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Peptidoglycan metabolism is controlled by the WalRK (YycFG) and PhoPR two‐component systems in phosphate‐limited Bacillus subtilis cells
Author(s) -
Bisicchia Paola,
Lioliou Efthimia,
Noone David,
Salzberg Letal I.,
Botella Eric,
Hübner Sebastian,
Devine Kevin M.
Publication year - 2010
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/j.1365-2958.2009.07036.x
Subject(s) - peptidoglycan , regulon , bacillus subtilis , biology , phosphate , biochemistry , metabolism , microbiology and biotechnology , in vitro , gene , gene expression , bacteria , genetics
Summary In Bacillus subtilis , the WalRK (YycFG) two‐component system controls peptidoglycan metabolism in exponentially growing cells while PhoPR controls the response to phosphate limitation. Here we examine the roles of WalRK and PhoPR in peptidoglycan metabolism in phosphate‐limited cells. We show that B. subtilis cells remain viable in a phosphate‐limited state for an extended period and resume growth rapidly upon phosphate addition, even in the absence of a PhoPR‐mediated response. Peptidoglycan synthesis occurs in phosphate‐limited wild‐type cells at ∼27% the rate of exponentially growing cells, and at ∼18% the rate of exponentially growing cells in the absence of PhoPR. In phosphate‐limited cells, the WalRK regulon genes yocH , cwlO ( yvcE ), lytE and ydjM are expressed in a manner that is dependent on the WalR recognition sequence and deleting these genes individually reduces the rate of peptidoglycan synthesis. We show that ydjM expression can be activated by PhoP∼P in vitro and that PhoP occupies its promoter in phosphate‐limited cells. However, iseA ( yoeB ) expression cannot be repressed by PhoP∼P in vitro , but can be repressed by non‐phosphorylated WalR in vitro . Therefore, we conclude that peptidoglycan metabolism is controlled by both WalRK and PhoPR in phosphate‐limited B. subtilis cells.