响应面优化脱酚棉籽粕制备棉籽多肽研究

棉籽粕经脱棉酚处理后,不经过提取棉籽蛋白的中间步骤,直接利用碱性蛋白酶酶解制备棉籽多肽。在单因素实验的基础上,选取酶解温度、酶解pH、加酶量、酶解时间为影响因素,应用响应面法的Box-Behnken中心组合实验进行设计,以棉籽多肽产率为响应值,对制备条件进一步优化。结果表明,采用响应面法得到的最佳制备工艺条件为:酶解温度56.4℃,酶解pH 9.7,加酶量8.4%,酶解时间4.1 h,底物浓度3%,此时的棉籽多肽产率为49.60%。     

两步酶法提取玉米胚芽蛋白的工艺研究

为确定更为温和、高效的玉米胚芽蛋白提取工艺,本实验采用纤维素酶和碱性蛋白酶对玉米胚芽进行两步酶法处理。通过单因素考察和正交实验设计对提取工艺参数进行优化。结果表明,纤维素酶酶解的最佳工艺为:pH4.5、酶解时间2.5h、加酶量0.3%(W/V);碱性蛋白酶酶解的最佳工艺为:pH9.0、酶解时间3h、加酶量4%(V/V)。在此条件下,玉米胚芽蛋白的提取率可达到83.7%±1.2%。     

小龙虾虾壳蛋白酶解条件的研究

文章主要介绍了以单酶、双酶协同分步酶解虾壳、虾头,以脱蛋白率(PR,%)为试验的衡量指标,对pH值、酶解温度、酶解时间、酶加量等试验条件进行考察。结果表明:胃蛋白酶的最优水解条件为pH值3.0,温度40℃,酶加量0.2%,水解时间4h,酶解液中蛋白质含量为4.243mg/mL,脱蛋白率最高达53.9%;碱性蛋白酶的最优水解条件为pH值7.5,温度55℃,酶加量0.3%,水解时间4h,酶解液中蛋白质含量为4.855mg/mL,脱蛋白率最高达61.9%;双酶协同分步酶解最优条件为碱性蛋白酶酶解3h(pH 7.5、温度40℃、酶加量0.3%),胃蛋白酶酶解1h(pH 3.0、温度40℃、酶加量0.2%),脱蛋白率为86.1%,酶解液中蛋白质含量为6.715mg/mL。     

微波辅助酶解棉籽粕的条件优化及酶解产物功能性质研究

研究了微波辅助碱性蛋白酶和风味蛋白酶双酶酶解棉籽粕的工艺条件.通过单因素实验确定了碱性蛋白酶酶解的最佳工艺条件为:微波温度60℃,微波功率500 W,酶加量5％(以底物质量计),酶解时间15 min;风味蛋白酶酶解的最佳工艺条件为:微波温度60℃,微波功率600W,酶加量5％(以底物质量计),酶解时间15 min.参照单因素优化条件,对棉籽粕进行连续酶解,酶解液多肽含量为13.32 mg/mL.棉籽粕经过微波连续双酶酶解后,吸油性、起泡性、乳化性等功能性质得到改善.     

联合酶法提取豆渣蛋白肽和可溶性膳食纤维

豆渣是大豆加工的主要副产物之一,含有丰富的蛋白质和膳食纤维。为促进豆渣高值化利用,采用联合酶法从豆渣中提取蛋白肽和可溶性膳食纤维（SDF）。首先用碱性蛋白酶酶解豆渣蛋白,以蛋白肽得率为指标,通过单因素试验优化了提取豆渣蛋白肽的工艺条件,再将脱蛋白豆渣用纤维素酶酶解制备SDF,以SDF提取率为指标,通过单因素试验优化提取SDF的工艺条件。结果表明：碱性蛋白酶酶解提取蛋白肽最佳工艺条件为料液比1∶ 35、酶与底物比2%、酶解时间5 h、酶解温度50 ℃、pH 95,在此条件下豆渣蛋白肽得率为66.81%;纤维素酶酶解提取SDF最佳工艺条件为料液比1∶ 30、酶与底物比3%、酶解温度50 ℃、酶解时间2 h、pH 4.0,在此条件下SDF提取率为1554%。利用碱性蛋白酶和纤维素酶依次酶解后,豆渣总利用率达到了89.81%,这为豆渣综合开发利用提供了一种新途径。     

