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A Novel Olive Oil Degrading Thermoactinomyces Species with a High Extremely Thermostable Lipase Activity

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dc.creator Hashwa, F. en_US
dc.creator Mroueh, M. en_US
dc.creator Al-Khudary, R. en_US
dc.date.accessioned 2016-12-20T13:03:50Z
dc.date.available 2016-12-20T13:03:50Z
dc.date.datecopyrighted 2004 en_US
dc.identifier.issn 1618-0240 en_US
dc.identifier.uri http://hdl.handle.net/10725/4958
dc.description.abstract A filamentous, Gram-positive, spore forming aerobic bacterium was isolated from olive oil contaminated soil (Al Koura, Lebanon) on rhodamine agar plates at 60 °C. The isolate, HRK-1 produced large quantities of an extracellular thermostable lipase which degrades olive oil. It was primarily classified as a Thermoactinomyces sp. due to the filamentous structure of its cells that bear one spore each on an un-branched sporophore, the resistance of its spores to boiling, utilisation of sucrose as a carbon source and production of dark pigments. The isolate grew optimally at a temperature of 60 °C, a pH of 7.3 and an orbital shaking of 250 rpm. It showed an efficient olive oil degrading ability. No traces of triolein were detected after a 36-h cultivation. A concentration of 10 % [v/v] olive oil did not inhibit its growth. Lipase production was constitutive, and did not depend on the presence of olive oil. The optimum concentration of olive oil for lipase activity was 1 % [v/v], and the activity was not enhanced at higher concentrations, but on the contrary, a decrease in enzyme activity was recorded. The lipase of HRK-1 was preliminarily characterised in the crude cell-free supernatant with a specific activity of 0.14 U/mg. It has an optimum activity at 60 °C and a pH of 8.0. This lipolytic enzyme showed resistance to boiling and to a wide range of metallic ions and inhibitors. The formation of this heat-stable lipase started in the early exponential growth phase, while a maximum extracellular enzyme activity was detected at the end of the decline phase, when most of the cells appeared as spherical spores. The exceptionally high activity of lipase (2.37 U/ml) produced by HRK-1 measured in the cell free supernatant clearly indicated the commercial importance of this isolate, especially after it showed great stability at elevated temperatures. en_US
dc.language.iso en en_US
dc.title A Novel Olive Oil Degrading Thermoactinomyces Species with a High Extremely Thermostable Lipase Activity en_US
dc.type Article en_US
dc.description.version Published en_US
dc.creator.school SAS en_US
dc.creator.school SOP
dc.creator.identifier 199390070 en_US
dc.creator.identifier 199590020 en_US
dc.creator.department Natural Sciences en_US
dc.description.embargo N/A en_US
dc.relation.ispartof Engineering in Life Sciences en_US
dc.description.volume 4 en_US
dc.description.issue 1 en_US
dc.article.pages 78-82 en_US
dc.identifier.doi http://dx.doi.org/10.1002/elsc.200400010 en_US
dc.identifier.ctation Al‐Khudary, R., Hashwa, F., & Mroueh, M. (2004). A novel olive oil degrading Thermoactinomyces species with a high extremely thermostable lipase activity. Engineering in life sciences, 4(1), 78-82. en_US
dc.creator.email fhashwa@lau.edu.lb en_US
dc.creator.email mmroueh@lau.edu.lb en_US
dc.description.tou http://libraries.lau.edu.lb/research/laur/terms-of-use/articles.php en_US
dc.identifier.url http://onlinelibrary.wiley.com/doi/10.1002/elsc.200400010/abstract en_US
dc.creator.ispartof Lebanese American University en_US


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