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Genotyping of HLA-DQ2 and DQ8 haplotypes is important for diagnosis or for screening of early risk detection of celiac disease or type 1 diabetes. Usually, venous blood DNA extraction and expensive and time consuming amplification are used, that hinder population-wide studies. We assayed a friendly HLA-DQ2 and DQ8 genotyping procedure using a combination of DNA from dried blood spot (DBS) and duplex allele-specific qPCR amplification using SYBR Green. DNA was extracted using home-made buffers and compared to an extraction commercial kit. Duplex reactions by qPCR were designed using each Tm allele amplicon for reference samples (positive HLA-DQ2 or DQ8) with allele-specific primers. DBS samples from 558 children (7.99 ± 2.47 y) were collected. The DNA final yield obtained by the home-made extractive procedure was higher than from the commercial kit (1.11 ± 0.56 vs 0.23 ± 0.14 µg), while the quality was similar for both DNA samples. There was concordance in the amplification profiles for DNA samples obtained with both methods. All of four alleles from DQ2 and DQ8 haplotypes were accurately identified in duplex reactions. By using DBS samples and DNA extraction home-made procedure, the costs were reduced by 60%. The whole procedure is cost-effective for HLA-DQ2 and DQ8 genotyping.
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Teste em Amostras de Sangue Seco/métodos , Técnicas de Genotipagem/métodos , Antígenos HLA-DQ/genética , Reação em Cadeia da Polimerase Multiplex/métodos , Reação em Cadeia da Polimerase em Tempo Real/métodos , Alelos , Benzotiazóis , Doença Celíaca/diagnóstico , Doença Celíaca/genética , Doença Celíaca/imunologia , Criança , Pré-Escolar , DNA/genética , Primers do DNA/química , Diabetes Mellitus Tipo 1/diagnóstico , Diabetes Mellitus Tipo 1/genética , Diabetes Mellitus Tipo 1/imunologia , Diaminas , Feminino , Testes Genéticos , Antígenos HLA-DQ/classificação , Haplótipos , Humanos , Masculino , Compostos Orgânicos/química , QuinolinasRESUMO
OBJECTIVE: To evaluate changes in weight and body fat of Mexican adolescent compared to those of adult lactating women from the Northwest (NM) and Central (CM) regions of Mexico in the first trimester postpartum. METHODS: A prospective design was used to evaluate 41 exclusively breastfeeding women (21 adolescents and 20 adults) recruited 1-2 days after delivering a healthy singleton at the Hospital Infantil del Estado de Sonora (Northwest Mexico) and Instituto Nacional de Perinatología, in Mexico City. Socioeconomic status, height, body weight and composition, dietary intake, physical activity, and milk volume (quantified by deuterium dilution method) were measured at the 1st and 3rd month postpartum. RESULTS: Women did not lose weight throughout the first trimester postpartum. Mean postpartum weight retention at the end of the study was 3.8 kg. No differences in weight and body mass index (BMI) were found between adolescent and adult women in both periods. Energy and macronutrient intakes, physical activity and milk volume were similar between the two groups of women. In both periods, adolescents from the CM region had lower weight, BMI, and body fat than adolescents from the NM region (P<0.05). At the 3rd month, pregestational weight (P < 0.0001) was a predictor of BMI, and region (P < 0.05) and milk volume (P < 0.01) were associated with percentage of body fat. CONCLUSIONS: Exclusively breastfeeding for 3 months did not reduce weight or body fat in the Mexican population of this study. Efforts to avoid weight retention in the lactation period may contribute to prevent overweight and obesity in women.
