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PublicationBiochim. Biophys. Acta
Year2009
Volume1794
Pages1099-1106
International

Study of a sterol esterase secreted by Ophiostoma piceae: sequence, model and biochemical properties

Authors:Olga Calero-Rueda , Victor Barba , Enrique Rodriguez , Francisco José Plou Gasca, A.T. Martinez , M.J. Martinez
Groups of research:Applied Biocatalysis
An extracellular sterol esterase from Ophiostoma piceae efficiently hydrolyzes sterol esters, triglycerides and p-nitrophenol esters. cDNA was screened with a probe obtained by PCR using as primers oligonucleotides corresponding to the N-terminal and internal mature enzyme sequences and complete sequence was obtained by 3′ rapid amplification of cDNA end (RACE) and inverse PCR. The O. piceaeesterase gene had a length of 1.8 kbp and lacked introns. A search for proteins with related amino acid sequences revealed around 40% identity with lipases from Candida rugosa and Geotrichum candidum.Modelling the O. piceae enzyme, using the crystal structures of Lip1 and Lip3 from C. rugosa as templates, revealed a similar substrate-binding site, but some changes affecting the flap zone and the aromatic region of the tunnel may be responsible for the wide substrate specificity of this interesting sterol esterase. The ability of the new fungal esterase to hydrolyze triglycerides and esters of p-nitrophenol and cholesterol was compared with those of commercial lipases and cholesterol esterases showing the new enzyme the highest efficiency hydrolyzing triglycerides and sterol esters in the conditions assayed (in presence of Genapol X-100). Finally, the O. piceae gene was successfully expressed in Pichia pastoris, as a model organism to express fungal enzymes, resulting in higher levels of esterase activity than those obtained in the O. piceaecultures. In spite of its higher glycosylation degree, the recombinant enzyme was able to hydrolyze more efficiently than native enzyme the assayed substrates.
Keywords:Ophiostoma piceae; Sterol ester; Triglyceride; Wood extractive; Pichia pastoris
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