复合酶对草莓出汁率和澄清度的影响

为提高草莓的出汁率和草莓汁的澄清度,该文以新鲜草莓为原料,研究单一酶（果胶酶、纤维素酶、木聚糖酶）和复合酶对出汁率和澄清度的影响。在单因素试验基础上,对复合酶添加量、复合酶质量比、酶解温度、酶解时间进行响应面优化,得到最佳酶解条件,并对酶解的草莓汁进行感官评价。结果表明,果胶酶和纤维素酶具有协同作用,可明显提高草莓的出汁率和澄清度,出汁率从64.16%（对照组）提高到87.38%,澄清度从2.34%提高到72.83%;经响应面优化试验,得到草莓汁最佳酶解条件为复合酶添加量0.17%、复合酶（果胶酶∶纤维素酶）质量比3∶1、酶解温度41℃、酶解时间35 min,此条件下草莓的出汁率为90.84%,草莓汁的澄清度为84.61%;与对照组相比,复合酶组的感官评分最高,整体风味及口感更优,表明果胶酶和纤维素酶可以有效提高草莓的出汁率和澄清度,且所得草莓清汁感官风味更佳。     

果胶酶处理对花红清汁出汁率和澄清度的影响

为提高花红果浆的出汁率,通过单因素试验和正交试验研究果胶酶对花红清汁出汁率的影响,并探讨最优酶解工艺条件对花红清汁澄清效果的影响。结果表明,最优酶解条件为:果胶酶添加量0.06%、酶解温度40℃、酶解时间90 min。与相同温度和时间但不经过酶解工艺相比,其澄清度极显著增加。     

不同酶解工艺对珍珠油杏出汁率的影响

试验以珍珠油杏为原料,经过清洗、解冻和打浆之后,加入酶进行酶解,分别对单一果胶酶酶解工艺和果胶酶与纤维素酶复配酶解工艺进行优化,考察优化条件对珍珠油杏杏浆出汁率的影响.经过单因素试验和正交优化试验,最终确定的最佳单一果胶酶酶解工艺条件是果胶酶添加量0.035％、酶解温度45℃、酶解时间120 min,此时珍珠油杏杏浆出...     

复合酶在野生樱桃李果汁澄清加工中的应用

选择果胶酶用量、α-淀粉酶用量、纤维素酶用量、酶解时间4个因素,在单因素试验基础上,设计四因素三水平正交试验,考察它们对出汁率和透光率的影响,研究复合酶澄清野生樱桃李果汁酶解工艺。结果表明:复合酶解最佳工艺条件为果胶酶用量0.06%, α-淀粉酶用量0.030%,纤维素酶用量0.045%,酶解时间125 min;在此条件下,野生樱桃李出汁率为90.1%,透光率为70.2%。     

白萝卜澄清汁的酶解工艺

以白萝卜为原料,采用双酶法酶解工艺,在单因素实验的基础上,采用正交实验设计,研究白萝卜澄清汁的酶解工艺。结果表明,白萝卜澄清汁的最佳酶解工艺为:果胶酶添加量0.2g/kg,纤维素酶添加量0.6g/kg,pH5.0,酶解温度45℃,酶解时间80min。在此工艺条件下生产的白萝卜澄清汁的出汁率为80.13%,透光率为89.2%。      

胡萝卜、番茄、黄瓜和西芹制汁过程中酶解工艺的优化

目的:优化胡萝卜、番茄、黄瓜和西芹这四种蔬菜制汁的酶解工艺。方法:榨汁过程中分别添加果胶酶或纤维素酶对蔬菜汁进行酶解处理,以出汁率和浊度为指标对酶解条件(酶解时间、酶添加量、酶解温度)进行单因素分析和正交实验优化。结果:四种蔬菜汁的最佳酶解工艺条件为:胡萝卜汁酶解时间60 min,果胶酶添加量0.4%,酶解温度40 ℃,在此条件下出汁率达到84.7%,浊度为54.3 NTU;番茄汁酶解时间40 min,果胶酶添加量0.2%,酶解温度40 ℃,在此条件下出汁率达到95.1%,浊度为36.3 NTU;黄瓜汁酶解时间60 min,果胶酶添加量0.5%,酶解温度40 ℃,在此条件下出汁率达到93.2%,浊度为60.7 NTU;西芹汁酶解时间60 min,纤维素酶添加量0.4%,酶解温度40 ℃,在此条件下出汁率达到92.1%,浊度为33.3 NTU。结论:在最佳酶解工艺条件下制得的蔬菜汁色泽清亮、甘甜爽口,具有一定的开发价值,可用于制备复合果蔬或蔬菜饮料的原料。

