Literature DB >> 5764340

Electron microscopy and viability of lysostaphin-induced staphylococcal spheroplasts, protoplast-like bodies, and protoplasts.

V T Schuhardt, T W Huber, L M Pope.   

Abstract

The cell walls of a selected isolate of Staphylococcus aureus FDA 209P were observed undergoing progressive disintegration when exposed to lysostaphin (1 unit/ml) in 24% NaCl solution. Electron micrographs of ultrathin sections of test cells after exposure to lysostaphin for 2 min showed only superficial evidence of lytic damage. However, an average of 89% of these cells were osmotically fragile, and 21% were damaged beyond their capacity to regenerate cell walls and to grow as normal staphylococci. The 68% (average) of the osmotically fragile cells which retained the capacity to revert to normal staphylococci were designated spheroplasts. Neither perforations of the cell walls nor separation of the cell walls from the plasma membranes were observed in the micrographs of these 2-min spheroplasts. Thus, it appears that the osmotic fragility of these and possibly all lysostaphin-induced staphylococcal spheroplasts results from the hydrolysis of a critical number of the pentapeptide cross-linkages of the murein of the cell wall. Electron micrographs of cells exposed to lysostaphin for 5 to 10 min showed perforations and more extensive damage, including the separation of walls from the plasma membranes and the disintegration of large sections of the walls. Smaller numbers of spheroplasts (21 and 8%) were recovered from these 5- and 10-min preparations; those recovered probably represent cells which were attacked more slowly than the majority by the lytic enzyme. The nonrevertible, osmotically fragile cells that retained segments of cell wall were designated protoplast-like bodies. After 20-min exposure to lysostaphin, all of the cell wall was digested away from most of the cells, and true staphylococcal protoplasts were produced. These lysostaphin-induced, osmotically fragile forms appear to have different osmotic properties from the staphylococcal "protoplasts" reported by other investigators and should serve as the basis for a variety of fundamental investigations.

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Year:  1969        PMID: 5764340      PMCID: PMC249619          DOI: 10.1128/jb.97.1.396-401.1969

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


  10 in total

1.  LYSOSTAPHIN: A NEW BACTERIOLYTIC AGENT FOR THE STAPHYLOCOCCUS.

Authors:  C A SCHINDLER; V T SCHUHARDT
Journal:  Proc Natl Acad Sci U S A       Date:  1964-03       Impact factor: 11.205

2.  PURIFICATION AND PROPERTIES OF LYSOSTAPHIN--A LYTIC AGENT FOR STAPHYLOCOCCUS AUREUS.

Authors:  C A SCHINDLER; V T SCHUHARDT
Journal:  Biochim Biophys Acta       Date:  1965-02-15

3.  LYSOSTAPHIN: ENZYMATIC MODE OF ACTION.

Authors:  H P BROWDER; W A ZYGMUNT; J R YOUNG; P A TAVORMINA
Journal:  Biochem Biophys Res Commun       Date:  1965-04-23       Impact factor: 3.575

4.  The localization of alkaline phosphatase in E. coli K12.

Authors:  M MALAMY; B L HORECKER
Journal:  Biochem Biophys Res Commun       Date:  1961-06-02       Impact factor: 3.575

5.  Autolytic release and osmotic properties of protoplasts from Staphylococcus aureus.

Authors:  P MITCHELL; J MOYLE
Journal:  J Gen Microbiol       Date:  1957-02

6.  The mechanism of sodium fluoride and cycloheximide inhibition of hemoglobin biosynthesis in the cell-free reticulocyte system.

Authors:  S Y Lin; R D Mosteller; B Hardesty
Journal:  J Mol Biol       Date:  1966-10-28       Impact factor: 5.469

7.  Osmotic fragility and viability of lysostaphin-induced staphylococcal spheroplasts.

Authors:  V T Schuhardt; P H Klesius
Journal:  J Bacteriol       Date:  1968-09       Impact factor: 3.490

8.  FORMATION OF "PROTOPLASTS" OF STAPHYLOCOCCUS AUREUS WITH A FUNGAL N-ACETYLHEXOSAMINIDASE.

Authors:  J H HASH; M WISHNICK; P A MILLER
Journal:  J Bacteriol       Date:  1964-02       Impact factor: 3.490

9.  The use of lead citrate at high pH as an electron-opaque stain in electron microscopy.

Authors:  E S REYNOLDS
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

10.  Electron microscope study of DNA-containing plasms. II. Vegetative and mature phage DNA as compared with normal bacterial nucleoids in different physiological states.

Authors:  E KELLENBERGER; A RYTER; J SECHAUD
Journal:  J Biophys Biochem Cytol       Date:  1958-11-25
  10 in total
  8 in total

1.  Isolation, structural and functional characterization of Staphylococcus aureus protoplasts obtained using lysoamidase.

Authors:  V V Petrov; E N Ratner; A I Severin; I S Kulaev
Journal:  Arch Microbiol       Date:  1991       Impact factor: 2.552

2.  Signal peptides direct surface proteins to two distinct envelope locations of Staphylococcus aureus.

Authors:  Andrea DeDent; Taeok Bae; Dominique M Missiakas; Olaf Schneewind
Journal:  EMBO J       Date:  2008-09-18       Impact factor: 11.598

3.  Electron microscopic localization of alpha toxin within the staphylococcal cell by ferritin-labeled antibody.

Authors:  J R Coulter; T M Mukherjee
Journal:  Infect Immun       Date:  1971-11       Impact factor: 3.441

4.  Electron microscopy of Staphylococcus aureus cells and cell walls after treatment with lysozyme Chalaropsis.

Authors:  J P Robinson; R D Robinson; J H Hash
Journal:  J Bacteriol       Date:  1974-02       Impact factor: 3.490

5.  Light and scanning-beam electron microscopy of wall-defective Staphylococcus aureus induced by lysostaphin.

Authors:  C Watanakunakorn; R J Fass; A S Klainer; M Hamburger
Journal:  Infect Immun       Date:  1971-07       Impact factor: 3.441

6.  Lysostaphin-induced, osmotically fragile Staphylococcus aureus cells.

Authors:  T W Huber; V T Schuhardt
Journal:  J Bacteriol       Date:  1970-07       Impact factor: 3.490

7.  Direct observation of Staphylococcus aureus cell wall digestion by lysostaphin.

Authors:  Grégory Francius; Oscar Domenech; Marie Paule Mingeot-Leclercq; Yves F Dufrêne
Journal:  J Bacteriol       Date:  2008-10-03       Impact factor: 3.490

8.  Functional Identification of Serine Hydroxymethyltransferase as a Key Gene Involved in Lysostaphin Resistance and Virulence Potential of Staphylococcus aureus Strains.

Authors:  Nayab Batool; Kwan Soo Ko; Akhilesh Kumar Chaurasia; Kyeong Kyu Kim
Journal:  Int J Mol Sci       Date:  2020-11-30       Impact factor: 5.923

  8 in total

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