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ANTIBACTERIAL AGENTS
I AM
ANTIBACTERIA..

I AM BACTERIA
…PLZ SPARE
ME….

BY: MINHAZ AHMED
Intgrated M.Sc 4th sem
BBI11014
What are antibacterial agents?
An antibacterial is an agent that inhibits bacterial growth or kills bacteria.
often used synonymously with the term antibiotic(s).
The term antibiotic was first used in 1942 by Selman Waksman.
WHY ANTIBACTERIALS?

Bacterial conjuctivities: pink eye

Bacterial Leaf Blight of soybean is
caused by the
bacterium Psuedomonas syringae

Skin spots by bacterial activities

Bacterial Canker
HOW ARE THEY CLASSIFIED?
on the basis of chemical/biosynthetic origin into
Natural (ex- penicillin)
 semisynthetic
 synthetic(ex-Sulfanilamide)
On biological activity; according to their biological effect on
microorganisms:
 bactericidal agents kill bacteria,
and bacteriostatic agents slow down or stall bacterial growth.
The bacterial cell
The success of antibacterial agents owes much to the fact that they can act
selectively
against bacterial cells rather than animal cells.
 This is largely due to the fact that
bacterial cells and animal cells differ both in their structure and in the biosynthetic
pathways which proceed inside them.
WHERE THEY WORK?

Rifamycins

Penicillins
Cephalosporins
cycloserine

capsule
Cell wall

cytoplasm

polymyxins
sulfonamides

Chloramphenicol
Streptomycin
tetracyclines

Ribosomes
MECHANISM OF ACTIONS

Inhibition of cell
wall synthesis
Penicillins
Cephalosphorins
Imipenem
Meropenem
Aztreonam
vancomycin

Inhibition of
bacterial protein
synthesis
Aminoglycosides
Chloramphenicol
Macrolides
Tetracycline
Streptogrmins
linezolid

Inhibition of
Nucleic Acid
Synthesis
Fluoroquinolones
Rifampin

Inhibition of
Folic Acid
Synthesis
Sulfonamides
Trimethoprim
Pyrimethamine
Inhibition of cell wall synthesis:
Penicillins, cephalosphorins, imipenem, meropenem, aztreonam,
vancomycin
bacteriocidal
Must have beta-lactum ring in them which binds and blocks
transpeptidases known as penicillin-binding proteins(PBP) which causes the
final cross links between the pentapeptides of peptidoglycan layer.
Mechanism of resistance:

Penicillin

Penicillinases: break the
beta lactam ring structure (
staphylococci)
Structural changes in PBP’s
(MRSA), S. pneumococci

cephalosporin

Change in porin structure:
concerns the gram negative
organism
Inhibition of bacterial protein synthesis
Aminoglycosides,Chloramphenicol,Macrolides,Tetracycline,Streptogrmins, Linezolid.
Bactericidal and bacteriostatic.
 The primary steps in the process that are attacked are
 the formation of the 30S initiation complex (made up of mRNA, the 30S ribosomal
subunit and formyl-methionyl-transfer RNA),ex Streptomycin (A-glycosides)
 the formation of the 70S ribosome by the 30S initiation complex and the 50S ribosome,ex
Kanamycin and tobramycin and
 the elongation process of assembling amino acids into a polypeptide.ex Lincomycin,
chloramphenicol.

RIBOSOME
Erythromycin:
Binds to 50S-rRNA &
prevents movement
along mrna
Mechanisms of resistance:

a mutation of ribosomal
binding site
enzymatic modification of
antibiotic
an active efflux of antibiotic
out of cell
Streptomycin
Inhibition of Nucleic Acid Synthesis
Fluoroquinolones(levofloxacin, norfloxacin),Rifampin
Bacteriocidal
Can inhibit DNA gyrase or RNA polymerase
Mechanism of resistance:
an alteration of alpha subunit of DNA gyrase
(chromosomal)
beta subunit of RNA polymerase (chromosomal) is
altered
Quinolones are a key group of antibiotics that interfere with DNA synthesis by
inhibiting topoisomerase, most frequently topoisomerase Iv and topoisomer ii (DNA
gyrase) , an enzyme involved in DNA replication. DNA gyrase relaxes supercoiled
DNA molecules and initiates transient breakages and rejoins phosphodiester bonds
in superhelical turns of closed-circular DNA. This allows the DNA strand to be
replicated by DNA or RNA polymerases.
Rifampicin blocks initiation of RNA synthesis by specifically inhibiting bacterial
RNA polymerase. It does not interact with mammalian RNA polymerases,
making it specific for Gram-positive bacteria and some Gram-negative
bacteria.

Mechanism of resistance:
an alteration of alpha subunit of DNA gyrase
(chromosomal)
beta subunit of RNA polymerase (chromosomal) is altered
Inhibition of Folic Acid Synthesis
Sulfonamides, Trimethoprim, Pyrimethamine
Bacteriostatic
Binds and blocks enzymes mainly pteridine synthesase, dihydrofolate
reductase responsible for folic acid synthesis.

What are Folic Acid?
Folic acid enzymes are nessary for the synthesis of amino acids, hence necessary for bacterial protein
synthesis.

