提高成熟温度对加速硬质干酪成熟的影响

本文通过对4 ℃、10 ℃、20 ℃条件下硬质干酪成熟90 d过程中干酪的成熟特性进行研究,通过测定干酪在成熟期间可溶性氮含量、微观结构改变情况、pH的值改变、游离脂肪酸含量的改变、风味物质种类和含量的变化、感官得分的变化分析表明：成熟温度的提高对干酪可溶性氮含量、游离脂肪酸含量、风味物质的种类和含量的增加都有显著的促进作用,其中10 ℃下经60 d成熟和20 ℃下经30 d成熟的干酪的可溶性氮含量、游离脂肪酸含量、风味物质种类已经等同于或者大于4 ℃下经90 d成熟的酪所具有的;而且提高成熟温度后,4 ℃成熟90 d的样品同10 ℃成熟60 d的样品以及20 ℃成熟30 d的样品微观结构相差不大。虽然20 ℃下也能在一定程度加速硬质干酪的成熟,但是会对风味和组织状态产生不良影响;所以可以将硬质干酪的成熟温度提高到10 ℃。     

水牛乳辣味适度成熟干酪的研制

通过对比不同成熟温度下,干酪成熟过程中硬度、弹性、微观结构、可溶性氮、感官评价等差异,研制一种水牛乳辣味适度成熟干酪,结果表明4℃下成熟90 d,8℃下成熟75 d,12℃下成熟60 d,均可获得品质良好的产品,干酪质地均匀,具有较浓郁的酸辣味、柔和的发酵风味。     

牦牛乳硬质乳酪成熟特性的研究

对牦牛乳硬质乳酪成熟特性进行研究。检测其成熟过程中感官指标、质构指标、营养成分、微生物指标、蛋白质与脂肪分解指标的变化,确定其成熟时间。结果表明:牦牛乳硬质乳酪在成熟过程中,质构指标呈先上升后下降的趋势,在(45~60)d范围内感官品质最佳;p H、水分、蛋白质及脂肪含量均呈下降趋势,灰分含量上升;蛋白质水解及脂肪分解反应在成熟过程中一直进行,并在(45~60)d阶段反应较快;微生物方面乳酸菌总数先上升后下降,而细菌总数呈下降趋势。综合考虑牦牛乳硬质乳酪成熟时间为60 d时品质最佳,风味最好,各项指标达到最优值。     

两种乳源切达干酪成熟期间蛋白质降解状况对比

为了了解中国特色水牛乳切达干酪成熟过程中蛋白质降解的情况,以荷斯坦牛乳切达干酪为对照,用凯氏定氮法研究两种干酪的磷钨酸可溶性氮(PTA-SN)、三氯乙酸可溶性氮(TCA-SN)和pH 4.6可溶性氮(pH 4.6-SN)在干酪成熟期间的变化情况.结果表明:在成熟期90 d内,两种切达干酪在成熟过程中PTA-SN、TCA-SN和pH 4.6-SN含量随着成熟时间的延长逐渐增大,且成熟温度越高,增加得越多,最终分别上升了约5％～10％,1％～10％,2％～5％.中国水牛乳切达干酪蛋白降解程度更深.     

新疆特色酸凝干酪成熟期间理化特性研究

对新疆特色酸凝干酪成熟50 d内理化特性研究结果表明:干酪成熟过程中水分含量减少,变化差异极显著(P<0.01);pH值在前20 d内下降较快,达到最低值;脂肪含量减少;pH4.6可溶性氮和12%TCA可溶性氮含量有不同程度的上升,且pH4.6可溶性氮比12%TCA可溶性氮含量高;通过SDS-PAGE图谱分析,得知干酪在成熟30 d之后蛋白质降解程度较深;乳糖含量在成熟前期下降较快,后期较慢。     

成熟温度对牦牛乳硬质干酪中乳酸菌自溶及氨肽酶活性的影响

通过动态监测5、10、15℃成熟牦牛乳硬质干酪在1~6个月成熟过程中乳酸菌总数、乳酸脱氢酶和氨肽酶活性等变化,探究提高成熟温度对其乳酸菌自溶和氨肽酶活性的影响。研究结果表明:成熟温度对p H值影响显著(P0.05)。干酪中乳酸菌在1~6个月成熟过程中其数量呈现降低趋势。p H值与乳酸菌总数之间存在负相关性。5、10、15℃成熟干酪中乳酸脱氢酶活力依次呈现增加趋势,15、10℃成熟干酪中氨肽酶活性高于5℃成熟干酪中氨肽酶活性。因此,15℃成熟干酪中乳酸菌自溶程度最强,其次为10℃成熟干酪,5℃成熟干酪中乳酸菌自溶程度最弱。15℃成熟干酪中广谱性氨肽酶(broad-specificity aminopeptidase,Pep N)和脯氨酸氨肽酶(X-prolyl-dipeptidlylaminopeptidase,Pep X)活性分别是10℃成熟干酪中Pep N和Pep X活性的2.19和2.64倍。5℃成熟干酪中Pep N、Pep X活性较低,分别没有超过0.29 U/g和0.4 U/g。     

