采后晾晒对油茶种仁油脂产量及组分的影响

油茶(Camellia oleifera)是我国大力推广的优质油料树种。本研究分别取花后150和170 d油茶果实,比较新鲜提取、自然晾晒及不同光质晾晒后种仁含油率及脂肪酸含量,旨在为合理采收处理提供科学依据。结果表明,晾晒能够显著提高花后150 d油茶种仁出油率,其中‘华鑫’种仁出油率的增加达5.35%。覆盖蓝色膜晾晒最有利于花后150 d的‘华硕’油茶油脂采后合成,种仁出油率高达52.42%。晾晒对花后170 d油茶种仁出油率影响不大。无论晾晒与否,脂肪酸成分不变,花后170 d较花后150 d油茶种仁中硬脂酸和油酸含量均有增加,但是品种间差异不显著。     

乌桕种子油脂含量与其水平地带性的关系

乌桕Sapium sebiferum (L.)Roxb.在现有栽培区域内,幼龄树的种仁含油率和种子含油率的高低与水平地带性变化差异不大。而种子含蜡率和种子含油脂率.则随纬度降低而极显著增高。     

绒毛番龙眼种仁油中脂肪酸组成和脂肪酸二氢(口恶)唑衍生物的GC-MS分析

本文报道绒毛番龙眼种仁油的脂肪酸组成脂肪酸双键位置,采用“远端基团修饰”的方法经GC/MS测定,它的种仁油的主要脂肪酸含量(%)如下:C16:0 3.94,C16:1(9)4.134,C18:0 3.31,C18:1(9) 19.18,C18:1(11) 13.49,C20:0 32.25,C20 :1(11) 2.21,C20:1(13) 8.43,C22:0 6.13,C22:1(13) 1.16,C22:1(15) 5.14.     

木鳖子种仁油中特殊脂肪酸成分的研究

<正> 葫芦科植物木鳖子Momordica cochinchinensis (Lour.) Spr.的种子入药,功能消肿、散结、祛毒。它分布于我国四川、湖北、河南、安徽,浙江、福建、广东、广西、贵州和云南等地。该种子富含油脂,种仁含油率高达41.2％。其化学组成,经气相色谱法鉴定其混合脂肪酸甲酯,紫外光谱和红外光谱测试其混合脂肪酸,同时制备其顺丁烯二酸酐的衍生物,通过熔点,红外光谱及质谱法鉴定此衍生物,证实该种子油中含有29.02％的α-桐酸组分。     

绒毛番龙眼种仁油中脂肪酸组成和脂肪酸二氢(口恶)唑衍生物的GC-MS分析

本文报道绒毛番龙眼种仁油的脂肪酸组成脂肪酸双键位置,采用“远端基团修饰”的方法经GC/MS测定,它的种仁油的主要脂肪酸含量(%)如下:C16:0 3.94,C16:1(9)4.134,C18:0 3.31,C18:1(9) 19.18,C18:1(11) 13.49,C20:0 32.25,C20 :1(11) 2.21,C20:1(13) 8.43,C22:0 6.13,C22:1(13) 1.16,C22:1(15) 5.14.     

