木瓜的营养保健功能及其产品的开发研究

介绍了木瓜的营养价值与保健功能，对木瓜果酒、木瓜保健果醋、低糖木瓜果脯、木瓜果酱、低糖木瓜罐头、木瓜果肉饮料、木瓜保健软糖等产品的开发研究进行了概述。     

木瓜酒生产包装后混浊的研究

<正>木瓜酒作为一种果酒,是营养丰富的酒,在实际生产销售过程中,只有确保酒体澄清透明,不仅可以保持木瓜酒外观品质,也可以,长期保持木瓜酒的稳定性。以下本篇研究木瓜酒生产包装后混浊的问题,并为此找出解决措施。据悉,木瓜酒包装后3个月,往往容易出现混浊的现象,这不仅严重影响木瓜酒的品质,也影响木瓜酒的销售市场。该项目主要研究木瓜酒后混浊产生的原因及解决办法。科学合理解决木瓜酒的沉淀问题,最大限度的保留其营养成分,使木瓜酒具有良     

木瓜酒和木瓜醋发酵工艺及其有机酸组成分析

以光皮木瓜为原料,发酵木瓜干酒,再通过液态深层发酵酿制木瓜醋,确定了木瓜干酒和木瓜醋的发酵工艺,并对木瓜酒和醋主要有机酸进行分析。光皮木瓜经榨汁、调整糖度后进入发酵工序,酒精发酵采用带皮渣半固态发酵方式,条件为加水比例1.5∶1（m/m）、初始糖度18%、果酒干酵母接种量0.1%、在24 ℃条件下发酵64 h,木瓜酒酒度（乙醇体积分数）为9.45%。醋酸发酵采用半连续式液态深层发酵法,调整初始酒度7%,醋酸菌接种量10%,在34 ℃条件下醋酸发酵80 h,木瓜醋总酸度为4.52%;分割留种发酵仅需24 h即可完成醋酸发酵。采用反相高效液相色谱法从木瓜干酒和木瓜醋中检出10 种有机酸,分别是草酸、酒石酸、甲酸、苹果酸、α-酮戊二酸、乳酸、醋酸、柠檬酸、富马酸和琥珀酸。实验确定的发酵工艺以及有机酸的分析与鉴定可为木瓜干酒及木瓜醋产品的开发提供理论依据。     

木瓜保健果醋的工艺研究

木瓜营养丰富,且具有良好的保健功能,以木瓜为原料,采用液态发酵法,经过酒精发酵和醋酸发酵,研制出风味独特、营养保健的木瓜醋,对开发木瓜保健调味品具有重要意义。该文对木瓜果汁浸提、酒精发酵、醋酸发酵等主要工艺进行了研究。     

木瓜入菜香

木瓜茶在台湾很流行。泡木瓜茶以选用圆形未熟的雌性果为佳，把一头切平做壶底，把另一头切开，掏除种子后直接放入茶叶，再把切去的顶端当成盖子盖上，过几分钟就可品尝到苦中带甜，充满木瓜清香的木瓜茶了。木瓜入菜做法更多。木瓜中含有特殊的木瓜酵素，对肉类有很强的软化作用，因此将肉类与木瓜同炖，     

木瓜椰油提取工艺的研究及其副产物分析

研究了用木瓜浆和果胶酶制备木瓜椰油并分析其副产物化学成分的变化。研究表明,制备木瓜椰油的最佳工艺为:椰奶经冷冻-解冻处理,反应体系中椰奶水分质量分数为65%,木瓜浆用量为40%(以椰奶质量计),果胶酶用量为1.0%(以木瓜浆质量计),不调节反应体系的pH,反应温度为45℃,反应时间为4 h。制备木瓜椰油后的副产物乳清营养丰富。     

凉菜的星味

木瓜冻烤鸭 把木瓜加少许精盐、糖粉打成木瓜汁,然后把烤鸭片成片,再贴上木瓜块和炸好的土豆片,配冰镇过的木瓜汁蘸食。     

皱皮木瓜真空冻干工艺优化及基于LF-NMR技术的复水特性研究

目的:对皱皮木瓜片的真空冷冻条件进行优化,研究木瓜片复水过程中水分状态变化。方法:采用单因素试验结合Box-Behnken响应面法,分别以复水比和色差值为指标,考察木瓜片厚度,真空冷冻干燥机的隔板温度以及真空度3个因素对冻干工艺的影响,优化皱皮木瓜片冻干工艺;利用低场核磁共振技术比较真空冷冻干燥和热风干燥的木瓜片成品复水过程中水分状态的变化情况。结果:确定皱皮木瓜真空冷冻干燥的复水比最佳工艺条件:木瓜片厚度4 mm,隔板温度40℃,真空度2.4 mbar;色差值最优的组合为:木瓜片厚度7.45 mm,隔板温度28.37℃,真空度2.02 mbar。NMR试验表明,复水过程中进入木瓜片中的水很快转化为不易流动水,结合水和自由水变化不大,且真空冷冻干燥的木瓜片中不易流动水增加较快,说明冻干比热风干燥的木瓜片品质好。结论:本研究结果为优化的皱皮木瓜真空冷冻干燥工艺参数,低场核磁共振技术可用于表征皱皮木瓜复水过程中水分状态的变化。     

