Processed turkey rolls were prepared with 1 or 3% whey protein concentrates WPC-50 (pH=5. 8 0) , WPC-60 (pH=4. 53) and WPC-75 (pH=6.85) containing 50, 60 and 75% protein along with controls (phosphate and no phosphate) . Control rolls made with 0.5% phosphate had the highest bind strength, and sensory evaluation scores. Only WPC-75 (1%) was acceptable as a binding agent and flavor enhancer. WPC-60 reduced pink discoloration of rolls, but flavor, bind and cohesiveness scores were unacceptably low. WPC-50 was not an effective binding agent. In general, rolls made with 3% WPC had lower scores for intensity of turkey flavor. Bind strength and sensory characteristics were compared for restructured beef rolls formulated with 1% salt, 0.375% sodium tripolyphosphate (STPP) or 0.07% sodium hydroxide (NaOH), and 5, 10 or 20% added water. Controls also had 1% x salt, but no STPP or NaOH. Relative bind strength of rolls was STPP > NaOH > controls. Addition of 20% water reduced bind strength. Cooked yield, moisture content, beef flavor and texture of NaOH rolls were similar to STPP rolls. Bind strength and cohesiveness of NaOH rolls were lower than STPP rolls, but still acceptable. For measuring bind strength of turkey and beef rolls, a sensitive and inexpensive penetrometer was developed. It was equipped with a top-loading balance, accessories, IBM-compatible personal computer and Quick-Basic program that allowed continuously collected penetration force data. at specific time intervals. Penetrometer bind strength and taste panel cohesiveness of turkey and beef rolls were highly correlated (r=0.89 and r=0.93, respectively).

Probiotic dairy foods, especially non- and low-fat dairy products, are becoming popular in the US. A non-fat goat's milk yogurt containing probiotics (Lactobacillus acidophilus and Bifidobacterium spp.) was developed using heat-treated whey protein concentrate (HWPC) as a fat replacer and pectin as a thickening agent. Yogurts containing non-heat treated whey protein concentrate (WPC) and pectin as well as one with only pectin were also produced. A fat-free cow's milk yogurt with pectin was also used as a control yogurt. The yogurts were analyzed for chemical composition, water holding capacity (syneresis), microstructure, changes in pH and viscosity, mold, yeast and coliform counts, and probiotic survivability during storage at 4°C for 10 weeks. The results showed that the non-fat goat's milk yogurt made with 12% HWPC (12.5% WPC solution heated at 85°C for 30 min at pH 8.5) and 0.35% pectin, had a significantly higher viscosity (P<0.01) than any of the other yogurts and low syneresis than the goat’s yogurt with only pectin added (P<0.01). After 10 weeks in storage, viscosity and pH remained constant throughout all of the yogurts. Mold, yeast, and coliform counts were negative throughout the 10 week study. Bifidobacterium spp. remained stable and counts remained above 10⁶CFU g⁻ ¹ during the 10 week storage. However, the population of Lactobacillus acidophilus dropped below 10⁶CFU g⁻ ¹ after 2 weeks of storage. Microstructure analysis of the non - fat goat’s milk yogurt determined by scanning electron microscopy revealed that HWPC interacted with casein micelles to form a more comprehensive network in the yogurt gel. The results indicate that HWPC could be used as a fat replacer to improve the consistency of non - fat goat’s milk yogurt and other products alike.

Eight samples of varying qualities and ages of surimi were used in the development of a new method for testing the quality of surimi. The effects of salt, pH, concentration, heating temperatures and times, and cooling times were observed. These results were used in the development of the McRae-Manning Test. By employing this method, it was possible to determine the difference between fresh high quality surimi, fresh low quality surimi, and old surimi. For this test, surimi was mixed at a 15% concentration, heated at 90 C for 20 minutes in plastic syringes, cooled and evaluated. The surimi was evaluated by emptying the samples onto prepared transparent sheets and measuring how far the sample spreads with time. The transparent sheets had circular measurements which indicated the amount of spread. Best results were obtained when the sheets were elevated at one end.