     

响应面试验优化桑葚汁复合酶解制备工艺及微滤技术对其品质的影响

以新鲜成熟桑葚果实为原料,桑葚出汁率为指标,通过单因素试验及响应面试验,确定果胶酶和纤维素酶酶解制备桑葚汁的最佳工艺参数,并进一步考察非热力杀菌微滤技术对桑葚汁杀菌、澄清、褐变抑制效果以及理化指标的影响。研究结果表明,适于实际生产的最佳酶解工艺为：果胶酶添加量0.42%、纤维素酶添加量1.84%、酶解时间101.26 min、酶解温度50 ℃、酶解pH 3.5～4.0（桑葚汁自然pH值）。在此条件下,桑葚出汁率为86.37%,与理论值88.10%接近。实验表明微滤技术对桑葚汁不仅有很好的抑菌效果,且对桑葚汁的褐变具有一定的抑制作用。     

几种酶对哈密大枣酶解特性研究

选择果胶酶、果汁酶、酸性果胶酶、淀粉酶和纤维素酶对哈密大枣进行酶解试验,酶添加量、酶解温度、pH和酶解时间单因素试验结果表明:酸性果胶酶效果明显优于其它酶类。同时,选择效果最好的酸性果胶酶进行正交优化试验,得出最佳工艺条件是:酸性果胶酶0.06%,酶解温度45℃,酶解时间1.0h,pH3.5,在此参数下酶解得到的出汁率高达94.67%。     

响应面试验优化胡萝卜浆复合酶解工艺

为优化胡萝卜制汁工艺,以出汁率为指标,通过单因素试验研究纤维素酶-果胶酶配比、酶解时间、酶解温度对胡萝卜出汁率的影响,再通过Box-Behnken试验法与响应面分析法,研究各自变量及其交互作用对胡萝卜出汁率的影响,建立了二次多项式回归预测模型。结果表明：复合酶酶解胡萝卜浆的最佳条件为纤维素酶-果胶酶配比2.2∶10（g/g）、复合酶添加量0.3%、酶解时间1.94 h、酶解温度41.67 ℃。在此酶解条件下,胡萝卜出汁率为（79.36±0.23）%,与响应面预测值79.06%拟合性较好,对实际生产有一定指导意义。     

响应面法优化酥李果汁的酶法提取工艺

目的:研究酶解提取酥李果汁的最佳工艺条件,为李深加工利用提供理论参考。方法:以酥李出汁率为指标,在单因素实验基础上采用响应面试验优化,对单一果胶酶、单一纤维素酶、复合酶（果胶酶和纤维素酶）提取酥李果汁的工艺条件分别进行优化。结果:不同加酶方式中对酥李出汁率的影响因素顺序均为酶解温度>加酶量>酶解pH>酶解时间;果胶酶酶解提取酥李果汁的最佳工艺条件为:加酶量0.45 g/L、酶解温度38 ℃、酶解pH3.8、酶解时间72 min,出汁率提高27.13%;维素酶酶解提取酥李果汁的最佳工艺条件为:加酶量0.55 g/L、酶解温度41 ℃、酶解pH4.2、酶解时间105 min,出汁率提高20.18%;复合酶酶解提取酥李果汁的最佳工艺条件为:果胶酶添加量0.45 g/L、纤维素酶添加量0.55 g/L、酶解温度41 ℃、酶解pH4.0、酶解时间87 min,出汁率提高31.79%。三种加酶方式中,回归模型均能较好地反应相应酶制备酥李果浆的出汁率,所得工艺合理可靠。结论:在酶法提取酥李果汁过程中,果胶酶和纤维素酶的不同添加方式均能有效提高酥李出汁率,其中采用复合酶提取酥李果汁效果最佳。本研究成果为贵州李产品开发提供了一定的技术参考。     

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.     

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     

Chinese CTP Market

According to Printing and Printing Equipment Industries Association of China（PEIAC）＇s statistics to the plate manufucturer in China, in 2013, the actual offset plate production has reached 346 million square meters in China. Among them, the CTP production volume was 245 million square meters, up by 11% than that of last year; the total sales of the CTP plate was 239 million square meters, up by 13%.     

Preparatory Work of Print China 2015 is Going Smoothly

正Held at Guangdong Modern International Exhibition Center,Print China 2015 will cover 7exhibition halls,besides the original Hall No.3,4,5,6,7,the newly built F zone of Hall 3 will be used too.The total area will be140,000 square meters.Hall 3:Offset and large printing equipment,package printing equipment,post press