Reference : Selection of new over-producing derivatives for the improvement of extracellular lipase ...
Scientific journals : Article
Life sciences : Microbiology
Life sciences : Biotechnology
http://hdl.handle.net/2268/29970
Selection of new over-producing derivatives for the improvement of extracellular lipase production by the non-conventional yeast Yarrowia lipolytica
English
Fickers, Patrick mailto [Université Libre de Bruxelles - ULB > > Centre d'ingénierie des protéines > > >]
Fudalej, F. [> > > >]
Nicaud, J. M. [> > > >]
Destain, Jacqueline mailto [Université de Liège - ULg > Gembloux Agro-Bio Tech > Gembloux Agro-Bio Tech >]
Thonart, Philippe mailto [Université de Liège - ULg > Département des sciences de la vie > Biochimie et microbiologie industrielles >]
Feb-2005
Journal of Biotechnology
Elsevier Science Bv
115
4
379-386
Yes (verified by ORBi)
International
0168-1656
Amsterdam
[en] Yarrowia lipolytica ; lipase production ; gene amplification ; bioreactor ; fed-batch
[en] The non-conventional yeast Yarrowia lipolytica produces an extracellular lipase encoded by the LIP2 gene. Mutant strains with enhanced productivity were previously obtained either by chemical mutagenesis or genetic engineering. In this work, we used one of these mutants, named LgX64.81 to select new overproducing strains following by amplification of the LIP2 gene. We also developed a process for lipase production in bioreactors and compared lipase production levels in batch and fed-batch cultures. Batch culture led to a lipase production of 26 450 U ml(-1) in a media containing olive oil and tryptone as carbon and nitrogen sources. Feeding of a combination of tryptone and olive oil at the end of the exponential growth phase yielded to lipase activity of 158 246 U ml(-1) after 80 h of cultivation. In addition this production system developed for the extracellular lipase could also be applied for other heterologous protein production since we have demonstrated that LgX64.81 is an interesting alternative host strain. (C) 2004 Elsevier B.V. All rights reserved.
http://hdl.handle.net/2268/29970
10.1016/j.jbiotec.2004.09.014

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