Replacement of fish meal as the primary protein source in diets for farmed carnivorous fish is a major priority for sustainability of the aquaculture industry. Three plant-based protein sources (soybeans, field peas, and canola) were investigated to compare their effects on the health and performance of rainbow trout (Oncorhynchus mykiss) and to identify significant anti-nutritional factors (ANFs). Six separate 8-week studies were conducted, over a period of one year, to assess the effects of protein source and processing level (meal versus protein concentrate) at dietary inclusion rates of 0 to 300 g kg-1. Abundance of inflammatory and immune marker transcripts including proliferating cell nuclear antigen (PCNA), immunoglobulin M (IgM), interleukin-1 beta (IL-1β), interleukin-8 (IL-8), and interleukin-10 (IL-10) was evaluated in distal intestinal tissue by quantitative PCR (qPCR) analysis. Activity of the pro-apoptotic enzyme caspase-3 was also assayed in distal intestinal tissue. Transcript abundance was highly variable and no suitable genes for the internal normalization of qPCR data could be identified. As a result, transcript copy numbers were reported per 50 ng of total RNA. At 300 g kg-1 inclusion, soybean meal (SBM) increased abundance of IL-8 and IgM, pea meal (PM) increased abundance of IL-10, and canola protein concentrate (CPC) increased abundance of IL-8. Pea protein concentrate (PPC) reduced IL-8 abundance and caspase-3 activity, while increasing abundance of IL-10. Canola meal (CM) and soy protein concentrate (SPC) did not significantly affect the transcript abundance of any assayed gene. Pearson correlation coefficients were determined between gene transcript abundance, performance parameters, protein source, inclusion level, and ANF content. Specific growth rate (SGR) was negatively correlated with the abundance of IL-1β and IgM. Dietary inclusion of SBM was positively correlated with all assayed proinflammatory markers and negatively correlated with SGR. Inclusion of PM was positively correlated with both SGR and the abundance of IL-10. The inclusion of CM was negatively correlated with average daily feed intake (ADFI) and with the abundance of both IL-8 and PCNA. Inclusion of PPC correlated positively with SGR and negatively with the activity of caspase-3. Correlation between transcript abundance and dietary content of putative ANFs suggested negative correlations between glucosinolate content, proinflammatory cytokine expression, SGR, and ADFI; whereas, isoflavone content was positively correlated with proinflammatory markers and negatively correlated with SGR. In conclusion, although high SBM and CM inclusion levels have been associated with reduced growth performance in trout, only SBM was associated with increased abundance of inflammatory marker transcripts. These contrasting responses may be mediated by CM glucosinolates, which could negatively affect palatability without inducing a pro-inflammatory response. Dietary PM was very well tolerated and may have promoted anti-inflammatory activity. Further processing of protein meals to concentrates markedly reduced any observable negative impact on performance parameters and the abundance of inflammatory marker mRNA transcripts. Interestingly, both PM and PPC were positively correlated with SGR and may contain a beneficial anti-inflammatory component.

The diploma thesis is focused on enzyme hydrolysis of potato protein concentrates and fractionation of obtained peptide fragments. Were used protein concentrate from tubers variety Ornella and protein concentrate obtained by swedish company Lyckeby Starch AB. The enzyme hydrolysis lasted 24 hours and were used the proteolytic enzyme alkalasa and trypsin. In this work were prove possitive effect of enzyme hydrolysis on solubility and antioxidative properties of potato protein isolates. The fractionation of obtained peptide hydrolysated was based on systém FPLC (Fast protein liquid chromatography). The fractions contained of peptide fragments about 1, 350 kDa or fragments of smaller moleculary weight. The antixodative activity of subfractions were determIne by method called DPPH. The highest values (2,2 and 2,6 TEAC g/kg) were accured at the subfractions which were separations from Ornella hydrolyzates digeste by enzyme alkalasa.

