Pierre Stallforth

The paper shows that Pseudomonas fluorescens protects Chlamydomonas reinhardtii from Pseudomonas protegens by inactivating its toxin protegencin in a tripartite microbial interaction.

The paper identifies a light-labile signal molecule that regulates secondary metabolite biosynthesis in Pseudomonas protegens by degrading in light and activating gene expression in the dark.

This study shows that fluorination of inhibitors can tune protein dimerization affinity by altering enzyme-inhibitor interactions and dynamics.

The paper investigates how bacterial toxin production and Allee effects influence predator-prey dynamics between Pseudomonas fluorescens and amoebae, revealing spatiotemporal regulation of toxin production.

This study enables functional reconstitution of type II PKS in vitro by engineering acyl carrier proteins to be activatable by Sfp.