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Title: Enabling microbial syringol conversion through structure-guided protein engineering

Abstract

Microbial conversion of aromatic compounds is an emerging and promising strategy for valorization of the plant biopolymer lignin. A critical and often rate-limiting reaction in aromatic catabolism is O -aryl-demethylation of the abundant aromatic methoxy groups in lignin to form diols, which enables subsequent oxidative aromatic ring-opening. Recently, a cytochrome P450 system, GcoAB, was discovered to demethylate guaiacol (2-methoxyphenol), which can be produced from coniferyl alcohol-derived lignin, to form catechol. However, native GcoAB has minimal ability to demethylate syringol (2,6-dimethoxyphenol), the analogous compound that can be produced from sinapyl alcohol-derived lignin. Despite the abundance of sinapyl alcohol-based lignin in plants, no pathway for syringol catabolism has been reported to date. Here we used structure-guided protein engineering to enable microbial syringol utilization with GcoAB. Specifically, a phenylalanine residue (GcoA-F169) interferes with the binding of syringol in the active site, and on mutation to smaller amino acids, efficient syringol O -demethylation is achieved. Crystallography indicates that syringol adopts a productive binding pose in the variant, which molecular dynamics simulations trace to the elimination of steric clash between the highly flexible side chain of GcoA-F169 and the additional methoxy group of syringol. Finally, we demonstrate in vivo syringol turnover in Pseudomonas putida KT2440more » with the GcoA-F169A variant. Taken together, our findings highlight the significant potential and plasticity of cytochrome P450 aromatic O -demethylases in the biological conversion of lignin-derived aromatic compounds.« less

Authors:
 [1];  [2];  [3];  [4]; ORCiD logo [5];  [3];  [6];  [1];  [3];  [2];  [3]; ORCiD logo [4]; ORCiD logo [7]; ORCiD logo [8];  [5]; ORCiD logo [9]; ORCiD logo [2];  [1]
  1. Department of Chemistry and Biochemistry, Montana State University, Bozeman, MT 59717,
  2. Centre for Enzyme Innovation, School of Biological Sciences, Institute of Biological and Biomedical Sciences, University of Portsmouth, Portsmouth PO1 2UP, United Kingdom,
  3. Biosciences Center, National Renewable Energy Laboratory, Golden, CO 80401,
  4. National Bioenergy Center, National Renewable Energy Laboratory, Golden, CO 80401,
  5. Department of Chemistry and Biochemistry, University of California, Los Angeles, CA 90095,
  6. National Bioenergy Center, National Renewable Energy Laboratory, Golden, CO 80401,, Department of Chemical Engineering, University of Kentucky, Lexington, KY 40506,
  7. Department of Microbiology, University of Georgia, Athens, GA 30602,
  8. Department of Chemical Engineering, University of Kentucky, Lexington, KY 40506,
  9. National Bioenergy Center, National Renewable Energy Laboratory, Golden, CO 80401,, Center for Bioenergy Innovation, Oak Ridge National Laboratory, Oak Ridge, TN 37830
Publication Date:
Research Org.:
National Renewable Energy Laboratory (NREL), Golden, CO (United States)
Sponsoring Org.:
USDOE Office of Energy Efficiency and Renewable Energy (EERE), Sustainable Transportation Office. Bioenergy Technologies Office (BETO); USDOE Office of Science (SC), Workforce Development for Teachers and Scientists (WDTS); USDOE Office of Science (SC), Biological and Environmental Research (BER)
OSTI Identifier:
1529168
Alternate Identifier(s):
OSTI ID: 1531144
Report Number(s):
NREL/JA-2A00-73031
Journal ID: ISSN 0027-8424
Grant/Contract Number:  
AC36-08GO28308; SC0014664
Resource Type:
Published Article
Journal Name:
Proceedings of the National Academy of Sciences of the United States of America
Additional Journal Information:
Journal Name: Proceedings of the National Academy of Sciences of the United States of America Journal Volume: 116 Journal Issue: 28; Journal ID: ISSN 0027-8424
Publisher:
Proceedings of the National Academy of Sciences
Country of Publication:
United States
Language:
English
Subject:
09 BIOMASS FUELS; aromatic catabolism; cytochrome P450; lignin valorization; protein engineering; Pseudomonas putida KT2440