酶法辅助提取、纯化米糠蛋白工艺优化

旨在为米糠副产品的精深加工利用提供指导,利用碱性蛋白酶辅助碱溶酸沉法提取米糠蛋白,并进一步以纤维素酶纯化米糠蛋白,在单因素实验的基础上通过正交实验优化提取、纯化工艺条件。结果表明：米糠蛋白提取的最佳工艺条件为酶解pH 10.5、酶解温度50℃、料液比1∶10、酶解时间120 min、加酶量2.5%,在此条件下米糠蛋白提取率为75.2%;米糠蛋白纯化的最佳工艺条件为酶解温度50℃、酶解pH 5.0、酶解时间60 min、加酶量4%、料液比1∶10,在此条件下米糠蛋白纯度为81.6%,提取率为72.6%。采用此方法可以得到提取率和纯度均较高的米糠蛋白。     

生物酶法制备香菇提取物的工艺研究

以香菇粉为对象,研究生物酶法制备香菇提取物的最佳工艺条件。主要采用纤维素酶、果胶酶、复合蛋白酶(蛋白酶H+风味蛋白酶)进行酶解,研究酶解温度、pH、加酶量、酶解时间分别对酶解过程的影响,以还原糖和氨基态氮为指标分析以上三种酶的最佳酶解条件。最后通过响应面法对多酶酶解体系进行初步研究,优化多酶酶解工艺。结果表明:多酶酶解香菇的最佳工艺条件:温度50℃,pH 7,酶解时纤维素酶添加量为0.6%,果胶酶添加量为0.3%,蛋白酶H加酶量0.4%,风味蛋白酶加酶量0.2%,酶解时间2.5h。     

双酶法水解双孢蘑菇蛋白的工艺研究

实验研究了纤维素酶和中性蛋白酶共同水解双孢蘑菇蛋白的水解工艺,以α-氨基氮含量为指标,确定了纤维素酶和中性蛋白酶的最佳水解条件为:先加纤维素酶,料液比1∶20,加酶量250 U/g,初始pH值6.0,酶解温度55℃,酶解时间120 min;后加中性蛋白酶,加酶量1500U/g,初始pH值6.5,酶解温度45℃,酶解时间150 min.经双酶水解后,α-氨基氮含量可达36.96mg/g.     

Alcalase 2.4L碱性内切酶和Flavourzyme风味酶酶解大豆分离蛋白及脱苦工艺优化

以大豆分离蛋白为原料,选用Alcalase 2.4L碱性内切酶和Flavourzyme风味蛋白酶对大豆分离蛋白进行酶法水解及脱苦工艺研究。以水解度和苦味分值为考察值,对酶解工艺进行优化,确定最佳条件。结果表明:Alcalase2.4L碱性内切酶最佳酶解条件为加酶量14 000 U/g、酶解温度60℃、酶解pH8.5、底物质量分数5%,酶解时间2h,最终水解度为45.34%,此时水解液苦味值为4。Flavourzyme风味蛋白酶对水解液进行二次水解的最优酶解条件为加酶量300 U/g、酶解温度55℃、酶解pH 7.0、酶解时间3 h,此条件下大豆分离蛋白水解液苦味值最低为1.2。Alcalase2.4L碱性内切酶和Flavourzyme风味蛋白酶水解大豆分离蛋白使水解度得到较大提高的同时也解决了水解液的苦味问题。     

复合酶水酶法提取大豆蛋白的工艺优化

采用复合酶水酶法提取大豆蛋白。水解酶选用碱性蛋白酶,复合酶采用纤维酶、半纤维酶、果胶酶。得出最优复合酶水酶法提取大豆蛋白工艺条件为料水比1:6(g/mL)、纤维素酶添加量0.64%、半纤维素酶添加量0.56%、酶解pH5、酶解温度37℃条件下水解0.75h后,再利用Alcalase碱性内切蛋白酶,加酶量1.85%、酶解温度50℃、酶解pH9.26、水解3.6h。经过验证实验可知,在最优酶解工艺条件下总蛋白提取率可达到极大值即85.78%。经过复合酶酶解预处理比传统的湿热预处理的总蛋白提取率提高了近10%,其原因经分析是经过复合酶酶解处理的豆粉其细胞结构充分破坏,使得酶的作用位点暴露更有利于蛋白酶的作用,具体的机理分析有待进一步研究。     

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.     

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.     

Contribution of European research to risk analysis

The European Commission's, Quality of Life Research Programme, Key Action 1—Health, Food & Nutrition is mission-oriented and aims, amongst other things, at providing a healthy, safe and high-quality food supply leading to reinforced consumer confidence in the safety of European food. Its objectives also include the enhancing of the competitiveness of the European food supply. Key Action 1 is currently supporting a number of different types of European collaborative projects in the area of risk analysis. The objectives of these projects range from the development and validation of prevention strategies including the reduction of consumers risks; development and validation of new modelling approaches; harmonization of risk assessment principles, methodologies, and terminology; standardization of methods and systems used for the safety evaluation of transgenic food; providing of tools for the evaluation of human viral contamination of shellfish and quality control; new methodologies for assessing the potential of unintended effects of genetically modified (genetically modified) foods; development of a risk assessment model for Cryptosporidium parvum related to the food and water industries; to the development of a communication platform for genetically modified organism, producers, retailers, regulatory authorities and consumer groups to improve safety assessment procedures, risk management strategies and risk communication; development and validation of new methods for safety testing of transgenic food; evaluation of the safety and efficacy of iron supplementation in pregnant women; evaluation of the potential cancer-preventing activity of pro- and pre-biotic ('synbiotic') combinations in human volunteers. An overview of these projects is presented here.     

