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• W566003893 abstract "Laccases are multi-copper oxidases that oxidize a broad range of substrates at the expense of molecular oxygen, without any need for co-factor regeneration. These enzymes bear high potential for the sustainable synthesis of fine chemicals and the modification of (bio)polymers. Here we describe cloning and expression of five novel bacterial laccase-like multi copper oxidases (LMCOs) of diverse origin which were identified by homology searches in online databases. Activity yields under different expression conditions and temperature stabilities were compared to three previously described enzymes from Bacillus subtilis, Bacillus pumilus and Bacillus clausii. In almost all cases, a switch to oxygen-limited growth conditions after induction increased volumetric activity considerably. For proteins with predicted signal peptides for secretion, recombinant expression with and without signal sequence was investigated. Bacillus CotA-type LMCOs outperformed enzymes from Streptomyces and Gram-negative bacteria with respect to activity yields in Escherichia coli and application relevant biochemical properties. The novel Bacillus coagulans LMCO combined high activity yields in E. coli with unprecedented activity at strong alkaline pH and high storage stability, making it a promising candidate for further development." @default.
• W566003893 created "2016-06-24" @default.
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• W566003893 date "2015-06-12" @default.
• W566003893 modified "2023-10-14" @default.
• W566003893 title "Biochemical properties and yields of diverse bacterial laccase-like multicopper oxidases expressed in Escherichia coli" @default.
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• W566003893 doi "https://doi.org/10.1038/srep10465" @default.
• W566003893 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4464401" @default.
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• W566003893 hasPublicationYear "2015" @default.
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