Author

C. M. Whitford

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 Bioengineering· 1

Signature Assays, Organisms & Methods

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Organism:bacteria (other)· 2 Approach:experimental assay· 2 Research Focus:cell type annotation· 1 Research Focus:clustering· 1 Organism:E. coli· 1 Approach:genetic perturbation / CRISPR· 1 Research Focus:genome assembly· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

T. S. Jorgensen· 3 shared T. Weber· 3 shared S. Y. Lee· 2 shared T. Gren· 2 shared E. B. Sterndorff· 1 shared E. E. Kontou· 1 shared J. B. Nielsen· 1 shared L. Ding· 1 shared

Activity by Year

2020-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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3 shared papersMicrobiology

T. S. Jorgensen

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Biosynthesis of the azoxy compound azodyrecin from Streptomyces mirabilis P8-A2

M. Maleckis, M. Wibowo, T. Gren, S. A. Jarmusch, E. B. Sterndorff, T. J. Booth, N. N. S. E. Henriksen, C. M. Whitford, X. Jiang, T. S. Jorgensen, L. Ding, T. Weber

This study identifies and characterizes the biosynthetic pathway for azodyrecin, an azoxy compound produced by Streptomyces mirabilis P8-A2, revealing key enzymes and gene cluster distribution across Streptomyces species.

bioRxiv · Oct 13, 2023Microbiology

Characterization and Engineering of Streptomyces griseofuscus DSM 40191 as a Potential Host for Heterologous Expression of Biosynthetic Gene Clusters

T. Gren, C. M. Whitford, O. S. Mohite, T. S. Jorgensen, E. E. Kontou, J. B. Nielsen, S. Y. Lee, T. Weber

This paper characterizes Streptomyces griseofuscus DSM 40191 as a potential heterologous host for biosynthetic gene clusters and demonstrates its ability to produce secondary metabolites.

bioRxiv · Nov 6, 2020Microbiology

CRISPR-nRAGE, a Cas9 nickase-reverse transcriptase assisted versatile genetic engineering toolkit for E. coli

Y. Tong, T. S. Jorgensen, C. M. Whitford, T. Weber, S. Y. Lee

CRISPR-nRAGE enables DSB-free, single-nucleotide resolution genome editing in E. coli by combining Cas9 nickase and reverse transcriptase, allowing substitutions, deletions, and insertions.

bioRxiv · Sep 2, 2020 · PreprintBioengineering