哈萨克羊不同部位脂肪溶剂法分提产物的性质分析

本文旨在研究新疆哈萨克羊不同部位脂肪经溶剂法分提改性后的变化,通过GC/MS法对其脂肪酸组成进行分析研究,为后续脂肪食用健康性的研究提供依据。结果表明:分提脂顺序为37℃固脂、17℃固脂、2℃固脂和2℃液脂,其熔点降低(p0.05),碘值则升高(p0.05);尾脂、肾周脂和网膜脂脂肪分提组分的脂肪酸含量变化趋势相同,其中分提组分饱和脂肪酸(SFA)的含量比原脂的SFA含量呈先下降后上升的趋势;不饱和脂肪酸(UFA)的变化趋势则和SFA相反。SFA中变化较明显的脂肪酸为棕榈酸(C16:0)和硬脂酸(C18:0);而UFA中变化较为明显的脂肪酸为油酸(C18:1n-9c)。结论:无论是从不饱和脂肪酸的含量,还是n-6/n-3的值来考虑,哈萨克羊尾脂处理组2℃液脂的食用健康性更加优秀,其16.67℃~17.07℃的低熔点、高不饱和脂肪酸(58.13%~59.65%)的特性,可作为商业色拉油的潜在替代品。     

哈萨克羊不同部位脂肪溶剂法分提产物性质分析

本文旨在研究新疆哈萨克羊不同部位脂肪经溶剂法分提改性后的变化,通过 GC/MS 法对其脂肪酸组成进行分析研究,为后续脂肪食用健康性的研究提供依据。结果表明：分提脂顺序为 37 ℃固脂、17 ℃固脂、2 ℃固脂和 2 ℃液脂,其熔点降低（plt;0.05）,碘值则升高（plt;0.05）;尾脂、肾周脂和网膜脂脂肪分提组分的脂肪酸含量变化趋势相同,其中分提组分饱和脂肪酸（SFA）的含量比原脂的 SFA 含量呈先下降后上升的趋势;不饱和脂肪酸（UFA）的变化趋势则和 SFA 相反。SFA 中变化较明显的脂肪酸为棕榈酸（C16:0）和硬脂酸（C18:0）;而 UFA 中变化较为明显的脂肪酸为油酸（C18:1n-9c）。结论：无论是从不饱和脂肪酸的含量,还是 n-6/n-3的值来考虑,哈萨克羊尾脂处理组 2 ℃液脂的食用健康性更加优秀,其 16.67 ℃~17.07 ℃的低熔点、高不饱和脂肪酸（58.13%~59.65%）的特性,可作为商业色拉油的潜在替代品。     

玛曲牦牛与康乐黄牛肠系膜脂肪和肾周脂肪中脂肪酸含量比较分析

分析了玛曲牦牛和康乐黄牛两个品种间肠系膜脂肪和肾周脂肪中脂肪酸的组成特点。利用冷抽提法,分别提取两个品种肠系膜脂肪和肾周脂肪中的脂肪酸,并进行甲酯化处理,最后采用气相色谱法(GC)对其脂肪酸组成及含量进行定性和定量的比较分析。结果显示:玛曲牦牛和康乐黄牛的肠系膜脂肪和肾周脂肪中脂肪酸含量均以饱和脂肪酸为主,牦牛肠系膜脂肪及肾周脂肪中饱和脂肪酸(SFA)含量均占总脂肪酸含量的近60%;黄牛肠系膜脂肪及肾周脂肪中饱和脂肪酸(SFA)含量均占总脂肪酸含量的近70%。其中,棕榈酸(C16∶0)和硬脂酸(C18∶0)含量较高,占饱和脂肪酸总量的50%以上。在饱和脂肪酸、单不饱和脂肪酸、多不饱和脂肪酸和功能性脂肪酸方面,两者差异显著(P0.05或P0.01);玛曲牦牛肠系膜脂肪和肾周脂肪中不饱和脂肪酸含量高于黄牛中的含量。这些对于玛曲牦牛的开发和品种选育具有重要的意义。     

