Engineering microbial cell viability for enhancing chemical production by second codon engineering.
Engineering second codon
Microbial cell factories
Microbial cell viability
ROS
Journal
Metabolic engineering
ISSN: 1096-7184
Titre abrégé: Metab Eng
Pays: Belgium
ID NLM: 9815657
Informations de publication
Date de publication:
09 2022
09 2022
Historique:
received:
26
10
2021
revised:
29
06
2022
accepted:
12
08
2022
pubmed:
21
8
2022
medline:
14
9
2022
entrez:
20
8
2022
Statut:
ppublish
Résumé
Microbial cell factories offer a promising strategy for the sustainable production of industrial chemicals from renewable biomass feedstock. However, their performance is often limited by poor microbial cell viability (MCV). Here, MCV was engineered to enhance chemical production by optimizing the regulation of lifespan-specific genes to reduce the accumulation of reactive oxygen species (ROS). In Escherichia coli, MCV was improved by reducing ROS accumulation using second codon engineering to regulate hypoxia-inducible transcription factor (arcA), resulting in lysine production up to 213 g L
Identifiants
pubmed: 35987432
pii: S1096-7176(22)00103-3
doi: 10.1016/j.ymben.2022.08.008
pii:
doi:
Substances chimiques
Codon
0
Reactive Oxygen Species
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
235-246Informations de copyright
Copyright © 2022 International Metabolic Engineering Society. Published by Elsevier Inc. All rights reserved.
Déclaration de conflit d'intérêts
Declaration of competing interest The authors declare that there are no competing interests.