Abstract

ABSTRACTAgrobacterium tumefaciens grows by addition of peptidoglycan (PG) at one pole of the bacterium. During the cell cycle, the cell needs to maintain two different developmental programs, one at the growth pole and another at the inert old pole. Proteins involved in this process are not yet well characterized. To further characterize the role of pole-organizing protein A. tumefaciens PopZ (PopZAt), we created deletions of the five PopZAt domains and assayed their localization. In addition, we created a popZAt deletion strain (ΔpopZAt) that exhibited growth and cell division defects with ectopic growth poles and minicells, but the strain is unstable. To overcome the genetic instability, we created an inducible PopZAt strain by replacing the native ribosome binding site with a riboswitch. Cultivated in a medium without the inducer theophylline, the cells look like ΔpopZAt cells, with a branching and minicell phenotype. Adding theophylline restores the wild-type (WT) cell shape. Localization experiments in the depleted strain showed that the domain enriched in proline, aspartate, and glutamate likely functions in growth pole targeting. Helical domains H3 and H4 together also mediate polar localization, but only in the presence of the WT protein, suggesting that the H3 and H4 domains multimerize with WT PopZAt, to stabilize growth pole accumulation of PopZAt.

Highlights

  • Agrobacterium tumefaciens grows by addition of peptidoglycan (PG) at one pole of the bacterium

  • The results show that H3 and H4 together mediate polar localization, but only in the presence of the WT protein, suggesting that the H3 and H4 domains are involved in multimerization with WT PopZAt

  • The increased length of the PED domain in PopZAt suggests that it may participate in additional functions or interactions compared to PopZCc

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Summary

Introduction

Agrobacterium tumefaciens grows by addition of peptidoglycan (PG) at one pole of the bacterium. Helical domains H3 and H4 together mediate polar localization, but only in the presence of the WT protein, suggesting that the H3 and H4 domains multimerize with WT PopZAt, to stabilize growth pole accumulation of PopZAt. IMPORTANCE Agrobacterium tumefaciens is a rod-shaped bacterium that grows by addition of PG at only one pole. The canonical proteins of the elongasome (which mediates dispersed growth), namely, MreB, MreC, MreD, RodA, RodZ, and PBP2, are not encoded in the A. tumefaciens genome [8,9,10], while most of the proteins of the division machinery (divisome), FtsZ, FtsA, PBP3, PBP1b, and FtsK, are conserved [8] These differences suggest that polar growth likely employs unique mechanisms to organize and regulate PG synthesis [11]. Many of the asymmetrically localized C. crescentus proteins are conserved in A. tumefaciens and may function in cellular polarization [9, 10, 17, 22]

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