Author

D. J. O'Connell

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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Microbiology· 2 Biochemistry· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:E. coli· 2 Research Focus:protein folding & dynamics· 2 Assay:proteomics· 2 Research Focus:cell-cell communication· 1 Organism:fungi (other)· 1 Organism:human· 1 Assay:metabolomics· 1

Frequent Co-Authors

A. G. Wilson· 1 shared C. D. Lynch· 1 shared C. Lynch· 1 shared D. C. Shields· 1 shared D. Matallanas· 1 shared E. R. Dorris· 1 shared F. Cerrone· 1 shared G. McGauran· 1 shared

Activity by Year

2019-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 18 mutual co-author links

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1 shared paperBiochemistry

A. G. Wilson

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Feeding secondary fermentations with mammalian and fungal culture waste streams increases productivity and resource efficiency

C. D. Lynch, F. Cerrone, K. E. O Connor, D. J. O'Connell

This paper demonstrates that waste streams from mammalian and fungal cell cultures can be used as feed for bacterial fermentations to increase productivity and resource efficiency in bioprocessing.

RSC Sustainability · Jan 1, 2024Peer-reviewedMicrobiology

Conversion of mammalian cell culture media waste to microbial fermentation feed efficiently supports production of recombinant protein by Escherichia coli

C. Lynch, D. J. O'Connell

This study shows that spent cell culture media can be reused as a feed for microbial fermentation to produce recombinant proteins with performance comparable to standard media.

bioRxiv · Jul 1, 2021Microbiology

The nuclear transport receptor TNPO1 binds macrophage immunometabolism regulator MACIR via a PY-NLS motif

G. McGauran, E. R. Dorris, R. Borza, N. Morgan, D. C. Shields, D. Matallanas, A. G. Wilson, D. J. O'Connell

The paper identifies TNPO1 as a binding partner of MACIR via a PY-NLS motif, revealing a potential mechanism for MACIR's role in macrophage immunometabolism.

bioRxiv · Nov 25, 2019 · PreprintBiochemistry