Characterization of Alkylguaiacol-Degrading Cytochromes P450 for the Biocatalytic Valorization of Lignin

Morgan M. Fetherolf, David J. Levy-Booth, Laura E. Navas, Jie Liu, Jason C. Grigg, Andrew Wilson, Rui Katahira, Gregg T. Beckham, William W. Mohn, Lindsay D. Eltis

Research output: Contribution to journalArticlepeer-review

39 Scopus Citations

Abstract

Cytochrome P450 enzymes have tremendous potential as industrial biocatalysts, including in biological lignin valorization. Here, we describe P450s that catalyze the O-demethylation of ligninderived guaiacols with different ring substitution patterns. Bacterial strains Rhodococcus rhodochrous EP4 and Rhodococcus jostii RHA1 both utilized alkylguaiacols as sole growth substrates. Transcriptomics of EP4 grown on 4-propylguaiacol (4PG) revealed the up-regulation of agcA, encoding a CYP255A1 family P450, and the aph genes, previously shown to encode a meta-cleavage pathway responsible for 4-alkylphenol catabolism. The function of the homologous pathway in RHA1 was confirmed: Deletion mutants of agcA and aphC, encoding the meta-cleavage alkylcatechol dioxygenase, grew on guaiacol but not 4PG. By contrast, deletion mutants of gcoA and pcaL, encoding a CYP255A2 family P450 and an orthocleavage pathway enzyme, respectively, grew on 4-propylguaiacol but not guaiacol. CYP255A1 from EP4 catalyzed the O-demethylation of 4-alkylguaiacols to 4-alkylcatechols with the following apparent specificities (kcat/KM): propyl > ethyl > methyl > guaiacol. This order largely reflected AgcA's binding affinities for the different guaiacols and was the inverse of GcoAEP4's specificities. The biocatalytic potential of AgcA was demonstrated by the ability of EP4 to grow on lignin-derived products obtained from the reductive catalytic fractionation of corn stover, depleting alkylguaiacols and alkylphenols. By identifying related P450s with complementary specificities for lignin-relevant guaiacols, this study facilitates the design of these enzymes for biocatalytic applications. We further demonstrated that the metabolic fate of the guaiacol depends on its substitution pattern, a finding that has significant implications for engineering biocatalysts to valorize lignin.

Original languageAmerican English
Pages (from-to)25771-25778
Number of pages8
JournalProceedings of the National Academy of Sciences of the United States of America
Volume117
Issue number41
DOIs
StatePublished - 13 Oct 2020

Bibliographical note

Publisher Copyright:
© 2020 National Academy of Sciences. All rights reserved.

NREL Publication Number

  • NREL/JA-2800-77914

Keywords

  • Biocatalysis
  • Cytochrome P450
  • Guaiacol
  • Lignin valorization
  • O-demethylase

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