红树植物红海榄脂肪酸的GC-MS分析

采用索氏提取法对红树植物红海榄(Rhizophora stylosa)叶中的脂肪酸进行提取,甲酯化后利用气相色谱-质谱联用仪对脂肪酸成分进行分离和鉴定,鉴定出了12种脂肪酸,占脂肪酸总量的84.95%,其中主要包括十六酸(棕榈酸)(40.49%),9-十八碳烯酸(油酸)(17.24%),9,12-十八碳二烯酸(亚油酸)(11.24%)等。     

猫儿屎和三叶木通种子油中脂肪酸成分的GC-MS分析

采用索氏提取法提取木通科植物猫儿屎和三叶木通种子的脂溶性成分,甲酯化处理后用气相色谱-质谱联用技术(GC-MS)分离和鉴定其组成和含量。从猫儿屎种子油中鉴定出9种脂肪酸,占检出物总质量分数的94.67%(其中饱和脂肪酸占12.63%,不饱和脂肪酸占82.04%),主要成分为9-十六烯酸(47.22%)、9-油酸(27.13%)、棕榈酸(10.75%)、亚油酸(7.47%)和硬脂酸(1.61%)。从三叶木通种子油中鉴定出10种脂肪酸,占检出物总质量分数的99.75%(其中饱和脂肪酸占23.39%,不饱和脂肪酸占76.36%),主要成分为11-油酸(47.63%)、亚油酸(27.05%)、棕榈酸(20.14%)、16-甲基-十七烷酸(3.03%)和8-油酸(1.07%)。结果表明,猫儿屎和三叶木通种子油中脂肪酸含量丰富,在食用、医疗保健等方面具有较高的应用潜力和综合开发前景。     

白马骨挥发性化学成分研究

采用水蒸气蒸馏法从白马骨中提取其挥发性成分,再通过气-质联用(GC-MS)技术对所提取的挥发性成分进行分离鉴定,共测定了其中的43种成分.已成功鉴定的成分占样品总量的88.87%,其主要成分为脂肪酸,占挥发性成分总量的52.12%,其次为烯烃化合物12.66%,醇类化合物8.97%,酮类化合物5.90%,酯类化合物3.84%,烷烃化合物3.28%,醛类化合物2.10%.     

超临界CO_2萃取韭菜籽油成分的GC-MS分析

以索氏提取法为对照,采用超临界二氧化碳(SC-CO_2)萃取韭菜籽油,气相色谱-质谱联用技术(GC-MS)对韭菜籽油成分进行分析,NIST 02质谱数据库对其进行分析和鉴定.结果表明,SC-CO_2萃取压力为22.25 MPa、温度为40.40℃条件下萃取86.7 min时,萃取得率为17.52%,共分离鉴定出17种物质,其中,饱和脂肪酸以棕榈酸(6.25%)为主,占脂肪酸总量的 9.05%;不饱和脂肪酸主要是亚油酸(69.71%)和油酸(19.53%),占脂肪酸总量的90.50%.采用索氏提取得率为16.50%,共鉴定出10种物质,饱和脂肪酸以棕榈酸(7.22%)为主,占总脂肪酸量的9.84%;不饱和脂肪酸主要是亚油酸(69.34%)和油酸(20.12%),不饱和脂肪酸占脂肪酸总量的90.16%.另外SC-CO_2萃取韭菜籽油还检出单不饱和脂肪酸7-棕榈烯酸、角鲨烯和β-谷甾醇.     

南五味子脂溶性成分的GC-MS分析

目的:对南五味子脂溶性成分进行研究。方法:采用索氏提取法提取脂溶性成分,甲酯化后用GC-MS联用技术分离鉴定其组成和含量。结果:脂溶性成分的得率为15．42％。鉴定了32个化合物,占样品总量的91．95％,其中脂肪酸成分的量占81．30％。含量较高的化合物为亚油酸(57．63％),油酸(13．37％),棕榈酸(7．16％)。结论:首次对南五味子脂溶性成分进行了分析,主要为脂肪酸,不饱和脂肪酸占优势。     

卷丝苣苔和勐醒芒毛苣苔脂肪酸成分的研究

用索氏提取法提取,甲酯化处理后采用气相色谱-质谱联用技术首次对卷丝苣苔(Corallodiscus kingianus)和勐醒芒毛苣苔(Aeschynanthus mengxingensis)中脂肪酸成分进行了分析.从卷丝苣苔的脂肪酸成分中鉴定出33个化合物,占检出物总质量分数的95.44%,主要成分为9,12-十八碳二烯酸、(Z,Z,Z)-9,12,15-十八碳三烯酸、十六烷酸.从勐醒芒毛苣苔的脂肪酸成分中鉴定出30个化合物,占检出物总质量分数的94.23%,主要成分为14-甲基-十五烷酸、(E)-9-十八碳烯酸、10,13-十八碳二烯酸.二者有15个组分是相同的.     

