Journal of Oleo Science
Online ISSN : 1347-3352
Print ISSN : 1345-8957
ISSN-L : 1345-8957
Volume 60, Issue 9
Displaying 1-7 of 7 articles from this issue
Oils and Fats
  • Yasushi Endo, Akira Ohta, Hirotsugu Kido, Masamitsu Kuriyama, Yasuhiko ...
    2011 Volume 60 Issue 9 Pages 451-456
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    Triacylglycerol (TAG) composition in vegetable oils was collaboratively analyzed in 9 laboratories using high-performance liquid chromatography (HPLC) equipped with a refractive index detector. Dococyl (C22) and triacontyl (C30) silica columns were used for analysis. The TAG molecular species in soybean, rapeseed, and palm oils were individually separated on the chromatogram. The collaborative study demonstrated that TAG composition in vegetable oils could be analyzed based on partition numbers (PN) between 38 and 50. In conclusion, the HPLC method using C22 and C30 silica columns would be useful for determining the TAG composition (%) in vegetable oils.
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  • Nagao Totani, Sayuri Tateishi, Tatsuya Takimoto, Yukari Maeda, Hideaki ...
    2011 Volume 60 Issue 9 Pages 457-462
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    Lifestyle-related diseases arise from obesity in 30 – 60% of cases. In recent years, food functions controlling the nutritional physiology of lipids have been a focus of disease prevention. Animal feeding experiments have revealed that esters made from gallic acid (GA) and (-)-epigallo-catechin (EGC) or linoleyl alcohol are more effective in weight-loss promotion and metabolic syndrome management than are intact GA and EGC. In this study, an ester (DOGGA) was chemically synthesized from GA and 1,2-dioleoyl glycerol and its effect was compared to that of octyl gallate (OG) and GA in male Wistar rats fed a powdered standard diet containing 7% frying oil for 12 weeks. Results revealed remarkably low body weight gains and food efficiency ratios in the DOGGA group, and the effects of OG were less pronounced than those of DOGGA. The GA group showed no difference from the control group. In addition, fecal lipid content in the DOGGA group was statistically higher than that in the control group, although organ weights and serum biochemical analyses did not differ between the groups. In conclusion, the data suggested that DOGGA promoted weight-loss more effectively than OG and GA did and that the alcohol moiety of gallate is not necessarily EGC and linoleyl alcohol.
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  • Yoshiharu Okada, Tomoyuki Motoya, Shinichi Tanimoto, Masato Nomura
    2011 Volume 60 Issue 9 Pages 463-467
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    Fatty acids of Euterpe oleracea Mart seeds were analyzed in hexane and diethyl ether extracts. The hexane extract contained dodecanoic acid (3), tetradecanoic acid (4), hexadecanoic acid (7), and 9-octadecenoic acid (10). The diethyl ether extract contained (10). The oil of Mart seeds was obtained firstly by methanol extract and further extracted with diethyl ether. The hexane and diethyl ether extracts were then analyzed for antioxidant effects. Both extracts demonstrated a 1,1-diphenyl-2-picrylhydrazyl radical elimination effect similar to that of α-tocopherol and an active oxygen inhibition effect. Significant quantities (0.6212 mg/mL) of polyphenol, in comparison to the standard rejected gallic acid, were found in the extract oil of Mart seeds by the methanol extraction.
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Detergents and Interface Science
  • Tsuyoshi Asakawa, Tadahiro Ozawa, Akio Ohta
    2011 Volume 60 Issue 9 Pages 469-474
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    We prepared a fluorinated gemini surfactant containing a disulfide bond in its spacer chain, [C8F17 (CH2)3N(CH3)2CH2CH2SSCH2CH2N(CH3)2(CH2)3C8F17]2Cl, and its analogue with a hexamethylene spacer. Monomeric thiol surfactant, [C8F17(CH2)3N(CH3)2CH2CH2SH]Cl, was readily produced by the cleavage of the gemini surfactant using dithiothreitol in water. The critical micelle concentration was determined using surface tension, conductivity, and fluorescence probe methods. The critical micelle concentration of the monomeric surfactant was significantly larger than that of the gemini surfactant. The surface tension of aqueous solution for the cleaved monomeric thiol surfactant returned gradually to the original value through the formation of the disulfide bond via air oxidation.
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Biochemistry and Biotechnology
  • Naoki Nagano, Keishi Sakaguchi, Yousuke Taoka, Yuji Okita, Daiske Hond ...
    2011 Volume 60 Issue 9 Pages 475-481
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    Heterotrophic marine protists known as thraustochytrids can synthesize polyunsaturated fatty acids (PUFAs) such as docosahexaenoic acid (DHA). The biosynthetic pathways of PUFAs in thraustochytrids are poorly understood, however. In this study, we attempted to reveal the enzymes involved in DHA synthesis in thraustochytrids. Nine thraustochytrid strains representing 3 genera (Aurantiochytrium, Schizochytrium, and Thraustochytrium) were used for PCR-based detection of the genes encoding Δ5-elongase and Δ4-desaturase and for fatty acid analysis. The degenerate primers were designed to amplify the Δ5-elongase and Δ4-desaturase genes, and the partial sequences of the enzymes were obtained from the genera Thraustochytrium and Schizochytrium. These fragments were identical to those of known Δ5-elongase and Δ4-desaturase. Neither Δ5-elongase nor Δ4-desaturase was detected in the strains belonging to the genus Aurantiochytrium, however, suggesting that this group likely synthesizes DHA not via the elongation/desaturation pathway but via an alternate pathway such as the polyketide synthase pathway. The fatty acid profiles of thraustochytrids were consistent with the presence of genes involved in PUFA biosynthesis in thraustochytrid genera. Thus, our findings suggest that two biosynthetic pathways for PUFAs exist in these organisms.
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General Subjects
  • Shun Sato, Hiroshi Habe, Tokuma Fukuoka, Dai Kitamoto, Keiji Sakaki
    2011 Volume 60 Issue 9 Pages 483-487
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    A novel derivative of glyceric acid (GA), dilinoleoyl-D-glyceric acid (LA2-DGA), was synthesized from D-GA calcium salt and linoleoyl chloride and evaluated for cytotoxicity. The D-GA calcium salt was first reacted with 4-methoxybezylchloride, and the resulting compound was esterified with linoleoyl chloride. This reaction was followed by hydrolysis of the 4-methoxybenzyl moiety, yielding LA2-DGA. LA2-DGA was then subjected to cytotoxicity testing using normal human dermal fibroblasts and primary normal human dermal microvascular endothelial cells. LA2-DGA showed no significant toxic effects in either type of cell.
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  • Hiroshi Habe, Shun Sato, Tokuma Fukuoka, Dai Kitamoto, Toshiharu Yakus ...
    2011 Volume 60 Issue 9 Pages 489-494
    Published: 2011
    Released on J-STAGE: August 19, 2011
    JOURNAL FREE ACCESS
    Acetobacter tropicalis NBRC16470 can produce highly enantiomerically pure D-glyceric acid (D-GA; >99 % enantiomeric excess) from glycerol. To investigate whether membrane-bound alcohol dehydrogenase (mADH) is involved in GA production in A. tropicalis, we amplified part of the gene encoding mADH subunit I (adhA) using polymerase chain reaction and constructed an adhA-disrupted mutant of A. tropicalisadhA). Because ΔadhA did not produce GA, we confirmed that mADH is essential for the conversion of glycerol to GA. We also cloned and sequenced the entire region corresponding to adhA and adhB, which encodes mADH subunit II. The sequences showed high identities (84–86 %) with the equivalent mADH subunits from other Acetobacter spp.
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