» Articles » PMID: 4982084

The Effect of Magnesium Ion Deprivation on the Synthesis of Mucopeptide and Its Precursors in Bacillus Subtilis

Overview
Journal Biochem J
Specialty Biochemistry
Date 1969 Nov 1
PMID 4982084
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

1. Mg(2+) or Mn(2+) starvation causes suspensions of Bacillus subtilis strain W 23 to accumulate bound amino sugars that are soluble in trichloroacetic acid. 2. The presence of chloramphenicol or puromycin produces higher intracellular concentrations of amino sugars during Mg(2+) starvation, but neither compound can stimulate the accumulation when Mg(2+) is present. 3. The major component of the amino sugar fraction extracted from cells deprived of Mg(2+) is a nucleotide containing uridine, phosphorus, N-acetylmuramic acid, alanine, glutamic acid and alphain-diaminopimelic acid in the molar proportions of 1:2:1:3:1:1. This compound represents at least 80% of the bound N-acetylhexosamine extracted by trichloroacetic acid. 4. Studies of the binding of this nucleotide with vancomycin support the proposal that it is the mucopeptide precursor UDP-N-acetylmuramyl-l-alanyl-d-glutaminyl- alphain-diaminopimelyl-d-alanyl-d-alanine. 5. A method is described for the isolation of this material labelled with [(3)H]alphain-diaminopimelic acid. 6. When Mg(2+) is supplied to cells previously starved of Mg(2+), the accumulated pool of amino sugars rapidly decreases. 7. The biosynthesis of mucopeptide is inhibited by 35-50% under conditions of Mg(2+) starvation. The presence of EDTA increases this inhibition to 70%. The amount of N-acetylhexosamine that accumulates is balanced exactly by the associated fall in mucopeptide synthesis. 8. ;Chase' experiments show that the accumulated N-acetylhexosamine compound is utilized in mucopeptide synthesis.

Citing Articles

Magnesium Modulates Bacillus subtilis Cell Division Frequency.

Guo T, Herman J J Bacteriol. 2022; 205(1):e0037522.

PMID: 36515540 PMC: 9879117. DOI: 10.1128/jb.00375-22.


Disruption of an M. tuberculosis membrane protein causes a magnesium-dependent cell division defect and failure to persist in mice.

Goodsmith N, Guo X, Vandal O, Vaubourgeix J, Wang R, Botella H PLoS Pathog. 2015; 11(2):e1004645.

PMID: 25658098 PMC: 4450064. DOI: 10.1371/journal.ppat.1004645.


Induced sensitivity of Bacillus subtilis colony morphology to mechanical media compression.

Polka J, Silver P PeerJ. 2014; 2:e597.

PMID: 25289183 PMC: 4183962. DOI: 10.7717/peerj.597.


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

Murray T, Popham D, Setlow P J Bacteriol. 1998; 180(17):4555-63.

PMID: 9721295 PMC: 107467. DOI: 10.1128/JB.180.17.4555-4563.1998.


Teicoplanin, a new antibiotic from Actinoplanes teichomyceticus nov. sp.

Somma S, Gastaldo L, Corti A Antimicrob Agents Chemother. 1984; 26(6):917-23.

PMID: 6240963 PMC: 180050. DOI: 10.1128/AAC.26.6.917.


References
1.
Rogers H, Perkins H . 5-Fluorouracil and mucopeptide biosynthesis by Staphylococcus aureus. Biochem J. 1960; 77:448-59. PMC: 1205056. DOI: 10.1042/bj0770448. View

2.
Park J, Strominger J . Mode of action of penicillin. Science. 1957; 125(3238):99-101. DOI: 10.1126/science.125.3238.99. View

3.
Webb M . The influence of certain trace metals on bacterial growth and magnesium utilization. J Gen Microbiol. 1968; 51(3):325-35. DOI: 10.1099/00221287-51-3-325. View

4.
Rogers H, Perkins H . Cell-wall mucopeptides of Staphyloccus aureus and Micrococcus lysodeikticus. Nature. 1959; 184:520-4. DOI: 10.1038/184520a0. View

5.
Hancock R, Park J . Cell-wall synthesis by Staphylococcus aureus in the presence of chloramphenicol. Nature. 1958; 181(4615):1050-2. DOI: 10.1038/1811050a0. View