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The Efficacy of Sodium Gluconate as a Calcium Lactate Crystal Inhibitor in Cheddar Cheese.

机译:葡萄糖酸钠作为切达干酪中乳酸钙晶体抑制剂的功效。

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摘要

Calcium and lactate are present in excess of their solubility in Cheddar cheese. Consequently, calcium lactate crystals are a common defect in Cheddar cheese. A novel approach for preventing calcium lactate crystals is the addition of sodium gluconate. Sodium gluconate has the potential to increase the solubility of calcium and lactate by forming soluble complexes with calcium and lactate ions, and preventing them from being available for the formation of calcium lactate crystals. This research project was to determine the efficacy of sodium gluconate as a calcium lactate crystal inhibitor in Cheddar cheese. The first part of this study was to determine if sodium gluconate could increase the solubility of calcium lactate. Seven calcium lactate solutions (5.31% w/w) with seven levels of sodium gluconate (0, 0.5, 1, 1.5, 2, 3, and 4% w/w) were made in triplicate. Solutions were stored at 7°C for 21 days, and were visually inspected for calcium lactate crystal formation. Subsequently, they were filtered to remove calcium lactate crystals and the supernatant was analyzed for lactic acid and gluconic acid by HPLC and for calcium by Atomic Absorption Spectroscopy. The visual inspection demonstrated that calcium lactate crystals were formed in the solution with 0% gluconate after the first day of storage and calcium lactate crystals continued to accumulate over time. A minute amount of calcium lactate crystals was also visible in the solution with 0.5% gluconate after 21 days of storage, while calcium lactate crystals were not visible in the other solutions. The HPLC results indicated that there was a higher concentration of calcium and lactic acid in the filtrate from the solutions containing added gluconate. Thus, sodium gluconate can increase the solubility of calcium lactate.;The second part of this study was to determine the manufacture and composition of Cheddar cheeses with different levels of sodium gluconate addition. Six Cheddar cheeses with two levels of salting (2 and 2.5%) and three sodium gluconate addition levels (0, 0.5 and 1%) were manufactured. All cheeses were made using a stirred-curd procedure and replicated three times. Two levels were obtained by dividing cheese curd (at pH 5.6) into two equal-weight halves; each half was salted with 2 and 2.5% (by weight of cheese curd) sodium chloride. Subsequently, each of the salted halves was separated into three equal-weight batches and mixed with 0 (control), 0.5, and 1.0% sodium gluconate, respectively. After sodium gluconate addition, the curds were hooped, pressed for 16 hour, vacuum-sealed in polyethylene bags, and transferred to a ripening room at 6 to 8°C. After 1 week of storage, compositional analyses (pH, moisture, salt, fat and protein) and gluconic acid concentration were determined. Mean pH, moisture, salt, fat and protein content of the cheeses ranged from 5.06 to 5.32, 36.98 to 38.15%, 1.65 to 2.13%, 30.96 to 32.98%, and 25.6 to 26.1%, respectively. At both salting levels, the pH and moisture contents were significantly (p0.05) increased in the treatments with added sodium gluconate. The concentration of gluconic acid in the low salt treatments was 0.33 and 0.59% for the 0.5 and 1.0% addition level, respectively, whereas the concentration in the high salt levels was 0.33 and 0.58%, respectively.;The third part of this study was to determine if the level and type of residual sugar and organic