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Cloning, Overexpression, and Characterization of a Thermostable, Organic Solvent-Tolerant Laccase from <i>Bacillus pumilus</i> ARA and Its Application to Dye Decolorization

Yunpeng Jiang, Junli Cai, Jianjun Pei, Qi Li, Linguo Zhao

2021ACS Omega24 citationsDOIOpen Access PDF

Abstract

, and 1.0 mM IPTG added into the culture. After 5 h, the final laccase production was 1283 U/mL. Moreover, the laccase activity increased to 4822 U/mL after follow-up 2 h stationary cultivation, with about a 3.76-fold increase. The purified B.P.Lacc was able to efficiently decolorize synthetic dyes combined with mediators. Adding 1.0 mM ABTS, more than 90% of BRRB was decolorized by the enzyme, whether at pH 4.0 or pH 7.9. The outstanding enzymatic properties suggested that B.P.Lacc may be suitable for a wide application in future biodegradation fields.

Topics & Concepts

Bacillus pumilusLaccaseCloning (programming)Characterization (materials science)ChemistrySolventOrganic solventMicrobiologyBiochemistryBiologyBacteriaEnzymeMaterials scienceNanotechnologyGeneticsChemical engineeringComputer scienceEngineeringProgramming languageEnzyme-mediated dye degradationbioluminescence and chemiluminescence researchDye analysis and toxicity
Cloning, Overexpression, and Characterization of a Thermostable, Organic Solvent-Tolerant Laccase from <i>Bacillus pumilus</i> ARA and Its Application to Dye Decolorization | Litcius