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Tecido Adiposo/metabolismo , Peso Corporal , Aleitamento Materno , Lactação , Adulto Jovem , Adolescente , Adulto , Antropometria , Composição Corporal , Índice de Massa Corporal , Feminino , Humanos , México , Estudos Prospectivos , Fatores de TempoRESUMO
Different formulations for chocolate pastries making (brownies) were prepared by substituting 15, 20, and 25% of the wheat flour by inulin. The batter characteristics of each formulation were evaluated and the batters were baked at 175 degrees C for 15 min. After baking, the brownies were allowed to cool, put into crystal polystyrene trays, and their texture after 1, 3, 7, and 15 days of storage at room temperature (25 degrees C) and 65% of relative humidity, was evaluated. Based on the evaluations of batter characteristics and brownies textural properties during storage, the formulation containing 20% of inulin was the best. Proximate analysis was determined, and total, soluble and insoluble dietary fiber were quantified for brownies control and 20% inulin ones, as well as commercial brownies. The brownies containing 20% inulin showed lower firmness, gumminess, and masticability than the control and higher protein and lower fat content (6,3 vs 26,3%) and caloric value (331,4 vs 467.9 kcal/100 g) in comparison to the commercial brownies. The brownie with 20% inulin had twice the total dietary fiber and 22 times more soluble fiber than the brownie control. The acceptability of the brownie with 20% inulin was similar to that of the control. The incorporation of inulin in the production of brownies allowed to reduce the caloric value and to increase the soluble fiber content without adverse effects in texture of the pastries.
Assuntos
Fibras na Dieta/normas , Manipulação de Alimentos/métodos , Tecnologia de Alimentos , Alimentos Formulados/normas , Inulina/normas , Fibras na Dieta/análise , Inulina/análise , Invenções/normas , Valor Nutritivo , PaladarRESUMO
INTRODUCTION: Introduction: nutritional therapy is essential for the treatment of critically ill patients, although its right application fails frequently, which increases the risk for undernutrition and complications. Objective: to evaluate the nutritional adequacy of patients with enteral nutritional support in an intensive care unit (ICU). Methods: a cohort study was conducted including adults admitted to the ICU with enteral support and stay ≥ 7 days. Demographic data, severity of the disease, and clinical and nutritional scores, including IL-6 levels and body composition, were evaluated at admission. Nutritional intake was recorded daily in relation to the target intake according to international guidelines, for calculation of caloric and protein deficiencies. Results: in all, 26 from 132 admitted patients were included. Their probability of mortality was 20-25 % due to disease severity by APACHE (16.6 ± 6.02) and SOFA (8 ± 4.4). Undernutrition risk was 5.6 ± 1.09 by NRS-2002 and 4.3 ± 1.2 by angle phase. Caloric deficiency was -674 kcal/day, with 13 % proteins (28 ± 11.5 g/d) and 42 % lipids, including 17.5 % of non-nutrient calories from propofol. NUTRIC was significantly associated with percentages of the caloric prescription at days 3 and 7 (R2 = 0.21, p = 0.01). Conclusion: patients had a caloric/protein deficit with critical protein deficit of -85.2 g/day, and an inadequate proportion between protein calories and non-protein calories, increasing their risk of complications.
INTRODUCCIÓN: Introducción: la terapia nutricional es esencial para tratar a pacientes críticos pero, si no es la adecuada, aumenta el riesgo de desnutrición y complica la evolución. Objetivo: evaluar la adecuación de la terapia nutricional enteral en una unidad de cuidados intensivos (UCI). Métodos: se evaluó una cohorte adulta ingresada a una UCI con nutrición enteral y estancia ≥ 7 días. Al ingreso se registraron la severidad de la enfermedad y los datos socio-demográficos, clínicos y nutricionales, con cribados que incluyeron la IL-6 y la composición corporal. Diariamente se evaluó el aporte de nutrientes con respecto al 70 % óptimo de lo prescrito por las guías internacionales, para estimar el déficit energético-proteico. Resultados: se incluyeron 26 de 132 pacientes ingresados. Su probabilidad de mortalidad era del 20-25 % debido a la severidad de su enfermedad por los sistemas APACHE (16,6 ± 6,0) y SOFA (8 ± 4,4); su riesgo de desnutrición era de 5,6 ± 1,09 puntos por el NRS-2002, con 4,3 ± 1,2 de ángulo de fase. El déficit energético promedio era de -674 kcal/día, con un 13 % en aporte proteico (28 ± 11,5 g/d) y un 42 % en lípidos, y con el 17,5 % proveniente del propofol. El NUTRIC se asoció significativamente con los porcentajes de prescripción calórica alcanzados los días 3 y 7 (R2 = 0,21, p = 0,01). Conclusión: los pacientes sufrieron déficit calórico/proteico, con déficit proteico crítico de > 85,2 g/día e inadecuada relación entre calorías proteicas y no proteicas, aumentando su riesgo de complicaciones.
