Literature DB >> 4331498

Changes in terminal respiratory pathways of Bacillus subtilis during germination, outgrowth and vegetative growth.

K Tochikubo.   

Abstract

The chemical and enzymatic properties of the cytochrome system in the particulate preparations obtained from dormant spores, germinated spores, young vegetative cells, and vegetative cells of Bacillus subtilis PCI219 were investigated. Difference spectra of particulate fractions from dormant spores of this strain suggested the presence of cytochromes a, a(3), b, c(+c(1)), and o. All of the cytochrome components were present in dormant spores and in germinated spores and vegetative cells at all stages which were investigated. Concentrations of cytochromes a, a(3), b, and c(+c(1)) increased during germination, outgrowth, and vegetative growth, but that of cytochrome o was highest in dormant spores. As the cytochrome components were reducible by reduced nicotinamide adenine dinucleotide (NADH), they were believed to be metabolically active. Difference spectra of whole-cell suspensions of dormant spores and vegetative cells were coincident with those of the particulate fractions. NADH oxidase and cytochrome c oxidase were present in dormant spores, germinated spores, and vegetative cells at all stages after germination, but succinate cytochrome c reductase was not present in dormant spores. Cytochrome c oxidase and succinate cytochrome c reductase activities increased with growth, but NADH oxidase activity was highest in germinated spores and lowest in vegetative cells. There was no striking difference between the effects of respiratory inhibitors on NADH oxidase in dormant spores and those on NADH oxidase in vegetative cells.

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Year:  1971        PMID: 4331498      PMCID: PMC247123          DOI: 10.1128/jb.108.2.652-661.1971

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


  14 in total

1.  Comparison of electron transport systems in vegetative cells and spores of Bacillus cereus.

Authors:  R H DOI; H HALVORSON
Journal:  J Bacteriol       Date:  1961-01       Impact factor: 3.490

2.  The chemical nature of the cytoplasmic membrane and cell wall of Bacillus megaterium, strain M.

Authors:  C WEIBULL; L BERGSTROM
Journal:  Biochim Biophys Acta       Date:  1958-11

3.  Photochemical determinations of the oxidases of bacteria.

Authors:  L N CASTOR; B CHANCE
Journal:  J Biol Chem       Date:  1959-06       Impact factor: 5.157

4.  Reactions of cytochromes a and a3. II. Studies with Micrococcus pyogenes var. albus and Bacillus subtilis.

Authors:  L SMITH
Journal:  J Biol Chem       Date:  1955-08       Impact factor: 5.157

5.  Bacterial cytochromes; difference spectra.

Authors:  L SMITH
Journal:  Arch Biochem Biophys       Date:  1954-06       Impact factor: 4.013

6.  [Bacterial metabolism of cytochromes and porphyrins. I. Partial disappearance of cytochromes in anaerobic culture in certain faculative aerobic bacteria].

Authors:  P SCHAEFFER
Journal:  Biochim Biophys Acta       Date:  1952-09

7.  The carbon monoxide compounds of the cytochrome oxidases. I. Difference spectra.

Authors:  B CHANCE
Journal:  J Biol Chem       Date:  1953-05       Impact factor: 5.157

8.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

9.  ELECTRON TRANSPORT SYSTEM IN VEGETATIVE CELLS AND MICROCYSTS OF MYXOCOCCUS XANTHUS.

Authors:  M DWORKIN; D J NIEDERPRUEM
Journal:  J Bacteriol       Date:  1964-02       Impact factor: 3.490

10.  EFFECT OF HEMIN ON THE FORMATION OF THE CYTOCHROME SYSTEM OF ANAEROBICALLY GROWN STAPHYLOCOCCUS EPIDERMIDIS.

Authors:  N J JACOBS; S F CONTI
Journal:  J Bacteriol       Date:  1965-03       Impact factor: 3.490

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  21 in total

1.  Structure and expression of the cytochrome aa3 regulatory gene ctaA of Bacillus subtilis.

Authors:  J P Mueller; H W Taber
Journal:  J Bacteriol       Date:  1989-09       Impact factor: 3.490

2.  Respiratory systems of the Bacillus cereus mother cell and forespore.

Authors:  J E Escamilla; R Ramírez; P Del-Arenal; A Aranda
Journal:  J Bacteriol       Date:  1986-08       Impact factor: 3.490

3.  Cloning and characterization of the hemA region of the Bacillus subtilis chromosome.

Authors:  M Petricek; L Rutberg; I Schröder; L Hederstedt
Journal:  J Bacteriol       Date:  1990-05       Impact factor: 3.490

4.  Cytochrome pigments in spores of Bacillus cereus T.

Authors:  G Bahnweg; H A Douthit
Journal:  J Bacteriol       Date:  1975-02       Impact factor: 3.490

5.  Respiratory system of vegetative and sporulating Bacillus cereus.

Authors:  J E Escamilla; M C Benito
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

6.  L-amino acid dehydrogenases in Bacillus subtilis spores.

Authors:  Y Nitta; Y Yasuda; K Tochikubo; Y Hachisuka
Journal:  J Bacteriol       Date:  1974-02       Impact factor: 3.490

7.  Changes in menaquinone concentration during growth and early sporulation in Bacillus subtilis.

Authors:  S K Farrand; H W Taber
Journal:  J Bacteriol       Date:  1974-01       Impact factor: 3.490

8.  Catabolite regulation of the Bacillus subtilis ctaBCDEF gene cluster.

Authors:  X Liu; H W Taber
Journal:  J Bacteriol       Date:  1998-12       Impact factor: 3.490

9.  Pleiotropic menaquinone-deficient mutant of Bacillus subtilis.

Authors:  S K Farrand; H W Taber
Journal:  J Bacteriol       Date:  1973-09       Impact factor: 3.490

10.  Regulation of the dicarboxylic acid part of the citric acid cycle in Bacillus subtilis.

Authors:  M Ohné
Journal:  J Bacteriol       Date:  1975-04       Impact factor: 3.490

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