酸木瓜浓缩提取物的制备及其在卷烟加料中的应用

用乙醇按物料比(14)的比例浸提酸木瓜3次,每次2h,得到的粗提浸膏经精制得到酸木瓜浓缩提取物.对酸木瓜浓缩提取物在卷烟加料中的应用效果作了试验,结果表明,酸木瓜浓缩提取物具有明显增补烟香、丰满烟气的作用.     

不同种类木瓜样品的总有机酸含量测定

建立木瓜中总有机酸含量的测定方法,并测定和比较皱皮木瓜和光皮木瓜共5个不同样品中的总有机酸含量.结果显示:24h内同一样品的测定结果稳定,RSD为1.28%,平均回收率为99.59%(n=6),RSD为1.548%;5个不同木瓜样品的总有机酸含量(以苹果酸酸计)在2.09%～3.47%之间.其中以皱皮木瓜1号的总有机酸含量最高(3.47%),皱皮木瓜4号最低(2.09%).     

内切葡聚糖酶在漂白硫酸盐浆酶法改性中的作用

最近,纤维素和半纤维素酶在浆纸工业的应用引起相当大的关注,并且有些纤维素酶已顺利地投入实际生产线。Pommier等人报道了一种利用Lifiase A-40酶改进浆料滤水性能的方法,]     

Textural Properties of Cold-set Gels Induced from Heat-denatured Whey Protein Isolates

A 9% whey protein (WP) isolate solution at pH 7.0 was heat-denatured at 80°C for 30 min. Size-exclusion HPLC showed that native WP formed soluble aggregates after heat-treatment. Additions of CaCl2 (10–40 mM), NaCl (50–400 mM) or glucono-delta-lactone (GDL, 0.4–2.0%, w/v) or hydrolysis by a protease from Bacillus licheniformis caused gelation of the denatured solution at 45°C. Textural parameters, hardness, adhesiveness, and cohesiveness of the gels so formed changed markedly with concentration of added salts or pH by added GDL. Maximum gel hardness occurred at 200 mM NaCl or pH 4.7. Increasing CaCl2 concentration continuously increased gel hardness. Generally, GDL-induced gels were harder than salt-induced gels, and much harder than the protease-induced gel.     

Review of techniques to manufacture micro-hydrogel particles for the food industry and their applications

Microgels are ‘soft’ microscopic cross-linked polymeric particles that are being increasingly exploited in a variety of industries for rheology control, encapsulation and targeted delivery. They are valued because of the ability to tune their functionality to address specific applications in oil recovery, coatings, drug delivery, cosmetics, personal care and foods. Food microgels are typically biopolymer hydrogels in the form of microspheres, nanospheres (also called nanogels), spheroids and fibres. The utilisation of engineered microgels in foods has so far been limited, despite their great potential to address several needs in the food industry, including: satiety control, encapsulation of phytonutrients and prebiotics, texture control for healthier food formulations (e.g. reduced fat products), and targeting delivery to specific areas in the digestive tract. We review the scientific and patent literature on the utilisation and manufacturing methods for producing microgels with an emphasis on micro-hydrogels for food applications.     

Occurrence of bisphenol-F-diglycidyl ether (BFDGE) in fish canned in oil

The levels of bisphenol-F-diglycidyl ether (BFDGE) were quantified as part of a European survey on the migration of residues of epoxy resins into oil from canned fish. The contents of BFDGE in cans, lids and fish collected from all 15 Member States of the European Union and Switzerland were analysed in 382 samples. Cans and lids were separately extracted with acetonitrile. The extraction from fish was carried out with hexane followed by re-extraction with acetonitrile. The analysis was performed by reverse phase HPL C with fluorescence detection. BFDGE could be detected in 12% of the fish, 24% of the cans and 18% of the lids. Only 3% of the fish contained BFDGE in concentrations considerably above 1mg/kg. In addition to the presented data, a comparison was made with the levels of BADGE (bisphenol-A-diglycidyl ether)analysed in the same products in the context of a previous study.     

Ramie fibre: part I. Chemical composition and chemical properties. A critical review of recent developments

The monograph deals with a critical review of the recent research work and development on ramie, a long vegetable bast fibre. The review is divided into two parts. Part I discusses the progress of recent work on ramie, chemical components like fibre degumming, its effects on fibre composition, chemical constituents, i.e. hemicellulose, cellulose, non-cellulosic and mineral matters. Besides various chemical properties of native and modified fibres such as accessibility, infrared, cellulose I-V, DP, grafting, cross linking and resin finishing and dyeing etc. are dealt with.     

