Literature DB >> 16561987

REVERSIBLE ACTIVATION FOR GERMINATION AND SUBSEQUENT CHANGES IN BACTERIAL SPORES.

W H Lee1, Z J Ordal.   

Abstract

Lee, W. H. (University of Illinois, Urbana) and Z. John Ordal. Reversible activation for germination and subsequent changes in bacterial spores. J. Bacteriol. 85:207-217. 1963.-It was possible to isolate refractile spores of Bacillus megaterium, from a calcium dipicolinate germination solution, that were activated and would germinate spontaneously in distilled water. Some of the characteristics of the initial phases of bacterial spore germination were determined by studying these unstable activated spores. Activated spores of B. megaterium were resistant to stains and possessed a heat resistance intermediate between that of dormant and of germinated spores. The spontaneous germination of activated spores was inhibited by copper, iron, silver, or mercury salts, saturated o-phenanthroline, or solutions having a low pH value, but not by many common inhibitors. These inhibitions could be partially or completely reversed by the addition of sodium dipicolinate. The activated spores could be deactivated and made similar to dormant spores by treatment with acid. Analyses of the exudates from the variously treated spore suspensions revealed that whatever inhibited the germination of activated spores also inhibited the release of spore material. The composition of the germination exudates was different than that of extracts of dormant spores. Although heavy suspensions of activated spores gradually became swollen and dark when suspended in solutions of o-phenanthroline or at pH 4, the materials released resembled those found in extracts of dormant spores rather than those of normal germination exudates.

Entities:  

Year:  1963        PMID: 16561987      PMCID: PMC278109          DOI: 10.1128/jb.85.1.207-217.1963

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


  17 in total

1.  Dependence of the heat resistance of bacterial endospores on their dipicolinic acid content.

Authors:  B D CHURCH; H HALVORSON
Journal:  Nature       Date:  1959-01-10       Impact factor: 49.962

2.  The water and solid content of living bacterial spores and vegetative cells as indicated by refractive index measurements.

Authors:  K F ROSS; E BILLING
Journal:  J Gen Microbiol       Date:  1957-04

3.  Effect of enzyme inhibitors on the germination and respiration of and growth from Bacillus cereus var. terminalis spores.

Authors:  G G KRISHNA MURTY; H O HALVORSON
Journal:  J Bacteriol       Date:  1957-02       Impact factor: 3.490

4.  Effect of temperature and hydrogen-ion concentration on the germination of spores of Bacillus cereus.

Authors:  K VAS; G PROSZT
Journal:  Nature       Date:  1957-06-22       Impact factor: 49.962

5.  A cell-wall lytic enzyme associated with spores of Bacillus species.

Authors:  R E STRANGE; F A DARK
Journal:  J Gen Microbiol       Date:  1957-02

6.  Method for removal of vegetative cells from Bacterial spore preparations.

Authors:  S K LONG; O B WILLIAMS
Journal:  J Bacteriol       Date:  1958-09       Impact factor: 3.490

7.  A paper chromatographic method for the quantitative estimation of amino-acids.

Authors:  A L LEVY
Journal:  Nature       Date:  1954-07-17       Impact factor: 49.962

8.  Biochemical changes occurring during the germination of bacterial spores.

Authors:  J F POWELL; R E STRANGE
Journal:  Biochem J       Date:  1953-05       Impact factor: 3.857

9.  Hexosamine-containing peptides in spores of Bacillus subtilis, B. megatherium and B. cereus.

Authors:  R E STRANGE; J F POWELL
Journal:  Biochem J       Date:  1954-09       Impact factor: 3.857

10.  Isolation of dipicolinic acid (pyridine-2:6-dicarboxylic acid) from spores of Bacillus megatherium.

Authors:  J F POWELL
Journal:  Biochem J       Date:  1953-05       Impact factor: 3.857

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  11 in total

1.  ACTIVATION OF BACTERIAL ENDOSPORES.

Authors:  A KEYNAN; Z EVANCHIK; H O HALVORSON; J W HASTINGS
Journal:  J Bacteriol       Date:  1964-08       Impact factor: 3.490

2.  Direct Transition of Outgrowing Bacterial Spores to New Sporangia Without Intermediate Cell Division.

Authors:  V Vinter; R A Slepecky
Journal:  J Bacteriol       Date:  1965-09       Impact factor: 3.490

3.  Study of Bacillus subtilis Endospores in Soil by Use of a Modified Endospore Stain.

Authors:  D A Mormak; L E Casida
Journal:  Appl Environ Microbiol       Date:  1985-06       Impact factor: 4.792

4.  Effects of added germination agents on loss of optical density in electron-irradiated spores.

Authors:  G Stogaitis; G M Lefebvre
Journal:  Appl Environ Microbiol       Date:  1976-08       Impact factor: 4.792

5.  Initiation of germination and inactivation of Bacillus pumilus spores by hydrostatic pressure.

Authors:  J G Clouston; P A Wills
Journal:  J Bacteriol       Date:  1969-02       Impact factor: 3.490

6.  Dipicolinate-induced germination of Bacillus stearothermophilus spores.

Authors:  M L Fields; H A Frank
Journal:  J Bacteriol       Date:  1969-01       Impact factor: 3.490

7.  Ultrahigh-temperature activation of a low-temperature Bacillus subtilis spore germination system.

Authors:  D M Adams; F F Busta
Journal:  Appl Microbiol       Date:  1972-09

8.  Spores of microorganisms. XXVI. Synthetic activities of germinating spores of Bacillus cereus prevented from outgrowth.

Authors:  J Stastná; V Vinter
Journal:  Folia Microbiol (Praha)       Date:  1975       Impact factor: 2.099

9.  Biochemical studies of bacterial sporulation and germination. XVII. Sulfhydryl and disulfide levels in dormancy and germination.

Authors:  P Setlow; A Kornberg
Journal:  J Bacteriol       Date:  1969-12       Impact factor: 3.490

10.  Water vapor, aqueous ethyl alcohol, and heat activation of Bacillus megaterium spore germination.

Authors:  M T Hyatt; H S Levinson
Journal:  J Bacteriol       Date:  1968-06       Impact factor: 3.490

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