocilloporidae, Poritidae, Faviidae, Dendrophylliidae, and Milleporidae) were separated by MSA according to the composition of their principal PUFAs. Therefore, PUFAs may serve as chemotaxonomic markers for reef-building corals at the family level. Family-specific compositions of coral zooxanthellae characterized by different PUFA profiles, which affect the PUFA content of whole coral colonies, were supposed to be the probable cause of the discovered chemotaxonomic distinctions between reef-building corals.

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The lipid classes and the fatty acid (FA) compositions of the zooxanthellae, the host tissue, and intact coral were determined for the first time in a soft coral, Sinularia sp. The contents of monoalkyldiacylglycerol (MADAG), triacylglycerol, and polar lipids differed significantly between the zooxanthellae and the host fractions. The zooxanthellae were rich in polar lipids, whereas neutral lipids were concentrated in the host. MADAG comprised 35% of the host lipids and was practically absent in zooxanthellae. Hence, MADAG is only synthesized in animal tissues and serves as a biomarker for the host in the host-zooxanthellae association of these soft corals. Similar to the zooxanthellae of reef-building corals, the main FA in the zooxanthellae of Sinularia sp. were 18:4n-3, 20:5n-3, and 22:6n-3. In addition, 16:3n-4 and 16:4n-1 (8.9% in total) were found in these zooxanthellae. The ratios of 16:3n-4, 16:4n-1, 18:4n-3, 20:5n-3, and 22:6n-3 in the zooxanthellae to those in the host tissue were 4.2, 11.2, 10.1, 11.0, and 9.1, respectively. The proportions of some FA and lipid classes in the intact coral and its fractions showed that zooxanthellate lipids comprised 36 ± 15% of the total lipids in Sinularia sp. Two tetracosapolyenoic acids (24:5n-6 and 24:6n-3) are proposed as a biomarkers of the animal tissue and indicators of the purity of the zooxanthellae fractions from soft corals.