2021
DOI: 10.1038/s42255-021-00453-0
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An orthogonal metabolic framework for one-carbon utilization

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Cited by 39 publications
(54 citation statements)
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References 66 publications
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“…The developed JST07 extract can be adapted for use for iPROBE prototyping of a wide range of biosynthetic pathways that use CoA ester intermediates and start with acetyl-CoA or pyruvate (e.g., isoprenoids, fatty acids, cannabinoids, polyketides). Additionally it has the potential to enable faster optimization of recently established CoA ester dependent new-to-nature/synthetic pathways like CETCH 33 and FORCE 34 . Second, by using this approach, we were able to tailor r-BOX to produce a single product at high selectivity.…”
Section: Discussionmentioning
confidence: 99%
“…The developed JST07 extract can be adapted for use for iPROBE prototyping of a wide range of biosynthetic pathways that use CoA ester intermediates and start with acetyl-CoA or pyruvate (e.g., isoprenoids, fatty acids, cannabinoids, polyketides). Additionally it has the potential to enable faster optimization of recently established CoA ester dependent new-to-nature/synthetic pathways like CETCH 33 and FORCE 34 . Second, by using this approach, we were able to tailor r-BOX to produce a single product at high selectivity.…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, it is also attractive to design synthetic routes using novel enzymes and novel combinations of well-studied enzymes. Well-designed synthetic routes can be superior to natural ones in: 1) circumventing the limitations of natural pathways, for example, the use of oxygen-tolerant enzymes makes rGlyP also functional in aerobic conditions ( Bang and Lee, 2018 ; Bang et al, 2020 ); 2) simplifying the metabolic pathway using less enzymes ( Xiao et al, 2022 ); 3) bypassing the host metabolism and regulations using orthogonal designs ( Chou et al, 2021 ); 4) achieving higher efficiency ( Schwander et al, 2016 ; Cai et al, 2021 ) or making the pathway more thermodynamically favourable ( Siegel et al, 2015 ).…”
Section: Metabolic Engineering Of Microbes To Use Next-generation Fee...mentioning
confidence: 99%
“…To overcome the technological challenges, researchers in metabolic engineering and synthetic biology have intelligently engineered and evolved microorganisms in laboratories to make best use of NGFs. For C1 feedstocks, current efforts are mainly spared on how to assimilate them faster and better into biomass and central metabolism of both naturally occurring microbes (e.g., chemoorganoautotrophs, methylotrophs) or synthetic model microbes, e.g., Escherichia coli ( Antonovsky et al, 2016 ; Yu and Liao, 2018 ; Gleizer et al, 2019 ; Chen F. Y.-H. et al, 2020 ; Chou et al, 2021 ) and yeasts ( Espinosa et al, 2020 ; Gassler et al, 2020 ). In contrast, industrial workhorse microbes can readily use C2 feedstocks without sophisticated genetic engineering or prolonged adaptive laboratory evolution (ALE).…”
Section: Introductionmentioning
confidence: 99%
“…At the same time, synthetic biotechnology was also employed to construct engineered bacteria by introducing the heterogeneous CO 2 fixation–related gene for carbon neutrality. Computational analysis was also another powerful tool to identify and design pathways with a more favorable thermodynamic driving force for CO 2 fixation ( Satanowski et al, 2020 ; Chou et al, 2021 ). Beyond that, electrically driven microbial and enzyme engineering was also suitable for CO 2 fixation with high efficiency.…”
Section: Conclusion and Perspectivementioning
confidence: 99%