蒙古斑点马不同部位脂肪和肌肉组织中脂肪酸组成的比较研究

通过对蒙古斑点马不同部位脂肪和肌肉组织中脂肪酸组成进行分析比较,旨在明确蒙古斑点马体脂脂肪酸组成特点。选择3 匹成年蒙古斑点马,屠宰后采集肾周、肠周和皮下脂肪以及肩肌、背最长肌和臀肌样品,利用气相色谱法测定脂肪酸组成及含量。结果表明：蒙古斑点马不同脂肪组织中均检出19 种脂肪酸,其中饱和脂肪酸（saturated fatty acid,SFA）含量34.77%～37.38%,不饱和脂肪酸（unsaturated fatty acid,UFA）含量达60%以上,UFA中单不饱和脂肪酸（monounsaturated fatty acid,MUFA）含量33.04%～36.39%,多不饱和脂肪酸（polyunsaturated fatty acid,PUFA）含量26.47%～27.51%,其中皮下脂肪C10:0、C18:0、C20:0含量显著低于肾周和肠周脂肪（P＜0.05）;MUFA在皮下脂肪的沉积程度较其他2 个部位高,但均无统计学差异;PUFA中C18:3 n-3含量最高,其在各脂肪组织间无显著差异。3 个不同部位肌肉中均检出15 种脂肪酸,其中SFA含量占总脂肪酸含量的38.32%～40.04%,MUFA含量占35.70%～40.19%,PUFA含量占15.25%～20.33%;SFA中背最长肌和臀肌C12:0含量显著高于肩肌（P＜0.05）,其余SFA在不同部位肌肉间无显著差异;MUFA中背最长肌C16:1含量显著高于肩肌和臀肌（P＜0.05）;肩肌n-6/n-3 PUFA比值显著高于背最长肌和臀肌（P＜0.05）;皮下脂肪的C18:3 n-3和总PUFA含量显著高于背最长肌（P＜0.05）。综上所述,蒙古斑点马不同部位脂肪和肌肉组织脂肪酸组成各具特点,但UFA含量均较高。     

3种淡水鱼油脂肪酸的含量分析

运用气相色谱质谱联用方法,分析了鲢鱼、罗非鱼和草鱼3种淡水鱼脂肪的脂肪酸组成。淡水鱼脂肪经氯仿/甲醇(体积比=2∶1)提取后,用三氟化硼甲醇溶液衍生,衍生物用气相色谱质谱法分析。结果显示,3种淡水鱼脂肪多不饱和脂脂酸(PUFA)含量为29.26%～41.49%,主要有亚油酸(C18∶2)、亚麻酸(C18∶3)、花生四烯酸(C20∶4)、二十二碳五烯酸(C20∶5,EPA)和二十二碳六烯酸(C22∶6,DHA);单不饱和脂肪酸(MUFA)的含量为26.46%～39.60%,主要有棕榈油酸(C16∶1)和油酸(C18∶1);饱和脂肪酸(SFA)的含量为23.35%～37.05%,主要有肉豆蔻酸(C14∶0)、棕榈酸(C16∶0)和硬脂酸(C18∶0)。3种淡水鱼脂肪SFA∶MUFA∶PUFA的比值,鲢鱼为0.56∶0.84∶1;罗非鱼为1.07∶1.35∶1;草鱼为1.02∶0.72∶1。鲢鱼、罗非鱼和草鱼脂肪的n-6/n-3脂肪酸比值分别为1.16,2.46和1.98。3种淡水鱼脂肪具有较高的营养和开发价值。     