76株薄壳山核桃实生单株的果实品质差异及综合评价

对南京地区种植的76株薄壳山核桃〔Carya illinoinensis(Wangenh.)K.Koch〕实生单株的8项果实性状和种仁中5种脂肪酸含量的差异以及各指标的相关性进行分析,并筛选出单项性状优良的单株;在此基础上,结合主成分分析结果,对供试76株单株的果实品质进行综合评价.结果显示:8项果实性状(包括坚果质量、种仁鲜质量、坚果壳厚度、坚果纵径、坚果横径、果形指数、出仁率和含油率)以及种仁中5种脂肪酸(包括棕榈酸、硬脂酸、油酸、亚油酸和亚麻酸)的含量均有较大变异,变异系数为663%~2899%,其中,出仁率的变异系数最小,亚麻酸含量的变异系数最大,8项果实性状的变异系数总体上小于5种脂肪酸含量的变异系数.部分果实性状间极显著或显著正相关,少数果实性状间极显著或显著负相关,而5种脂肪酸含量间均极显著正相关,但脂肪酸含量与果实性状间总体上无显著相关性.主成分分析结果表明:在8项果实性状中,与坚果大小有关的性状较为重要;而5种脂肪酸含量均同等重要.对果实性状和脂肪酸含量的主成分分析结果显示:第1主成分的决定指标包括含油率以及棕榈酸、硬脂酸、油酸、亚油酸和亚麻酸的含量,第2主成分的决定指标包括坚果质量、种仁鲜质量、坚果壳厚度和坚果横径,说明薄壳山核桃果实评价的首要指标为种仁中脂肪酸含量,其次为果实大小.在利用坚果质量、种仁鲜质量、坚果壳厚度、出仁率、含油率、果形指数、油酸含量和不饱和脂肪酸含量8个单项指标优选单株的基础上,结合主成分分析结果,71号单株的综合得分较高,其种仁鲜质量、含油率以及油酸和不饱和脂肪酸的含量均较高,可作为优良品种选育的首选候选单株.根据上述研究结果,建议在薄壳山核桃不同育种目标的优良品种选育工作中,将主成分分析法作为单项性状筛选法的有效补充方法.     

囊状黄丝藻在不同初始氮浓度条件下特殊的油脂积累规律

对不同初始氮浓度条件下囊状黄丝藻(Tribonema utriculosum SAG22.94)的生长状况、油脂含量和脂肪酸组成与含量进行研究。结果显示,囊状黄丝藻在氮浓度为3.0 mmol/L时,获得生物质浓度最高,为6.39 g/L;氮浓度为18.0 mmol/L时获得总脂和总脂肪酸含量最高,分别为细胞干重的44.62%和42.21%;上述3个指标单位体积的产率均在氮浓度3.0 mmol/L时达到最高值,分别为0.538、0.209和0.206 g·L~(-1)·d~(-1)。在4种初始氮浓度条件下,囊状黄丝藻油脂和脂肪酸含量可随着氮浓度增加而增加。脂肪酸含量分析结果显示,该藻的主要脂肪酸为豆蔻酸(C14∶0)、棕榈酸(C16∶0)、棕榈油酸(C16∶1ω7)、花生四烯酸(C20∶4ω6)和二十碳五烯酸(C20∶5ω3,EPA)。其中棕榈油酸含量最高,占总脂肪酸含量的36.53%~50.08%。研究结果表明囊状黄丝藻在不同初始氮浓度条件下具有特殊的油脂积累规律,是一株具有重要应用价值的产油丝状微藻。     

石油油脂酵母及其应用研究I．利用油脂酵母发酵正烷烃生产脂肪酸的研究

用C13-11．为主成分的正烷烃为原料,从两千多株菌中,筛选出产脂肪酸量较高的解脂假丝酵母AS2．1207。改进了影响产酸的条件,脂肪酸产量由3毫克／毫升提高至13—14毫克／毫升,组分主要为C13-10．酸,尤以C17-18。酸含量最大,其次为C16酸,C16-18。酸占总酸量的80％以上。不饱和酸占总酸的80％,以C17：1含量最高。每次发酵生成的脂肪酸的组分较稳定。这些脂肪酸主要以油脂状态积累于胞内。菌株具有一定的稳定性。     

斑点叉尾鮰鱼油脂成分分析

采用铁锅炼制提取斑点叉尾鮰内脏鱼油,然后加酸使其甲酯化,以气相色谱/质谱法分析鱼油中的脂肪酸.结果斑点叉尾鮰内脏纯油脂中鱼油达到99%.从鱼油中共鉴定出15种成分,有饱和脂肪酸及不饱和脂肪酸,还有少量烷烃类物质.不饱和脂肪酸含量为76.40%,其中多不饱和脂肪酸为18.03%,以C18∶ 2(16.23%)为主,单不饱和脂肪酸为58.37%,以C18∶ 1(54.88%)为主.饱和脂肪酸含量为20.91%,主要有C16∶ 0 (15.84%)和C18∶ 0(4.29%),多是低于C18以上的中长链脂肪酸.因此斑点叉尾鮰油脂可作功能性脂肪酸的重要膳食来源.     

