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. 1965 Aug 1;26(2):657–667. doi: 10.1083/jcb.26.2.657

THE INITIAL STRUCTURAL LESION OF PENICILLIN ACTION IN BACILLUS MEGATERIUM

Philip Fitz-James 1, Ronald Hancock 1
PMCID: PMC2106740  PMID: 4956030

Abstract

The effect of penicillin on the structure of Bacillus megaterium cells was followed in media with and without osmotic stabilization. In peptone without osmotic support the cells showed a distortion of the normal membrane-wall relationship by 20 minutes. This appeared to be a combination of both membrane distortion and cytoplasmic leakage. Lytic changes quickly followed. With osmotic support a clean-cut lesion at the transverse-septal site developed by 10 minutes' growth in penicillin. The membrane lost its normal relationship to the cell wall and formed a pocket which was filled with a fibrous material which appeared to be unorganized wall mucopeptide. The pocket of fibers enlarged until the cell either lysed or formed a protoplast.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. COLLINS J. F., RICHMOND M. H. A structural similarity between N-acetylmuramic acid and penicillin as a basis for antibiotic action. Nature. 1962 Jul 14;195:142–143. doi: 10.1038/195142a0. [DOI] [PubMed] [Google Scholar]
  2. FITZ-JAMES P. C. Cytological and chemical studies of the growth of protoplasts of Bacillus megaterium. J Biophys Biochem Cytol. 1958 May 25;4(3):257–266. doi: 10.1083/jcb.4.3.257. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. FITZ-JAMES P. C. Participation of the cytoplasmic membrane in the growth and spore fromation of bacilli. J Biophys Biochem Cytol. 1960 Oct;8:507–528. doi: 10.1083/jcb.8.2.507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. FITZ-JAMES P. FATE OF THE MESOSOMES OF BACILLUS MEGATERIUM DURING PROTOPLASTING. J Bacteriol. 1964 Jun;87:1483–1491. doi: 10.1128/jb.87.6.1483-1491.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Fitz-James P. Electron microscopy of Bacillus megaterium undergoing isolation of its nuclear bodies. J Bacteriol. 1964 May;87(5):1202–1210. doi: 10.1128/jb.87.5.1202-1210.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Hancock R., Fitz-James P. C. Some differences in the action of penicillin, bacitracin, and vancomycin on Bacillus megaterium. J Bacteriol. 1964 May;87(5):1044–1050. doi: 10.1128/jb.87.5.1044-1050.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. MURRAY R. G., FRANCOMBE W. H., MAYALL B. H. The effect of penicillin on the structure of staphylococcal cell walls. Can J Microbiol. 1959 Dec;5:641–648. doi: 10.1139/m59-078. [DOI] [PubMed] [Google Scholar]
  8. PARK J. T. Uridine-5'-pyrophosphate derivatives. III. Amino acid-containing derivatives. J Biol Chem. 1952 Feb;194(2):897–904. [PubMed] [Google Scholar]
  9. RYTER A., KELLENBERGER E. L'inclusion au polyester pour l'ultramicrotomie. J Ultrastruct Res. 1958 Dec;2(2):200–214. doi: 10.1016/s0022-5320(58)90018-2. [DOI] [PubMed] [Google Scholar]
  10. RYTER A., LANDMAN O. E. ELECTRON MICROSCOPE STUDY OF THE RELATIONSHIP BETWEEN MESOSOME LOSS AND THE STABLE L STATE (OR PROTOPLAST STATE) IN BACILLUS SUBTILIS. J Bacteriol. 1964 Aug;88:457–467. doi: 10.1128/jb.88.2.457-467.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. SALTON M. R. Studies of the bacterial cell wall. IV. The composition of the cell walls of some Gram-positive and Gram-negative bacteria. Biochim Biophys Acta. 1953 Apr;10(4):512–523. doi: 10.1016/0006-3002(53)90296-0. [DOI] [PubMed] [Google Scholar]
  12. STROMINGER J. L., PARK J. T., THOMPSON R. E. Composition of the cell wall of Staphylococcus aureus: its relation to the mechanism of action of penicillin. J Biol Chem. 1959 Dec;234:3263–3268. [PubMed] [Google Scholar]

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