Edam牦牛干酪成熟过程中品质变化及蛋白质降解

为研究Edam牦牛半硬质干酪成熟机理，分别测定成熟0、20、40、60、80 d Edam牦牛干酪的感官、理化、物性、蛋白质和脂肪分解指标，采用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳和傅里叶变换红外光谱等方法研究酪蛋白降解情况，通过Pearson相关性分析成熟时间与各指标间的相关性。结果表明：随着成熟时间延长，感官评分先下降后上升；水分含量、pH值下降；亮度值（L*）下降，红度值（a*）和黄度值（b*）值上升；硬度、弹性、胶黏性均上升，凝聚性逐渐下降；储能模量和损耗模量升高，损耗角正切值始终小于1；成熟时间与总氮含量、pH 4.6和12%三氯乙酸条件下干酪中可溶性氮含量等呈极显著正相关（P<0.01）；脂肪含量先升高后降低，游离脂肪酸含量和硫代巴比妥酸值逐渐增加。酪蛋白（casein,CN）降解研究结果表明：αs1-CN、αs2-CN、β-CN及κ-CN均随成熟时间延长而不断降解，成熟80 d时大分子蛋白降解明显；成熟过程中β-折叠、α-螺旋逐渐向无规卷曲转化；成熟时间与羰基含量、表面疏水性呈极显著正相关（P<0.01），与总巯基含量呈显著负相关（P<0.05）。     

发酵剂的添加量对半硬质干酪品质影响研究

研究发酵剂的添加量对半硬质干酪品质的影响,以确定其最佳添加量。采用单因素试验设计,发酵剂的添加量(体积比)分别为1%、2%、3%、4%、5%。在其他工艺条件相同的情况下,分别加工一批干酪,然后测定成熟干酪的性能指标。结果表明,随着发酵剂添加量的增加,干酪的感官评定值先升高后降低;干酪的硬度和pH 值逐渐降低;总酸度、pH4.6 可溶性氮含量、游离氨基酸总量和水分含量逐渐增加。以感官评定值为主要指标,结合其他性能指标,确定发酵剂的最佳添加量为2%～3%。     

混合型大豆干酪成熟中蛋白质降解特性的研究

对混合型大豆干酪成熟过程中蛋白质的降解及感官特性变化进行了研究。检测了混合型大豆干酪成熟过程中pH4．6水溶性氮、12％三氯乙酸氮、5％磷钨酸氮和游离氨基酸含量的变化；在不同成熟时间下对混合型大豆干酪进行了感官评定。结果表明，随着成熟时间的延长，混合型大豆干酪的pH4．6水溶性氮、12％三氯乙酸氮、5％磷钨酸氮的含量增大；游离氨基酸含量变化较为显著；8℃下成熟30d时，混合型大豆干酪的感官特性最好。     

脂质体微胶囊化中性蛋白酶在Cheddar干酪快速成熟中的应用

尝试通过添加不同剂量的脂质体微胶囊化中性蛋白酶来加快Cheddar干酪的成熟;测定了不同成熟期内干酪的pH值、可溶性氮含量以及干酪的质构的变化,经过综合感官分析,确定了最适添加量。结果表明,添加脂质体微胶囊中性蛋白酶加快了干酪的成熟,其中,0.01%的添加量既加快了干酪成熟,又没有导致干酪在风味、质构等品质方面的缺陷。     

海藻酸钠固定化乳酸菌促熟干酪效果的研究

对海藻酸钠固定化乳酸菌促熟干酪的效果进行了研究。结果表明，在干酪粒中添加10^6CFU／g固定化乳酸菌，水溶性氮（WSN）、三氯乙酸氮（TCASN）和磷钨酸氮（PTASN）含量较对照组明显增大；ADV值在添加固定化乳酸菌干酪中成熟初期变化不大，45d后明显增大；感官评定结果表明，干酪粒中添加10^5CFU／g固定化乳酸菌干酪成熟60d时风味和质地较好，可比对照组干酪成熟期缩短30d左右。     

