四种真菌油脂提取方法的比较研究*

采用索氏法、超临界CO₂ 萃取法、酸热法和有机溶剂法分别提取雅致枝霉、拉曼被孢霉、少根根霉、畸雌腐霉和橙黄红酵母的油脂 ,从样品要求、最小样品量、仪器要求、处理样品能力及油脂得率等方面对 4种提取方法进行综合评价 ,并对索氏法、超临界CO₂萃取法和酸热法提取的雅致枝霉油脂的脂肪酸组成进行气相色谱分析。索氏法的油脂得率最高 ,但耗时较长 ;超临界CO₂ 萃取法和酸热法的油脂得率相近 ,较索氏法略低 ,但酸热法更为简便 ,单位时间内样品处理能力     

超临界CO2萃取真菌油脂及其脂肪酸组成分析

采用超临界CO2萃取雅致枝霉的油脂,从最小样品需要量、处理样品能力及油脂得率等方面将其与索氏提取法进行综合对比评价,并对两种方法提取的雅致枝霉油脂的脂肪酸组成进行气相色谱分析.索氏法的油脂得率最高,但耗时较长(＞6h),样品需要量大(＞2000mg),且提取的油脂中杂质较多;超临界CO2萃取法油脂得率较索氏法低,但提取的油脂中杂质较少,单位时间内样品处理能力强,是索氏法的6倍,且可处理微量样品(50mg).气相色谱分析结果表明两种方法提取的油脂,均含12种已知脂肪酸,且每种脂肪酸的含量相近.综合各项指标考虑,超临界CO2萃取法优于索氏法,是一种简便、有效的真菌油脂提取方法,适合油脂及多不饱和脂肪酸高产株菌筛选的实际应用需要.     

超临界CO2萃取真菌油脂及其脂肪酸组成分析

采用超临界CO2 萃取雅致枝霉的油脂 ,从最小样品需要量、处理样品能力及油脂得率等方面将其与索氏提取法进行综合对比评价 ,并对两种方法提取的雅致枝霉油脂的脂肪酸组成进行气相色谱分析。索氏法的油脂得率最高 ,但耗时较长 (>6h) ,样品需要量大 (>2 0 0 0mg) ,且提取的油脂中杂质较多 ;超临界CO2 萃取法油脂得率较索氏法低 ,但提取的油脂中杂质较少 ,单位时间内样品处理能力强 ,是索氏法的 6倍 ,且可处理微量样品 (5 0mg)。气相色谱分析结果表明两种方法提取的油脂 ,均含 12种已知脂肪酸 ,且每种脂肪酸的含量相近。综合各项指标考虑 ,超临界CO2 萃取法优于索氏法 ,是一种简便、有效的真菌油脂提取方法 ,适合油脂及多不饱和脂肪酸高产株菌筛选的实际应用需要     

白果油的提取工艺及其化学成分研究

采用正交实验对超临界CO2萃取白果油的工艺条件进行优化,比较超声波提取、索氏提取、超临界CO2萃取3种方式对白果油提取率的大小,用最佳提取方式分析不同品种白果中油脂的含量,并用GC-MS分析其成分.结果表明: (1)3种提取方式对白果油提取率的大小顺序为:超临界CO2萃取(添加夹带剂)＞索氏提取＞超声波提取.(2)超临界CO2萃取白果油的最佳工艺条件为:温度40℃、压力20 MPa、流速15 L/h、时间3 h并添加石油醚夹带剂,不同品种白果干粉中油脂得率为3.6%～7.11%.(3)GC-MS分析表明:从超临界萃取白果油中鉴定出17种化学成分,其中不饱和脂肪酸占85.4%;超声波和索氏提取相似,分别从提取的白果油中鉴定出10种和9种化学成分,其中不饱和脂肪酸含量分别为90.3%和90.1%;不饱和脂肪酸以十六、十八碳的为主.     

侧柏树干的超临界CO_2萃取物组分分析及双条杉天牛的EAG反应

利用超临界CO2萃取法和索氏提取法分别提取侧柏Platycladus orientalis(L.)的韧皮部和木质部挥发物,经GC/MS分析其成分,结果表明:超临界CO2萃取物中检测到的21种组分中以倍半萜烯及其氧化物为主,没有检测到单萜类物质;索氏提取法检测到23种组分,韧皮部中检测到的组分以高沸点的树脂酸和二萜等为主,单萜烯和倍半萜及其氧化物含量较低;木质部中以倍半萜烯及其氧化物为主。将不同提取样品进行双条杉天牛Semanotus bifasciatus(Motschulsky)的触角电位反应,结果表明:2种方法的萃取物均能引起天牛的EAG反应,但以超临界萃取物引起的EAG反应较强,且与索氏提取物的反应值差异显著。罗汉柏烯和雪松醇可能是侧柏植物中引诱双条杉天牛的重要活性组分。     

