Skip to main content
  • 110 Accesses

Abstract

In the search for differences between microbial pathogens and animal cells that could provide the basis for selective antimicrobial attack, one evident distinction lies in their general structure. The animal cell is relatively large and has a complex organization; its biochemical processes are compartmentalized and different functions are served by the nucleus with its surrounding membrane, by the mitochondria and by various other organelles. The cytoplasmic membrane is thin and lacks rigidity. The cell exists in an environment controlled in temperature in mammals and birds and also in osmolarity. It is constantly supplied with nutrients from the extracellular fluid. Bacteria and fungi live in variable and often hostile environments and they must be able to withstand considerable changes in external osmolarity. Some micro-organisms have relatively high concentrations of low molecular weight solutes in their cytoplasm. Such cells suspended in water or in dilute solutions develop a high internal osmotic pressure. This would inevitably disrupt the cytoplasmic membrane unless it were provided with a tough, elastic outer coat. This coat is the cell wall, a characteristic of bacteria and fungi which is entirely lacking in animal cells. It has a protective function but at the same time it is vulnerable to attack, and a number of antibacterial and antifungal drugs owe their action to their ability to disturb the processes by which the walls are synthesized. Since there is no parallel biosynthetic mechanism in animal cells, substances affecting this process may be highly selective in their antimicrobial action.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 84.99
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Further reading

  • Brennan, P.J. (1995). The envelope of mycobacteria. Ann. Rev. Biochem. 64, 29–63.

    Article  Google Scholar 

  • Debono, M. and Gordee, R.S. (1994). Antibiotics that inhibit fungal cell wall development. Ann. Rev. Microbiol. 48, 471–97.

    Article  Google Scholar 

  • Doyle, R.J. and Marquis, R.E. (1994). Elastic, flexible peptidoglycan and bacterial cell wall properties. Trends Microbiol. 2, 57–60.

    Article  Google Scholar 

  • Georgopapadakou, N.H. and Tkacz, J.S. (1995). The fungal cell wall as a drug target. Trends Microbiol. 3, 98.

    Article  Google Scholar 

  • Ghuysen, J.-M. (1991). Serine ß-lactamases and penicillin-binding proteins. Ann. Rev. Microbiol. 45, 37–67.

    Article  Google Scholar 

  • Ghuysen, J.-M. et al. (1996). Penicillin and beyond: evolution, protein fold, multimodular polypeptides and multiprotein complexes. Microb. Drug Resist. 2, 163–75.

    Article  Google Scholar 

  • Hancock, R.E. (1997). The bacterial outer membrane as a drug permeability barrier. Trends Microbiol. 5, 37–42.

    Article  Google Scholar 

  • Johnsson, K. and Schulz, PG. (1994). Mechanistic studies of the oxidation of isoniazid by the catalase-peroxidase from Mycobacterium tuberculosis. J. Am. Chem. Soc. 116, 7425–6.

    Article  Google Scholar 

  • Kurtz, M.B. and Douglas, C.M. (1997). Lipopeptide inhibitors of fungal glucan synthase. J. Med. Vet. Mycol. 35, 79.

    Article  Google Scholar 

  • Prescott, L.M., Harley, J.P and Klein, D.A. (1996). Microbiology, Wm. C. Brown, Dubuque IA.

    Google Scholar 

  • Schaffet, L.M., Schneider, T.R and Sheldrick G.M. (1996). Crystal structure of vancomycin. Structure 4, 1509–15.

    Article  Google Scholar 

  • Skarzynski, T. et al. (1996). Structure of UDP-N-acetyl glucosamine enol pyruvyl transferase: an enzyme essential for the synthesis of bacterial peptidoglycan, complexed with substrate UDP-N-acetyl glucosamine and the drug fosfomycin. Structure 4, 1465–74.

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 1998 The Kluwer Academic Publishers

About this chapter

Cite this chapter

Franklin, T.J., Snow, G.A. (1998). Vulnerable shields — the cell walls of bacteria and fungi. In: Biochemistry and Molecular Biology of Antimicrobial Drug Action. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-9127-5_2

Download citation

  • DOI: https://doi.org/10.1007/978-94-010-9127-5_2

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-0-412-82190-5

  • Online ISBN: 978-94-010-9127-5

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics