High production of laccase B from Trametes sp. in Pichia pastoris

The coding sequence of a laccase isozyme from Trametes sp. AH28-2 was cloned in pPIC9K vector and heterologously overexpressed in the yeast Pichia pastoris strain GS115. In the minimal medium containing 0.3 mM CuSO₄ and 0.6% alanine, the maximum yield of the recombinant laccase rLacB reached 32,000...

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Veröffentlicht in:World journal of microbiology & biotechnology 2007-05, Vol.23 (5), p.741-745
Hauptverfasser: Li, J. F, Hong, Y. Z, Xiao, Y. Z, Xu, Y. H, Fang, W
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Sprache:eng
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Zusammenfassung:The coding sequence of a laccase isozyme from Trametes sp. AH28-2 was cloned in pPIC9K vector and heterologously overexpressed in the yeast Pichia pastoris strain GS115. In the minimal medium containing 0.3 mM CuSO₄ and 0.6% alanine, the maximum yield of the recombinant laccase rLacB reached 32,000 U/l (1,012 U/mg), slightly higher than that of the native enzyme nLacB (~30,000 U/l, 1,356 U/mg). The enzymatic properties of rLacB were different from those of nLacB as well. Regardless of the inferior thermal stability, rLacB had much better stability at both neutral and basic pH range compared to nLacB. In addition, the dye decolorization potential of rLacB was similar to that of nLacB.
ISSN:0959-3993
1573-0972
DOI:10.1007/s11274-006-9286-2