灰树花粗多糖的提取方法比较及其分离纯化

比较了几种常规粗多糖提取法与超临界CO2提取法对灰树花粗多糖提取的差异,同时对灰树花粗多糖进行脱蛋白、脱色研究。试验结果表明:热水浸提法所得灰树花粗多糖得率最高,为28.1%,而超临界CO2提取法所得粗多糖纯度最高,为39.3%。聚酰胺法脱蛋白及脱色效果较好,蛋白脱除率及脱色率分别为69.9%、61.9%,且多糖吸附率较低。将超临界CO2法提取的灰树花粗多糖采用聚酰胺法脱蛋白及脱色后,多糖得率为79.3%,纯度为50.1%。因此聚酰胺法是分离纯化灰树花粗多糖的一种简便、高效的方法。     

不同方法提取组培百里香精油质量及成分的比较分析

采用水蒸气蒸馏法、有机溶剂萃取法、CO2超临界萃取法3种提取方法提取组培百里香精油,比较分析精油得率、精油化学成分以及相对含量,以期得出最佳提取方法。结果表明：水蒸气蒸馏法提取的百里香精油得率为O．21％,主要化学成分为：百里酚（36．53％）、间伞花烃（14．13％）、松油烯（8．09％）和石竹烯（4．14％）;有机溶剂萃取法提取的精油得率为0．19％,主要化学成分为：1,2-苯二甲酸-单-2-乙基己基酯（55．23％）、百里酚（873％）、松油烯（5．23％）;CO2超临界萃取法提取的精油得率为0．27％,主要化学成分为：百里酚（26．68％）、3-苯基-2-丙烯酸-甲酯（21．55％）、间伞花烃（9．69％）。从精油得率、精油质量以及精油主要化学成分综合比较3种方法,水蒸气蒸馏法是提取百里香精油的最佳方法。     

超临界二氧化碳法萃取丝状真菌油脂及其成分测定

采用超临界二氧化碳装置萃取被孢霉油脂,研究了萃取温度、萃取压力、萃取时间和原料粒度对被孢霉油脂得率的影响。通过四因素三水平的正交试验确定了超临界萃取被孢霉油脂的最佳条件：温度40℃、压力20MPa、时间120min、原料粒度20～40目,油脂得率为46．08％（质量分数）。气相色谱检测油脂成分,其中棕榈酸占24．2％、油酸54．2％、亚油酸11．3％、γ-亚麻酸2．8％。     

石香薷挥发油提取的比较研究

利用GC-MS对石香薷挥发油进行了定性、定量分析。采取超临界CO2萃取、水蒸气蒸馏和有机溶剂石油醚萃取这三种方法提取石香薷挥发油。这三种方法提取石香薷挥发油的主要成分基本相似,主要为含氧化合物(香薷酮、百里香酚和香荆芥酚)等,采取超临界CO2萃取和水蒸气蒸馏的石香薷挥发油品质较优。超临界CO2萃取法为提取石香薷挥发油的理想方法。     

山胡椒挥发油的提取及其抑菌活性研究

目的:研究山胡椒中挥发油最佳提取方法和其抑菌作用。方法:采用水蒸汽蒸馏法、微波萃取法和超临界CO2萃取法三种方法提取干山胡椒果实中的挥发油,研究山胡椒挥发油对7种细菌、4种霉菌、2种酵母的抑菌活性及其最低抑菌浓度(MIC)。结果:水蒸汽蒸馏法提取的山胡椒挥发油为淡黄色液体,提取率为10.0%;微波萃取法提取的山胡椒挥发油为黄褐色液体,提取率为11.6%;超临界CO2萃取的山胡椒挥发油为亮黄色液体,提取率为14.7%。山胡椒挥发油经固相和气相扩散,对细菌、酵母有较强的抑菌能力,对霉菌具有很强的抑制能力。对所有供试菌的最低抑菌浓度(MIC)为0.2%。结论:提取干山胡椒果实中的挥发油的最好方法是超临界CO2萃取法。山胡椒挥发油有较强的抑菌能力,最低抑菌浓度(MIC)为0.2%。     

破壁马尾松花粉中脂肪酸的成分分析

以石油醚为溶剂,采用索氏抽提法提取破壁马尾松花粉中的粗脂肪,进行甲酯化处理,并用GC-MS技术对脂肪酸甲酯进行分离鉴定,共鉴定出11种脂肪酸;测定其相对含量,不饱和脂肪酸相对含量高达73.14%,其中亚油酸相对含量最高,达36.53%.     

