Rv3722c governs aspartate-dependent nitrogen metabolism inMycobacterium tuberculosis

Abstract

AbstractOrganisms are defined by their genomes, yet many distinguishing features of a given organism are encoded by genes that are functionally unannotated.Mycobacterium tuberculosis(Mtb), the leading cause of death due to a single microbe, co-evolved with humans as its only known natural reservoir, yet the factors mediatingMtb’spathogenicity remain incompletely defined.rv3722cis a gene of unknown function predicted to encode a pyridoxal phosphate binding protein and to be essential forin vitrogrowth ofMtb. Using metabolomic, genetic and structural approaches, we show that Rv3722c is the primary aspartate aminotransferase ofMtband mediates an essential but underrecognized role in metabolism: nitrogen distribution. Together with the attenuation of Rv3722c-deficientMtbin macrophages and mice, these results identify aspartate biosynthesis and nitrogen distribution as potential species-selective drug targets inMtb.