中国大鲵肌内脂肪酸组成及其抗氧化研究

分析中国大鲵肌内脂肪酸的组成,并研究肌内脂肪酸抗氧化,提供肌内脂肪酸开发利用的基础理论。通过气相色谱/质谱联用技术分析肌内脂肪酸的组成;通过Schaal烘箱法(63±1℃)研究肌内脂肪酸的抗氧化特性。GC-MS分析结果表明:肌内脂肪主要含13种脂肪酸,其含量由高到低依次为,C18∶124.2%,C16∶015.4%,C16∶113.7%,C18∶28.2%,C20∶56.7%,C18∶34.5%,C22∶64.3%,C14∶13.0%,C18∶02.8%,C22∶52.6%,C20∶42.2%,C17∶02.0%,C17∶11.9%。饱和脂肪酸(SFA)为20.2%,不饱和脂肪酸(UFA)达71.3%。单不饱和脂肪酸(MUFA)为42.8%,多不饱和脂肪酸(PUFA)为28.5%,具有保健功能性作用的ω-6型PUFA为13.0%,ω-3型PUFA为15.5%。ω-6型与ω-3型PUFA比为0.8。Schaal烘箱法研究结果表明:抗氧化剂二丁基对甲苯酚(BHT)、没食子酸丙酯(PG)、特丁基对苯二酚(TBHQ)对肌内脂肪酸有明显的抗氧化作用,其中特丁基对苯二酚抗氧化效果较佳。中国大鲵肌内脂肪富含ω-3和ω-6型...     

栉孔扇贝和海湾扇贝脂质及其脂肪酸组成分析

以栉孔扇贝和海湾扇贝为研究对象,采用Folch法提取两种扇贝肌肉和内脏中的总脂,并对其脂质和脂肪酸组成进行分析。结果表明:两种扇贝的肌肉总脂含量显著低于内脏,且肌肉总脂以磷脂为主,而内脏总脂以甘油三酯为主。两种扇贝的脂肪酸组成特征为多不饱和脂肪酸(PUFA)>饱和脂肪酸(SFA)>单不饱和脂肪酸(MUFA),其中,PUFA以n-3系列为主,主要为C20∶5n-3(16.58%~19.00%)和C22∶6n-3(11.49%~21.18%);肌肉中的n-3/n-6比值高于内脏,尤其C22∶6n-3含量显著高于内脏(P<0.01)。同时从两种扇贝中鉴定出6种脂肪醛二甲基缩醛(DMA),总量在7.77%~11.20%,并以C18∶0DMA(3.05%~6.89%)和C20∶1DMA(1.55%~4.25%)为主,且肌肉中DMA含量高于内脏,表明两种扇贝总脂中含有丰富的缩醛磷脂,肌肉总脂中的缩醛磷脂百分含量高于内脏。     

5种不同植物油脂氧化程度与脂肪酸比例变化的相关性研究

选取椰子油、大豆油、玉米油、葵花籽油、菜籽油5种植物油脂为研究对象,在180℃加热氧化的过程中,测定不同油脂中脂肪酸比例变化规律,与共轭二烯值(CDV)、p-茴香胺值(p-AV)和己醛含量进行相关性分析。结果表明:加热相同时间油脂的氧化程度与脂肪酸组成有显著性差异,含多不饱和脂肪酸油脂的氧化敏感性较高;对CDV、p-AV和己醛含量与脂肪酸比例之间相关性分析可知椰子油的SFA/UFA比例与CDV、p-AV和己醛含量相关性R值在0.9以上;大豆油、玉米油C18∶0/C18∶1,C18∶1/C18∶2脂肪酸比例与CDV、p-AV和己醛含量之间相关性R值在0.8以上,葵花籽油的C16∶0/C18∶2,C18∶0/C18∶2与CDV、p-AV和己醛含量之间的相关性在0.85以上,而菜籽油的脂肪酸比例C16∶0/C18∶1,C18∶0/C18∶1,C18∶1/C18∶2,SFA/UFA与CDV、p-AV和己醛含量之间的相关性R≥0.8。油脂中脂肪酸比例与油脂氧化指标的相关性研究表明,利用不同特征脂肪酸比例参数可以表征不同植物油脂的氧化程度,为油脂氧化研究提供参考。     

