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prevalence of toxigenic bacteria in some egyptian food abstract ...

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116PREVALENCE OF TOXIGENIC BACTERIA IN SOME EGYPTIAN FOODPhoto(2): Polyacrylamide gel electrophoresis show<strong>in</strong>g the prote<strong>in</strong> pattern <strong>of</strong> cell free filtrates <strong>of</strong> the selected <strong>toxigenic</strong> isolates.M: prote<strong>in</strong> marker (mixture <strong>of</strong> 7 purified prote<strong>in</strong>s with mol. wt. 116,97.4,66.2,37.6,28.5,18.4 and 14 kDa.Lanes (1,2,3 &4): B.cereus stra<strong>in</strong>sCH, GT1,LB3 & G8 and lanes (5,6,7,&8) :S.aureus stra<strong>in</strong>s S, S1, S2, S3.Table(5): Similarity percentage betweenselected B. cereus stra<strong>in</strong>sStra<strong>in</strong>s CH GT1 LB3 G8CH 100 80 60 60GT1 80 100 80 60LB3 43 57 100 71.4G8 50 50 83.3 100Table(6): Similarity percentage betweenselected S. aureus stra<strong>in</strong>sStra<strong>in</strong>s S S1 S2 S3S 100 100 66.7 66.7S1 75 100 50 50S2 50 50 100 50S3 50 50 50 100Also, the pro-analysis <strong>of</strong> the extracellular prote<strong>in</strong> bands <strong>of</strong> the tested isolates revealedvary<strong>in</strong>g similarity between the virulent stra<strong>in</strong>s rang<strong>in</strong>g between50 to 83.3% <strong>in</strong> B. cereus andbetween 50 to 75% <strong>in</strong> S. aureus (tables5&6). Photo (2) showed obvious prote<strong>in</strong> bands <strong>in</strong> lanes1,2,3&4 hav<strong>in</strong>g molecular weights (19.26, 30.24, 33.98, 53.44 & 72.59 kDa) ; (19.6, 30. 12,33, 75, 35.53 & 53.19 kDa); (22.11, 30. 03, 33,67, 35.08, 43.24, 53.14 & 234.36 kDa)&(19.63,22.77, 30. 93, 33,53, 43.23 & 234.36 kDa); <strong>in</strong> case <strong>of</strong> B. cereus stra<strong>in</strong>s CH,GT1,LB3&G8, respectively. Meanwhile S. aureus stra<strong>in</strong>s S, S1, S2&S3 possessedextracellular prote<strong>in</strong>s with molecular weights (43.23, 93.486& 234.36kDa); (22.82, 43.54,53.676& 234.36kDa); (22.67, 33.21, 43.57 & 92.19kDa) & (30.39, 33.31, 43.74 &234.36kDa), respectively.Beecher and MacMillan (1990&1991) reported that molecular weights <strong>of</strong> B. cereusenterotox<strong>in</strong> prote<strong>in</strong>s were 35, 36 and 45 kDa for b<strong>in</strong>d<strong>in</strong>g prote<strong>in</strong> B, lytic prote<strong>in</strong> L1 (HBLD)and lytic prote<strong>in</strong> L2 (HBLC), respectively. Beecher and Wong (1994) also found that themolecular weight <strong>of</strong> B component was 37.8kDa, L1 was 38.5kDa and L2 was 43.2kDa.Schoeni and Wong (1999) reported that the three components isolated from prototype stra<strong>in</strong><strong>of</strong> B. cereus F837/76 have molecular weights <strong>of</strong> 37.5, 38.2 and 43.5 kDa, respectively. Theyalso added that an <strong>in</strong>dividual stra<strong>in</strong> could produce s<strong>in</strong>gle or multiple bands <strong>of</strong> eachcomponent. They observed two bands (38&42kDa) for B prote<strong>in</strong>, two L1prote<strong>in</strong>s(38&41kDa) and two L2 prote<strong>in</strong>s (both 43kDa) <strong>in</strong> a soil isolate encoded S1C stra<strong>in</strong>.

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