Seeds from nine kenaf genotypes (Cubano, Everglades 41, Everglades 71, GR2563, Guatemala 48, Indian, 178-18RS-10, Tainung #l, and Tainting #2) were evaluated for oil, fatty acid, phospholipid, and sterol content. Oil content ranged from 21.4 to 26.4% with a mean of 23.7%. Total phospholipids ranged from 3.9 to 10.3% of the oil, with a mean of 6.0%. Mean sterol percent was 0.9 and ranged from 0.6% of the total oil for 178-18RS-10 accession to 1.2% for Everglades 71. Palmitic (20.1% of the total fatty acids), oleic (29.2%), and linoleic (45.9%) were the major fatty acids, and palmitoleic (1.6%), linolenic (0.7%), and stearic (3.5%) were the minor components. Medium (Ci2-Ci4) and long (C22-C24) chain fatty acids were less than 1%. Sphingomyelin (4.42% of the total phospholipids), phosphatidyl ethanolamine (12.8%), phosphatidyl choline (21.9%), phosphatidyl serine (2.9%), phosphatidyl inositol (2.7%), lysophosphatidyl choline (5.3%), phosphatidyl glycerol (8.9%), phosphatidic acid (4.9%), and cardiolipin (3.6%) were identified in the nine genotypes. Phosphatidyl choline, phosphatidyl ethanolamine, and phosphatidyl glycerol were the dominant phospholipids. In addition, eight unidentified phospholipids were also found. /I-sitosterol (72.3% of the total sterols), campsterol (9.9%), and stigmasterol (6.07%) were prevalent among kenaf genotypes. Kenaf's relatively high oil content and its similarity to cottonseed oil suggest that the seed oil may be used as a source of edible oil. The variation among genotypes indicates potential for genetic improvement in oil yield and quality.
There is little information available about phytosterols in canola (Brassica napa L.) oil and the effects of genotype and growing locations from Virginia and the mid-Atlantic region of the United States, a potential area for the establishment of domestic production to provide edible oil. Our objectives were to characterize the phytosterols, phospholipids, unsaponifiable matter, and FA in oil from Virginia-grown canola. Among 11 canola genotypes grown at two locations during 1995-1996 significant variations existed for oil content and FA profiles, but not for contents of phospholipids, unsaponifiable matter, total phytosterols, campesterol, stigmasterol, and βsitosterol. Total phytosterol content in the oil of Virginia-grown canola varied from 0.7 to 0.9% with a mean of 0.8%. This concentration compared favorably with oil from Canadian canola, which typically contains 0.5 to 1.1% total phytosterols. The mean contents of brassicasterol, campesterol, stigmasterol, βsitosterol, ∆ 5 -avenasterol, and ∆ 7 -stigmastenol as percentages of total phytosterols in Virginia-grown canola were: 9.7, 32.0, 0.6, 49.3, 4.99, and 3.5%, respectively. Growing location did not affect phytosterols in Virginia-grown canola oil but had significant effects on contents of phospholipids, and saturated (myristic, stearic, and arachidic) and unsaturated (palmitoleic, linoleic, linolenic, eicosenoic, and erucic) FA.
This study was conducted to determine effects of genotypes and growing environment on phytosterols, triterpene alcohols, and phospholipids (PL) in lupin (Lupinus albus L.) oil from seven genotypes grown in Maine and Virginia. The unsaponifiable lipid (UNSAP) and phospholipid (PL) fractions ranged from 2.1 to 2.8% and from 2.6 to 2.8% of oil, respectively. UNSAP in lupin oil contained 19.9 to 28.7% sterols and 17.3 to 22.0% triterpene alcohols. Growing location significantly affected contents of total PL, PS, phosphatidylglycerol, β‐sitosterol, campesterol, and β‐amyrin. Genotypic effects were significant for stigmasterol. PC (32.6 to 46.3% of PL), PE (21.6 to 32% of PL), and PS (11.2 to 17.9% of PL) were the major PL in lupin oil. The concentration of PL classes in lupin oil were in the following descending order: PC>PE>PS>PI>phosphatidic acid > lysophosphatidylcholine > phosphatidylglycerol > diphosphatidylglycerol. In descending order of abundance, the sterols present in lupin oil were: β‐sitosterol > campesterol > stigmasterol > Δ5‐avenasterol > Δ7‐stigmastenol Lupeol was the most prominent triterpene alcohol in lupin seed oil. In general, growing environment had a much greater influence on lupin oil characteristics than the genotypes.
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