posted on 2016-01-27, 00:00authored byAndrew
W. Robertson, Stephanie M. Forget, Camilo F. Martinez-Farina, Nicole E. McCormick, Raymond T. Syvitski, David L. Jakeman
We report that JadX, a protein of
previously undetermined function
coded for in the jadomycin biosynthetic gene cluster of Streptomyces venezuelae ISP5230, affects both chloramphenicol
and jadomycin production levels in blocked mutants. Characterization
of recombinant JadX through protein–ligand interactions by
chemical shift perturbation and WaterLOGSY NMR spectroscopy resulted
in the observation of binding between JadX and a series of jadomycins
and between JadX and chloramphenicol, another natural product produced
by S. venezuelae ISP5230. These results
suggest JadX to be an unusual class of natural product binding protein
involved in binding structurally disparate natural products. The ability
for JadX to bind two different natural products in vitro and the ability
to affect production of these secondary metabolites in vivo suggest
a potential role in regulation or signaling. This is the first example
of functional characterization of these JadX-like proteins, and provides
insight into a previously unobserved regulatory process.