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Ingestão de Energia , Unidades de Terapia Intensiva , Adulto , Estudos de Coortes , Cuidados Críticos , Estado Terminal , Humanos , Apoio NutricionalRESUMO
Bifidobacterium animalis subsp. lactis Bb12 is a widely used probiotic that provides numerous health benefits to its host, many due to its immunomodulatory properties. Although the precise mechanism of modulation is still under investigation, several reports associate the interaction of TLR2 with components of the bacterial cell wall inducing a signaling cascade that culminates with the production of cytokines and co-stimulatory molecules. MicroRNAs (miRNAs) have emerged as important post-transcriptional regulators of immune responses, including those toward probiotics. In this study, we analyzed the miRNA expression profile in swine monocytes exposed to Bb12 by using an anti-TLR2 blocking strategy and Bb12 involvement in the regulation of the TLR2 pathway. As a result, the expression of 40 miRNAs was influenced by the treatments (p < 0.01), and 15 differentially expressed miRNAs with validated miRNA-mRNA interactions with around 26 proteins related to the TLR2 pathway were identified. The miRNAs upregulated in response to Bb12 included miR-15a-5p, miR-16-5p, miR-26a-5p, miR-29b-3p, and miR-30d-5p, and the following showed downregulation: miR-181a-5p, miR-19b-3p, miR-21-5p, miR-23a-5p, and miR-221-3p. The expression of let-7c-5p, let-7f-5p, miR-146b-5p, miR-150-5p, and miR-155-5p was increased by Bb12 only when TLR2 was blocked. The identified miRNA common targets were downstream proteins from bacterial recognition via TLR2, such as MyD88, TRAF6, and MAPK members; transcription factors such as NF-κB and AP-1; and cytokines such as IL-6, IL-10, and TNF-α. TLR2 participation was abrogated by anti-TLR2 antibody and suggests that bacterial recognition is complemented by other receptors since there were still changes in the microtranscriptome.
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Bifidobacterium animalis , MicroRNAs , Animais , Bifidobacterium animalis/genética , Citocinas/genética , Imunidade , Imunomodulação , MicroRNAs/genética , MicroRNAs/metabolismo , Monócitos , Suínos , Receptor 2 Toll-Like/genéticaRESUMO
A weekly conference series paired with lectures entitled "Microbiome-MX: exploring the Microbiota and Microbiome Research in Mexico" was organized to provide a multidisciplinary overview of the most recent research done in Mexico using high-throughput sequencing. Scientists and postgraduate students from several disciplines such as microbiology, bioinformatics, virology, immunology, nutrition, and medical genomics gathered to discuss state of the art in each of their respective subjects of expertise, as well as advances, applications and new opportunities on microbiota/microbiome research. In particular, high-throughput sequencing is a crucial tool to understand the challenges of a megadiverse developing country as Mexico, and moreover to know the scientific capital and capabilities available for collaboration. The conference series addressed three main topics important for Mexico: i) the complex role of microbiota in health and prevalent diseases such as obesity, diabetes, inflammatory bowel disease, tuberculosis, HIV, autoimmune diseases and gastric cancer; ii) the use of local, traditional and prehispanic products as pre/probiotics to modulate the microbiota and improve human health; and iii) the impact of the microbiota in shaping the biodiversity of economically important terrestrial and marine ecosystems. Herein, we summarize the contributions that Mexican microbiota/microbiome research is making to the global trends, describing the highlights of the conferences and lectures, rather than a review of the state-of-the-art of this research. This meeting report also presents the efforts of a multidisciplinary group of scientist to encourage collaborations and bringing this research field closer for younger generations.
