891 resultados para Meat cuts


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Receipt from D. Bryant, St. Catharines for meat, May 16, 1887.

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Receipt from D. Bryant, St. Catharines for meat, July 16, 1887.

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Receipt from D. Bryant, St. Catharines for meat, Oct. 18, 1887.

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Receipt from D. Bryant, St. Catharines for meat, Jan. 26, 1888.

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Receipt from D. Bryant, St. Catharines for meat, Feb. 15, 1888.

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Receipt from D. Bryant, St. Catharines for meat, March 28, 1888.

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Receipt from D. Bryant, St. Catharines for meat, Apr. 17, 1888.

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Receipt from Parsons and Harvey, Guelph for meat, May 5, 1888.

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Texte issu d’une conférence donnée à Brown University : Bauer, O. (2014, 23-25 octobre). Bagel, Bagelry, Smoked Meat and Deli as the Jewish Part of Montreal’s Culinary Heritage. Communication présenté lors du colloque Food Heritage, Hybridity & Locality: An International Conference, Brown University.

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In recent years, we observed a significant increase of food fraud ranging from false label claims to the use of additives and fillers to increase profitability. Recently in 2013, horse and pig DNA were detected in beef products sold from several retailers. Mass spectrometry has become the workhorse in protein research and the detection of marker proteins could serve for both animal species and tissue authentication. Meat species authenticity will be performed using a well defined proteogenomic annotation, carefully chosen surrogate tryptic peptides and analysis using a hybrid quadrupole-Orbitrap mass spectrometer. Selected mammalian meat samples were homogenized, proteins were extracted and digested with trypsin. The samples were analyzed using a high-resolution mass spectrometer. The chromatography was achieved using a 30 minutes linear gradient along with a BioBasic C8 100 × 1 mm column at a flow rate of 75 µL/min. The mass spectrometer was operated in full-scan high resolution and accurate mass. MS/MS spectra were collected for selected proteotypic peptides. Muscular proteins were methodically analyzed in silico in order to generate tryptic peptide mass lists and theoretical MS/MS spectra. Following a comprehensive bottom-up proteomic analysis, we were able to detect and identify a proteotypic myoglobin tryptic peptide [120-134] for each species with observed m/z below 1.3 ppm compared to theoretical values. Moreover, proteotypic peptides from myosin-1, myosin-2 and -hemoglobin were also identified. This targeted method allowed a comprehensive meat speciation down to 1% (w/w) of undesired product.

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In this thesis all these aspects are taken into consideration. Extensive studies were conducted on all aspects of processing of crabs, mussels and clams. The species taken for studies are commercially used ones namely Scylla sereta, perna viridis, and villorita cyprinoids. In Chapter 4.1 with regard to crab) the following aspects on their handling and processing are reported seasonal variation of chemical constituents, changes taking place during ice storage, freezing, canning etc. In Chapter 4._2 with regard to mussel, the relation between age (size) and chemical constituents, changes taking place during ice storage, freezing, canning etc. are reported and in Chapter 4.3 the changes taking place in clam muscle during icing and freezing are reported and the ame rebility of ice stored clams for canning purpose is reported.The interference of high concentration of glycogen in mussel and clam muscles during the colour development of ribose (Me-jbaum's method) is observed and remedial step are taken to minimise the interference.

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To elucidate the effect of washing, on flesh components, mrigal flesh was washed through one, two and three washing cycles. Washing resulted in absorption of water (1-3%) and loss of fat (49%). 35% loss of soluble protein (SP) was noticed in the first washing itself and the loss is almost equally shared by the sarcoplasmic (18% of SP) and the myofibrillar proteins (17% of SP). The subsequent washings removed small portions of water-soluble sarcoplasmic proteins resulting in the concentration of myofibrillar proteins. 73% of the soluble protein was retained in the flesh after three washing cycles. The protein had undergone marginal conformational changes as reflected by the decrease in the actomyosin Ca super(2+) ATPase activity The rheological properties of the washed flesh were,however, significantly better than that of the unwashed mince

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El presente trabajo investigativo busca brindar al lector las herramientas necesarias para poder exportar carne fresca al mercado Canadiense mediante la implementación de un plan detallado, que involucrando el proceso de producción de animales óptimos para la producción de carne, pueda cumplir con el objetivo de expandir la disponibilidad de cortes finos de carne en el mercado extranjero. Por una parte, se hace una explicación detallada del producto, del proceso de producción y del sector cárnico en Colombia. Se hace una exposición de las condiciones en las cuales debe crecer un animal para llegar a producir carne de la mejor calidad. Así mismo, se informa sobre la situación actual del sector cárnico y las debilidades y fortalezas que tiene para poder expandirse al mercado internacional. Posteriormente se hace una investigación de marcados en el país objeto de estudio, para mostrar las oportunidades y posibles obstáculos que se pueden encontrar en Canadá. En segundo lugar, se analiza la competencia a la que se enfrentaría el producto colombiano, que comprende el análisis de las cifras de exportación de los socios comerciales de Canadá para la venta del producto objeto de análisis, para finalmente diseñar un documento dirigido a emprendedores, empresarios y/o ganaderos que busquen la manera de expandir su negocio a Canadá, con todos los pasos necesarios para poder realizar el proceso de exportación de la manera más productiva y eficaz.