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Effects of dietary n-3 polyunsaturated fatty acids and ... - FINS

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1 st WorkshopXIII International Feed Technology SymposiumPreparation <strong>of</strong> starch hydrolyzates from corn meal <strong>and</strong> triticale [8,9]Starch hydrolyzates were obtained by a two step hydrolysis (liquefaction <strong>and</strong>saccharification). A 100 g <strong>of</strong> corn meal was mixed with water at the weight ratio 1:3, <strong>and</strong>60 ppm <strong>of</strong> Ca 2+ (as CaCl 2 ) ions was added. The liquefaction was carried out at 85ºC <strong>and</strong>pH=6.0 for 1h by adding 0.026% (v/w starch) enzyme Termamyl SC. The liquefiedmash was saccharified at 55ºC <strong>and</strong> pH=5.0 for 4h with 0.156% (v/w starch) enzymeSAN Extra L. The hydrolysis was performed in flasks in a thermostated water bath withshaking at 150 rpm.Grinded <strong>and</strong> mashed triticale samples were mixed with water warmed at 50 C in metallicjars, keeping the sample to water ratio at 1:3. After mixing <strong>of</strong> the samples with waterTerm amyl 120 L was added. The samples were held in a water bath with mixing(150 rpm) for 30 min at 50 C. After that triticale samples were heated to 60 C. At thistemperature the samples were held for 60 min with mixing. Temperature was thenlowered to 55 C <strong>and</strong> SAN Super 240 L was added. Samples were held on thistemperature for 30 min after which the temperature was lowered to 30 C.Laboratory preparation <strong>of</strong> cell culture [8]Saccharomyces cerevisiae was used for the fermentation <strong>of</strong> the hydrolyzed corn meal<strong>and</strong> triticale samples. The culture originated from the collection <strong>of</strong> BIB-TMF, Belgrade,<strong>and</strong> was maintained on a malt agar slant. Before use as an inoculum for the fermentation,the culture was aerobically propagated in 500 ml flasks in a shaking bath at 30ºC for 24h <strong>and</strong> then separated by centrifugation.Ethanol fermentation <strong>of</strong> starch hydrolyzatesStarch hydrolyzates were subjected to ethanol fermentation by Saccharomycescerevisiae under anaerobic conditions (pH=5.0; 30ºC). The initial yeast concentrationwas 2%. Fermentation time was 36 hours.Separation <strong>of</strong> stillage after distillationAfter ethanol distillation, the stillages <strong>of</strong> corn <strong>and</strong> triticale were removed bycentrifugation. The solid samples were dried at 60 0 C <strong>and</strong> used for chemical analysis.Enrichment <strong>of</strong> corn stillage with yeastDried corn stillage was enriched with spray dried Saccharomyces cerevisiae (1%w/wstillage) [10].RESULTS AND DISCUSSIONThe results <strong>of</strong> the chemical composition <strong>of</strong> corn stillage, the stillage <strong>of</strong> triticale <strong>and</strong> thecorn stillage enriched with yeast are presented in Table 1.301

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