Preprint
Investigating the potential of division of labour in synthetic bacterial communities for the production of violacein
- Abstract:
- With advancements in synthetic biology and metabolic engineering, microorganisms can now be engineered to perform increasingly complex functions, which may be limited by the resources available in individual cells. Division of labour in synthetic microbial communities offers a promising approach to enhance metabolic efficiency and resilience in bioproduction. By distributing complex metabolic pathways across multiple subpopulations, the resource competition and metabolic burden imposed on an individual cell is reduced, potentially enabling more efficient production of target compounds. Violacein is a high-value pigment with anti-tumour properties that exemplifies such a challenge due to its complex bioproduction pathway, imposing a significant metabolic burden on host cells. In this study we investigated the benefits of division of labour for violacein production by splitting the violacein bioproduction pathway between two subpopulations of Escherichia coli based synthetic communities. We tested several pathway splitting strategies and reported that splitting the pathway into two subpopulations expressing VioABE and VioDC at a final composition of 60:40 yields a 2.5 fold increase in violacein production as compared to a monoculture. We demonstrated that the coculture outperforms the monoculture when both subpopulations exhibit similar metabolic burden levels, resulting in comparable growth rates, and when both subpopulations are present in sufficiently high proportions.
- Publication status:
- Published
- Peer review status:
- Not peer reviewed
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- Files:
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(Preview, Pre-print, pdf, 849.7KB, Terms of use)
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- Preprint server copy:
- 10.1101/2025.01.07.631562
Authors
+ European Commission
More from this funder
- Funder identifier:
- https://ror.org/00k4n6c32
- Funding agency for:
- Ledesma-Amaro, R
- Grant:
- 101098826
+ European Research Council
More from this funder
- Funder identifier:
- https://ror.org/0472cxd90
- Funding agency for:
- Ledesma-Amaro, R
- Grant:
- 949080
+ Engineering and Physical Sciences Research Council
More from this funder
- Funder identifier:
- https://ror.org/0439y7842
- Funding agency for:
- Ledesma-Amaro, R
- Grant:
- EP/Y014073/1
+ Biotechnology and Biological Sciences Research Council
More from this funder
- Funder identifier:
- https://ror.org/00cwqg982
- Funding agency for:
- Jimenez, J
- Ledesma-Amaro, R
- Grant:
- BB/T011289/2
- BB/R01602X/1
- BB/T013176/1
- BB/T011408/1
- BB/Y008510/1
- BB/X01911X/1
+ Royal Academy of Engineering
More from this funder
- Funder identifier:
- https://ror.org/0526snb40
- Funding agency for:
- Stan, G-B
- Programme:
- RAE Chair in Emerging Technologies RAEng CiET 1819/5
- Preprint server:
- bioRxiv
- Publication date:
- 2025-01-10
- DOI:
- Language:
-
English
- Pubs id:
-
2354148
- UUID:
-
uuid_69b0af7a-6e20-448c-bbee-a8e3e471d863
- Local pid:
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pubs:2354148
- Source identifiers:
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W4406258131
- Deposit date:
-
2025-12-23
- ARK identifier:
Terms of use
- Copyright holder:
- Mehta et al.
- Copyright date:
- 2025
- Rights statement:
- The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC-ND 4.0 International license.
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