Journal
JOURNAL OF BACTERIOLOGY
Volume 193, Issue 4, Pages 896-908Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/JB.00594-10
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Funding
- NSF [ID 0744872]
- ARCS
- NIH [T32GM007757]
- National Institute of Allergy and Infectious Diseases [AI060744]
- Div Of Molecular and Cellular Bioscience
- Direct For Biological Sciences [0744872] Funding Source: National Science Foundation
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Bacteria must accurately replicate and segregate their genetic information to ensure the production of viable daughter cells. The high fidelity of chromosome partitioning is achieved through mechanisms that coordinate cell division with DNA replication. We report that YycJ (WalJ), a predicted member of the metallo-beta-lactamase superfamily found in most low-G+C Gram-positive bacteria, contributes to the fidelity of cell division in Bacillus subtilis. B. subtilis Delta walJ (Delta walJ(Bsu)) mutants divide over unsegregated chromosomes more frequently than wild-type cells, and this phenotype is exacerbated when DNA replication is inhibited. Two lines of evidence suggest that WalJ(Bsu) and its ortholog in the Gram-positive pathogen Streptococcus pneumoniae, WalJ(Spn) (VicX), play a role in cell wall metabolism: (i) strains of B. subtilis and S. pneumoniae lacking walJ exhibit increased sensitivity to a narrow spectrum of cephalosporin antibiotics, and (ii) reducing the expression of a two-component system that regulates genes involved in cell wall metabolism, WalRK (YycFG), renders walJ essential for growth in B. subtilis, as observed previously with S. pneumoniae. Together, these results suggest that the enzymatic activity of WalJ directly or indirectly affects cell wall metabolism and is required for accurate coordination of cell division with DNA replication.
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