A surfactant tolerant laccase of <Emphasis Type="Italic">Meripilus giganteus</Emphasis> |
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Authors: | Gunnar Schmidt Ulrich Krings Manfred Nimtz Ralf G Berger |
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Institution: | 1.Institut für Lebensmittelchemie, Gottfried Wilhelm Leibniz Universit?t Hannover,Hannover,Germany;2.Helmholtz Zentrum für Infektionsforschung,Braunschweig,Germany |
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Abstract: | A laccase (Lcc1) from the white-rot fungus Meripilus giganteus was purified with superior yields of 34% and 90% by conventional chromatography or by foam separation, respectively. Size
exclusion chromatography (SEC) and sodium dodecylsulfate-polyacrylamide gel electrophoresis (SDS-PAGE) yielded a molecular
mass of 55 kDa. The enzyme possessed an isoelectric point of 3.1 and was able to oxidize the common laccase substrate 2,2′-azino-bis(3-ethylbenzothiazoline-6-sulfonic
acid) (ABTS) at a pH of 2.0, whereas the enzyme was still able to oxidize ABTS and 2,6-dimethoxyphenol (DMP) at pH 6.0. Lcc1
exhibited low K
m
values of 8 μM (ABTS) and 80 μM (DMP) and remarkable catalytic efficiency towards the non-phenolic substrate ABTS of 37,437
k
cat/k
m (s−1 mM−1). The laccase showed a high stability towards high concentrations of various metal ions, EDTA and surfactants indicating
a considerable biotechnological potential. Furthermore, Lcc1 exhibited an increased activity as well as a striking boost of
stability in the presence of surfactants. Degenerated primers were deduced from peptide fragments. The complete coding sequence
of lcc1 was determined to 1,551 bp and confirmed via amplification of the 2,214 bp genomic sequence which included 12 introns. The
deduced 516 amino acid (aa) sequence of the lcc1 gene shared 82% identity and 90% similarity with a laccase from Rigidoporus microporus. The sequence data may aid theoretical studies and enzyme engineering efforts to create laccases with an improved stability
towards metal ions and bipolar compounds. |
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Keywords: | |
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