A Regulatory Pathway That Selectively Up-regulates Elongasome Function in the Absence of Class A PBPs

Overview

Journal Elife

Specialty Biology

Date 2020 Sep 8

PMID 32897856

Citations 20

Authors

Yesha Patel

Heng Zhao

John D Helmann

Affiliations

Soon will be listed here.

Abstract

Bacteria surround themselves with peptidoglycan, an adaptable enclosure that contributes to cell shape and stability. Peptidoglycan assembly relies on penicillin-binding proteins (PBPs) acting in concert with SEDS-family transglycosylases RodA and FtsW, which support cell elongation and division respectively. In , cells lacking all four PBPs with transglycosylase activity (aPBPs) are viable. Here, we show that the alternative sigma factor σ is essential in the absence of aPBPs. Defects in aPBP-dependent wall synthesis are compensated by σ-dependent upregulation of an MreB homolog, MreBH, which localizes the LytE autolysin to the RodA-containing elongasome complex. Suppressor analysis reveals that cells unable to activate this σ stress response acquire gain-of-function mutations in the essential histidine kinase WalK, which also elevates expression of , and . These results reveal compensatory mechanisms that balance the directional peptidoglycan synthesis arising from the elongasome complex with the more diffusive action of aPBPs.

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