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Bactérias/classificação , Biologia Computacional/métodos , Microbioma Gastrointestinal/fisiologia , Bactérias/genética , Bactérias/isolamento & purificação , Sequenciamento de Nucleotídeos em Larga Escala , Humanos , México , Saúde Pública/métodosRESUMO
BACKGROUND: Consumption of seafood can produce allergic symptoms in susceptible individuals and crustacean allergies are the most frequently reported causes of allergic reactions. METHODS: An allergen from the muscle of the white shrimp Litopenaeus vannamei was purified by ion exchange chromatography and identified by mass spectrometry of tryptic peptides and its specific enzymatic activity. Moreover, the corresponding full-length cDNA was obtained from an L. vannamei muscle cDNA library. RESULTS: A 40-kDa protein was purified and identified as arginine kinase and its cDNA of 1.4 kb encoded a 356 amino acid protein. The obtained arginine kinase was recognized by IgE in serum from shrimp-allergic individuals using ELISA and immunoblotting analysis. CONCLUSIONS: This is the first allergen reported for the Pacific white shrimp species; it was named Lit v 2 and has a 96% identity to Pen m 2 from Penaeus monodon.
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Alérgenos/química , Arginina Quinase/química , Arginina Quinase/imunologia , Hipersensibilidade Alimentar/imunologia , Penaeidae/enzimologia , Penaeidae/imunologia , Alérgenos/genética , Alérgenos/imunologia , Sequência de Aminoácidos , Animais , Arginina Quinase/genética , Sequência de Bases , Hipersensibilidade Alimentar/enzimologia , Humanos , Imunoglobulina E/biossíntese , Dados de Sequência Molecular , Penaeidae/genéticaRESUMO
INTRODUCTION: Entamoeba histolytica, E. dispar, and E. moshkovskii are morphologically identical, but intestinal amebiasis is caused only by E. histolytica. Mexico is among the countries with high amebae infection rates, although the contribution of pathogenic amoeba to the total detected cases remains unknown, especially in the northwestern dry region. Therefore, the aim of this study was to identify the actual prevalence of E. histolytica using real-time polymerase chain reaction (PCR) in schoolchildren of northwestern Mexico. METHODOLOGY: Participants were children from five public elementary schools in the low-socioeconomic-level suburban areas of Hermosillo, Sonora, Mexico. One stool sample was collected from each child and analyzed by the Faust technique for Entamoeba spp. and by real-time PCR for E. histolytica. RESULTS: Analysis of stool samples from 273 children (9.0 ± 1.5 years of age) resulted in 25 (9.2%) positive for E. histolytica/E. dispar/E. moshkovskii by the Faust technique; of these, 3 were positive for E. histolytica by real-time PCR. In addition, 2 samples that were negative for E. histolytica/E. dispar/E. moshkovskii by the Faust technique were positive by real-time PCR. CONCLUSIONS: The actual prevalence of E. histolytica in our study population was 1.8%, which is lower than those reported in previous studies in other Mexican regions.
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AIM: To study the histological and pancreatitis-associated protein mRNA accumulation changes of pancreas from acute phase of caerulin-induced pancreatitis to recuperation in rats. METHODS: Acute pancreatitis was induced by caerulein in male Wistar rats and followed up for 90 d by histological and mRNA analyses of pancreas. Pancreases were dissected at 0, 9, 24 h and 3, 5, 15, 30, 60, 90 d post-induction. Edema (E), polymorphonuclear neutrophil (PMN) infiltration, cytoplasmic vacuolization (V), zymogen granule depletion (ZD) and acinar disorganization (AD) were microscopically evaluated. Accumulation of pancreatitis-associated protein (PAP) and L13A mRNAs were quantified by real-time PCR. RESULTS: The main histological changes appeared at 9 h post-induction for PMN infiltration and cytoplasmic V, while at 24 h and 3 d for E and ZD, respectively. All the parameters were recovered after 5 d, except for ZD which delayed more than 30 d. The main AD was observed after 15 d and values returned to normal after 30 d. Similarly to histological changes, accumulation of the PAP mRNA was increased at 9 h with the highest accumulation at 24 h and differences disappeared after 5 d. CONCLUSION: From the acute phase to recuperation of pancreatitis, regeneration and re-differentiation of pancreas occur and PAP expression is exclusively an acute response of pancreatitis.
