Literature DB >> 13950913

Cell division in a species of Erwinia. V. Effect of metabolic inhibitors on terminal division and composition of a "division" medium.

E A GRULA, M M GRULA.   

Abstract

Grula, E. A. (Oklahoma State University, Stillwater) and Mary M. Grula. Cell division in a species of Eriwinia. V. Effect of metabolic inhibitors on terminal division and composition of a "division" medium. J. Bacteriol. 84:492-499. 1962.-Terminal division in Erwinia spp. involves a triggering action and subsequent septum synthesis. It is a metabolic process requiring organic nitrogen and carbon and energy. The process, when triggered by pantoic acid or pantoyl lactone, is inhibited strongly by 2,4-dinitrophenol, hydroxylamine, mitomycin C, and Hg ion and to a lesser degree by cyanide, azide, 5-fluorouracil, and diisopropylfluorophosphate. Ethylenediaminetetraacetic acid completely inhibits division only when calcium ion is the triggering agent. Heating of the cells at 43 C for 10 to 20 min also completely inhibits division. Hydroxylamine, iodoacetate, and mitomycin C cause extensive lysis of growing cells. No evidence has been obtained to demonstrate the need for protein or normal ribonucleic acid synthesis in terminal division. Requirement for intact deoxyribonucleic acid (DNA) or DNA synthesis is questionable; -SH groups are not directly involved. Once triggering has occurred, septum formation appears to require synthesis of at least cell-wall mucopeptide. A "division" medium is reported and discussed.

Entities:  

Keywords:  ANTIMETABOLITES; BUTYRATES; CALCIUM; CELL DIVISION; ERWINIA; LACTONES

Mesh:

Substances:

Year:  1962        PMID: 13950913      PMCID: PMC277904          DOI: 10.1128/jb.84.3.492-499.1962

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


  28 in total

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3.  Increase in ribonucleic acid in the bacterial chromatin body during chloramphenicol treatment.

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4.  Cell division in a species of Erwinia. I. Inhibition of division by D-amino acids.

Authors:  E A GRULA
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5.  5-Fluorouracil and mucopeptide biosynthesis by Staphylococcus aureus.

Authors:  H J ROGERS; H R PERKINS
Journal:  Biochem J       Date:  1960-12       Impact factor: 3.857

6.  Degradation of deoxyribonucleic acid in Escherichia coli cells treated with mitomycin C.

Authors:  H KERSTEN; H M RAUEN
Journal:  Nature       Date:  1961-06-24       Impact factor: 49.962

7.  Effect of folic acid analogues on growth and cell division of nonexacting microorganisms.

Authors:  W J NICKERSON; M WEBB
Journal:  J Bacteriol       Date:  1956-02       Impact factor: 3.490

8.  THE MODE OF ACTION OF 5-FLUOROURACIL AND ITS DERIVATIVES.

Authors:  S S Cohen; J G Flaks; H D Barner; M R Loeb; J Lichtenstein
Journal:  Proc Natl Acad Sci U S A       Date:  1958-10-15       Impact factor: 11.205

9.  Reversal of toxicity of 5-fluorouracil and 5-fluorodeoxyuridine for Candida albicans by pyridoxine and pyridoxamine.

Authors:  M L LITTMAN; T MIWATANI
Journal:  Nature       Date:  1961-12-23       Impact factor: 49.962

10.  Cell division in a species of Erwinia III. Reversal of inhibition of cell division caused by D-amino acids, penicillin, and ultraviolet light.

Authors:  E A GRULA; M M GRULA
Journal:  J Bacteriol       Date:  1962-05       Impact factor: 3.490

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  4 in total

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Journal:  J Bacteriol       Date:  1975-08       Impact factor: 3.490

Review 2.  Control of cell division in bacteria.

Authors:  M Slater; M Schaechter
Journal:  Bacteriol Rev       Date:  1974-06

3.  Filament formation in Clostridium acidiurici under conditions of elevated temperatures.

Authors:  D R Terry; A Gaffar; R D Sagers
Journal:  J Bacteriol       Date:  1966-04       Impact factor: 3.490

4.  Inhibitory effects of mitomycin-related compounds lacking the C1-C2 aziridine ring.

Authors:  C M Mercado; M Tomasz
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  4 in total

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