贮藏条件对红薯叶酸菜品质的影响

目的:探寻乳酸菌发酵红薯叶酸菜的贮藏条件及贮藏期间品质变化规律。方法:真空包装后以常温25℃、低温4℃、80℃—15 min巴氏杀菌后4℃、85℃-10 min巴氏杀菌后4℃贮藏,比较4个条件下红薯叶酸菜pH值、乳酸含量、亚硝酸盐含量、菌落数、色差值及感官评分。结果:25℃下贮藏亮度下降最快,第60天色泽明显变深;4℃下贮藏第30天的酵母菌数量最多,第45天的乳酸菌数量最多;80℃-15 min杀菌后贮藏第90天的大肠杆菌数量最少,感官评分达到食用临界值;85℃-10 min杀菌后贮藏第75天的总菌数量最少,感官评分及格。pH值与亚硝酸盐含量呈极显著负相关,与L值、感官评分呈极显著正相关;乳酸菌数与酵母菌、大肠杆菌、总菌数呈极显著正相关,其中感官评分在第一主成分中的载荷量最大。结论:80℃-15 min杀菌后4℃贮藏,其主要微生物为乳酸菌,其他指标均符合安全标准,感官品质稳定,更适合作为酸菜的贮藏条件,贮藏期可达90 d。     

非发酵剂乳酸菌A-3和D-3对半硬质山羊奶干酪成熟的影响

目的获得加速半硬质山羊奶干酪成熟的非发酵剂乳酸菌菌株(non-starterlacticacidbacteria,NSLAB)。方法以前期分离自地中海地区山羊奶干酪中的2株优良NSLAB菌株为研究对象,测定其对干酪成熟过程中组成成分、微生物菌群、蛋白质水解和质构的影响。结果添加NSLAB菌株对干酪组成成分没有显著影响, NSLAB菌株没有影响乳球菌生长,在干酪成熟期间pH 4.6-SN和12%TCA-SN逐渐增加,且添加NSLAB的干酪在成熟30 d后显著增加了pH 4.6-SN和12%TCA-SN含量, 5%PTASN/TN的增加主要是由于乳酸菌中肽酶作用的结果, SDS-PAGE电泳结果说明添加NSLAB菌株的干酪中小分子多肽含量明显比对照干酪多,RP-HPLC分析得出干酪水溶性中肽的数量随着成熟时间增加。添加NSLAB菌株A-3没有改变干酪的硬度,使干酪的弹性增加。结论添加菌株A-3作为NSLAB的干酪样品中微生物自溶率高,蛋白水解程度强,质构性能良好,具有加速干酪成熟的潜力,是山羊奶干酪工业化生产的优良NSLAB。     

驼乳干酪的工艺优化及成熟期间的理化特性

研究了驼乳干酪最佳加工工艺及成熟期间理化和微生物指标的变化。确定了驼乳干酪的最佳工艺参数:发酵剂的添加量为0.006%,CaC12的添加量为0.03 g/L,pH值为6.1,凝乳酶的添加量为0.06 g/L,凝乳温度为35℃。驼乳干酪的干物质质量分数约为45%,随成熟时间的延长,驼乳干酪的蛋白质、脂肪、乳糖、水分,质量分数下降;硬度、咀嚼性升高,但黏着性和弹性降低;pH4.6-SN的质量分数、12%TCA-SN和5%PTA-SN的质量分数都有不同程度的上升;发酵剂乳酸菌数在逐渐降低,非发酵剂活菌数却在逐渐增高。     

Influence of microflora on texture and contents of amino acids, organic acids, and volatiles in semi-hard cheese made with DL-starter and propionibacteria

The microflora of semi-hard cheese made with DL-starter and propionic acid bacteria (PAB) is quite complex, and we investigated the influence of its variation on texture and contents of organic acids, free amino acids, and volatile compounds. Variation in the microflora within the normal range for the cheese variety Grevé was obtained by using a PAB culture in combination with different DL-starters and making the cheeses at 2 dairy plants with different time and temperature profiles during ripening. Propionic acid bacteria dominated the microflora during ripening after a warm room period at levels of log 8 to log 9 cfu/g, which was about 1 log unit higher than the total number of starter bacteria and about 2 log units higher than the number of nonstarter lactic acid bacteria. Eye formation was observed during the warm room period and further ripening (at 8 to 10°C). The amounts of acetate, propionate, total content of free amino acids, 2-propanol, and ethyl propionate in the ripened cheeses were related to the number of PAB. A decrease in the relative content of Asp and Lys and increase of Phe over the ripening time were different from what is observed in semi-hard cheese without PAB. The occurrence of cracks was higher in cheeses with more hydrolyzed α_S1- and β-casein, higher content of free amino acids, lower strain at fracture (shorter texture), and a greater number of PAB.     