高寒草原地区安格斯和西门塔尔母牛血液及肌内脂肪酸组成特性

随机采集48 月龄安格斯和西门塔尔母牛各37 头血液样品以及用于肉质分析的各5 头母牛背最长肌肉样。样品经过前处理和甲酯化后,利用气相色谱-质谱联用仪测定脂肪酸组成和含量,对血液和肌内脂肪酸组成特性进行分析。结果表明：安格斯和西门塔尔母牛血液和肌内脂肪中均测得36 种脂肪酸,样品中均含有51%以上的高含量饱和脂肪酸（saturated fatty acids,SFA）,且具有以棕榈酸和硬脂酸为主的组成特点,二者总含量分别约占血液和肌内脂肪SFA的92%和89%;不饱和脂肪酸（unsaturated fatty acids,UFA）中油酸相对含量最高,其次为亚油酸;血液和肌内脂肪的油酸含量均约占单不饱和脂肪酸总量的87%,UFA中各主要脂肪酸组成在血液中有显著性差异,而在肌内脂肪中无显著性差异;血液和肌内脂肪中n-6/n-3 PUFA均符合联合国粮农组织（United Nations Food Agriculture Organization,FAO）推荐比例（5～10）,血液中P/S高于世界卫生组织（World Health Organization,WHO）推荐标准（≥0.4）。综上所述,高寒草原饲养的纯种安格斯和西门塔尔母牛血液和肌内脂肪酸组成特性相似,UFA符合FAO和WHO理想比值及推荐标准,具有较高的营养价值。     

不同热加工温度对牛肉干脂肪酸及脂肪氧化的影响

采用气相色谱-质谱联用技术,测定牛肉干中脂肪酸的组成,研究失水率相同时,不同干燥温度（25、55 ℃）及熟制温度（85、150 ℃）对牛肉干中脂肪酸组成和脂肪氧化的影响。结果表明：经热加工后,牛肉干的脂肪酸含量和脂肪氧化程度均有不同程度的变化。经55 ℃干燥后,不饱和脂肪酸（unsaturated fatty acid,UFA）、多不饱和脂肪酸（polyunsaturated fatty acid,PUFA）和单不饱和脂肪酸（monounsaturated fattyacid,MUFA）含量显著低于25 ℃干燥（P＜0.01）,饱和脂肪酸（saturated fatty acid,SFA）含量显著高于25 ℃干燥（P＜0.01）,且脂肪氧化程度低于25 ℃干燥;熟制阶段,25 ℃干燥后熟制,SFA、UFA、MUFA和PUFA含量变化不显著（P＞0.05）,而55 ℃干燥后,经150 ℃熟制,UFA、MUFA和PUFA含量显著低于85 ℃熟制（P＜0.01）,SFA含量显著高于85 ℃熟制（P＜0.01）,且脂肪氧化程度高。综上所述,不同干燥温度及熟制温度对牛肉干脂肪酸及脂肪氧化的影响不同,干燥阶段,较高温度（55 ℃）干燥对牛肉干脂肪氧化的影响小于25 ℃干燥;熟制阶段,较低温度（85 ℃）熟制对牛肉干脂肪氧化影响较小。因此,55 ℃干燥、85 ℃熟制得到的牛肉干产品,其UFA、MUFA和PUFA含量最高,SFA含量最低,脂肪氧化程度最小,牛肉干营养价值损失最小。     

Reliable identification of grapevine rootstock varieties using RAPD PCR on woody samples

Since grapevine ( Vitis spp .) rootstock material is being traded increasingly as disbudded woody material a lack of distinctive morphological features on such material necessitates an alternative and reliable means of identification. Methods described here were developed for rapid and efficient extraction of DNA from woody samples rich in phenolic compounds and polysaccharides, and for subsequent identification of varieties by RAPD PCR. Using these methods, and with the application of only one selected RAPD primer, we were able to differentiate sixteen rootstock varieties, including the seven varieties most commonly used in Germany. Problems commonly encountered with reproducibility of RAPD patterns were avoided by choosing primers with a dinucleotide sequence and a high G/C content that allowed a rather high annealing temperature of 45°C. Methods described here should also be useful for other horticultural crops, especially those with woody tissues rich in phenolic compounds and polysaccharides.     