两种海桐属植物种子油脂肪酸组成的分析评价

采用有机溶剂抽提了海桐属 2种植物 (海桐和皱叶海桐 )的籽油 ,使用气相色谱法 (GC)分析鉴定了其油脂的脂肪酸组分。 2种籽油均含有 6种脂肪酸 ,主要脂肪酸成分均为软脂酸 (C16∶0 )和油酸 (C18∶1)。其含量 ( % )分别为 :软脂酸 (C16∶0 ) 2 9.66,3 4 .72 ;油酸 (C18∶1) 66.4 3 ,62 .54。这两种油脂中 ,单不饱和脂肪酸油酸占优势 ,因而品质优良。提示海桐属植物籽油可作为保健型食用油研究和开发利用     

Genetic enhancement of palmitic acid accumulation in cotton seed oil through RNAi down‐regulation of ghKAS2 encoding β‐ketoacyl‐ACP synthase II (KASII)

Palmitic acid (C16:0) already makes up approximately 25% of the total fatty acids in the conventional cotton seed oil. However, further enhancements in palmitic acid content at the expense of the predominant unsaturated fatty acids would provide increased oxidative stability of cotton seed oil and also impart the high melting point required for making margarine, shortening and confectionary products free of trans fatty acids. Seed‐specific RNAi‐mediated down‐regulation of β‐ketoacyl‐ACP synthase II (KASII) catalysing the elongation of palmitoyl‐ACP to stearoyl‐ACP has succeeded in dramatically increasing the C16 fatty acid content of cotton seed oil to well beyond its natural limits, reaching up to 65% of total fatty acids. The elevated C16 levels were comprised of predominantly palmitic acid (C16:0, 51%) and to a lesser extent palmitoleic acid (C16:1, 11%) and hexadecadienoic acid (C16:2, 3%), and were stably inherited. Despite of the dramatic alteration of fatty acid composition and a slight yet significant reduction in oil content in these high‐palmitic (HP) lines, seed germination remained unaffected. Regiochemical analysis of triacylglycerols (TAG) showed that the increased levels of palmitic acid mainly occurred at the outer positions, while C16:1 and C16:2 were predominantly found in the sn‐2 position in both TAG and phosphatidylcholine. Crossing the HP line with previously created high‐oleic (HO) and high‐stearic (HS) genotypes demonstrated that HP and HO traits could be achieved simultaneously; however, elevation of stearic acid was hindered in the presence of high level of palmitic acid.     

Isolation and Identification of Fatty Acid Component from Seed Oil of Microula sikkimensis (Clarke) Hemsl

The seed oil content of Microula sikkimensis (Clarke) Hemsl. is up to 45% There is 8.1% of γ-linolenic acid which has the pharmacological action in the fatty acids composition, It has showed that this oil has a stronger effect on reducing triglyceride in serum. Fifteen different kinds of fatty acids were analysed. The unsaturated C20, C22, C24 acid, C18 triene-acid and tetraene-acid of the seed oil were separated on AgNO3-silica gel column and HPLC. and were identified by Periodata-Permanganate Oxidation, GLC, IR, UV, and MS. They are cis-11-eicosenoic, cis-13-docosenoic, cis-15-tetracosenoic, cis-6,9,12-octadecatrienoic and cis-6,9,12,15- octadecatetraenoic acids.     

Physicochemical properties of cold pressed sunflower,peanut, rapeseed,mustard and olive oils grown in the Eastern Mediterranean region

Fatty acid composition and stability of vegetable oils have taken more attention as an essential source of biologically active compounds in a good balanced diet. The purpose of the study was to determine peroxide value, free fatty acids, unsaponifiable matter, total carotenoid content, iodine value and fatty acid composition of sunflower, rapeseed, mustard, peanut and olive oils. Rapeseed and peanut oils had the highest peroxide values, while sunflower oil had the lowest peroxide values. The free fatty acid value of the tested oils varied between 0.43 and 1.36% oleic. The peanut oil had the highest free acid value and the mustard oil had the lowest one. Total carotenoid contents of mustard and rape seed oil were higher than those of the other oils tested. Palmitic acid (C16:0), oleic acid (C18:1) and stearic acid (C18:0) were the common main fatty acid components of the vegetable oils tested. Followed by linoleic acid, the amount of oleic acid was the highest among other fatty acid components. Mustard oil had the highest erucic acid (C22:1) with the amount of 11.38%, indicating that it cannot be used for human consumption. Among the oils investigated, sunflower and mustard oils were more stable than rapeseed, peanut and olive oils.     