菘蓝种子脂肪酸的GC-MS分析

目的:分析菘蓝种子中的脂肪酸。方法:分别利用索氏提取法,运用气相色谱-质谱(GC-MS)联用技术,计算机检索和人工解析对菘蓝种子中的脂肪酸进行分析和鉴定。结果:鉴定了11种脂肪酸成分。结论:菘蓝种子中脂肪酸成分主要是亚麻酸(24．72%)、芥酸(23．9%)、油酸(19．11%)和亚油酸(10．76%)。     

缺萼枫香叶挥发油的化学成分研究

以水蒸气蒸馏法提取缺萼枫香叶中的挥发油,首次以气相色谱-质谱联用技术对其化学成分进行分离、鉴定,共分离出44个成分,鉴定了其中的29个成分,占挥发油总量的81.04%,主要成分为n-棕榈酸(27.03%)和9,12,15-十八酸(13.35%)。     

开封产两个菊花品种的脂溶性成分的GC-MS分析

以索氏提取法提取白菊花和紫白菊花的脂溶性成分,采用气相色谱-质谱分析鉴定。从白菊花中共分离得到46个化学成分,鉴定了其中的39个,占色谱总出峰面积的97．05％;从紫白菊花中共分离得到61个化学成分,鉴定了其中的49个,占色谱总出峰面积的90．17％。白色菊花和紫白色菊花在脂肪酸含量和烃类成分含量具有显著性差异。     

侧柏叶子与种子脂肪酸的GC-MS比较分析研究

目的:研究柏子仁与侧柏叶的脂肪酸组成.方法:用GC-MS方法对侧柏叶子与种子油进行定性鉴定和定量分析.结果:鉴定了柏子仁油中的8种脂肪酸,占脂溶性成分的93.56%;侧柏叶子油中12种脂肪酸,占脂溶性成分的93.39%.柏子仁饱和脂肪酸主要是十六烷酸(8.11%)、硬脂酸(6.08%);不饱和脂肪酸主要为亚油酸(24.59%)、亚麻酸(59.77%),占脂肪酸的83.14%.侧柏叶子饱和脂肪酸饱和脂肪酸主要为十六烷酸(14.70%)、乙酸(3.20%)、十七烷酸(2.50%);不饱和脂肪酸主要为二十二碳四烯酸(40.48%)、亚油酸(10.69%)、亚麻酸(17.62%).结论:柏子仁和侧柏叶均含有合理的脂肪酸组成.     

播娘蒿种子脂肪油组分的GC-MS分析

播娘蒿[Descurainia sophia（L．）Webb ex Prantl]为十字花科（Cruciferae）播娘蒿属（Descuainia Webb et Berth）1～2年生草本植物,其成熟的种子俗称南葶苈子,为临床常用中药材。葶苈子味辛、苦、大寒,具泻肺降气、祛痰平喘、行水消肿之功效。用于痰涎壅肺、喘咳痰多、胸肋胀满、胸腹水肿、小便不利、肺原性心脏病水肿等症。     

杨梅核脂肪酸及蜡质成分分析

采用GC-MS联用技术,对杨梅(Myrica rubra)核中的脂肪酸及蜡质成分进行了分析.结果表明,杨梅核中脂肪酸和蜡质的总含量为31.10%,其中含有8种脂肪酸和3种长链烷烃,主要为棕榈酸(C16:0)28.22%、亚油酸(C182)14.4%、顺式-油酸(C18:1)25.74%、芥酸(C22:1)15.68%、十七烷5.2%、十八烷5.87%和十九烷4.71%,是一种优质和价廉的脂肪酸来源.     

