Literature DB >> 4303541

Fractionation and characterization of the plasma and mesosome membrane of Listeria monocytogenes.

B K Ghosh, R G Murray.   

Abstract

Protoplasts of Listeria monocytogenes strain 42 were fractionated after control lysis on a Ficoll (a polysucrose) density gradient. Visually, five zones could be recognized in the gradient. The first one was composed of amorphous cytoplasmic solutes (fraction 1a) and a mixture of particles (fraction 1b). These were: (i) light particles that were lipase-sensitive and composed of six subunits and (ii) heavy particles, sensitive to ribonuclease and devoid of fine structure. The second zone consisted of tubules and vesicles still harboring cytoplasmic components (fraction 2), whereas the third zone contained only empty vesicles and protoplast ghosts (fraction 3). The material congregating into the fourth zone was morphologically identical to that of the third (fraction 3a). The fifth and heaviest zone contained a mixture of (i) particles without any substructure and (ii) partly lysed protoplasts (fraction 4). Fractions 1b and 4 were the richest in nucleic acids (ribonucleic acid, 11.4 and 9.4%, respectively; deoxyribonucleic acid, 5.1 and 4.8%, respectively), whereas fraction 1b had the highest protein contents (74.6%). Phospholipids were mainly found in fractions 2 and 3. Except for fraction 1, all materials contained significant amounts of protein-bound phosphorus. The main concentrations of four enzymes were: glucose-6-phosphate dehydrogenase (fraction 1a); adenosine triphosphatase and reduced nicotinamide adenine diphosphate oxidase (fraction 3); nitro blue tetrazolium chloride reductase (fraction 2). Fractionation of strain 42 after addition of (32)P during the mid-log phase of growth revealed that the radio-activity was mainly detected in fraction 1b, when growth in the presence of the marker was allowed for 10 min, and in fraction 2, when growth was allowed for 90 min. The vesicles of fraction 2, often tubular, are probably of mesosomal origin, whereas those of fraction 3, which are always spherical, represent, most likely, the bulk of the cell plasma membrane. Our data showed slight chemical differences between these two fractions, but the differences in enzymatic activities and lipid-phosphorus incorporation during long pulse experiments were most dramatic.

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Year:  1969        PMID: 4303541      PMCID: PMC249627          DOI: 10.1128/jb.97.1.426-440.1969

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


  34 in total

1.  Intracellular location of carotenoid pigments and some respiratory enzymes in Sarcina lutea.

Authors:  M M MATHEWS; W R SISTROM
Journal:  J Bacteriol       Date:  1959-12       Impact factor: 3.490

2.  Tellurite reductase from Mycobacterium avium.

Authors:  T TERAI; T KAMAHORA; Y YAMAMURA
Journal:  J Bacteriol       Date:  1958-05       Impact factor: 3.490

3.  Electron microscopy of ultra-thin sections of bacteria I. Cellular division in Bacillus cereus.

Authors:  G B CHAPMAN; J HILLIER
Journal:  J Bacteriol       Date:  1953-09       Impact factor: 3.490

4.  Characteristics of isolated and purified preparations of the outer and inner membranes of mitochondria.

Authors:  D F Parsons; G R Williams; B Chance
Journal:  Ann N Y Acad Sci       Date:  1966-07-14       Impact factor: 5.691

5.  [Localization of the cytochromes of Bacillus subtilis in mesosomal structures].

Authors:  B Ferrandes; P Chaix; A Ryter
Journal:  C R Acad Hebd Seances Acad Sci D       Date:  1966-11-21

6.  The interaction of guanofuracin and Listeria monocytogenes.

Authors:  E G Murray; B K Ghosh; R G Murray
Journal:  Can J Microbiol       Date:  1966-04       Impact factor: 2.419

Review 7.  Symposium on the fine structure and replication of bacteria and their parts. II. Bacterial cytoplasm.

Authors:  W van Iterson
Journal:  Bacteriol Rev       Date:  1965-09

8.  Isolation, composition, and structure of membrane of Listeria monocytogenes.

Authors:  B K Ghosh; K K Carroll
Journal:  J Bacteriol       Date:  1968-02       Impact factor: 3.490

9.  ELECTRON MICROSCOPE OBSERVATIONS ON INTACT CELLS, PROTOPLASTS, AND THE CYTOPLASMIC MEMBRANE OF BACILLUS STEAROTHERMOPHILUS.

Authors:  D ABRAM
Journal:  J Bacteriol       Date:  1965-03       Impact factor: 3.490

10.  A CYTOCHEMICAL LOCALIZATION OF REDUCTIVE SITES IN A GRAM-POSITIVE BACTERIUM. TELLURITE REDUCTION IN BACILLUS SUBTILIS.

Authors:  W LEENE
Journal:  J Cell Biol       Date:  1964-03       Impact factor: 10.539

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  12 in total

Review 1.  Mesosomes: membranous bacterial organelles.

Authors:  J W Greenawalt; T L Whiteside
Journal:  Bacteriol Rev       Date:  1975-12

2.  Isolation, partial characterization of the cytoplasmic membrane fraction of Streptomyces albus G and DD-carboxypeptidase localization.

Authors:  E Muñoz; A Marquet; V Larraga; J Coyette
Journal:  Arch Mikrobiol       Date:  1972

3.  Growth, structure, and classification of Selenomonas.

Authors:  V V Kingsley; J F Hoeniger
Journal:  Bacteriol Rev       Date:  1973-12

4.  Electron-dense particles resembling ribosomes in mesosomes of Bacillus subtilis.

Authors:  A Matheson; M C Kwong
Journal:  J Bacteriol       Date:  1972-05       Impact factor: 3.490

5.  Electron microscopy during release and purification of mesosomal vesicles and protoplast membranes from Staphylococcus aureus.

Authors:  T J Popkin; T S Theodore; R M Cole
Journal:  J Bacteriol       Date:  1971-09       Impact factor: 3.490

6.  Isolation and properties of mesosomal membrane fractions from Micrococcus lysodeikticus.

Authors:  P Owen; J H Freer
Journal:  Biochem J       Date:  1972-10       Impact factor: 3.857

7.  Factors influencing the activity of succinate dehydrogenase in membrane preparations from Micrococcus lysodeikticus.

Authors:  P Owen; J H Freer
Journal:  Biochem J       Date:  1970-11       Impact factor: 3.857

8.  Purification of a monocytosis-producing activity from Listeria monocytogenes.

Authors:  S B Galsworthy; S M Gurofsky; R G Murray
Journal:  Infect Immun       Date:  1977-02       Impact factor: 3.441

9.  Streptococcus pneumoniae proteins released into medium upon inhibition of cell wall biosynthesis.

Authors:  R Hakenbeck; C Martin; G Morelli
Journal:  J Bacteriol       Date:  1983-09       Impact factor: 3.490

10.  Protein and fatty acid composition of mesosomal vesicles and plasma membranes of Staphylococcus aureus.

Authors:  T S Theodore; C Panos
Journal:  J Bacteriol       Date:  1973-11       Impact factor: 3.490

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