低温带皮菜籽粕微粉的不同粒级部分的功能特性

为研究低温带皮菜籽粕微粉的不同粒级部分的功能特性,以经低温脱脂的带皮菜籽粕为原料,经微粉碎后筛分成212~425μm、150~212μm和106~150μm的3个不同粒级的微粉样品,检测这些样品的吸水性、吸油性、乳化性和乳化稳定性、蛋白质体外消化率。结果表明:1 3个不同粒级的微粉样品之间的粗纤维含量存在显著差异,表明三者的结构组成成分有一定差异。23个微粉样品的乳化活性和乳化稳定性随粒度级别的减小而显著增加(P0.01)。33个微粉样品的蛋白质体外消化率随粒度级别的减小而显著增加(P0.01)。4不同粒级带皮菜籽粕微粉样品的吸水性与吸油性受其结构组成物质不同和粒度的双重影响,与粒度的相关性不明显。     

Microbiology of food taints

Fresh and processed foods are often spoilt by the presence of undesirable flavours and odours caused by microbial action. The aim of this paper is to review the current knowledge of microbiologically induced taints that occur in a wide range of foodstuffs, including meats, poultry, fish, crustaceans, milk, dairy products, fruits, vegetables, cereals and cereal products. Examples have been chosen where the compounds responsible for the taint have been identified and sufficient data obtained to demonstrate the involvement of microorganisms. However, in some cases the full identity of the causative organism may not have been elucidated. The types of microorganisms covered by this review include bacteria, fungi, yeasts, actinomycetes and cyanobacteria. Although cyanobacteria do not in general infect foods, their presence in aqueous systems and water supplies can lead to off-flavours in aquatic organisms and processed foodstuffs. Several examples of each of these processes are discussed. Wherever possible, the likely biosynthetic pathway used by the microorganism to produce the offending compound in a foodstuff is indicated.     

Analysis for organic residues from aids to polymerization used to make plastics intended for food contact

Polymers intended for food contact use have been analysed for organic residues which could be attributed to a range of substances employed as polymerization aids (e.g. initiators and catalysts). A wide range of polymers was extracted with solvents and the extracts analysed by gas chromatography-mass spectrometry (GC-MS). The overwhelming majority of substances identified were not derived from aids to polymerization but were oligomers, additives and adventitious contaminants. However, a small number of substances were identified as initiator residues. These included tetramethylsuccinonitrile (TMSN) which was observed in two polymers and it derived from recombination of two azobisisobutyronitrile (AIBN) initiator radicals. Methyl benzoate, benzoic acid, biphenyl and phenyl benzoate were detected in one poly(methyl methacrylate) sample and in two polyvinylchlorides and they are thought to be derived from benzoyl peroxide initiator. TMSN was subsequently targeted for analysis of poly-(methyl methacrylate) plastics using proton nuclear magnetic resonance spectrometry (¹     

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

Experiments were performed to characterize the kinetics of the permeation of different medium molecular weight model permeants: bisphenol A, warfarin and anthracene, from liquid paraffin, through a surrogate potential functional barrier (25 microns-thick orientated polypropylene--OPP) into the food simulants olive oil and 3% (w/v) acetic acid. The characterization of permeation kinetics generally observed the permeation models previously reported to explain the experimental permeation results obtained for a low molecular weight group of model permeants. In general, the model permeants exhibited behaviour consistent with their relative molecular weights with respect to (a) the time taken to attain steady-state permeation into the food simulant in which they were more soluble, (b) their subsequent steady-state permeation rates, and (c) their partition between liquid paraffin and the OPP membrane.     

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.     

Focus on China's Paper Industry

In the English section of this issue, 〈China Paper Newsletters〉 will introduce ＂National Development and Reform Commission Issued Announcement for Selection of Major Preliminary Research Projects for the ＇13th Five-Year Plan＇＂, ＂2013 Annual Report of China＇s Paper Industry＂, and news of projects and other policies.     

Listen to downstream & search for innovation

正Nowadays,textile enterprises are all taking efforts in transformation and upgrading,like improving producing capacity and optimizing production structure to face market downturn.It claimed a higher request to the standard of textile equipments.In the upcoming of ITMA ASIA+CITME 2014exhibition,this magazine have interviewed several branch associations and a series of relative enterprises,to summarize industrial developing status