Ripening Profile of Semi-Hard Standard Goat Cheese Made From Pasteurized Milk

The microbial groups, physico-chemical characteristics, proteolysis, lipolysis, and rheological properties over a 30-day ripening period of a semi-hard cheese from pasteurized goat's milk were investigated. The count of aerobic mesophilic flora was high in cheese throughout ripening with lactic acid bacteria being the main microbial group. Halophilic bacteria, yeast and molds showed initial low counts but maintained their levels relatively constant during the ripening period. The main biochemical modification of cheese during ripening was related to the extent of proteolysis. The water soluble nitrogen in the semi-hard cheese increased during ripening. Lipolysis also occurred throughout the ripening period, with the major constituents being the palmitic, oleic, myristic, capric, and lauric acids. The rheological study suggested that the most important factors influencing the texture of the goat cheese is the level of total solids, and the extent of protein degradation recorded as soluble nitrogen during the ripening period. Rheological properties of goat cheese showed a transformation from a soft and elastic consistency to a hard and brittle body as a function of aging.     

The effect of three different ripening/storage conditions on the distribution of selected parameters in individual parts of Dutch‐type cheese

The aim of the study was (i) to detect changes of dry matter, NaCl and twenty‐two free amino acids contents, pH and levels of selected microorganisms in four layers of cheese (from edge to core) during ripening and storage period and (ii) to describe the changes of the above‐mentioned parameters caused by early relocation of cheese from optimum ripening conditions to refrigeration temperatures. The number of mesophilic aerobic and facultative anaerobic bacteria and lactic acid bacteria differed significantly (P < 0.05) during the experiment dependent on the analysed layer and ripening/storage conditions. The free amino acid content differed significantly in individual analysed layers of cheese and also according to individual ripening/storage conditions. The highest content of free amino acids was found in samples stored at optimal ripening temperatures. Cheese hardness was also analysed and the lowest one was detected in samples ripened under optimal temperatures for the whole period. Early release of cheeses into storage rooms with lower temperature significantly affected properties of these products.     

Characterisation of the microflora during ripening of a Norwegian semi-hard cheese with adjunct culture of propionic acid bacteria

The microflora of a semi-hard, washed curd, Norwegian cheese with an added adjunct culture of propionic acid bacteria (PAB) was investigated throughout ripening by phenotypic and physiological tests, API test and 16S rRNA sequencing. Cheeses were made at two commercial Norwegian dairies using different milk treatments (pasteurisation versus microfiltration plus pasteurisation) and the same type of starter cultures. Microflora in the cheese varied according to different plant site, milk treatment, and ripening time. PAB dominated the microflora throughout the ripening process. Leuconostoc spp., most probably from the starter, dominated among the isolates from the cheese using microfiltered and pasteurised milk; however, after 40 weeks of ripening non-starter lactic acid bacteria specie Lactobacillus casei/paracasei and Leuconostoc spp. dominated at the dairy using pasteurised milk. Cheese made at the two plants on two subsequent days showed almost identical microflora throughout ripening.     

Changes in physicochemical and organoleptic properties of traditional Iranian cheese Lighvan during ripening

Lighvan cheese was studied to determine the physicochemical and biochemical changes over 90 days of ripening in brine. Acidity, pH, dry matter, fat values, lipolysis level, water‐soluble nitrogen (WSN), total nitrogen (TN), ripening index (RI), trichloroacetic acid‐soluble nitrogen (TCA‐SN) and organoleptic assessments were analysed. Dry matter and fat values decreased during ripening. Lipolysis level, RI, TCA‐SN values and salt content increased continuously until the end of the ripening period, but total nitrogen decreased throughout a 90‐day storage period. The ripening stage was the main factor affecting the cheese’s sensory properties.     

Probiotic cheese production using Lactobacillus casei cells immobilized on fruit pieces

Lactobacillus casei cells were immobilized on fruit (apple and pear) pieces and the immobilized biocatalysts were used separately as adjuncts in probiotic cheese making. In parallel, cheese with free L. casei cells and cheese only from renneted milk were prepared. The produced cheeses were ripened at 4 to 6°C and the effect of salting and ripening time on lactose, lactic acid, ethanol concentration, pH, and lactic acid bacteria viable counts were investigated. Fat, protein, and moisture contents were in the range of usual levels of commercial cheeses. Reactivation in whey of L. casei cells immobilized on fruit pieces after 7 mo of ripening showed a higher rate of pH decrease and lower final pH value compared with reactivation of samples withdrawn from the remaining mass of the cheese without fruit pieces, from cheese with free L. casei, and rennet cheese. Preliminary sensory evaluation revealed the fruity taste of the cheeses containing immobilized L. casei cells on fruit pieces. Commercial Feta cheese was characterized by a more sour taste, whereas no significant differences concerning cheese flavor were reported by the panel between cheese containing free L. casei and rennet cheese. Salted cheeses scored similar values to commercial Feta cheese, whereas unsalted cheese scores were significantly lower, but still acceptable to the sensory panelists.