Assuntos
Antígenos de Neoplasias/metabolismo , Biomarcadores Tumorais/metabolismo , Lectinas Tipo C/metabolismo , Pâncreas/metabolismo , Pâncreas/patologia , Pancreatite/metabolismo , Pancreatite/patologia , Recuperação de Função Fisiológica/fisiologia , Animais , Ceruletídeo , Expressão Gênica , Masculino , Pancreatite/induzido quimicamente , Proteínas Associadas a Pancreatite , Reação em Cadeia da Polimerase , RNA Mensageiro/metabolismo , Ratos , Ratos WistarRESUMO
BACKGROUND: Type 1 diabetes (T1D) is currently an autoimmune disease occurring more frequently and early in life. T1D development requires genetic predisposition and environmental factors, which influence the gut microbiota in early infancy and could increase the risk for T1D-associated autoimmunity. In Mexico there are no published microbiota studies in children <6 years old with T1D. CASE REPORTS: We report two contrasting Mexican T1D cases of children <6 years of age and a third case of a healthy child prior to autoimmunity and T1D onset. Perinatal factors, feeding regimes in the first year of life and gut microbiota composition are discussed and related to the T1D onset. The three cases show a particular microbiota profile with decreased bacterial diversity as compared with healthy children, which could be related to environmental factors prior to the development of T1D and disease control. CONCLUSIONS: T1D infant cases presented a decreased bacterial diversity, which appeared before autoimmunity and T1D onset. Glycemic control could tend to correct the gut dysbiosis in T1D children. Prospective studies are needed to follow-up healthy children at high genetic risk to assess factors related to the microbiota structure.
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Measurements of deuterium oxide concentrations (DOC) in saliva by infrared spectroscopy (IRS) and isotope ratio mass spectrometry (IRMS) were compared for the calculation of infants' milk intake and maternal body fat. Deuterium oxide (30 g) was given to the mother. DOC by IRS and IRMS were 340 +/- 209 and 345 +/- 202 ppm. The mean difference between both methods (4.62 +/- 76.3) was not different from zero (p = .57). Bland and Altman analysis showed no significant overall bias (r = 0.10; p = .33), but dispersion within the limits of agreement. The mean milk intake in the infants' by IRS and IRMS were 624 +/- 296 g/day and 634 +/- 327 g/day (p = .642) and the mothers' mean body fat were 31.3 +/- 12% and 31.5 +/- 13% (p = .755). The results appear to be the same for milk intake and body fat by the two methods and no evidence of bias was found.
Assuntos
Tecido Adiposo/metabolismo , Composição Corporal/fisiologia , Óxido de Deutério , Espectrometria de Massas/métodos , Leite Humano , Espectroscopia de Luz Próxima ao Infravermelho/métodos , Adolescente , Adulto , Água Corporal/metabolismo , Feminino , Humanos , Técnicas de Diluição do Indicador , Lactente , Recém-Nascido , Lactação , Saliva/químicaRESUMO
Thirty four subjects (13 men and 21 women), 24 to 70 years old from northern Mexico, were measured for body density by air displacement plethysmography (ADP) with the BOD-POD, and for total body water by deuterium oxide dilution and infrared spectroscopy (IRS-DOD). Subjects were given a 30 g dose of deuterium oxide. Saliva samples were filtered, sublimated, and deuterium was measured using a Miran 1 FF, IRS. Linear regression of the fat mass (FM) derived from both methods showed that the intercept (0.071) was not different from zero (p = .96) and the slope was 0.96 (p < .0001) demonstrating the techniques to be equivalent. Further, mean FM was 26.7 +/- 12.4 and 25.6 +/- 12.4 kg, for IRS-DOD and ADP techniques, respectively (p = .08). Precision analysis by the model R2 showed that 92.3% of the variability was explained (SEM = 3.4 kg). Bland-Altman analysis showed no significant bias (r = 0.017; p = .93). Mean difference between methods was -1.08 (CI: -2.3 to + 0.13) kg FM.
