Abstract
In this study, we tried to decolorize synthetic dyes using small laccase (SLAC) from Streptomyces coelicolor, which is resistant to pH, temperature change, and traditional inhibitors for the actual industrial applications using spore surface display system. We inserted SLAC-His6 tag at the C-terminal of CotE anchoring motif. The proper surface expression of CotE-SLAC fusion protein on the surface of Bacillus subtilis spore was verified with flow cytometry using FITC labeled anti-His6 tag antibody. After 6 h of reaction, more than 90% of Indigo carmine was decomposed using recombinant SLAC displaying Bacillus spore, whereas less than 10% of Indigo carmine was decomposed with wild type spore. Over 70% of laccase activity was retained with recombinant SLAC displaying spore, which was heat-treated for 3 h at 90°C. For eight rounds of repeated decomposition of Indigo carmine, no significant decrease of enzymatic activity was observed. This showed the robust characteristics of spore display format for repeated and harsh condition reactions.