Partial hydrolysates of two types potato protein concentrates were produced by four selected food proteases. Commercialy produced (company Lyckeby) protein concentrate and laboratory prepared concentrate from tubers of Ornella cultivar were subjected of enzymatic hydrolysis by Fromase 220TL, Fromase 220XLG, Maxiren XDS (commercialy available forms of chymosin) and Neutral protases from bacterial Bacillus subtilis. Protein profile of hydrolysates was created using SDS-PAGE. All hydrolysates were determined by solubility and antioxidant activity using DPPH method. The main aim of this study was to evaluate the efficiency of digestion potato protein concentrate by these selected proteases. Based on the results, the most effective enzyme used for hydrolysis of PC was Neutral proteases form Bacillus subtilis.

Many sources of protein have been investigated to reduce the use of fish meal (FM) in aquaculture feeds, including soybean meal (SBM). However, FM replacement in feeds for carnivorous species is limited by problems with feed intake, growth rate, and overall health associated with reduced digestibility and anti-nutritional factors found in SBM. However, soy processing strategies can reduce the effects of anti-nutritional factors and improve utilization. Therefore, we examined the possibility of further FM replacement in SBM maximized feeds for hybrid striped bass using refined soy products, soy protein concentrate (SPC) and soy protein isolate (SPI). Results indicate that further FM sparing is possible, beyond what can be achieved with SBM. For example, it is possible to reduce dietary FM content as low as 5% using SPC, and though this negatively affects growth rate, this effect may be reversed by the addition of a betaine-based attractant. Replacement with SPI resulted in such a degree of feeding reluctance that starvation and cannibalization became issues during the trial. Reducing FM content below 5-10% resulted in more variable production performance and, when using SPI, increased incidence of cannibalism. No differences in stress tolerance were observed during the trials; however, there was a trend of increasing handling mortality in fish fed the SPC diets. Refined soy proteins can be used in conjunction with SBM to spare FM, but the cost of these products, along with their acceptability to aquatic livestock, will determine the extent of their utilization in aquafeeds.

The present study aimed at assessing the zootechnical parameters, metabolic responses and body nutrient deposition in silver catfish (Rhamdia quelen) regarding partial substitution of fish meal to intermediary residue from rice alcohol distilleries (IRAD). A total of 375 silver catfish juveniles were distributed in 15 boxes of 125 L each (25 fish/box) connected with a water recirculation system during 60 days. Three isoproteic and isoenergetic diets (IRAD0: without IRAD addition, IRAD25 - 25% substitution of PB of fish meal with PB from IRAD, and IRAD50 - 50% substitution of PB of fish meal with PB from IRAD) were formulated. The animals were fed three times a day until apparent satiety. At the end of the experiment (60 days), zootechnical parameters (full length, total weight, weight gain, specific growth rate, feed conversion ratio, final biomass and food intake) and somatic indexes digestivesomatic, hepatosomatic and intestinal quotient were evaluated. Glucose, total proteins, albumin, total cholesterol and triglycerides in the blood, and glucose, glycogen, proteins and free amino acids in the hepatic tissue were also evaluated. In addition, the body composition of nutrients (moisture, ash, fat and protein), protein deposition and body fat were evaluated. Animals fed the IRAD0 presented significantly higher (P <0.5) total consumption, followed by treatments IRAD25 and IRAD50, respectively. Likewise, significant differences (P <0.05) were found for the final weight (FW), final biomass (FB), weight gain (WG) and specific growth rate (SGR), where treatment animals IRAD0 presented the best values in animal performance when compared to those submitted to IRAD25 and IRAD50 treatments, which in turn presented a significant reduction with the increasing inclusion of IRAD. The highest feed conversion rate (FCR) was observed for the IRAD50 treatment, differing from the treatments IRAD0 and IRAD25. The highest levels of glucose, total proteins and plasmatic albumin were observed in fish fed with IRAD50. The levels of hepatic glycogen, glucose, free amino acids and hepatic protein were higher in fish fed with IRAD50 diet compared to the animals that received the IRAD0 and IRAD25 diets. The IRAD0 treatment presented the highest level of PD, differing from IRAD50 treatment. The other evaluated parameters did not differ between them. Even though IRAD presented a high protein concentration, for this study, it negatively affected fish performance. Thus, further studies on assessing the protein quality of IRAD are necessary in order to effectively apply it on fish nutrition. / Este trabalho teve como objetivo avaliar parâmetros zootécnicos, respostas metabólicas e deposição corporal de nutrientes de jundiás (Rhamdia quelen) em resposta à substituição parcial da farinha de peixe pelo resíduo intermediário de destilarias de álcool de arroz (RIDA). Ao todo 375 juvenis de jundiá (3,56±0,6 g) foram distribuídos em 15 caixas de 125 L (25 peixes/caixa) interligadas em um sistema de recirculação de água por um período de 60 dias. Foram formuladas três dietas isoproteicas e isoenergéticas (RIDA0: sem adição do RIDA, RIDA25 - 25% da PB da farinha de peixe substituída pela PB do RIDA e RIDA50 - 50% da PB da farinha de peixe substituída pela PB do RIDA). Os animais foram alimentados três vezes ao dia, até a saciedade aparente. Ao final do período experimental (60 dias), foram avaliados os parâmetros zootécnicos (comprimento total, peso final, ganho em peso, taxa de crescimento específico, conversão alimentar aparente, biomassa final e o consumo de alimento) e índices digestivo somáticos, hepatossomático e quociente intestinal. Também foram avaliados glicose, proteínas totais, albumina, colesterol total e triglicerídeos no plasma e glicose, glicogênio, proteínas e aminoácidos livres no tecido hepático. Além disso, foi avaliada a composição corporal de nutrientes (umidade, cinzas, gordura e proteína), deposição de proteína (DPC) e gordura corporal (DGC). Os animais alimentados com a ração RIDA0 apresentaram significativamente maior consumo total, seguido pelos tratamentos RIDA25 e RIDA50, respectivamente. Da mesma forma, foram encontradas diferenças para as variáveis peso final (PF), biomassa final (BF), ganho em peso (GP) e taxa de crescimento específico (TCE), onde os animais do tratamento RIDA0 apresentaram valores superiores quando comparado aos animais submetidos aos tratamentos RIDA25 e RIDA50 que, por sua vez, apresentaram redução significativa nestes parâmetros com a inclusão crescente do RIDA. A conversão alimentar (CAA) mais elevada foi observada para o tratamento RIDA50, diferindo dos tratamentos RIDA0 e RIDA25. Foram observados níveis mais elevados de glicose, proteínas totais e albumina plasmática nos peixes alimentados com a dieta RIDA50. Os níveis de glicogênio hepático, glicose, aminoácidos livres e proteína hepática foram mais elevados nos peixes alimentados com a dieta RIDA50 comparado aos animais que receberam as dietas RIDA0 e RIDA25. O tratamento RIDA0 apresentou o nível mais elevado de DPC, diferindo do tratamento RIDA50. Os demais parâmetros avaliados não diferiram entre si. Apesar do RIDA apresentar alta concentração de proteína, neste estudo, afetou negativamente o desempenho dos peixes. Diante disso, ainda são necessários novos estudos visando avaliar a qualidade da proteína deste ingrediente para aplica-lo de forma eficiente na nutrição de peixes.

