Abstrakt
How bacteria control proper septum placement at midcell, to guarantee the generation of identical daughter cells, is still largely unknown. Although different systems involved in the selection of the division site have been described in selected species, these do not appear to be widely conserved.
Here we report that LocZ (Spr0334), a newly identified cell division protein, is involved in proper septum placement in Streptococcus pneumoniae. We show that locZ is not essential, but its deletion results in cell division defects and shape deformation, causing cells to divide asymmetrically and generate unequally-sized, occasionally anucleated, daughter cells.
LocZ has a unique localization profile. It arrives early at midcell, before FtsZ and FtsA, and leaves the septum early, apparently moving along with the equatorial rings that mark the future division sites.
Consistently, cells lacking LocZ also show misplacement of the Z-ring, suggesting that it could act as a positive regulator to determine septum placement. LocZ was identified as a substrate of the Ser/Thr protein kinase StkP, which regulates cell division in S. pneumoniae.
Interestingly, homologues of LocZ are found only in streptococci, lactococci and enterococci, indicating that this close phylogenetically related group of bacteria evolved a specific solution to spatially regulate cell division.