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New Researches in Biotechnology - Facultatea de Biotehnologii ...

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Proceed<strong>in</strong>g of the 4 rd International Symposium“NEW RESEARCH IN BIOTECHNOLOGY” USAMV Bucharest, Romania, 2011(manometric method). These tests were ma<strong>de</strong> us<strong>in</strong>g Lyssy L80-5000 water vaporpermeability tester and Lyssy L100-5000 manometric gas permeability tester both fromPBI Dansensor.Physico-chemical analysesWater activity was <strong>de</strong>term<strong>in</strong>ed at basel<strong>in</strong>e, before the wash<strong>in</strong>g process, and that onevery test<strong>in</strong>g day, us<strong>in</strong>g the Aquaspector AQS-2-TC <strong>de</strong>vice.Homogeneous samples were obta<strong>in</strong>ed by cutt<strong>in</strong>g the lettuce leafs with a sterilescalpel.Evi<strong>de</strong>nce of weight loss as a result of <strong>de</strong>hydration vegetables dur<strong>in</strong>g storage was<strong>de</strong>term<strong>in</strong>ed by weigh<strong>in</strong>g with the electronic balance Kern EW1500-2M. Salads were firstweighed.To <strong>de</strong>term<strong>in</strong>e the pH 10g of homogeneous sample were weighed, then 100mLdistillated water were ad<strong>de</strong>d. It was used the Inolab pH meter with comb<strong>in</strong>ed electro<strong>de</strong> andthe samples were homogenized us<strong>in</strong>g a Circular Seward 400 Stomacher.Microbiological analysesSamples were <strong>in</strong>itially analyzed, after the wash<strong>in</strong>g process, consi<strong>de</strong>red day 0, andthen on day 1, 3, 5, 7 and 10. For the microbiological analyses, 10g of lettuce were weighedand then homogenized with 90mL peptone water us<strong>in</strong>g the Circular Seward 400 Stomacherfor 30 seconds. Serial dilutions (1:10) of each homogenized sample were ma<strong>de</strong>. Totalaerobic mesophiles and psychrotrophs were <strong>de</strong>term<strong>in</strong>ed accord<strong>in</strong>g to SR EN ISO4833/2003, us<strong>in</strong>g Plate Count Agar (PCA, Biokar Diagnostics) and <strong>in</strong>cubated at 30°C for 3days. The yeasts and moulds were <strong>de</strong>term<strong>in</strong>ed accord<strong>in</strong>g to SR ISO 21527-1/2009, us<strong>in</strong>gDichloran-Rose Bengal Chlormaphenicol agar (DRBC agar, Biokar Diagnostics), <strong>in</strong>cubatedat 25 °C for 5 days. Coliform bacteria were <strong>de</strong>term<strong>in</strong>ed us<strong>in</strong>g Violet Red Bile Agar withLactose, VRBL (Biokar Diagnostics) – <strong>in</strong>cubated 24h at 37 °C STAS ISO 4832/2009.Escherichia coli was <strong>de</strong>term<strong>in</strong>e accord<strong>in</strong>g to SR ISO 16649-2/2007 us<strong>in</strong>g Tryptone BileGlucuroni<strong>de</strong>, TBX (Lab M Harlequ<strong>in</strong>) – <strong>in</strong>cubated 24h at 44 °C.Sensory qualityThere were evaluated changes <strong>in</strong> visual quality, texture, flavour, off-odours andbrown<strong>in</strong>g.1583. RESULTS AND DISCUSSIONSBarrier properties analysisThe barrier properties to water vapor and gas (oxygen, nitrogen and carbondioxi<strong>de</strong>) are presented <strong>in</strong> Table 1.Effect of storage on water lossIn terms of water activity, there was neither significant difference betweenthe salads packaged <strong>in</strong> different film bags, and the perforations didn’t have any significantrelevance. The <strong>in</strong>itial lettuce water activity, at basel<strong>in</strong>e, before wash<strong>in</strong>g, was 1.023. Thevalues registered on the test<strong>in</strong>g days are listed <strong>in</strong> table 1.The lowest water activity values were registered for sample 1, especially <strong>in</strong> thefirst days of storage. In fig. 1 there can be observed that all the tested lettuce samplesregistered an <strong>in</strong>crease of the water activity values <strong>in</strong> the first 3 days, reach<strong>in</strong>g the maximum

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