Orientador: Helena Maria Andre Bolini / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Engenharia de Alimentos / Made available in DSpace on 2018-08-12T13:31:07Z (GMT). No. of bitstreams: 1 Melo_LauroLuisMartinsMedeirosde_D.pdf: 959944 bytes, checksum: ee44eced3d2acbc8900f5441b96782b5 (MD5) Previous issue date: 2008 / Resumo: Atualmente, há um interesse crescente de consumidores do mundo todo por alimentos e bebidas com menores quantidades de calorias. Neste contexto, a Análise Sensorial é a única forma de se determinar a aceitação e o perfil em relação à aparência, aroma, sabor e textura de alimentos e bebidas, sendo, portanto, uma ferramenta insubstituível. Com base nestes fundamentos, o objetivo do presente projeto foi realizar a determinação de doçura ideal, doçura equivalente de diferentes edulcorantes, análise descritiva quantitativa (ADQ) e análise de aceitação (com mapas de prerência interno, extendido e análise de regressão de mínimos quadrados parciais, Partial Least Squares - PLS) de chocolates adoçados com diferentes edulcorantes (estévia e sucralose) e sacarose (convencional), e com substituto de gordura (concentrado de soro de leite, WPC), comparando seus comportamentos sensoriais, para a obtenção de uma formulação de alta qualidade sensorial. Também foi incluída ao estudo uma amotra diet (em sacarose) comercial. A ADQ e a análise de aceitação foram conduzidas ao longo da estocagem dos chocolates a 20 °C em 0, 3, 6 e 9 meses. A análise de aceitação foi conduzida tanto com consumidores não-diabéticos quanto com diabéticos. Também foram realizadas análises no NCSU Sensory Service Center da North Carolina State University nos Estados Unidos, incluindo análise descritiva, aceitação e conjoint analysis. Foi possível produzir chocolates ao leite diet (em sacarose) e diet (em sacarose)/light (em calorias) com sucralose e estévia como substitutos da sacarose e WPC como substituto parcial de gordura com curvas tempointensidade do gosto doce similares à curva tempo-intensidade do chocolate ao leite convencional de melhor aceitação dentre os testados (43% de sacarose). Houve poucas alterações nos chocolates desenvolvidos em relação ao chocolate convencional. A amostra de chocolate ao leite convencional adoçada com sacarose caracteriza-se mais pelos atributos aroma doce e doçura. As amostras adoçadas com sucralose e sucralose/WPC são caracterizadas, principalmente, pelo atributo sabor de leite em pó (aumentado pelos agentes de corpo lactitol/polidextrose e pelo substituto de gordura WPC). As amostras com estévia se caracterizam pelos atributos amargor e residual amargo. A amostra comercial foi caracterizada por aroma de manteiga de cacau e derretimento na boca. A maioria dos atributos sensoriais das amostras não foi significativamente alterada até o término do estudo aos 9 meses. A comparação das equipes de provadores do Brasil e dos Estados Unidos mostrou que equipes de provadores altamente treinadas usando terminologia padronizada e representativa podem fornecer resultados similares. As amostras convencional e comercial apresentaram as maiores aceitações entre consumidores não-diabéticos. As alterações observadas nos perfis sensoriais não foram suficientes para provocar mudança na aceitação das amostras durante o período de estocagem, o que garante uma vida-de-prateleira efetiva de pelo menos 9 meses. Análise de cluster dividiu os consumidores em dois grupos. As médias de aceitação das amostras convencional e comercial para o grupo 2 foram significativamente maiores. Para o grupo 1, não houve diferença entre as médias de aceitação das amostras convencional, sucralose e sucralose/WPC. As amostras produzidas com sucralose são tão bem aceitas quanto à amostra comercial entre consumidores diabéticos. Todos os chocolates desenvolvidos (diet em sacarose e diet em sacarose/light em calorias, com sucralose ou estévia) apresentaram médias de aceitação estatisticamente maiores entre diabéticos do que entre não-diabéticos. Os consumidores se dividiram principalmente para a amostra convencional e para a amostra comercial. A doçura foi o atributo mais importante para o primeiro grupo enquanto os atributos derretimento na boca e aroma de manteiga de cacau foram mais importantes para o segundo grupo. Estas tendências se mantiveram até o fim do estudo de tempo de estocagem aos 9 meses. Para consumidores dos Estados Unidos, o atributo declaração sobre açúcar é mais importante para