Cargando…

Enzyme engineering and in vivo testing of a formate reduction pathway

Formate is an attractive feedstock for sustainable microbial production of fuels and chemicals, but its potential is limited by the lack of efficient assimilation pathways. The reduction of formate to formaldehyde would allow efficient downstream assimilation, but no efficient enzymes are known for...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Jue, Anderson, Karl, Yang, Ellen, He, Lian, Lidstrom, Mary E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511477/
https://www.ncbi.nlm.nih.gov/pubmed/34651085
http://dx.doi.org/10.1093/synbio/ysab020
_version_ 1784582771604193280
author Wang, Jue
Anderson, Karl
Yang, Ellen
He, Lian
Lidstrom, Mary E
author_facet Wang, Jue
Anderson, Karl
Yang, Ellen
He, Lian
Lidstrom, Mary E
author_sort Wang, Jue
collection PubMed
description Formate is an attractive feedstock for sustainable microbial production of fuels and chemicals, but its potential is limited by the lack of efficient assimilation pathways. The reduction of formate to formaldehyde would allow efficient downstream assimilation, but no efficient enzymes are known for this transformation. To develop a 2-step formate reduction pathway, we screened natural variants of acyl-CoA synthetase (ACS) and acylating aldehyde dehydrogenase (ACDH) for activity on one-carbon substrates and identified active and highly expressed homologs of both enzymes. We then performed directed evolution, increasing ACDH-specific activity by 2.5-fold and ACS lysate activity by 5-fold. To test for the in vivo activity of our pathway, we expressed it in a methylotroph which can natively assimilate formaldehyde. Although the enzymes were active in cell extracts, we could not detect formate assimilation into biomass, indicating that further improvement will be required for formatotrophy. Our work provides a foundation for further development of a versatile pathway for formate assimilation.
format Online
Article
Text
id pubmed-8511477
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-85114772021-10-13 Enzyme engineering and in vivo testing of a formate reduction pathway Wang, Jue Anderson, Karl Yang, Ellen He, Lian Lidstrom, Mary E Synth Biol (Oxf) Research Article Formate is an attractive feedstock for sustainable microbial production of fuels and chemicals, but its potential is limited by the lack of efficient assimilation pathways. The reduction of formate to formaldehyde would allow efficient downstream assimilation, but no efficient enzymes are known for this transformation. To develop a 2-step formate reduction pathway, we screened natural variants of acyl-CoA synthetase (ACS) and acylating aldehyde dehydrogenase (ACDH) for activity on one-carbon substrates and identified active and highly expressed homologs of both enzymes. We then performed directed evolution, increasing ACDH-specific activity by 2.5-fold and ACS lysate activity by 5-fold. To test for the in vivo activity of our pathway, we expressed it in a methylotroph which can natively assimilate formaldehyde. Although the enzymes were active in cell extracts, we could not detect formate assimilation into biomass, indicating that further improvement will be required for formatotrophy. Our work provides a foundation for further development of a versatile pathway for formate assimilation. Oxford University Press 2021-09-24 /pmc/articles/PMC8511477/ /pubmed/34651085 http://dx.doi.org/10.1093/synbio/ysab020 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Jue
Anderson, Karl
Yang, Ellen
He, Lian
Lidstrom, Mary E
Enzyme engineering and in vivo testing of a formate reduction pathway
title Enzyme engineering and in vivo testing of a formate reduction pathway
title_full Enzyme engineering and in vivo testing of a formate reduction pathway
title_fullStr Enzyme engineering and in vivo testing of a formate reduction pathway
title_full_unstemmed Enzyme engineering and in vivo testing of a formate reduction pathway
title_short Enzyme engineering and in vivo testing of a formate reduction pathway
title_sort enzyme engineering and in vivo testing of a formate reduction pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511477/
https://www.ncbi.nlm.nih.gov/pubmed/34651085
http://dx.doi.org/10.1093/synbio/ysab020
work_keys_str_mv AT wangjue enzymeengineeringandinvivotestingofaformatereductionpathway
AT andersonkarl enzymeengineeringandinvivotestingofaformatereductionpathway
AT yangellen enzymeengineeringandinvivotestingofaformatereductionpathway
AT helian enzymeengineeringandinvivotestingofaformatereductionpathway
AT lidstrommarye enzymeengineeringandinvivotestingofaformatereductionpathway