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Composição Corporal/fisiologia , Óxido de Deutério , Pletismografia/métodos , Espectroscopia de Luz Próxima ao Infravermelho/métodos , Tecido Adiposo/metabolismo , Adulto , Idoso , Feminino , Humanos , Masculino , México , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Sensibilidade e EspecificidadeRESUMO
Due to an increasing incidence of celiac disease (CD) and other gluten-related disorders, different gluten-free breads have been developed using starches and additives as a substitute for gluten. Thus, patients miss not only the taste and aroma of wheat bread but also risk their sensitive intestines. Therefore, modifying gluten to avoid an immune response in CD and its application to baking is in progress. The aim of the study was to enzymatically modify gluten on wheat flour, during bread-making avoiding the use of additives, to reduce immunoreactivity, preserving its properties. Microbial transglutaminase (mTG) or chymotrypsin (ChT) was used to bind lysine or valine to gluten proteins in a model system. The best conditions were directly applied to wheat flour for bread-making with and without punching at 45 min. Subsequently, the rheological properties of the doughs, specific volume of the loaves, immunoreactive gluten content and modification of the extracted proteins were evaluated. ChT-treated breads presented a better appearance with a more homogeneous crumb, higher specific volume values (3.34-4.25 cm(3) g(-1)) and higher reactive gluten reduction (up to 71%) than the mTG-treated ones (1.23-2.66 cm(3) g(-1)) with only a 42% reactive gluten reduction. Thus, transpeptidation during bread-making is a promising technology, although it is necessary to improve the modification process to obtain the reactive gluten reduction required in breads for the treatment of CD patients and other gluten-related disorders.
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Pão/análise , Farinha/análise , Manipulação de Alimentos/métodos , Gliadina/química , Glutens/química , Triticum/química , Aminoácidos/química , Quimotripsina/metabolismo , Fermentação , Reologia , Amido/química , Transglutaminases/metabolismoRESUMO
AbstractBackground: Type 1 diabetes (T1D) is currently an autoimmune disease occurring more frequently and early in life. T1D development requires genetic predisposition and environmental factors, which influence the gut microbiota in early infancy and could increase the risk for T1D-associated autoimmunity. In Mexico there are no published microbiota studies in children <6 years old with T1D.Case reports:We report two contrasting Mexican T1D cases of children <6 years of age and a third case of a healthy child prior to autoimmunity and T1D onset. Perinatal factors, feeding regimes in the first year of life and gut microbiota composition are discussed and related to the T1D onset. The three cases show a particular microbiota profile with decreased bacterial diversity as compared with healthy children, which could be related to environmental factors prior to the development of T1D and disease control.Conclusions:T1D infant cases presented a decreased bacterial diversity, which appeared before autoimmunity and T1D onset. Glycemic control could tend to correct the gut dysbiosis in T1D children. Prospective studies are needed to follow-up healthy children at high genetic risk to assess factors related to the microbiota structure.
ResumenIntroducción: La diabetes tipo 1 (DT1) es una enfermedad autoinmune que cada vez es más frecuente y se presenta a edades más tempranas. Su desarrollo requiere de predisposición genética y factores ambientales que influyen sobre la microbiota intestinal en la infancia temprana que pudieran aumentar el riesgo de autoinmunidad asociada con DT1. En México no existen publicaciones de estudios de microbiota en niños menores de 6 años con DT1.Casos clínicos: Se reportan dos casos de DT1 contrastantes de niños mexicanos menores de 6 años de edad y un tercer caso de un niño sano, previo al desarrollo de autoinmunidad y DT1. Se discuten los factores perinatales, los regímenes de alimentación en el primer año de vida y la microbiota intestinal en relación con el desarrollo de DT1. Los tres casos presentaron una microbiota particular con disminución de la diversidad bacteriana en comparación con los niños sanos, lo cual pudiera estar relacionado con factores ambientales previos al desarrollo de la enfermedad y con el control de la DT1.Conclusiones: Los niños con DT1 presentaron una diversidad bacteriana disminuida que aparece antes de la autoinmunidad y DT1. El control glucémico podría corregir la disbiosis intestinal en DT1. Faltan estudios prospectivos que den seguimiento a niños sanos con alto riesgo genético y evalúen factores relacionados con la estructura de la microbiota.