diabéticos do que para não-diabéticos enquanto que o tipo de edulcorante e a redução calórica têm a mesma importância para ambos os grupos. Teoricamente, um chocolate com declaração ¿livre de açúcar¿, edulcorante natural e 25% de redução calórica seria a melhor combinação. Os consumidores dos Estados Unidos foram divididos em três grupos, sendo que o grupo 1 se assemelha mais aos diabéticos em geral, e os grupos 2 e 3, aos nãodiabéticos. A principal diferença entre os grupos 2 e 3 está no fato de o grupo 2 ser mais atento ao consumo de calorias. Nos Estados Unidos, convencional, sucralose e sucralose/WPC foram as amostras com melhor aceitação entre não-diabéticos e sucralose, sucralose/WPC e comercial, entre diabéticos, não confirmando o resultado teórico da conjoint analysis. Os consumidores diabéticos são mais receptivos a chocolates ao leite diet (em sacarose) e diet (em sacarose)/light (em calorias) do que consumidores não-diabéticos / Abstract: Nowadays, there is an increasing interest in foods and beverages with smaller amounts of calories. Then, Sensory Evaluation is the most important tool for evaluation of acceptance and sensory characteristics regarding appearance, aroma, flavor and texture of foods. Therefore, objective of the current study was determination of the most accepted sweetness, equi sweet concentration for different sweeteners, quantitative descriptive analysis (QDA) and acceptance testing (using internal and extended preference mappings and PLS regression) of chocolates sweetened with differente sweeteners (steviosídeo and sucralose) and sucrose (conventional), and with whey protein concentrate (WPC) as fat replacer, comparing their sensory characteristics, in order to get a high sensory quality recipe. This research also included a commercial sugra-free sample. QDA and acceptance testing were performed during storage time at 20 °C after 0, 3, 6 and 9 months. Acceptance testing was performed with both non-diabetic and diabetic consumers. In addition, some analyses were carried out at NCSU Sensory Service Center at North Carolina State University, in the USA, including descriptive analysis, acceptance testing, and conjoint analysis. Lab developed prototypes sugar-free and reduced calorie milk chocolates with sucralose or stevioside and WPC as fat replacer presented time-intensity curves similar to most accepted chocolate with sucrose (43%). There were few changes comparing lab developed prototypes to convencional chocolate. Sweet aroma and sweetness were the most important attributes for conventional milk chocolate sweetened with sucrose while milky flavor (increased by bulking agents lactitol/polydextrose and by fat replacer WPC) was the most important attribute for samples sweetened with sucralose and sucralose/WPC. Bitterness and bitter aftertaste were the most important attributes for samples sweetened with stevioside. Regarding commercial sample, cocoa butter aroma and melting rate were the most important attributes. There were not significant changes in most of sensory attributes during 9-month storage time. Comparisons with Brazilian and USA panels showed that highly trained panels using standardized, representative languages can provide comparable results. Conventional and commercial chocolates presented higher acceptance means for non-diabetic consumers. Effects of aging on some sensory characteristics of chocolates were not enough to change consumer acceptance over time, which assures a realistic shelf life for at least 9 months. Cluster analysis presented two groups. Conventional and commercial chocolates presented higher acceptance means for group 2. For group 1, there was no difference between acceptance means for conventional, sucralose, and sucralose/WPC. Diabetic consumers accept samples produced with sucralose so well as they accept commercial sample. All lab developed prototypes presented higher acceptance means among diabetics compared to non-diabetics. Consumers presented preferences especially for conventional sample or for commercial sample. Sweetness was the most important attribute for the first group while melting rate and cocoa butter aroma were the most important attributes for the second group. These results lasted until the end of storage time (9 months). For USA consumers, sugar claim attribute is more important for diabetics than for non-diabetics while sweetener type and calorie reduction attributes have the same importance for both