Citation Formats

Machovina, Melodie M., Mallinson, Sam J. B., Knott, Brandon C., Meyers, Alexander W., Garcia-Borràs, Marc, Bu, Lintao, Gado, Japheth E., Oliver, April, Schmidt, Graham P., Hinchen, Daniel J., Crowley, Michael F., Johnson, Christopher W., Neidle, Ellen L., Payne, Christina M., Houk, Kendall N., Beckham, Gregg T., McGeehan, John E., and DuBois, Jennifer L. Enabling microbial syringol conversion through structure-guided protein engineering. United States: N. p., 2019. Web. doi:10.1073/pnas.1820001116.
Machovina, Melodie M., Mallinson, Sam J. B., Knott, Brandon C., Meyers, Alexander W., Garcia-Borràs, Marc, Bu, Lintao, Gado, Japheth E., Oliver, April, Schmidt, Graham P., Hinchen, Daniel J., Crowley, Michael F., Johnson, Christopher W., Neidle, Ellen L., Payne, Christina M., Houk, Kendall N., Beckham, Gregg T., McGeehan, John E., & DuBois, Jennifer L. Enabling microbial syringol conversion through structure-guided protein engineering. United States. https://doi.org/10.1073/pnas.1820001116
Machovina, Melodie M., Mallinson, Sam J. B., Knott, Brandon C., Meyers, Alexander W., Garcia-Borràs, Marc, Bu, Lintao, Gado, Japheth E., Oliver, April, Schmidt, Graham P., Hinchen, Daniel J., Crowley, Michael F., Johnson, Christopher W., Neidle, Ellen L., Payne, Christina M., Houk, Kendall N., Beckham, Gregg T., McGeehan, John E., and DuBois, Jennifer L. Mon . "Enabling microbial syringol conversion through structure-guided protein engineering". United States. https://doi.org/10.1073/pnas.1820001116.
@article{osti_1529168,
title = {Enabling microbial syringol conversion through structure-guided protein engineering},
author = {Machovina, Melodie M. and Mallinson, Sam J. B. and Knott, Brandon C. and Meyers, Alexander W. and Garcia-Borràs, Marc and Bu, Lintao and Gado, Japheth E. and Oliver, April and Schmidt, Graham P. and Hinchen, Daniel J. and Crowley, Michael F. and Johnson, Christopher W. and Neidle, Ellen L. and Payne, Christina M. and Houk, Kendall N. and Beckham, Gregg T. and McGeehan, John E. and DuBois, Jennifer L.},
abstractNote = {Microbial conversion of aromatic compounds is an emerging and promising strategy for valorization of the plant biopolymer lignin. A critical and often rate-limiting reaction in aromatic catabolism is O -aryl-demethylation of the abundant aromatic methoxy groups in lignin to form diols, which enables subsequent oxidative aromatic ring-opening. Recently, a cytochrome P450 system, GcoAB, was discovered to demethylate guaiacol (2-methoxyphenol), which can be produced from coniferyl alcohol-derived lignin, to form catechol. However, native GcoAB has minimal ability to demethylate syringol (2,6-dimethoxyphenol), the analogous compound that can be produced from sinapyl alcohol-derived lignin. Despite the abundance of sinapyl alcohol-based lignin in plants, no pathway for syringol catabolism has been reported to date. Here we used structure-guided protein engineering to enable microbial syringol utilization with GcoAB. Specifically, a phenylalanine residue (GcoA-F169) interferes with the binding of syringol in the active site, and on mutation to smaller amino acids, efficient syringol O -demethylation is achieved. Crystallography indicates that syringol adopts a productive binding pose in the variant, which molecular dynamics simulations trace to the elimination of steric clash between the highly flexible side chain of GcoA-F169 and the additional methoxy group of syringol. Finally, we demonstrate in vivo syringol turnover in Pseudomonas putida KT2440 with the GcoA-F169A variant. Taken together, our findings highlight the significant potential and plasticity of cytochrome P450 aromatic O -demethylases in the biological conversion of lignin-derived aromatic compounds.},
doi = {10.1073/pnas.1820001116},
journal = {Proceedings of the National Academy of Sciences of the United States of America},
number = 28,
volume = 116,
place = {United States},
year = {Mon Jun 24 00:00:00 EDT 2019},
month = {Mon Jun 24 00:00:00 EDT 2019}
}

Journal Article:
Free Publicly Available Full Text
Publisher's Version of Record
https://doi.org/10.1073/pnas.1820001116

Citation Metrics:
Cited by: 34 works
Citation information provided by
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Figures / Tables:

Scheme 1 Scheme 1: O-demethylation of A) guaiacol to form catechol and formaldehyde or B) syringol to form pyrogallol and two formaldehydes. The singly demethylated species, 3-methoxycatechol (3MC), is expected to form as an intermediate in reaction B). See Figure 1.

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Figures/Tables have been extracted from DOE-funded journal article accepted manuscripts.