An internet compendium of analytical methods and spectroscopic information for monomers and additives used in food packaging plastics

An internet website (http://cpf.jrc.it/smt/) has been produced as a means of dissemination of methods of analysis and supporting spectroscopic information on monomers and additives used for food contact materials (principally packaging). The site which is aimed primarily at assisting food control laboratories in the European Union contains analytical information on monomers, starting substances and additives used in the manufacture of plastics materials. A searchable index is provided giving PM and CAS numbers for each of 255 substances. For each substance a data sheet gives regulatory information, chemical structures, physico-chemical information and background information on the use of the substance in particular plastics, and the food packaging applications. For monomers and starting substances (155 compounds) the infra-red and mass spectra are provided, and for additives (100 compounds); additionally proton NMR are available for about 50% of the entries. Where analytical methods have been developed for determining these substances as residual amounts in plastics or as trace amounts in food simulants these methods are also on the website. All information is provided in portable document file (PDF) format which means that high quality copies can be readily printed, using freely available Adobe Acrobat Reader software. The website will in future be maintained and up-dated by the European Commission's Joint Research Centre (JRC) as new substances are authorized for use by the European Commission (DG-ENTR formerly DGIII). Where analytical laboratories (food control or other) require reference substances these can be obtained free-ofcharge from a reference collection housed at the JRC and maintained in conjunction with this website compendium.     

Aroma characterization of various apricot varieties using headspace–solid phase microextraction combined with gas chromatography–mass spectrometry and gas chromatography–olfactometry

The characterization of the aromatic profile of several apricot cultivars with molecular tracers in order to obtain objective data concerning the aromatic quality of this fruit was undertaken using headspace–solid phase microextraction (HS–SPME). Six apricot cultivars were selected according to their organoleptic characteristics: Iranien, Orangered, Goldrich, Hargrand, Rouge du Roussillon and A4025. The aromatic intensity of these varieties measured by HS–SPME–Olfactometry were defined and classified according to the presence and the intensity of grassy, fruity and apricot like notes. In the six varieties, 23 common volatile compounds were identified by HS–SPME–GC–MS. Finally, 10 compounds, ethyl acetate, hexyl acetate, limonene, β-cyclocitral, γ-decalactone, 6-methyl-5-hepten-2-one, linalool, β-ionone, menthone and (E)-hexen-2-al were recognized by HS–SPME–GC–O as responsible of the aromatic notes involved in apricot aroma and considered as molecular tracers of apricot aromatic quality which could be utilized to discriminate apricot varieties.     

Tests of potential functional barriers for laminated multilayer food packages. Part I: Low molecular weight permeants

The advent of the functional barrier concept in food packaging has brought with it a requirement for fast tests of permeation through potential barrier materials. In such tests it would be convenient for both foodstuffs and materials below the functional barrier (sub-barrier materials) to be represented by standard simulants. By means of inverse gas chromatography, liquid paraffin spiked with appropriate permeants was considered as a potential simulant of sub-barrier materials based on polypropylene (PP) or similar polyolefins. Experiments were performed to characterize the kinetics of the permeation of low molecular weight model permeants (octene, toluene and isopropanol) from liquid paraffin, through a surrogate potential functional barrier (25 μm-thick oriented PP) into the food simulants olive oil and 3% (w/v) acetic acid. These permeation results were interpreted in terms of three permeation kinetic models regarding the solubility of a particular model permeant in the post-barrier medium (i.e. the food simulant). The results obtained justify the development and evaluation of liquid sub-barrier simulants that would allow flexible yet rigorous testing of new laminated multilayer packaging materials.     