Redirection of metabolic flux for high levels of omega‐7 monounsaturated fatty acid accumulation in camelina seeds

Seed oils enriched in omega‐7 monounsaturated fatty acids, including palmitoleic acid (16:1?9) and cis‐vaccenic acid (18:1?11), have nutraceutical and industrial value for polyethylene production and biofuels. Existing oilseed crops accumulate only small amounts (<2%) of these novel fatty acids in their seed oils. We demonstrate a strategy for enhanced production of omega‐7 monounsaturated fatty acids in camelina (Camelina sativa) and soybean (Glycine max) that is dependent on redirection of metabolic flux from the typical ?9 desaturation of stearoyl (18:0)‐acyl carrier protein (ACP) to ?9 desaturation of palmitoyl (16:0)‐acyl carrier protein (ACP) and coenzyme A (CoA). This was achieved by seed‐specific co‐expression of a mutant ?9‐acyl‐ACP and an acyl‐CoA desaturase with high specificity for 16:0‐ACP and CoA substrates, respectively. This strategy was most effective in camelina where seed oils with ~17% omega‐7 monounsaturated fatty acids were obtained. Further increases in omega‐7 fatty acid accumulation to 60–65% of the total fatty acids in camelina seeds were achieved by inclusion of seed‐specific suppression of 3‐keto‐acyl‐ACP synthase II and the FatB 16:0‐ACP thioesterase genes to increase substrate pool sizes of 16:0‐ACP for the ?9‐acyl‐ACP desaturase and by blocking C18 fatty acid elongation. Seeds from these lines also had total saturated fatty acids reduced to ~5% of the seed oil versus ~12% in seeds of nontransformed plants. Consistent with accumulation of triacylglycerol species with shorter fatty acid chain lengths and increased monounsaturation, seed oils from engineered lines had marked shifts in thermotropic properties that may be of value for biofuel applications.     

千年桐种子油提取工艺研究及其主要脂肪酸成分分析

本文以氯仿、石油醚和正己烷-异丙醇(3:2,v/v)三种不同溶剂对千年桐种子油进行提取,比较了不同溶剂对种子出油率的影响,结果表明以氯仿为溶剂时出油率最高,达到了35％;并考查了提取时间和提取溶剂体积对出油率的影响.最终优化的提取工艺为:以氯仿为溶剂,液料比为12:1(v/w),提取时间6h,出油率达到了37％.提取的种子油经转酯化后,GC-MS分析其主要脂肪酸组分,结果表明千年桐种子油中总脂肪酸占总油酯的90.55％,其中棕榈酸3.87％,硬脂酸4.11％,亚油酸12.15％,油酸13.31％,亚麻酸12.09％,共轭亚麻酸51.20％和EPA(二十碳五烯酸)3.30％.千年桐种子油中富含不饱和脂肪酸,是一种良好的干性油.     

华山松籽油的制取及性质研究

华山松籽有机溶剂萃取出油率为41％。油的相对密度(25℃)0.9243、折光率(25℃)1.4770、皂化值153.4、酸值0.24、碘值142.1,过氧化值9.9。油的主要脂肪酸有:亚油酸(44.60％)、油酸(22.42％)、亚麻油酸(19.14％)、异油酸(4.68％)、棕榈酸(4.62％)、硬脂酸(1.87％)、花生酸(2.02％)和其他酸(2.61％)。不饱和脂肪酸含量较高(占90.9％)。与药用沙棘籽油进行了性质和脂肪酸组成比较,初步证明其质量指标优于沙棘油,脂肪酸组成与沙棘油相似。推断华山松籽油可作为医疗保健、食品工业等油源加以开发利用。     

七种植物籽油中脂肪酸成分的比较分析(英文)

