Enrico Orsi
@eorsi.bsky.social
470 followers 37 following 48 posts
Bolognese 🇮🇹 in Copenhagen 🇩🇰 I engineer and optimize the metabolism of nonmodel C1-trophic bacteria for novel biotechnological applications Metabolic Engineering | Green Economy | CO2 valorization | DTU Biosustain
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eorsi.bsky.social
Thanks! First challenge is to expand the substrate acceptance range in the cell factory
eorsi.bsky.social
Please repost!

Postdoc in adaptive laboratory evolution and C1 synthetic metabolism!

Location: DTU Biosustain

🦠🧬🔬

Starting in 01/2026!

Fell free to reach out if you have questions!
efzu.fa.em2.oraclecloud.com/hcmUI/Candid...
efzu.fa.em2.oraclecloud.com
eorsi.bsky.social
🧪 We're hiring a #Postdoc in Bioprocess Engineering!
Excited about scaling CO₂-based biomanufacturing from bench to pilot scale?
Join our group working on converting CO₂ + renewable electricity → polymers 💡🌱 👇
Reposted by Enrico Orsi
gerrich.bsky.social
#ME16

This is quite subjective , but imo
@helenasm.bsky.social just gave the most impressive talk of the conference so far and she is "only" in the third year of her PhD.

If you are interested in synthetic pathway engineering or C1 fixation you should check out her research.
scholar.google.com
eorsi.bsky.social
🎉 Excited to share that I’ve received an Emerging Investigator Grant from the Novo Nordisk Foundation! I’ll start my research group in Jan 2026 to develop universal cell factories for P2X & CO₂-based biomanufacturing 🌱🔬
👉 researchleaderprogramme.com/recipients/e...
Reposted by Enrico Orsi
ari-satanowski.bsky.social
Excited to share a main project from my PhD, out now in
@naturecomms.bsky.social! 📝
We've designed and brought to life the “CORE cycle” – a new-to-nature pathway that provides a novel route for biological CO2 capture 🦠🌱
nature.com/articles/s41...
Take a look! Thread below... 🧵
Reposted by Enrico Orsi
Reposted by Enrico Orsi
copabio.bsky.social
Excited to see our SIBR work out in Trends in Biotechnology :)
doi.org/10.1016/j.ti...

This is the first study I have coordinated from start to finish, and it brings me immense satisfaction to see it published.

For a brilliant description of the tech check this: www.linkedin.com/feed/update/...
Redirecting
doi.org
eorsi.bsky.social
We had great support from our labs in developing this toolkit. Thanks to @pabnik.bsky.social, @nicoc-micsynmet.bsky.social, Sjoerd, Luc, Angela, Chase, Harrison, Raymond, John, and Wei!

The plasmids will be available on Addgene. Feel free to reach out in case you want to try them!
eorsi.bsky.social
These results demonstrates that a new state-of-the-art is available for making gene deletions in this promising bug.
With a turnaround time that is 50% shorter than the current systems available, we believe that SIBR-Cas9 and SIBR2.0-Cas12a will help using C. necator in new P2X applications! 8/n
eorsi.bsky.social
SIBR2.0 was then functional and we moved testing it for Cas12a. The new architectures revealed to be tight, allowing precise and controllable induction of cas12a as well, with similar efficiencies to the ones observed for Cas9! 7/n
eorsi.bsky.social
Here is where SIBR2.0 comes into place. Simona and Costas developed a script for strategically moving the intron position within the CDS to get rid of such hidden translation initiation starts. This was tested first in E. coli using GFP as readout. 6/n
eorsi.bsky.social
Then, we moved at testing if SIBR would work also on Cas12a. To our surprise, induction during the targeting assay revealed a leaky cas12a expression despite the presence of the intron with the STOP codon. This was because of a hidden translation start site that required some adjustments. 5/n
eorsi.bsky.social
We started by testing the SIBR setup on Cas9. This was because we already had evidence that it worked before, although poorly www.sciencedirect.com/science/arti...
Targeting worked fine & by combining SIBR w/ Cas9, we achieved high editing efficiencies of >80% in two loci! Great start! 4/n
eorsi.bsky.social
Teaming up with Simona and Costas, we decided to apply the SIBR technology that Costas developed during his PhD to "pause" Cas counter-selection and allow endogenous homologous recombination (HR) to happen first. Our suspect was that C. necator is also poor at HR academic.oup.com/nar/article/... 3/n
Streamlined CRISPR genome engineering in wild-type bacteria using SIBR-Cas
Abstract. CRISPR-Cas is a powerful tool for genome editing in bacteria. However, its efficacy is dependent on host factors (such as DNA repair pathways) an
academic.oup.com
eorsi.bsky.social
C. necator holds potential for the conversion and valorization of CO2 for its ability to grow on this substrate using power-to-X feedstocks (like hydrogen or formate). However, making gene deletions in this organism has always been a pain due to its limited gene deletion toolkit 2/n
Reposted by Enrico Orsi
beaubd.bsky.social
Check out Sebastians crazy effort to engineer E. coli to grow on formate via the synthetic Serine-Threonine-Cycle. In contrast to the rGlyp the STC works even at ambient CO2!🔥
sebwenk.bsky.social
Interested in Sustainability, Metabolic Engineering and Evolution?
Check out how we convinced E. coli to grow on the CO2-derived substrate formic acid using the synthetic Serine Threonine Cycle! ♻️🌱🦠

OPEN ACCESS publication to be found here:
🚨 doi.org/10.1016/j.ym... 🚨

#MEvoSky #microsky

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Reposted by Enrico Orsi
sebwenk.bsky.social
Interested in Sustainability, Metabolic Engineering and Evolution?
Check out how we convinced E. coli to grow on the CO2-derived substrate formic acid using the synthetic Serine Threonine Cycle! ♻️🌱🦠

OPEN ACCESS publication to be found here:
🚨 doi.org/10.1016/j.ym... 🚨

#MEvoSky #microsky

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