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Goat’s milk, despite its similarity to cow’s milk in chemical composition, shows a significant difference in terms of the structure and composition of the fat. Milk fat globules in goat’s milk, with an approximate size of 2.76 µm (ranging from 0.73 to 8.58 µm), are smaller than those in cow’s milk, in which their size is approximately 3.51 µm (ranging from 0.92 to 15.75 µm). Moreover, goat’s milk is characterized by a generally lower cholesterol level (16.90 - 18.09 mg/100 g milk) than cow’s milk (25.60-31.40 mg/100 g of milk). Compared to cow’s milk fat, goat’s milk fat contains 54.6% more of C6:0, 69.9% more of C8:0, 80.2% more of C10:0, and 56.3% more of CLA, but 75% less of C4:0. Nutrition is an important factor modifying the fatty acid profile of goat’s milk. Pasture feeding, compared with green forage feeding, exerts a positive influence on the proportion of n6/n3 fatty acids and increases the content of the fatty acids C18:1 t6-11, C18:1 t12-14 + c6-8, C18:1 c14 + t16, C18:2 t11c15, and C18:2 c9t13 + t8c12, as well as that of the isomers CLA c9t11 + t7c9 + t8c10 and t11c13 + c9c11. Goats fed higher doses of concentrate (65%) produced milk with higher contents of C4:0 and C6:0 fatty acids and a significantly higher content of C18:0 and all trans C18 fatty acid, i.e. C18:1, C18:2 c9, t11. The addition of rapeseed results in a higher content of C18:0, vaccenic acid C18:1 t11 and some of cis C18 fatty acids (C18:1 c9, C18:2 c9,t11 and C18:3 c9,c12,c15). Goats fed corn silage produced milk containing more of the following fatty acids: C16:1ɷ7, C17:0, C18:1ɷ9 and C20:0. The study also showed the effect of various feed additives, such as garlic oil, on the fatty acid profile. An increased amount of garlic oil in the diet was followed by a reduction in non-esterified fatty acids (including C14:0, C15:0 and C16:0) and a proportional increase in C18 fatty acids, both monounsaturated and polyunsaturated, mainly CLA c9, t11 and CLA c12, t10. The fatty acid composition of goat’s milk is therefore not constant, as it depends mainly on the fodder content. It should be noted, however, that pasture feeding is the easiest and cheapest feeding system, which increases the content of polyunsaturated fatty acids, including CLA.
The calpain family includes proteolytic enzymes, which have a high capacity to degrade cytoskeletal and muscle fibre proteins. Thus they play an important role in the fusion of myoblasts and in cell proliferation and growth. The CAPN1 gene has been selected as a ‘candidate gene’ for meat quality in many domestic animals, including chickens. Consequently, the aim of our study was to identify new polymorphisms in the promoter region of the CAPN1 gene in broilers and to investigate their impact on CAPN1 transcript abundance in breast muscles. The experiment used broilers of two genetic lines, fast- and slow-growing. Five new polymorphisms in the promoter region of the CAPN1 gene were identified, all of them in linkage disequilibrium (P<0.05). However, the results obtained for their association with expression level were doubtful. Therefore, we surmise that the newly discovered polymorphisms, although they alter the potential sequence binding of transcription factors, probably have just a weak effect on the level of CAPN1 expression in broiler chickens at the investigated stage of ontogenesis.
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