Jessica C. Seeliger

This paper shows that disrupting riboflavin biosynthesis in Mycobacterium tuberculosis leads to metabolic changes and loss of infectivity in mice.

This study identifies the C-terminal domain of MmpL11 as required for its interaction with MSMEG_0240 using biotin proximity labeling assays in Mycobacterium smegmatis.

This study measures membrane fluidity in live mycobacteria using C-Laurdan, revealing subcellular variation and pole-selective responses to mycomembrane perturbations.

The paper uses metabolic tagging to identify surface-associated lipoproteins in mycobacteria, revealing their presence without known transporters.

The paper shows that synonymous mutations in mycobacteria can create new transcription start sites within genes, leading to smaller protein isoforms.