Synergistic substrate cofeeding stimulates reductive metabolism.


Journal

Nature metabolism
ISSN: 2522-5812
Titre abrégé: Nat Metab
Pays: Germany
ID NLM: 101736592

Informations de publication

Date de publication:
06 2019
Historique:
received: 10 08 2018
accepted: 13 05 2019
entrez: 23 7 2020
pubmed: 23 7 2020
medline: 7 1 2021
Statut: ppublish

Résumé

Advanced bioproduct synthesis via reductive metabolism requires coordinating carbons, ATP and reducing agents, which are generated with varying efficiencies depending on metabolic pathways. Substrate mixtures with direct access to multiple pathways may optimally satisfy these biosynthetic requirements. However, native regulation favouring preferential use precludes cells from co-metabolizing multiple substrates. Here we explore mixed substrate metabolism and tailor pathway usage to synergistically stimulate carbon reduction. By controlled cofeeding of superior ATP and NADPH generators as 'dopant' substrates to cells primarily using inferior substrates, we circumvent catabolite repression and drive synergy in two divergent organisms. Glucose doping in Moorella thermoacetica stimulates CO

Identifiants

pubmed: 32694804
doi: 10.1038/s42255-019-0077-0
pii: 10.1038/s42255-019-0077-0
doi:

Substances chimiques

NADP 53-59-8
Adenosine Triphosphate 8L70Q75FXE
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

643-651

Auteurs

Junyoung O Park (JO)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, Los Angeles, CA, USA.

Nian Liu (N)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

Kara M Holinski (KM)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

David F Emerson (DF)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

Kangjian Qiao (K)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

Benjamin M Woolston (BM)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

Jingyang Xu (J)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Key Laboratory of Drug Prevention and Control Technology of Zhejiang Province, Zhejiang Police College, Hangzhou, China.

Zbigniew Lazar (Z)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Department of Biotechnology and Food Microbiology, Wroclaw University of Environmental and Life Sciences, Monskiego, Wroclaw, Poland.

M Ahsanul Islam (MA)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.
Department of Chemical Engineering, Loughborough University, Loughborough, UK.

Charles Vidoudez (C)

Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA.

Peter R Girguis (PR)

Department of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA, USA.

Gregory Stephanopoulos (G)

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA. gregstep@mit.edu.

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Classifications MeSH