- Beta-lactam
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-|A beta-lactam ring (β-lactam) or penam is alactam with aheteroatomic ring structure , consisting of threecarbon atoms and onenitrogen atom [Heterocyclic chemistry T.L. Gilchrist ISBN 0-582-01421-2 ] .Clinical significance
The beta-lactam ring is part of the structure of several
antibiotic families, principally thepenicillin s,cephalosporins ,carbapenem s andmonobactam s, which are therefore also called "beta-lactam antibiotic s". These antibiotics work by inhibiting the bacterialcell wall synthesis. This has a lethal effect on bacteria, especially onGram-positive ones. Bacteria can become resistant against beta-lactam antibiotics by expressingbeta-lactamase .History
The first synthetic β-lactam ever was prepared by
Hermann Staudinger in 1907 by reaction of theSchiff base ofaniline andbenzaldehyde withdiphenylketene ["Hugo (Ugo) Schiff, Schiff Bases, and a Century of b-Lactam Synthesis" Thomas T. TidwellAngew. Chem. Int. Ed. 2008, 47, 1016–1020 DOI|10.1002/anie.200702965 ] [H. Staudinger, Justus Liebigs Ann. Chem. 1907, 356, 51 – 123.] in a [2+2]cycloaddition ::Beta-lactam resistance
Because of the popularity of beta-lactam drugs, certain bacteria have been able to develop counter-measures to traditional drug therapies. An enzyme called
beta-lactamase is present in many different types of bacteria, which serves to 'break' the beta lactam ring, which effectively nullifies the antibiotic's effectiveness.As a response to bacterial resistance to beta-lactam drugs, there are drugs, such as
Augmentin , which are designed to disable the beta-lactamase enzyme.Augmentin is made ofamoxicillin , a beta-lactam antibiotic, andclavulanic acid , a beta-lactamase inhibitor. The clavulanic acid is designed to overwhelm all beta-lactamase enzymes, bind irreversibly to them, and effectively serve as an antagonist so that the amoxicillin is not affected by the beta-lactamase enzymes.Secondary beta-lactam drug resistance
As a response to decreased efficacy of beta-lactamase, some bacteria have changed the proteins that beta-lactam antibiotics bind, the
penicillin binding proteins (PBPs). Since the PBPs no longer recognize the beta-lactams, the antibiotics are essentially useless. This is the mechanism behind the methicillin-resistant Staphylococcus aureus (MRSA).See also
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ATC code J01#J01C Beta-lactam antibacterials.2C penicillins
*Bacteria External links
* [http://www.organic-chemistry.org/synthesis/heterocycles/lactams/beta-lactams.shtm Synthesis of beta-lactams]
References
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