Polymerization Potential of a Bacterial CotA-laccase for β-naphthol: Enzyme Structure and Comprehensive Polymer Characterization

Overview

Journal Front Microbiol

Specialty Microbiology

Date 2024 Dec 6

PMID 39640860

Authors

Marina Refaat

Marwa T ElRakaiby

Mustapha El Hariri El Nokab

Julien Es Sayed

Ahmed Elshewy

Khaled O Sebakhy

Nayera Moneib

Tuo Wang

Thomas J Smith

Mohamed H Habib

Affiliations

Soon will be listed here.

Abstract

Introduction: Laccases are blue-multicopper containing enzymes that are known to play a role in the bioconversion of recalcitrant compounds. Their role in free radical polymerization of aromatic compounds for their valorization remains underexplored. In this study, we used a pBAD plasmid containing a previously characterized CotA laccase gene (abbreviated as -Lacc) from strain ATCC 9945a to express this enzyme and explore its biotransformation/polymerization potential on β-naphthol.

Methods: The protein was expressed from TOP10 cells of after successful transformation of the plasmid. Immobilized metal affinity chromatography (IMAC) was used to generate pure protein. The biocatalytic polymerization reaction was optimized based on temperature, pH and starting enzyme concentration. H and C solution nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy (FTIR), and solid-state NMR (ssNMR) were used to characterize the formed polymer. A one-gram conversion reaction was done to explore applicability of the reaction in a pilot-scale.

Results: The polymerization reaction generated a brown precipitate, and its chemical structure was confirmed using H and C NMR and FTIR. SsNMR revealed the presence of two different orientational hydroxyl functional groups in the polymer in addition to the presence of a very small amount of ether linkages (< 2%). This analysis elucidated that polymerization occurred mainly on the carbons of the aromatic rings, rather than on the carbons attached to the hydroxyl groups, resulting in a condensed ring or polynuclear aromatic structure. The reaction was optimized, and the highest yield was attained under conditions of 37°C, pH 10 and a starting enzyme concentration of 440 nM in 50 mM phosphate buffer. A one-gram conversion yielded 216 mg of polymer as dry mass. The crystal structure of the enzyme was solved at 2.7 Å resolution using X-ray crystallography and presented with a hexagonal space group. The final structure was deposited in the Protein Databank (PDB) with an ID-9BD5.

Discussion: This article provides a green/enzymatic pathway for the remediation of phenolics and their valorization into potential useful polymeric materials. The comprehensive analysis of the formed polymer provides insight into its structure and functional moieties present. Based on the yield of the one-gram conversion, this synthetic method proves useful for a pilot-scale production level and opens opportunities to invest in using this polymer for industrial/environmental applications.

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