Expression and characterization of a thermostable organic solvent-tolerant laccase from Bacillus licheniformis ATCC 9945a

• Published in: Journal of molecular catalysis. B, Enzymatic Enzymatic, 2016-12, Vol.134, p.390-395
• Main Authors: Lončar, Nikola, Božić, Nataša, Vujčić, Zoran
• Format: Article
• Language: English
• Subjects: Bacillus licheniformis; Laccase; Lignin; Oxidation; Thermostable enzyme
• ISSN: 1381-1177; 1873-3158
• DOI: 10.1016/j.molcatb.2016.06.005

[Display omitted] •Bacillus licheniformis 9945a laccase is overexpressed in E. coli with yield 50mg/L.•Temperature optimum of laccase is 90°C and pH optimum is 7.0.•Enzyme is thermostable with a melting temperature of 79°C at pH 7.0.•Presence of organic solvents reduces melting temperature but activity remains impaired.•Lignin model compounds are dimerized after one electron oxidation of phenolic group. Bacterial laccases have proven advantages over fungal and plant counterparts in terms of wider pH optimum, higher stability and broader biocatalytic scope. In this work, Bacillus licheniformis ATCC 9945a laccase is produced heterologously in Escherichia coli. Produced laccase exhibits remarkably high temperature optimum at 90°C and possess significant thermostability and resistance to inactivation by organic solvents. Laccase has an apparent melting temperature of 79°C at pH 7.0 and above 70°C in range of pH 5.0–8.0, while having half-life of 50min at 70°C. Presence of 10% organic solvents such as acetonitrile, dimethylformamide, dimethylsulfoxide or methanol reduces melting temperature to 45–52°C but activity remains practically unimpaired. With 50% of acetonitrile and methanol laccase retained ∼40% of initial activity. EDTA and 300mM sodium-chloride have positive effect on activity. Enzyme is active on syringaldazine, ABTS, phenols, amines, naphthol, lignin and lignin model compounds and mediates CC bond formation via oxidative coupling after one electron oxidation of phenolic group. Successful polymerization of 2-naphthol was achieved with 77% conversion of 250mg/L 2-naphtol in only 15min which may further expand substrate scope of this enzyme towards polymer production and/or xenobiotics removal for environmental applications.