Evaluation of extraction methods for recovery of fatty acids from lipid-producing microheterotrophs

The effect of different extraction techniques on the recovery of fatty acids from freeze-dried biomass of two lipid-producing microheterotrophs was examined. Two procedures were used: the extraction of lipids from biomass followed by transesterification of the fatty acids (extraction-transesterification); and the direct transesterification of biomass to produce fatty acid methyl esters (i.e. without the initial extraction step). Variable factors in the extraction-transesterification experiment were the sequence in which solvents were added to the samples, the relative amount of methanol in the solvent mix, and sonication of biomass while in the solvent mix. Variable factors in the direct transesterification experiment were sample size, and reaction duration. Statistical analysis of data (level of significance P<0.05) showed that: (1) extraction of total fatty acids prior to transesterification was significantly more efficient when solvents were added in the order of increasing polarity; (2) neither sonication nor increasing the proportion of methanol in the extraction solvent significantly affected extraction of fatty acids prior to transesterification; (3) efficiency of direct transesterification of fatty acids increased significantly with reaction time; (4) efficiency of direct transesterification of fatty acids was not significantly affected by sample size; (5) the most efficient method for extraction of fatty acids prior to transesterification yielded significantly less fatty acids than the most effective direct transesterification method. While the study examined only two strains, our results suggest that fatty acid analysis methodology for microheterotrophs under consideration for biotechnological exploitation requires optimisation and validation.     

Efficacy of extraction methods for lipid and fatty acid composition from fungal cultures

The efficacy of three extraction methods for determining the lipid and fatty acid composition of six fungal cultures was studied. The extraction methods were: chloroform/methanol (2:1), hexane/isopropanol (3:2) and Soxhlet extraction by using hexane. The total lipid and fatty acid composition varied in fungal cultures depending on the extraction conditions. Of the three methods, chloroform/methanol (2:1) was found to be the best for extraction of lipid and fatty acids from fungal cultures.     

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.     

Optimizing a continuous flow lipid extraction system (CFLES) used for extracting microalgal lipids

A laboratory‐made continuous flow lipid extraction system (CFLES) was devised to extract lipids from microalgae Nannochloropsis sp., a potential feedstock for biodiesel fuel, with a focus to assess the workable temperatures and pressures for future industrial applications. Using conventional solvents, the CFLES recovered 100% of the lipids extracted with conventional Soxhlet extraction. The optimum temperature and pressure were found to be 100 °C and 50 psi, respectively; conditions significantly lower than those normally used in pressurized liquid extractions requiring specialized equipment. Approximately 87% of the extracted oil was successfully transesterified into biodiesel fuel (fatty acid methyl esters). Preliminary calculations based on the tested lab‐scale system indicated savings in energy, solvent consumption, and extraction time as 96%, 80%, and more than 90%, respectively, as compared to Soxhlet extraction. However, the true cost savings can only be assessed at scaled up level. Energy efficiency of CFLES was calculated as 48.9%. Residual water (~70%) in the biomass had no effect on the extraction performance of CFLES, which is expected to help the process economics at scaled up application. The effect of temperature and pressure on the fatty acids profile of Nannochloropsis sp. is also discussed. Based on the existing literature, the authors believe that a pressurized liquid extraction system with continuous solvent flow has not been reported for lipid extraction from Nannochloropsis sp.     

Analysis of Fatty Acid Content and Composition in Microalgae

A method to determine the content and composition of total fatty acids present in microalgae is described. Fatty acids are a major constituent of microalgal biomass. These fatty acids can be present in different acyl-lipid classes. Especially the fatty acids present in triacylglycerol (TAG) are of commercial interest, because they can be used for production of transportation fuels, bulk chemicals, nutraceuticals (ω-3 fatty acids), and food commodities. To develop commercial applications, reliable analytical methods for quantification of fatty acid content and composition are needed. Microalgae are single cells surrounded by a rigid cell wall. A fatty acid analysis method should provide sufficient cell disruption to liberate all acyl lipids and the extraction procedure used should be able to extract all acyl lipid classes.With the method presented here all fatty acids present in microalgae can be accurately and reproducibly identified and quantified using small amounts of sample (5 mg) independent of their chain length, degree of unsaturation, or the lipid class they are part of.This method does not provide information about the relative abundance of different lipid classes, but can be extended to separate lipid classes from each other.The method is based on a sequence of mechanical cell disruption, solvent based lipid extraction, transesterification of fatty acids to fatty acid methyl esters (FAMEs), and quantification and identification of FAMEs using gas chromatography (GC-FID). A TAG internal standard (tripentadecanoin) is added prior to the analytical procedure to correct for losses during extraction and incomplete transesterification.     