Chlorohydrins of bisphenol A diglycidyl ether (BADGE) and of bisphenol F diglycidyl ether (BFDGE) in canned foods and ready-to-drink coffees from the Japanese market

BADGE.2HCl and BFDGE.2HCl were determined in 28 samples of ready-to-drink canned coffee and 18 samples of canned vegetables (10 corn, 5 tomatoes and 3 others), all from the Japanese market. HPLC was used as the principal analytical method and GCMS for confirmation of relevant LC fractions. BADGE.2HCl was found to be present in one canned coffee and five samples of corn, BFDGE.2HCl in four samples of canned tomatoes and in one canned corn. No sample was found which exceeded the 1mg/kg limit of the EU for the BADGE chlorohydrins. However the highest concentration was found for the sum of BFDGE.2HCl and BFDGE.HCl.H₂O at a level of 1.5mg/kg. A Beilstein test confirmed that all cans containing foods contaminated with BADGE.2HCl or BFDGE.2HCl had at lest one part coated with a PVC organosol.     

European priorities for research to support legislation in the area of food contact materials and articles

A strong science base is required to underpin the planning and decision-making process involved in determining future European community legislation on materials and articles in contact with food. Significant progress has been made in the past 5 years in European funded work in this area, with many developments contributing to a much better understanding of the migration process, and better and simpler approaches to food control. In this paper this progress is reviewed against previously identified work-areas (identified in 1994) and conclusions are reached about future requirements for R&D to support legislation on food contact materials and articles over the next 5 or so years.     

Analysis of benzo[a]pyrene in spiked fatty foods by second derivative synchronous spectrofluorimetry after microwave-assisted treatment of samples

A simple, rapid and inexpensive method has been developed for the determination of benzo[a     

The development of reference materials for paralytic shellfish poisoning toxins in lyophilized mussel. II: Certification study

This paper describes the second part of a project undertaken to develop certified mussel reference materials for paralytic shellfish poisoning toxins. In the first part two interlaboratory studies were undertaken to investigate the performance of the analytical methodology for several PSP toxins, in particular saxitoxin and decarbamoyl-saxitoxin in lyophilized mussels, and to set criteria for the acceptance of results to be applied during the certification exercise. Fifteen laboratories participated in this certification study and were asked to measure saxitoxin and decarbamoyl-saxitoxin in rehydrated lyophilized mussel material and in a saxitoxin-enriched mussel material. The participants were allowed to use a method of their choice but with an extraction procedure to be strictly followed. The study included extra experiments to verify the detection limits for both saxitoxin and decarbamoyl-saxitoxin. Most participants (13 of 15) were able to meet all the criteria set for the certification study. Results for saxitoxin.2HCl yielded a certified mass fraction of <0.07 mg/kg in the rehydrated lyophilized mussels. Results obtained for decarbamoyl-saxitoxin.2HCl yielded a certified mass fraction of 1.59+/-0.20 mg/kg. The results for saxitoxin.2HCl in enriched blank mussel yielded a certified mass fraction of 0.48 +/- 0.06 mg/kg. These certified reference materials for paralytic shellfish poisoning toxins in lyophilized mussel material are the first available for laboratories to test their method for accuracy and performance.     

Announcing a new international peer-reviewed journal:Food Science and Human Wellness now accepting manuscript submission in English

<正>We are pleased to announce the launch of a new international peer-reviewed journal-Food Science and Human Wellness,ISSN 2213-4530,which is an open access journal,produced and hosted by Elsevier B.V.on behalf of Beijing Academy of Food Sciences.Food Science and Human Wellness is an international peer-reviewed English journal that provides a forum for the dissemination of the