acids produced during ripening was impacted by sodium gluconate addition to Cheddar cheeses. Six cheeses with two salting rates (2 and 2.5%) and three sodium gluconate addition levels (0, 0.5 and 1%) were manufactured. The cheeses were analyzed for lactose and water-soluble organic acids (acetic, butanoic, citric, formic, gluconic, lactic, orotic, propanoic, and uric) at 1-week, 3-month and 6-month, 9-month, and 12-month of ripening by using a cation-exchange-column HPLC externally equipped with a refractive index detector . The organic acids were detected using the UV detector set at 210 and 285 nm, and the refractive index was used for quantification of lactose. The results indicated that at 1-week of ripening, Cheddar cheeses with a higher concentration of gluconic acid had lower concentration of lactic acid, but higher concentration of lactose, while there were no differences in acetic, butanoic, citric, formic, orotic, propanoic and uric acids among treatments at all ripening times. The concentrations of butanoic and propanoic acids gradually increased over time in all treatments, whereas the concentrations of orotic acid and lactose gradually decreased over time. Minor changes in the levels of acetic, citric, formic, lactic, and uric were also observed throughout ripening in all treatments.;The fourth part of this study was to determine the effect of sodium gluconate on pH, lactose, lactic acid, and WSC changes during Cheddar cheese ripening. Six Cheddar cheeses with two salting levels (2 and 2.5%) and three sodium gluconate levels (0, 0.5 and 1%) were manufactured in triplicate. Composition and chemical analysis was performed at 1 week of ripening, and at 3, 6, 9, and 12 months of ripening. Cheeses were analyzed for pH, lactose and lactic acid, and WSC. Compositional analyses at 1 week indicated that sodium gluconate addition had a significant effect on cheese pH, moisture, Na, lactose, and lactic acid. Cheddar cheeses from both 2% and 2.5% salt levels with 0.5 and 1.0% sodium gluconate exhibited higher pH than the control cheeses throughout the ripening time. HPLC results from Cheddar cheeses from both 2% and 2.5% salt levels indicated that cheeses with higher concentration of sodium gluconate addition had a higher concentration of lactose, but lower concentration of lactic acid when compared to the control cheeses throughout the ripening time. WSC results indicated that Cheddar cheeses from both 2% and 2.5% salt levels with higher concentration of sodium gluconate addition had lower WSC concentration when compared to the control cheeses throughout the ripening time. From the results, we concluded that sodium gluconate could have an effect on starter culture activity and could also act as buffering agent, which would cause a higher cheese pH. A higher cheese pH resulted in less soluble of calcium in the cheese serum; thus, resulting in less calcium and lactate ions in the cheese serum.;The final part of this study was to determine the effect of sodium gluconate on the extent of proteolysis, textural properties and sensory evaluation during Cheddar cheese ripening. Six Cheddar cheeses with two salting levels (2 and 2.5%) and three sodium gluconate levels (0, 0.5 and 1%) were manufactured in triplicate. Cheeses were analyzed for the extent of proteolysis by measuring pH 4.6 soluble N and 12% TCA soluble N at 3, 6, 9, and 12-month of ripening. Textural properties were determined by Texture Profile Analysis (TPA) using a TA.XTplus Texture Analyzer at 3, 6, 9, and 12-month of ripening. TPA parameters generated were fracturability, hardness, cohesiveness, springiness, chewiness, and