Comparison of methods for the extraction of plant lipids

The ability of a number of different solvent systems to extract lipid from a range of plant tissues was compared by measurement of phospholipid, glycolipid, sterol lipid and total acyl lipid content. A chloroform-methanol extraction method based upon the principles of Bligh and Dyer was considered to be the most efficient system for use with the majority of plant tissues. Cereal seeds were anomalous in that water saturated n- butanol was the preferred solvent system due to its superior ability to extract bound lysophospholipids present in large amounts in the endosperm portion of the tissue.     

Ultrasonic-Assisted Extraction of Raspberry Seed Oil and Evaluation of Its Physicochemical Properties,Fatty Acid Compositions and Antioxidant Activities

Ultrasonic-assisted extraction was employed for highly efficient separation of aroma oil from raspberry seeds. A central composite design with two variables and five levels was employed and effects of process variables of sonication time and extraction temperature on oil recovery and quality were investigated. Optimal conditions predicted by response surface methodology were sonication time of 37 min and extraction temperature of 54°C. Specifically, ultrasonic-assisted extraction (UAE) was able to provide a higher content of beneficial unsaturated fatty acids, whereas conventional Soxhlet extraction (SE) resulted in a higher amount of saturated fatty acids. Moreover, raspberry seed oil contained abundant amounts of edible linoleic acid and linolenic acid, which suggest raspberry seeds could be valuable edible sources of natural γ-linolenic acid products. In comparison with SE, UAE exerted higher free radical scavenging capacities. In addition, UAE significantly blocked H₂O₂-induced intracellular reactive oxygen species (ROS) generation.     

Rose hip (Rosa canina L.) oil obtained from waste hip seeds by different extraction methods

From the rose hip seed, which is generally a waste material, valuable oil can be obtained for medicinal use. Various extraction methods have been compared: traditional solvent extraction with ultrasound-, microwave-, sub- and supercritical fluid extraction (SFE). Unsaturated fatty acid (UFA: oleic-, linoleic- and linolenic acid; 16.25-22.11%, 35.94-54.75%, 20.29-26.48%) and polyunsaturated fatty acid (PUFA:linoleic- and linolenic acid) content were over 90% and 60% in the recovered oils. The oils contained different amounts of metals. The concentration of some metals, particularly iron in microwave oil (27.11 microg g(-1)) is undesirable from the aspect of stability. By traditional solvent extraction, oil was obtained in 4.85 wt/wt%. Subcritical FE appeared to be the best method for the recovery of rose hip oil with highest oil yield (6.68 wt/wt%), carotene- (145.3 microg g(-1)) and linoleic acid content (54.75%). Supercritical FE without organic solvent is suitable for mild recovery of oil. The oil was rich in UFA and PUFA (92.7% and 76.25%) and contained the lowest amount of carotene and pheophytin (36.3 and 45.8 microg g(-1)). Oil yield in most new extraction methods (microwave extraction, super- and subcritical FE) was higher than in the case of traditional Soxhlet extraction. The main benefit of supercritical FE with CO2 is the solvent free oil while in the case of other extractions evaporation of the solvent is needed. Although the content of bioactive compounds in oils was different, all oils may be appropriate for medicinal use.     

Analysis of fatty acids in A. szechenyianum Gay. by microwave‐assisted extraction and gas chromatography‐mass spectrometry

Introduction – Aconitum szechenyianum Gay. is a traditional Chinese medicinal herb with the detumescent and styptic effects and antitumor activity. There have been only a few researches on its chemical components, but no detailed report has appeared on its fatty acids. Objective – To develop a simple and effective method for the extraction of fatty acids from A. zechenyianum Gay. and then to investigate the fatty acid components. Methodology – Microwave‐assisted extraction (MAE) was optimized with response surface methodology, and the fatty acid compositions of extract were determined by GC–MS with previous derivatisation to fatty acid methyl esters (FAMEs). The results were compared with that obtained by classical Soxhlet extraction (SE). Results – Compared with SE, MAE showed significantly higher fatty acid yields, shorter extraction time, and lower energy and solvent consumption. The major fatty acids in A. szechenyianum Gay. are linoleic acid, palmitic acid, linolenic acid, oleic acid and stearic acid, and the unsaturated fatty acids occupy 66.4% of the total fatty acids. Copyright © 2010 John Wiley & Sons, Ltd.