Unknown

Dataset Information

0

An Engineered Laccase from Fomitiporia mediterranea Accelerates Lignocellulose Degradation.


ABSTRACT: Laccases from white-rot fungi catalyze lignin depolymerization, a critical first step to upgrading lignin to valuable biodiesel fuels and chemicals. In this study, a wildtype laccase from the basidiomycete Fomitiporia mediterranea (Fom_lac) and a variant engineered to have a carbohydrate-binding module (Fom_CBM) were studied for their ability to catalyze cleavage of β-O-4' ether and C-C bonds in phenolic and non-phenolic lignin dimers using a nanostructure-initiator mass spectrometry-based assay. Fom_lac and Fom_CBM catalyze β-O-4' ether and C-C bond breaking, with higher activity under acidic conditions (pH < 6). The potential of Fom_lac and Fom_CBM to enhance saccharification yields from untreated and ionic liquid pretreated pine was also investigated. Adding Fom_CBM to mixtures of cellulases and hemicellulases improved sugar yields by 140% on untreated pine and 32% on cholinium lysinate pretreated pine when compared to the inclusion of Fom_lac to the same mixtures. Adding either Fom_lac or Fom_CBM to mixtures of cellulases and hemicellulases effectively accelerates enzymatic hydrolysis, demonstrating its potential applications for lignocellulose valorization. We postulate that additional increases in sugar yields for the Fom_CBM enzyme mixtures were due to Fom_CBM being brought more proximal to lignin through binding to either cellulose or lignin itself.

SUBMITTER: Pham LTM 

PROVIDER: S-EPMC10968408 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

altmetric image

Publications

An Engineered Laccase from <i>Fomitiporia mediterranea</i> Accelerates Lignocellulose Degradation.

Pham Le Thanh Mai LTM   Deng Kai K   Choudhary Hemant H   Northen Trent R TR   Singer Steven W SW   Adams Paul D PD   Simmons Blake A BA   Sale Kenneth L KL  

Biomolecules 20240308 3


Laccases from white-rot fungi catalyze lignin depolymerization, a critical first step to upgrading lignin to valuable biodiesel fuels and chemicals. In this study, a wildtype laccase from the basidiomycete <i>Fomitiporia mediterranea</i> (Fom_lac) and a variant engineered to have a carbohydrate-binding module (Fom_CBM) were studied for their ability to catalyze cleavage of β-O-4' ether and C-C bonds in phenolic and non-phenolic lignin dimers using a nanostructure-initiator mass spectrometry-base  ...[more]

Similar Datasets

| S-EPMC9549746 | biostudies-literature
| S-EPMC10218912 | biostudies-literature
| S-EPMC11233627 | biostudies-literature
| PRJNA59449 | ENA
2022-09-27 | PXD036889 | Pride
| S-EPMC11457069 | biostudies-literature
| PRJNA1125291 | ENA
| PRJNA653411 | ENA
| PRJNA653412 | ENA
| PRJNA653415 | ENA