Ben Rebah_2008_Lett.Appl.Microbiol_47_549

Reference

Title : Culture of Staphylococcus xylosus in fish processing by-product-based media for lipase production - Ben Rebah_2008_Lett.Appl.Microbiol_47_549
Author(s) : Ben Rebah F , Frikha F , Kamoun W , Belbahri L , Gargouri Y , Miled N
Ref : Lett Appl Microbiol , 47 :549 , 2008
Abstract :

AIMS: The objective of this study was to demonstrate that fish-processing by-products could be used as sole raw material to sustain the growth of Staphylococcus xylosus for lipase production. METHODS AND RESULTS: Bacterial growth was tested on supernatants generated by boiling (100 degrees C for 20 min) of tuna, sardine, cuttlefish and shrimp by-products from fish processing industries. Among all samples tested, only supernatants generated from shrimp and cuttlefish by-products sustained the growth of S. xylosus. Shrimp-based medium gave the highest growth (A(600) = 22) after 22 h of culture and exhibited the maximum lipase activity (28 U ml(-1)). This effect may be explained by better availability of nutrients, especially, in shrimp by-products. Standard medium (SM) amendments to sardine and tuna by-product-based media stimulated the growth of S. xylosus and the highest A(600) values were obtained with 75% SM. Lipase activity, however, remained below 4 U ml(-1) for both sardine and tuna by-product-based media. CONCLUSIONS: Fish by-products could be used for the production of highly valuable enzymes. SIGNIFICANCE AND IMPACT OF THE STUDY: The use of fish by-products in producing S. xylosus-growth media can reduce environmental problems associated with waste disposal and, simultaneously, lower the cost of biomass and enzyme production.

PubMedSearch : Ben Rebah_2008_Lett.Appl.Microbiol_47_549
PubMedID: 19120924

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Citations formats

Ben Rebah F, Frikha F, Kamoun W, Belbahri L, Gargouri Y, Miled N (2008)
Culture of Staphylococcus xylosus in fish processing by-product-based media for lipase production
Lett Appl Microbiol 47 :549

Ben Rebah F, Frikha F, Kamoun W, Belbahri L, Gargouri Y, Miled N (2008)
Lett Appl Microbiol 47 :549