resilience. Descriptive sensory analysis was used to monitor Cheddar cheese flavors in this study at 6 and 12-month of ripening. An increase in soluble N and decreases in textural properties (fracturability, hardness, cohesiveness, springiness, gumminess, chewiness, and resilience) were observed throughout the ripening time for all treatments. At both salting levels, cheeses with added sodium gluconate exhibited a trend for a higher level of proteolysis and lower TPA hardness at 6 and 9 months. The overall flavor intensity scores at 6 months of ripening were lower in cheeses with added sodium gluconate, which could relate to their lower bitterness scores. A similar trend was observed at 12 months of ripening, where cheeses with sodium gluconate addition had lower overall flavor intensity and lower bitterness scores. This present study provides an understanding of how sodium gluconate impacts cheese characteristics during ripening.
机译:钙和乳酸的含量超过了它们在切达干酪中的溶解度。因此,乳酸钙晶体是切达干酪的常见缺陷。防止乳酸钙晶体的一种新方法是添加葡萄糖酸钠。葡萄糖酸钠具有通过与钙和乳酸离子形成可溶性络合物并防止其可用于形成乳酸钙晶体的方式来增加钙和乳酸的溶解度的潜力。该研究项目旨在确定葡萄糖酸钠作为切达干酪中乳酸钙晶体抑制剂的功效。这项研究的第一部分是确定葡萄糖酸钠是否可以增加乳酸钙的溶解度。一式三份制备具有七个水平的葡萄糖酸钠(0、0.5、1、1.5、2、3和4%w / w)的七个乳酸钙溶液(5.31%w / w)。将溶液在7℃下储存21天,并目视检查乳酸钙晶体的形成。随后,将它们过滤以除去乳酸钙晶体,并通过HPLC分析上清液中的乳酸和葡萄糖酸,并且通过原子吸收光谱法分析其钙。目视检查表明,在储存的第一天后,在含有0%葡萄糖酸盐的溶液中形成了乳酸钙晶体,并且随着时间的推移,乳酸钙晶体继续积累。储存21天后,在含0.5%葡萄糖酸盐的溶液中也可见少量的乳酸钙晶体,而在其他溶液中则看不见乳酸钙晶体。 HPLC结果表明,含有葡萄糖酸盐的溶液的滤液中钙和乳酸的浓度较高。因此,葡萄糖酸钠可以增加乳酸钙的溶解度。本研究的第二部分是确定添加不同葡萄糖酸钠含量的切达干酪的制造和组成。制造了六种具有两个盐度水平(2%和2.5%)和三个葡萄糖酸钠添加度(0%,0.5%和1%)的切达干酪。所有奶酪均采用搅拌固化程序制作,并重复三次。将干酪凝乳(pH 5.6)分为两个等重的一半,可得到两个水平。每一半用2和2.5%(按干酪凝乳的重量计)氯化钠腌制。随后,将每个盐渍的半部分分成三等份,并分别与0(对照),0.5和1.0%的葡萄糖酸钠混合。加入葡萄糖酸钠后,将凝乳箍紧,压紧16小时,在聚乙烯袋中真空密封,然后转移至6至8°C的成熟室。储存1周后,确定成分分析(pH,水分,盐,脂肪和蛋白质)和葡萄糖酸浓度。奶酪的平均pH,水分,盐,脂肪和蛋白质含量分别为5.06至5.32、36.98至38.15%,1.65至2.13%,30.96至32.98%和25.6至26.1%。在两种盐浓度下,添加葡萄糖酸钠的处理均显着提高了pH和水分含量(p <0.05)。在0.5和1.0%的添加量下,低盐处理中的葡萄糖酸浓度分别为0.33和0.59%,而在高盐处理中的葡萄糖酸浓度分别为0.33和0.58%。确定在成熟过程中产生的残留糖和有机酸的水平和类型是否受到切达干酪中添加葡萄糖酸钠的影响。制造了六种具有两种盐化率(2%和2.5%)和三种葡萄糖酸钠添加水平(0%,0.5%和1%)的奶酪。在1周,3个月和6个月,9个月和9周对奶酪和奶酪中的乳糖和水溶性有机酸(乙酸,丁酸,柠檬酸,甲酸,葡萄糖酸,乳酸,乳清,牛磺酸,丙酸和尿酸)进行了分析。通过使用外部装有折射率检测器的阳离子交换柱HPLC进行12个月的熟化。使用设置在210和285 nm的UV检测器检测有机酸,并将折射率用于定量乳糖。结果表明,在成熟的1周内,葡萄糖酸含量较高的切达干酪的乳酸含量较低,而乳糖含量较高,而乙酸,丁酸,柠檬酸,甲酸,乳清,丙酸和丙酸均无差异。在所有成熟时间的处理中都含有尿酸和尿酸。在所有处理中,丁酸和丙酸的浓度随时间逐渐增加,而乳清酸和乳糖的浓度随时间逐渐减少。在所有处理中,在整个成熟过程中,醋酸,柠檬酸,甲酸,乳酸和尿酸的含量也发生了微小变化。这项研究的第四部分是确定葡萄糖酸钠对pH,乳糖,乳酸的影响,并且在切达干酪成熟期间WSC发生变化。一式三份地制作了六种具有两个盐含量(2%和2.5%)和三个葡萄糖酸钠含量(0、0.5和1%)的切达干酪。在成熟的1周和成熟的3、6、9和12个月时进行成分和化学分析。分析奶酪的pH,乳糖和乳酸以及WSC。 1周时的成分分析表明,添加葡萄糖酸钠对奶酪的pH,水分,Na,乳糖和乳酸有显着影响。在整个成熟过程中,盐含量分别为2%和2.5%的切达干酪和0.5%和1.0%的葡萄糖酸钠均显示出比对照干酪更高的pH值。切达干酪的盐含量分别为2%和2.5%的HPLC结果表明,与整个成熟时间相比,与对照干酪相比,添加较高浓度葡萄糖酸钠的干酪的乳糖浓度较高,但乳酸浓度较低。 WSC结果表明,与2%和2.5%盐水平的切达干酪相比,添加较高浓度的葡萄糖酸钠时,与整个成熟期间的对照干酪相比,WSC浓度较低。从结果可以得出结论,葡萄糖酸钠可能对发酵剂的发酵活性有影响,并且还可以充当缓冲剂,从而导致更高的奶酪pH值。较高的奶酪pH值导致奶酪血清中钙的溶解度降低;本研究的最后一部分是确定葡萄糖酸钠对切达干酪成熟期间蛋白水解程度,质地特性和感官评估的影响。一式三份地制作了六种具有两个盐含量(2%和2.5%)和三个葡萄糖酸钠含量(0、0.5和1%)的切达干酪。通过在成熟期3、6、9和12个月测量pH 4.6可溶性N和12%TCA可溶性N来分析干酪的蛋白水解程度。在成熟的3、6、9和12个月时,使用TA.XTplus纹理分析仪通过纹理轮廓分析(TPA)来确定纹理特性。生成的TPA参数是可断裂性,硬度,内聚性,弹性,耐嚼性和回弹性。描述性感官分析用于监测切达干酪在成熟期6和12个月时的风味。在所有处理的整个熟化时间内,均观察到可溶性氮的增加和质地特性(断裂性,硬度,内聚性,弹性,胶粘性,耐嚼性和回弹性)的降低。在两个盐含量下,添加葡萄糖酸钠的奶酪在6和9个月时都呈现出更高的蛋白水解水平和更低的TPA硬度趋势。添加葡萄糖酸钠的奶酪在成熟6个月时的总体风味强度评分较低,这可能与其苦味评分较低有关。在成熟的12个月时观察到类似的趋势,其中添加葡萄糖酸钠的奶酪的总体风味强度较低,而苦味评分较低。本研究提供了对葡萄糖酸钠在成熟过程中如何影响奶酪特性的理解。

著录项

  • 作者

    Phadungath, Chanokphat.;

  • 作者单位

    University of Minnesota.;

  • 授予单位 University of Minnesota.;
  • 学科 Agriculture Food Science and Technology.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 287 p.
  • 总页数 287
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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