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Se prepararon distintas formulaciones para pastelillos de chocolate (brownies) sustituyendo 15, 20 y 25% de la harina de trigo con inulina. Se evaluaron las características del batido de cada una de las formulaciones y se sometieron al proceso de horneado a 175 oC por 45 min. Después del horneado, los brownies se dejaron enfriar por 1 h y posteriormente se empacaron en charolas de poliestireno cristal y se les evaluó textura a los 1, 3, 7 y 15 días de almacenamiento a temperatura ambiente (25 oC) y 65% de humedad relativa. En base a las evaluaciones del batido y a las propiedades texturales de los brownies durante el almacenamiento, se seleccionó la formulación con 20% inulina como la mejor. Se analizó composición proximal y cuantificó fibra dietética total, soluble e insoluble, tanto al brownie control y al de 20% de inulina, como a un brownie comercial. El brownie con 20% de inulina presentó menor firmeza, gomosidad y masticabilidad que el control, mayor contenido de proteína y menor contenido de grasa (6,3 vs 26,3%) y aporte calórico (331,4 vs 467,9 kcal/100 g) con respecto al brownie comercial. El brownie con 20% de inulina mostró el doble de fibra dietética total y 22 veces más fibra soluble que el brownie control. La aceptabilidad del brownie con 20% inulina fue similar a la del brownie control. La incorporación de inulina en la elaboración de brownies permitió reducir el aporte calórico y aumentar el contenido de fibra soluble, sin afectar adversamente la textura de los pastelillos.
Formulation and elaboration of lowenergy and high fiber-containing brownies. Different formulations for chocolate pastries making (brownies) were prepared by substituting 15, 20, and 25% of the wheat flour by inulin. The batter characteristics of each formulation were evaluated and the batters were baked at 175 oC for 15 min. After baking, the brownies were allowed to cool, put into crystal polystyrene trays, and their texture after 1, 3, 7, and 15 days of storage at room temperature (25 oC) and 65% of relative humidity, was evaluated. Based on the evaluations of batter characteristics and brownies textural properties during storage, the formulation containing 20% of inulin was the best. Proximate analysis was determined, and total, soluble and insoluble dietary fiber were quantified for brownies control and 20% inulin ones, as well as commercial brownies. The brownies containing 20% inulin showed lower firmness, gumminess, and masticability than the control and higher protein and lower fat content (6,3 vs 26,3%) and caloric value (331,4 vs 467.9 kcal/100 g) in comparison to the commercial brownies. The brownie with 20% inulin had twice the total dietary fiber and 22 times more soluble fiber than the brownie control. The acceptability of the brownie with 20% inulin was similar to that of the control. The incorporation of inulin in the production of brownies allowed to reduce the caloric value and to increase the soluble fiber content without adverse effects in texture of the pastries.
Assuntos
Fibras na Dieta/normas , Tecnologia de Alimentos , Manipulação de Alimentos/métodos , Alimentos Formulados/normas , Inulina/normas , Fibras na Dieta/análise , Inulina/análise , Invenções/normas , Valor Nutritivo , PaladarRESUMO
A gene coding for lysozyme from the insect Manduca sexta (Ms-lyz) was expressed in Escherichia coli. The protein was produced as an insoluble cytoplasmic inclusion body which was denatured in 8 M: guanidine-HCl, renatured and purified by affinity and ion-exchange chromatography. The N-terminal sequence and the activity of the recombinant protein against Micrococcus luteus confirmed that correct expression had occurred. When Ms-lyz activity was compared to hen egg white lysozyme, the insect lysozyme was active at lower temperatures. These results demonstrate the feasibility of producing a disulfide-bonded lysozyme enzyme in bacteria and suggest that the insect Ms-lyz is an interesting system for further development of an antibacterial functional at low temperatures.