罗勒籽脂肪酸及其对蛋白酪氨酸磷酸酯酶1B(PTP1B)抑制作用的研究

利用索氏提取法提取罗勒籽油,向罗勒籽油加入氢氧化钾甲醇溶液后并用水浴加热,加入正已烷和蒸馏水萃取,上清液即为罗勒籽油中脂肪酸,用气相色谱质谱法(CC/MS)对脂肪酸进行鉴定.共鉴定出了4种脂肪酸,其中α-亚麻酸为62.88％、亚油酸为20.66％、棕榈酸为10.67％、硬脂酸为5.79％.对罗勒籽脂肪酸进行PTP1B的抑制作用研究,结果表明脂肪酸对PTP1B有较强的抑制作用,其IC50为11.12 μg/mL.该研究为深入研究罗勒籽的药理作用提供了科学依据.     

Chemical C2-elongation of polyunsaturated fatty acids

Three fatty acids were synthesized from commercially available alpha-linolenic, stearidonic and eicosapentaenoic acids by C2-elongation using a four step preparative technique. The parent fatty acid methyl esters were reduced to alcohols with LiAlH(4), converted to bromides by treatment with triphenylphosphine dibromide, coupled with a lithiated C2-elongation block--2,4,4-trimethyl-2-oxazoline--to form the corresponding 2,2-dimethyloxazolines of C2-elongated fatty acids, and finally, converted to the target polyunsaturated fatty acids by acidic alcoholysis. Yields of more than 60% were achieved on a gram scale. The resulting 11Z,14Z,17Z-eicosatrienoic, 8Z,11Z,14Z,17Z-eicosatetraenoic and 7Z,10Z,13Z,16Z,19Z-docosapentaenoic acids were obtained as colorless oils with >98% purity and could be used for biochemical investigations without additional purification. The elongated fatty acids were free of byproducts that could result from Z-E isomerization or migration of double bonds.     

Metabolism of polyunsaturated fatty acids by rabbit reticulocytes

Rabbit reticulocytes obtained by repeated bleeding metabolize exogenous [1-14C]linoleic acid and [1-14C]arachidonic acid by three different pathways. 1. Incorporation into cellular lipids: 50% of the fatty acids metabolized are incorporated into phospholipids, mainly phosphatidylcholine (32.8%) but also into phosphatidylethanolamine (12%), whereas about 10% of the radioactivity was found in the neutral lipids (mono- di- and triacylglycerols, but not cholesterol esters). 2. Formation of lipoxygenase products: 30% of the fatty acids metabolized are converted via the lipoxygenase pathway mainly to hydroxy fatty acids. Their formation is strongly inhibited by lipoxygenase inhibitors such as 5,8,11,14-eicosatetraynoic acid or nordihydroguaiaretic acid. Inhibition of the lipoxygenase pathway results in an increase of the incorporation of the fatty acids into cellular lipids. 15-Hydroxy-5,8,11,13(Z,Z,Z,E)eicosatetraenoic acid and 13-hydroxy-9,11(Z,E)-octadecadienoic acid are incorporated by reticulocytes into cellular lipids and also are metabolized via beta-oxidation. The metabolism of arachidonic acid and linoleic acid is very similar except for a higher incorporation of linoleic acid into neutral lipids. 3. beta-Oxidation of the exogenous fatty acids: about 10% of the polyenoic fatty acids are metabolized via beta-oxidation to 14CO2. Addition of 5,8,11,14-eicosatetraynoic acid strongly increased the 14CO2 formation from the polyenoic fatty acids whereas antimycin A completely abolished beta-oxidation. Erythrocytes show very little incorporation of unsaturated fatty acids into phospholipids and neutral lipids. Without addition of calcium and ionophore A23187 lipoxygenase metabolites could not be detected.     