为寻求新的食用油资源,发展了一种快速可靠的气相色谱-质谱联用方法,用于植物籽油中脂肪酸成分的定性鉴定和含量测定。所建立的方法成功用于葡萄籽、南瓜籽和猕猴桃籽等七种植物籽油中的棕榈酸、十八烷酸、油酸、亚油酸和α-亚麻酸的定性定量分析。结果表明,刺葡萄籽油、普通葡萄籽油、国外葡萄籽油、南瓜籽油、枸杞籽油和西番莲籽油均具有相似的脂肪酸谱,尽管其中它们所含上述五种脂肪酸含量不同,由于均存在人体所必需的饱和与不饱和脂肪酸,故可以用作替代食用油。猕猴桃籽油因为其存在高含量的α-亚麻酸成分,可能是更好的食用油和营养油资源。本文首次对枸杞籽油、西番莲籽油和猕猴桃籽油脂肪酸成分进行绝对含量分析,为新的食用油资源的开发提供了重要的依据。     

Production of butter fat rich in trans10-C18:1 for use in biomedical studies in rodents

Trans fatty acids are suspected to be detrimental to health, particularly to cardiovascular function. Trans fatty acids include a wide range of fatty acids, with isomers of C18:1, conjugated and non-conjugated C18:2 as major components. A vaccenic acid (trans11-C18:1) + rumenic acid (cis9,trans11-CLA)-rich butter has been shown previously to exhibit health beneficial effects, but less is known concerning another trans-C18:1 present in hydrogenated vegetable oil-based products and sometimes in milk fat, the trans10-isomer. The present experiment was conducted to produce butters from milk of variable fatty acid composition for use in biomedical studies with rodents, with the overall aim of evaluating the specific effect of trans10-C18:1 and trans11-C18:1 + cis9,trans11-CLA on cardiovascular function. Milks from lactating dairy cows fed two types of maize-based diets supplemented (5% of dry matter)--or not--with sunflower oil were collected, and used to manufacture butters either rich in trans10-C18:1 (14% of total fatty acids, 64.5% of fat content) or rich in trans11-C18:1 + cis9,trans11-CLA (7.4 and 3.1% of total fatty acids, respectively, 68.5% of fat content), or with standard fatty acid composition (70% of fat content). Additionally, total saturated fatty acid percentage was reduced by more than one third in the enriched butters compared with the standard butter. An understanding of the role of nutrition on milk fatty acid composition in cows allows for the production of dairy products of variable lipid content and composition for use in biomedical studies in animal models and human subjects.     

Epistatic interaction among loci controlling the palmitic and the stearic acid levels in the seed oil of sunflower

Two sunflower (Helianthus annuus L.) mutants with high concentrations of saturated fatty acids in their seed oil have been identified and studied extensively. The mutant line CAS-5 has high concentrations of palmitic acid (C16:0) (>25% compared with 7% in standard sunflower seed oil) and low-C18:0 values (3%). CAS-3 is characterized by its high levels of stearic acid (C18:0) (>22% compared with 4% in standard sunflower seed oil) and a low-C16:0 content (5%). CAS-5 also possesses elevated levels of palmitoleic acid (C16:1) (>5%), which is absent in standard sunflower seed oil. The objective of this study was to determine the relationships between the loci controlling the high-C16:0 and the high-C18:0 traits in these mutants. Plants of both mutants were reciprocally crossed. Gas chromatographic analyses of fatty acids from the seed oil of F₁, F₂, F₃ and the BC₁F₁ to CAS-5 generations indicated that the loci controlling the high-C16:0 trait exerted an epistatic effect over the loci responsible for the high-C18:0 character. As a result, the phenotypic combination containing both the high-C16:0 levels of CAS-5 and the high-C18:0 levels of CAS-3 was not possible. However, phenotypes with a saturated fatty acid content of 44% (34.5% C16:0+9.5% C18:0) were identified in the F₃ generation. These are the highest saturated (C16:0 and C18:0) levels reported so far in sunflower seed oil. When F₃ C16:0 segregating generations in both a high- and a low-C18:0 background were compared, the high-C16:1 levels were not expressed as expected in the high-C18:0 background (CAS-3 background). In this case, the C16:1 content decreased to values below 1.5%, compared with >5% in a low-C18:0 background. As the stearoyl-ACP desaturase has been reported to catalyze the desaturation from C16:0-ACP to C16:1-ACP, these results suggested that a decrease in its activity was involved in the accumulation of C18:0 in the high-C18:0 mutant CAS-3. Received: 10 March 1999 / Accepted: 16 June 1999