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Bactérias/metabolismo , Manduca/enzimologia , Muramidase/metabolismo , Proteínas Recombinantes/química , Animais , Aspergillus/enzimologia , Bioquímica/métodos , Reatores Biológicos , Cromatografia , Cromatografia de Afinidade , Cromatografia por Troca Iônica , Citoplasma/metabolismo , Dissulfetos , Eletroforese em Gel de Poliacrilamida , Escherichia coli/metabolismo , Guanidina/química , Insetos , Muramidase/química , Dobramento de Proteína , Estrutura Terciária de Proteína , TemperaturaRESUMO
Objetivo. Determinar la frecuencia de uso, el contenido y la composición de proteínas de los productos para lactancia en Hermosillo, Sonora, México. Material y métodos. Se revisaron encuestas sobre prácticas de lactancia (1986-1994). En muestras de sucedáneos y leche humana se cuantificó proteína total (microKjeldhal) y se analizó la proporción de éstas separadas por electroforesis, con un programa computacional. Resultados. Once fórmulas y tres leches enteras fueron las más utilizadas en infantes de 0-6 meses. El contenido de proteínas en las fórmulas de inicio y seguimiento fue acorde con el etiquetado comercial y cumplió con lo estipulado por la regulación sanitaria. La cantidad de caseína, una de las proteínas de la leche, fue de 40 por ciento en la leche humana, fórmulas de inicio 44 por ciento, fórmulas de seguimiento y leches enteras 60 por ciento y fórmulas especiales > 70 por ciento. Conclusiones. En la lactancia se usan productos no recomendables; en algunos su composición proteica es diferente a la de la leche humana, aunque la regulación sanitaria no los proscribe
Objective. To determine the frequency of utilization of milk surrogates as well as their protein contents and composition. Material and methods. Interview data on lactation patterns previously recorded (1986-1994) in Hermosillo, Mexico, were reviewed. Both human and surrogate milk fluids were tested; total protein contents were quantified by microKjeldhal and protein composition was determined by electrophoresis computer densitometry. Results. Eleven milk formulas and three whole cow milks were used more frequently for infants aged 0-6 months. Total protein contents of modified and follow-up formulas were the same as reported on the label, in compliance with sanitary regulation. Casein content of human milk was 40%, and modified formulas contained 44%; follow-up formulas and whole milks were 60% and special formulas contained more than 70%. Conclusions. Products used for lactation seem to be inadequate for infant nutrition. In addition, the protein composition of some products was quite different that of human milk, and they are not proscribed from official regulation.
Assuntos
Substitutos do Leite Humano/análise , Substitutos do Leite Humano/normas , Proteínas/análise , Tabela de Composição de AlimentosRESUMO
En la producción de fórmulas hipoalergénicas, bebidas fortificadas y nutracéuticos para alimentación especial, se requieren ingredientes ideales. En este estudio, se obtuvieron ingredientes proteicos por medio de hidrólisis y síntesis enzimática con metionina a la proteína de soya. La hidrólisis se realizó al 4 por ciento (p/v) con enzimas pancreáticas porcinas al 4 por ciento (p/p), 50ºC, 6h y pH 8. El hidrolizado seco se resuspendió al 20 por ciento (p/v) e incubó con 7,6 por ciento de metiléster de metionina (p/p), quimotripsina al 1 por ciento (p/p) y glicerol 3 M, 37ºC, 3 h y pH 7.0. Ates y después del enriquecimiento (E), el hidrolizado se fraccionó en 3 partes por ultrafiltración (UF): FI>10, 10>FII>3 y 3>FIII>1 kDa. A la proteína nativa y todas las fracciones se les evaluaron propiedades funcionales, aminoácidos, factores antifisiológicos y antigenicidad; así como la calidad proteica y características sensoriales a 2 de ellas. La hidrólisis y síntesis modificaron las propiedades proteicas y el enriquecimiento se dio en un mínimo de tiempo y metionina añadida. Después de la UF, las fracciones menores de 10 kDa presentaron solubilidad completa (pH 4 y 7), buena claridad y regular capacidad espumante. La FIII-E por su calidad nutricia, nulas antigenicidad y actividad antifisiológica, puede utilizarse en fórmulas infantiles hipoalergénicas. La FII-E por su composición de aminóacidos es adecuada para formúlas fortificadas solubles y como única proteína en nutracéuticos. La FI, semejante al aislado comercial, es utilizable amortizando costos. La FI-E por su contenido de metionina, la estabilidad de su espuma, su actividad emulsificante y buen sabor, puede utilizarse en papillas infantiles