Literature DB >> 9721295

Bacillus subtilis cells lacking penicillin-binding protein 1 require increased levels of divalent cations for growth.

T Murray1, D L Popham, P Setlow.   

Abstract

Bacillus subtilis strains lacking penicillin-binding protein 1 (PBP1), encoded by ponA, required greater amounts of Mg2+ or Ca2+ for vegetative growth or spore outgrowth than the wild-type strain and strains lacking other high-molecular-weight (HMW) PBPs. Growth of ponA cells in a medium low in Mg2+ also resulted in greatly increased cell bending compared to wild-type cells or cells lacking other HMW PBPs. The addition of high levels of Mg2+ to growth media eliminated these phenotypes of a ponA mutant. In contrast to the effects of divalent cations, NaCl did not restore ponA cell growth in a divalent-cation-deficient medium. Surprisingly, wild-type cells swelled and then lysed during both vegetative growth and spore outgrowth when 500 mM NaCl was included in a divalent-cation-deficient medium. Again, Mg2+ addition was sufficient to allow normal vegetative growth and spore outgrowth of both wild-type and ponA cells in a medium with 500 mM NaCl. These studies demonstrate that (i) while HMW PBPs possess largely redundant functions in rich medium, when divalent cations are limiting, PBP1 is required for cell growth and spore outgrowth; and (ii) high levels of NaCl induce cell lysis in media deficient in divalent cations during both vegetative growth and spore outgrowth.

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Year:  1998        PMID: 9721295      PMCID: PMC107467     

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  47 in total

1.  Differential effect of mutational impairment of penicillin-binding proteins 1A and 1B on Escherichia coli strains harboring thermosensitive mutations in the cell division genes ftsA, ftsQ, ftsZ, and pbpB.

Authors:  F García del Portillo; M A de Pedro
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

2.  Analysis of the peptidoglycan structure of Bacillus subtilis endospores.

Authors:  D L Popham; J Helin; C E Costello; P Setlow
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

3.  Structural analysis of Bacillus subtilis 168 endospore peptidoglycan and its role during differentiation.

Authors:  A Atrih; P Zöllner; G Allmaier; S J Foster
Journal:  J Bacteriol       Date:  1996-11       Impact factor: 3.490

4.  dacD, an Escherichia coli gene encoding a novel penicillin-binding protein (PBP6b) with DD-carboxypeptidase activity.

Authors:  M R Baquero; M Bouzon; J C Quintela; J A Ayala; F Moreno
Journal:  J Bacteriol       Date:  1996-12       Impact factor: 3.490

5.  Isolation and sequence analysis of dacB, which encodes a sporulation-specific penicillin-binding protein in Bacillus subtilis.

Authors:  C E Buchanan; M L Ling
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

6.  Lytic response of Escherichia coli cells to inhibitors of penicillin-binding proteins 1a and 1b as a timed event related to cell division.

Authors:  F García del Portillo; M A de Pedro; D Joseleau-Petit; R D'Ari
Journal:  J Bacteriol       Date:  1989-08       Impact factor: 3.490

7.  Lysis of Escherichia coli by beta-lactam antibiotics: deletion analysis of the role of penicillin-binding proteins 1A and 1B.

Authors:  S Y Yousif; J K Broome-Smith; B G Spratt
Journal:  J Gen Microbiol       Date:  1985-10

8.  The divIVB region of the Bacillus subtilis chromosome encodes homologs of Escherichia coli septum placement (minCD) and cell shape (mreBCD) determinants.

Authors:  A W Varley; G C Stewart
Journal:  J Bacteriol       Date:  1992-11       Impact factor: 3.490

9.  The effect of magnesium ion deprivation on the synthesis of mucopeptide and its precursors in Bacillus subtilis.

Authors:  A J Garrett
Journal:  Biochem J       Date:  1969-11       Impact factor: 3.857

10.  Germination of Bacillus megaterium spores after various extraction procedures.

Authors:  J C Vary
Journal:  J Bacteriol       Date:  1973-11       Impact factor: 3.490

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  27 in total

1.  Penicillin-binding protein-related factor A is required for proper chromosome segregation in Bacillus subtilis.

Authors:  L B Pedersen; P Setlow
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

Review 2.  The bacterial actin-like cytoskeleton.

Authors:  Rut Carballido-López
Journal:  Microbiol Mol Biol Rev       Date:  2006-12       Impact factor: 11.056

3.  Life without a wall or division machine in Bacillus subtilis.

Authors:  M Leaver; P Domínguez-Cuevas; J M Coxhead; R A Daniel; J Errington
Journal:  Nature       Date:  2009-02-12       Impact factor: 49.962

4.  The cell wall regulator {sigma}I specifically suppresses the lethal phenotype of mbl mutants in Bacillus subtilis.

Authors:  Kathrin Schirner; Jeff Errington
Journal:  J Bacteriol       Date:  2008-12-29       Impact factor: 3.490

5.  Evidence that the extracytoplasmic function sigma factor sigmaE is required for normal cell wall structure in Streptomyces coelicolor A3(2).

Authors:  M S Paget; L Chamberlin; A Atrih; S J Foster; M J Buttner
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

6.  Analysis of outgrowth of Bacillus subtilis spores lacking penicillin-binding protein 2a.

Authors:  T Murray; D L Popham; C B Pearson; A R Hand; P Setlow
Journal:  J Bacteriol       Date:  1998-12       Impact factor: 3.490

7.  Discovery of novel cell wall-active compounds using P ywaC, a sensitive reporter of cell wall stress, in the model gram-positive bacterium Bacillus subtilis.

Authors:  T L Czarny; A L Perri; S French; E D Brown
Journal:  Antimicrob Agents Chemother       Date:  2014-03-31       Impact factor: 5.191

8.  Analysis of the role of Bacillus subtilis σ(M) in β-lactam resistance reveals an essential role for c-di-AMP in peptidoglycan homeostasis.

Authors:  Yun Luo; John D Helmann
Journal:  Mol Microbiol       Date:  2012-01-04       Impact factor: 3.501

9.  Identification of Mycobacterium tuberculosis RNAs synthesized in response to phagocytosis by human macrophages by selective capture of transcribed sequences (SCOTS).

Authors:  J E Graham; J E Clark-Curtiss
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

10.  Dynamic localization of MreB in Vibrio parahaemolyticus and in the ectopic host bacterium Escherichia coli.

Authors:  Shen-Wen Chiu; Shau-Yan Chen; Hin-chung Wong
Journal:  Appl Environ Microbiol       Date:  2008-09-12       Impact factor: 4.792

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