groups. A chocolate with sugar-free claim, natural sweetener and 25% calorie reduction would be theoretically the best combination. USA consumers were segmented in 3 clusters and cluster 1 was more similar to diabetics while clusters 2 and 3 were more similar to non-diabetics. The main difference between clusters 2 and 3 is consumers in cluster 2 are more concerned about calorie consumption. In the USA, conventional, sucralose, and sucralose/WPC were the most accepted samples among nondiabetics and sucralose, sucralose/WPC, and commercial were the most accepted samples among diabetics, which did not confirm theorical results of conjoint analysis. Diabetic consumers are more accepting than non-diabetic consumers of diabetic and diabetic/reduced calorie milk chocolates / Doutorado / Consumo e Qualidade de Alimentos / Doutor em Alimentos e Nutrição

Master of Science / Food Science Institute / Jayendra K. Amamcharla / Milk protein concentrate (MPC) powders are high-protein dairy ingredients obtained from membrane filtration processes and subsequent spray drying. MPC powders have extensive applications due to their nutritional, functional, and sensory properties. However, their flow properties, rehydration behavior, and morphological characteristics are affected by various factors such as processing, storage, particle size, and composition of the powder. Literature has shown that knowledge about the powder flowability characteristics is critical in their handling, processing, and subsequent storage. For this study, FT4 powder rheometer (FT4, Freeman Technologies, UK) was used to characterize the flowability of MPC powders during storage. This study investigated the flowability and morphological characteristics of commercial MPC powders with three different protein contents (70, 80, and 90%, w/w) after storage at 25ºC and 40ºC for 12 weeks. Powder flow properties (basic flowability energy (BFE), flow rate index (FRI), permeability, etc.) and shear properties (cohesion, flow function, etc.) were evaluated. After 12 weeks of storage at 40ºC, the BFE and FRI values significantly increased (P < 0.05) as the protein content increased from 70 to 90% (w/w). Dynamic flow tests indicated that MPC powders with high protein contents displayed higher permeability. Shear tests confirmed that samples stored at 40ºC were relatively less flowable than samples stored at 25ºC. Also, the lower protein content samples showed better shear flow behavior. The results indicated that MPC powders stored at 40ºC had more cohesiveness and poor flow characteristics than MPC powders stored at 25ºC. The circle equivalent diameter, circularity, and elongation of MPC powders increased as protein content and storage temperature increased, while the convexity decreased as protein content and storage temperature increased. Overall, the MPC powders evidently showed different flow properties and morphological characteristics due to their difference in composition and storage temperature. Literature has shown various methods for determining the solubility of dairy powders, but it requires expensive instruments and skilled technicians. The front-face fluorescence spectroscopy (FFFS) coupled with chemometrics could be used as an efficient alternative, which is commonly used as fingerprints of the various food products. To evaluate FFFS as a useful tool for the non-destructive measurement of solubility in the MPC powders, commercially procured MPC powders were stored at two temperatures (25 and 40ºC) for 1, 2, 4, 8, and 12 weeks to produce powders with different rehydration properties, which subsequently influenced their fluorescence spectra. The spectra of tryptophan and Maillard products were recorded and analyzed with principal components analysis. The solubility index and the relative dissolution index (RDI) obtained from focused beam reflectance measurement was used to predict solubility and dissolution changes using fluorescence spectra of tryptophan and Maillard products. The solubility index and RDI showed that the MPC powders had decreased solubility as the storage time and temperature increased. The results suggest that FFFS has the potential to provide rapid, nondestructive, and accurate measurements of rehydration behavior in MPC powders. Overall, the results indicated that solubility and dissolution behavior of MPC powders were related to protein content and storage conditions that could be measured using FFFS.