Laccases have been predominantly reported in fungi, and
primarily,
fungal laccases are currently exploited in industrial applications.
However, extremophilic bacterial laccases possess immense potential,
as they can withstand extreme temperatures, pH, and salt concentrations.
In addition, unlike fungal laccases, the production of bacterial laccases
is cost-effective. Therefore, bacterial laccases are gaining significant
attention for their large-scale applications. Previously, we reported
a novel thermostable laccase (LacT) from
Brevibacillus
agri
. Herein, we have confirmed that LacT shares a
high sequence similarity with CotA laccase from
Bacillus
amyloliquefaciens
. Peptide mass fingerprinting of
LacT was conducted via matrix-assisted laser desorption ionization-time-of-flight
mass spectrometry (MALDI-TOF/MS-MS). Inductively coupled plasma-optical
emission spectroscopic (ICP-OES) analysis revealed the presence of
∼3.95 copper ions per protein molecule. Moreover, the secondary
and tertiary structure of LacT was studied using circular dichroism
(CD) and fluorescence spectroscopy. The absence of notable shifts
in CD and fluorescence spectra with an increase in temperature established
that LacT remains intact even at elevated temperatures. Analysis of
the thermal denaturation profile of LacT by thermogravimetric analysis
(TGA) also confirmed its temperature stability. Thereafter, we exploited
LacT in its application for the bioremediation of phenolic endocrine
disruptors, namely, triclosan, 4,4′-dihydroxybiphenyl, and
dienestrol. LacT oxidizes 4,4′-dihydroxybiphenyl and triclosan
but no LacT activity was detected with dienestrol. The rate of biotransformation
of 4,4′-dihydroxybiphenyl and triclosan increased in the presence
of CuSO
4
and a redox mediator, ABTS. Transformation of
dienestrol was observed only with LacT in the presence of ABTS. This
study establishes the application of LacT for the bioremediation of
phenolic compounds.