AI Article Synopsis

  • White-rot fungi, known for their ability to efficiently degrade lignin, produce enzymes like lignin peroxidases and manganese peroxidases that help break down lignin into aromatic compounds.
  • This study focused on the characterization of two specific enzymes, PcHGD1 and PcHGD2, from a certain white-rot fungus, which are responsible for cleaving the aromatic rings of methoxyhydroquinone (MHQ) and dimethoxyhydroquinone (DMHQ), showing a strong preference for MHQ.
  • The research identifies these enzymes as potential candidates for biotechnological applications due to their efficient degradation capabilities and broad substrate spectra, marking a significant advancement in understanding lignin degradation processes.

Article Abstract

White-rot fungi, such as , are the most efficient degraders of lignin, a major component of plant biomass. Enzymes produced by these fungi, such as lignin peroxidases and manganese peroxidases, break down lignin polymers into various aromatic compounds based on guaiacyl, syringyl, and hydroxyphenyl units. These intermediates are further degraded, and the aromatic ring is cleaved by 1,2,4-trihydroxybenzene dioxygenases. This study aimed to characterize homogentisate dioxygenase (HGD)-like proteins from that are strongly induced by the G-unit fragment of vanillin. We overexpressed two homologous recombinant HGDs, PcHGD1 and PcHGD2, in . Both PcHGD1 and PcHGD2 catalyzed the ring cleavage in methoxyhydroquinone (MHQ) and dimethoxyhydroquinone (DMHQ). The two enzymes had the highest catalytic efficiency (/) for MHQ, and therefore, we named PcHGD1 and PcHGD2 as MHQ dioxygenases 1 and 2 (PcMHQD1 and PcMHQD2), respectively, from . This is the first study to identify and characterize MHQ and DMHQ dioxygenase activities in members of the HGD superfamily. These findings highlight the unique and broad substrate spectra of PcHGDs, rendering them attractive candidates for biotechnological applications.IMPORTANCEThis study aimed to elucidate the properties of enzymes responsible for degrading lignin, a dominant natural polymer in terrestrial lignocellulosic biomass. We focused on two homogentisate dioxygenase (HGD) homologs from the white-rot fungus, , and investigated their roles in the degradation of lignin-derived aromatic compounds. In the genome database, PcMHQD1 and PcMHQD2 were annotated as HGDs that could cleave the aromatic rings of methoxyhydroquinone (MHQ) and dimethoxyhydroquinone (DMHQ) with a preference for MHQ. These findings suggest that MHQD1 and/or MHQD2 play important roles in the degradation of lignin-derived aromatic compounds by . The preference of PcMHQDs for MHQ and DMHQ not only highlights their potential for biotechnological applications but also underscores their critical role in understanding lignin degradation by a representative of white-rot fungus, .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10880611PMC
http://dx.doi.org/10.1128/aem.01753-23DOI Listing

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