THE FASHION CONSUMER IN THE GLOBAL MARKETPLACE

Abstract

This monograph traces the various means by which flax fibre is transformed into linen yarns and fabrics. The principal innovations and developments of the past fifty years are identified. An extensive range of relevant literature is reviewed. Details are given of how the fibre is extracted from the stem of the flax plant and of the stages of yarn and fabric production. An explanation is given of how yarns are produced from short fibres (known as tow) using carding, drafting and dry spinning, and from long fibres (known as line) using hackling, drafting, doubling, roving and wet spinning in warm water. Further areas covered include yarn winding, linen weaving, dyeing and finishing. New applications for flax fibre, beyond traditional uses in apparel or furnishing fabrics, are also identified.     

Analysis of raw materials, intermediates and subsidiary colours in Food Yellow No. 5 (Sunset Yellow FCF) by LC/MS

Raw materials, intermediates and subsidiary colours in Food Yellow No. 5 (Sunset Yellow FCF) were determined using liquid chromatography/mass spectrometry (LC/MS) with electrospray ionization. A gradient consisting of acetonitrile and 0.04% aqueous ammonium carbonate solution was used for the HPL C mobile phase. Quasi-molecular ions of impurities were used as monitor ions. It was necessary to use fragment ions of the sodium salts of 6-hydroxy-5-phenylazo-2-naphthalenesulphonic acid (SS-AN) and 4-(2- hydroxy-1- naphthylazo) benzenesulphonic acid (2N-SA) as monitor ions because the compounds are not resolved by chromatography and have the same molecular weight. Fifteen samples of commercial Sunset Yellow FCF were examined. The results obtained by UV-Vis spectroscopy were in good agreement with the results of LC/MS analyses. The detection limits of the impurities in Sunset Yellow FCF ranged from 0.01 to 0.1%.     

Comparison of the affinity and selectivity of insoluble fibres and commercial proteins for wine proanthocyanidins

The fining action of commercial proteins and insoluble fibres for wine proanthocyanidin (PA) were compared. Fibres were prepared from fresh apple and grape sources, and their corresponding pomaces. PA removal by fibre was via adsorption, and required a higher dose to achieve a fining effect comparable with proteins. A principal component analysis data model revealed that PA molecular mass was significant in defining the fining response, and reflected changes in the proportion of the dominant terminal PA subunits catechin and epicatechin, but not epicatechin-3-O-gallate. For PA extension subunits, changes in epigallocatechin were inversely correlated with epicatechin and epicatechin-3-O-gallate. Generally, the application of proteins and fibres reduced PA molecular mass. Selectivity for PAs by subunit composition was variable between treatments, but differences were minor. This work demonstrates the potential use of fibres as an alternative to proteins in winemaking. Benefits, and possible limitations of such an approach are discussed.     

The development of reference materials for paralytic shellfish poisoning toxins in lyophilized mussel. I: Interlaboratory studies of methods of analysis

This paper describes the first part of a project undertaken to develop mussel reference materials for Paralytic Shellfish Poisoning (PSP) toxins. Two interlaboratory studies were undertaken to investigate the performance of the analytical methodology for several PSP toxins, in particular saxitoxin (STX) and decarbamoyl-saxitoxin (dc-STX) in lyophilized mussels, and to set criteria for the acceptance of results to be applied during the second part of the project: the certification exercise. In the first study, 18 laboratories were asked to measure STX and dc-STX in rehydrated lyophilized mussel material and to identify as many other PSP toxins as possible with a method of their choice. In the second interlaboratory study, 15 laboratories were additionally asked to determine quantitatively STX and dc-STX in rehydrated lyophilized mussel and in a saxitoxin-enriched mussel material. The first study revealed that three out of four postcolumn derivatization methods and one pre-column derivatization method sufficed in principle to determine STX and dc-STX. Most participants (13 of 18) obtained acceptable calibration curves and recoveries. Saxitoxin was hardly detected in the rehydrated lyophilized mussels and results obtained for dc-STX yielded a CV of 58% at a mass fraction of 1.86 mg/kg. Most participants (14 out of 18) identified gonyautoxin-5 (GTX-5) in a hydrolysed extract provided. The first study led to provisional criteria for linearity, recovery and separation. The second study revealed that 6 out of 15 laboratories were able to meet these criteria. Results obtained for dc-STX yielded a CV of 19% at a mass fraction of 3.49mg/kg. Results obtained for STX in the saxitoxin-enriched material yielded a CV of 19% at a mass fraction of 0.34mg/kg. Saxitoxin could not be detected in the PSP-positive material. Hydrolysis was useful to confirm the identity of GTX5 and provided indicative information about C1 and C2 toxins in the PSP-positive material. The methods used in the second interlaboratory study showed sufficiently consistent analysis results to undertake a certification exercise to assign certified values for STX and dc-STX in lyophilized mussel.     

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.