Lipid analysis of the sex pheromone gland of the moth Heliothis virescens

The sex pheromone gland of female Heliothis virescens was analyzed for fatty acid and lipid content. Base methanolysis of the gland showed a large amount of methyl (Z)-11-hexadecenoate (Z11-16:Acyl), the fatty acyl analog of the major pheromone component, (Z)-11-hexadecenal, as well as a small amount of methyl (Z)-11-octadecenoate. Methyl esters of various common fatty acids were also observed. HPTLC analysis of the glandular lipids revealed large quantities of triacylglycerols (TGs), and lesser amounts of 1,2-diacylglycerols (1,2-DGs), 2-monoacylglycerols (2-MGs), phosphatidyl ethanolamines, and phosphatidyl cholines. The greatest amount of Z11-16:Acyl in these lipids was in the TGs, with lesser amounts in the two phospholipid classes and only trace amounts in the other neutral lipids. The glands of females at various ages and photoperiodic times were extracted, fractionated into neutral and polar fractions by silica SPE, and fatty acid titers in these fractions determined. All fatty acids, but notably Z11-16:Acyl, showed significant total and neutral lipid fraction peaks at mid scotophase for 2-day-old females; a less dramatic, but significant, Z11-16:Acyl peak in the polar fraction was also observed. However, only a relatively small proportion (<50%) of this acid was recovered from the silica at all times. This "non-recoverable" Z11-16:Acyl showed a dramatic and significant peak at mid scotophase for 2-day females, corresponding roughly with maximal pheromone titer. All other acids in the gland were recovered in high proportions, and their respective "non-recoverable" titers were not different at any of the times analyzed. Based on previous work, this non-recoverable Z11-16:Acyl is likely the CoA ester. Therefore, it appears that the pheromone gland of H. virescens maintains pools of Z11-16:Acyl in both CoA ester and TG forms, which are available for biosynthesis of pheromone. These pools are greatest during maximal pheromone production when the biosynthetic enzymes, possibly the fatty acid reductase, are unable to utilize rapidly enough the quantities of Z11-16:Acyl biosynthesized.     

Fatty acid constituents of Peganum harmala plant using Gas Chromatography–Mass Spectroscopy

Fatty acid contents of the Peganum harmala plant as a result of hexane extraction were analyzed using GC–MS. The saturated fatty acid composition of the harmal plant was tetradecanoic, pentadecanoic, tridecanoic, hexadecanoic, heptadecanoic and octadecanoic acids, while the saturated fatty acid derivatives were 12-methyl tetradecanoic, 5,9,13-trimethyl tetradecanoic and 2-methyl octadecanoic acids. The most abundant fatty acid was hexadecanoic with concentration 48.13% followed by octadecanoic with concentration 13.80%. There are four unsaturated fatty acids called (E)-9-dodecenoic, (Z)-9-hexadecenoic, (Z,Z)-9,12-octadecadienoic and (Z,Z,Z)-9,12,15-octadecatrienoic. The most abundant unsaturated fatty acid was (Z,Z,Z)-9,12,15-octadecatrienoic with concentration 14.79% followed by (Z,Z)-9,12-octadecadienoic with concentration 10.61%. Also, there are eight non-fatty acid compounds 1-octadecene, 6,10,14-trimethyl-2-pentadecanone, (E)-15-heptadecenal, oxacyclohexadecan-2 one, 1,2,2,6,8-pentamethyl-7-oxabicyclo[4.3.1]dec-8-en-10-one, hexadecane-1,2-diol, n-heneicosane and eicosan-3-ol.     

Metabolism of 6,9,12-octadecatrienoic acid in the red alga Lithothamnion corallioides: mechanism of formation of a conjugated tetraene fatty acid.

Incubation of [1-14C]6(Z),9(Z),12(Z)-octadecatrienoic acid with an enzyme preparation from the red alga Lithothamnion corallioides Crouan led to the formation of two new compounds, i.e. the conjugated tetraene 6(Z),8(E),10(E),12(Z)-octadecatetraenoic acid and the bis-allylic hydroxy acid 11(R)-hydroxy-6(Z),9(Z),12(Z)-octadecatrienoic acid. These two compounds were formed by independent pathways and were not interconvertible by the enzyme preparation. Experiments with stereospecifically deuteriated 6,9,12-octadecatrienoic acids demonstrated that formation of 6,8,10,12-octadecatetraenoic acid was accompanied by loss of the pro-S and pro-R hydrogens from C-8 and C-11, respectively, whereas formation of 11-hydroxy-6,9,12-octadecatrienoic acid proceeded with loss of the pro-S hydrogen from C-11. Biosynthesis of 6,8,10,12-octadecatetraenoic acid was dioxygen-dependent and was accompanied by production of hydrogen peroxide. A number of artificial electron acceptors supported formation of 6,8,10,12-octadecatetraenoic acid under anaerobic conditions. The existence in Lithothamnion corallioides of a fatty acid oxidase that catalyzes the oxidation of certain poly-unsaturated fatty acids into conjugated tetraene fatty acids is postulated.