Author

Y.-S. Jin

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Bioengineering· 2 Microbiology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:yeast· 2 Approach:biophysical modeling· 1 Research Focus:cancer & tumor microenvironment· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:host-pathogen & immune response· 1 Assay:metabolomics· 1 Organism:mouse· 1

Frequent Co-Authors

D. P. Procopio· 2 shared A. Damasio· 1 shared A. Hamm· 1 shared A. J. Steelman· 1 shared A. M. Abdel-Hamid· 1 shared A. Osswald· 1 shared C. Greening· 1 shared C. Welsh· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersBioengineering

D. P. Procopio

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Author profile →

3 papers

Recent·Most cited

Engineering Xylose Fermentation in an Industrial Yeast: Continuous Cultivation as a Tool for Selecting Improved Strains

T. Basso, D. P. Procopio, T. Petrin, T. Giacon, Y.-S. Jin, T. Basso, L. Basso

The paper engineers an industrial yeast strain to improve xylose fermentation through CRISPR-Cas9 and continuous cultivation, resulting in a 70% increase in xylose consumption rate.

Letters in Applied Microbiology · Jul 6, 2023Peer-reviewedBioengineering

Metabolic engineering of Saccharomyces cerevisiae for second-generation ethanol production from xylo-oligosaccharides and acetate

D. P. Procopio, J. W. Lee, J. Shin, R. Tramontina, P. F. Avila, L. B. Brenelli, F. M. Squina, A. Damasio, S. C. Rabelo, R. Goldbeck, T. T. Franco, D. Leak, Y.-S. Jin, T. O. Basso

This study engineers Saccharomyces cerevisiae to simultaneously ferment xylo-oligosaccharides, xylose, and acetate, producing 60% more ethanol and 12% less xylitol than the control strain.

bioRxiv · Feb 4, 2023 · PreprintBioengineering

Gut bacteria convert cortisol into a distinct hostsignalling molecule

M. Freiberg, T. Wang, R. S. d. L. Rosa, A. Osswald, M. C. R. Melo, D. G. Stouffer, P. S. Buobu, C. Welsh, L. Yang, A. M. Abdel-Hamid, H. L. Doden, S. Devendran, R. M. Pollet, S. Goldberg, L. Ray, , J. M. Ridlon

The paper shows gut bacteria convert cortisol into 20-dihydrocortisol, a distinct host signalling molecule that reprograms colonic transcription and activates inflammatory pathways via NR4A3.

bioRxiv · Jun 12, 2020 · PreprintMicrobiology