Minggu, 10 Juni 2012

LACTAM


Beta-lactam ring structure.
Beta-lactam antibiotics are a class of antibiotics that have a common structural component in the form of beta-lactam ring and is commonly used to treat bacterial infections .There are approximately ± 56 kinds antibotik beta-lactam antimicrobials that have activity in the beta-laktamnya ring and if the ring is cut by microorganisms, there will be resistance to these antibiotics.
The types of
Beta-lactam antibiotics is divided into four main groups, namely penicillin, cephalosporin, carbapenem, and monobactam .

Amoxicillin is one example of penicillin
Based on the spectrum antimikrobialnya activity, penicillin is divided into 4 groups, namely penicillin early (earlier), penicillin spektruk broad, anti-staphylococcal penicillins, and anti-pseudomonal penicillin (expanded spectrum) .Early penicillin is actively able to fight bacteria that are sensitive, such as beta-hemolytic Streptococcus group, alpha-hemolytic Streptococcus in combination with an aminoglycoside), pneumococcus, meningococcus, and Clostridium groups other than C. difficile .Examples of previous penicillin is penicillin G and penicillin V .Broad-spectrum penicillins have the ability to fight and the enteric bacteria more easily absorbed by the gram-negative bacteria but is still susceptible to the degradation of beta-lactamase, such as ampicillin, amoxicillin, mesilinam, bacampicillin, etc. Anti-staphylococcal penicillin was developed in the 1950s to cope with S. aureus that produce beta-lactamase and has the advantage of resistance to beta-lactamase activity. Examples of this group are methicillin and cloxacillin .Anti-pseudomonal penicillin made ​​to overcome the bacterial infection gram negative bacilli, including Pseudomonas aeruginosa, an example of this group are penicillin carbenicillin, ticarcillin, Azlocillin, and piperacillin

Cephalosporin
Antibioik divided into 3-generation cephalosporins, cephalothin and the first is that cephaloridine is not widely used .The second generation (among others: cefuroxime, cefaclor, cefadroxil, cefoxitin, etc..) Is widely used to address severe infections and some of which have activity against anaerobic bacteria .The third generation of cephalosporins (among them: ceftazidime, cefotetan, latamoxef, cefotetan, etc..) Made in the 1980s to cope with severe systemic infections due to gram-negative bacilli

Carbapenem
There is only one class of carbapenem antibiotic agents that are used for clinical care, namely imipenem has excellent antibacterial ability against gram-negative bacilli (including P. aeruginosa, Staphylococcus, and Bacteroides) .The use of imipenem must be combined with specific enzyme inhibitors to protect it from degragasi of liver enzymes in the body [
Monobactam
This group has the structure of beta-lactam ring is not bound to the second ring in the molecule
.One of this class of antibiotics commonly used is the aztreonam is active against many gram-negative bacteria, including P. Aeruginosa.
Mechanism of action
Beta-lactamase antibiotics work by killing bacteria menginhibisi cell wall synthesis. In the process of cell wall formation, a reaction catalyzed by the enzyme transpeptidasi transpeptidase and produce a bond between two peptide chains cross-glucan. Transpeptidase enzyme which is located on the cytoplasmic membrane of bacteria can also bind to beta-lactam antibiotics that cause the enzyme is not able to catalyze the reaction of the cell wall transpeptidasi although still continue to be formed. Cell wall is formed has no crosslinking and peptidoglycan formed is not perfect so much weak and easily degraded. In normal conditions, the difference in osmotic pressure within cells and gram-negative bacteria in the environment will make the occurrence of cell lysis .In addition, the complex protein transpeptidase and beta-lactam antibiotics will stimulate autolisin compounds that can mendigesti the bacterial cell wall .Thus, the loss of bacterial cell walls or through lysis will die.

mechanisms of resistance
Degradation mechanisms of beta-lactam antibiotics by the enzyme beta-lactamase.

Some bacteria are known to have resistance to beta-lactam antibiotics, one of which is the class of methicillin-resistant S. aureus (methicillin resistant Staphylococcus aureus / MRSA) . Bacteria that are resistant to beta-lactam antibiotics has three mechanisms of resistance, the destruction of the beta-lactamase antibiotics, reduce the penetration of antibiotic to bind to the protein transpepidase, and lower binding affinity of these binding proteins with antibiotic compounds . Some bacteria such as Haemophilus influenzae, Staphylococcus group, and most of the rod-shaped enteric bacteria have beta-lactamase enzymes that break down beta-lactam ring in antibiotics and makes it inactive. In detail, the mechanisms that occur beginning with the termination of the CN bond in the ring beta-lactam antibiotics and the resulting protein can not bind to transpeptdase resulting in loss of ability to menginhibisi formation of bacterial cell wall . Some studies suggest that in addition found naturally on gram positive and negative bacteria, the gene encoding the enzyme beta-lactamase was also found on the plasmid and the transposon so that it can be transferred between species of bacteria. This causes the resistance ability of the beta-lactam antibiotics would be able to spread rapidly. Diffusion of beta-lactam antibiotics into bacterial cells occurs through the mediation of transmembrane proteins called porine and diffusion capacity is influenced by size, charge, and the hydrophilic nature of the antibiotic.


Overcoming beta-lactam antibiotic resistance
Clavulanic acid, beta-lactamase inhibitor.
To overcome the degradation of beta-lactam cincing, some beta-lactam antibiotics combined with the enzyme inhibitor compounds such as beta-lactamase clavulanat acid, tazobactam, or sulbactam. One of the beta-lactam antibiotic-resistant beta-lactamase is augmentin, Amoxycillin and clavulanic acid combination. Augmentin has been proven to successfully overcome the bacterial infection in the urinary tract and skin [10]. Yng clavulanic acid is produced from the fermentation of Streptomyces clavuligerus has the ability to inhibit the enzyme beta-lactamase active, causing the enzyme to be inactive. Some types of beta-lactam antibiotics (eg, nafcillin) also have properties resistant to beta-lactamase because it has a side chain with a specific location.


references
http://id.wikipedia.org/wiki/Antibiotik_beta-laktam

2 komentar:

  1. whether you can explain how betalactam work as an antibiotic

    BalasHapus
    Balasan
    1. β-Lactam antibiotics are bacteriocidal, and act by inhibiting the synthesis of the peptidoglycan layer of bacterial cell walls. The peptidoglycan layer is important for cell wall structural integrity, especially in Gram-positive organisms, being the outermost and primary component of the wall. The final transpeptidation step in the synthesis of the peptidoglycan is facilitated by transpeptidases [disambiguation needed ] known as penicillin-binding proteins (PBPs). PBPs vary in their affinity for binding penicillin or other β-lactam antibiotics. The amount of PBPs varies among bacterial species.

      β-Lactam antibiotics are analogues of d-alanyl-d-alanine—the terminal amino acid residues on the precursor NAM/NAG-peptide subunits of the nascent peptidoglycan layer. The structural similarity between β-lactam antibiotics and d-alanyl-d-alanine facilitates their binding to the active site of PBPs. The β-lactam nucleus of the molecule irreversibly binds to (acylates) the Ser403 residue of the PBP active site. This irreversible inhibition of the PBPs prevents the final crosslinking (transpeptidation) of the nascent peptidoglycan layer, disrupting cell wall synthesis.
      thanks before via,,,,,
      you can visit this link to get more information,
      http://en.wikipedia.org/wiki/Beta-lactam_antibiotic

      Hapus