Folic acid
Sulfonamide functional group

trimethoprim

Pyrimethamine

Pyrimethamine

Mechanism of resistance:
Mutations in the gene for
dihydrofolate reductase
decreasing binding affinity .
Some Side affects of antibacterial agents
ANTIBACTERIAL AGENTS

SIDE EFFECTS

Aminoglycosides

renal (kidney) toxicity, ototoxicity (hearing
loss), dizziness, nausea/vomiting,
nystagmus

Sulfonamides

nausea/vomiting, diarrhea, anorexia,
abdominal pain, rash, photosensitivity,
headache, dizziness

Tetracyclines

nausea/vomiting, diarrhea, anorexia,
abdominal pain, tooth discoloration in
children < 8 years, liver toxicity

Quinolones

nausea/vomiting, diarrhea, abdominal
pain, headache, lethargy, insomnia,
photosensitivity (can be severe)
Antibacterial agents

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Antibacterial agents

  • 1. ANTIBACTERIAL AGENTS I AM ANTIBACTERIA.. I AM BACTERIA …PLZ SPARE ME…. BY: MINHAZ AHMED Intgrated M.Sc 4th sem BBI11014
  • 2. What are antibacterial agents? An antibacterial is an agent that inhibits bacterial growth or kills bacteria. often used synonymously with the term antibiotic(s). The term antibiotic was first used in 1942 by Selman Waksman.
  • 3. WHY ANTIBACTERIALS? Bacterial conjuctivities: pink eye Bacterial Leaf Blight of soybean is caused by the bacterium Psuedomonas syringae Skin spots by bacterial activities Bacterial Canker
  • 4. HOW ARE THEY CLASSIFIED? on the basis of chemical/biosynthetic origin into Natural (ex- penicillin)  semisynthetic  synthetic(ex-Sulfanilamide) On biological activity; according to their biological effect on microorganisms:  bactericidal agents kill bacteria, and bacteriostatic agents slow down or stall bacterial growth.
  • 5. The bacterial cell The success of antibacterial agents owes much to the fact that they can act selectively against bacterial cells rather than animal cells.  This is largely due to the fact that bacterial cells and animal cells differ both in their structure and in the biosynthetic pathways which proceed inside them.
  • 6. WHERE THEY WORK? Rifamycins Penicillins Cephalosporins cycloserine capsule Cell wall cytoplasm polymyxins sulfonamides Chloramphenicol Streptomycin tetracyclines Ribosomes
  • 7. MECHANISM OF ACTIONS Inhibition of cell wall synthesis Penicillins Cephalosphorins Imipenem Meropenem Aztreonam vancomycin Inhibition of bacterial protein synthesis Aminoglycosides Chloramphenicol Macrolides Tetracycline Streptogrmins linezolid Inhibition of Nucleic Acid Synthesis Fluoroquinolones Rifampin Inhibition of Folic Acid Synthesis Sulfonamides Trimethoprim Pyrimethamine
  • 8. Inhibition of cell wall synthesis: Penicillins, cephalosphorins, imipenem, meropenem, aztreonam, vancomycin bacteriocidal Must have beta-lactum ring in them which binds and blocks transpeptidases known as penicillin-binding proteins(PBP) which causes the final cross links between the pentapeptides of peptidoglycan layer. Mechanism of resistance: Penicillin Penicillinases: break the beta lactam ring structure ( staphylococci) Structural changes in PBP’s (MRSA), S. pneumococci cephalosporin Change in porin structure: concerns the gram negative organism
  • 9.
  • 10. Inhibition of bacterial protein synthesis Aminoglycosides,Chloramphenicol,Macrolides,Tetracycline,Streptogrmins, Linezolid. Bactericidal and bacteriostatic.  The primary steps in the process that are attacked are  the formation of the 30S initiation complex (made up of mRNA, the 30S ribosomal subunit and formyl-methionyl-transfer RNA),ex Streptomycin (A-glycosides)  the formation of the 70S ribosome by the 30S initiation complex and the 50S ribosome,ex Kanamycin and tobramycin and  the elongation process of assembling amino acids into a polypeptide.ex Lincomycin, chloramphenicol. RIBOSOME
  • 11. Erythromycin: Binds to 50S-rRNA & prevents movement along mrna
  • 12. Mechanisms of resistance: a mutation of ribosomal binding site enzymatic modification of antibiotic an active efflux of antibiotic out of cell Streptomycin
  • 13. Inhibition of Nucleic Acid Synthesis Fluoroquinolones(levofloxacin, norfloxacin),Rifampin Bacteriocidal Can inhibit DNA gyrase or RNA polymerase Mechanism of resistance: an alteration of alpha subunit of DNA gyrase (chromosomal) beta subunit of RNA polymerase (chromosomal) is altered
  • 14. Quinolones are a key group of antibiotics that interfere with DNA synthesis by inhibiting topoisomerase, most frequently topoisomerase Iv and topoisomer ii (DNA gyrase) , an enzyme involved in DNA replication. DNA gyrase relaxes supercoiled DNA molecules and initiates transient breakages and rejoins phosphodiester bonds in superhelical turns of closed-circular DNA. This allows the DNA strand to be replicated by DNA or RNA polymerases.
  • 15. Rifampicin blocks initiation of RNA synthesis by specifically inhibiting bacterial RNA polymerase. It does not interact with mammalian RNA polymerases, making it specific for Gram-positive bacteria and some Gram-negative bacteria. Mechanism of resistance: an alteration of alpha subunit of DNA gyrase (chromosomal) beta subunit of RNA polymerase (chromosomal) is altered
  • 16. Inhibition of Folic Acid Synthesis Sulfonamides, Trimethoprim, Pyrimethamine Bacteriostatic Binds and blocks enzymes mainly pteridine synthesase, dihydrofolate reductase responsible for folic acid synthesis. What are Folic Acid? Folic acid enzymes are nessary for the synthesis of amino acids, hence necessary for bacterial protein synthesis. Folic acid
  • 17. Sulfonamide functional group trimethoprim Pyrimethamine Pyrimethamine Mechanism of resistance: Mutations in the gene for dihydrofolate reductase decreasing binding affinity .
  • 18. Some Side affects of antibacterial agents ANTIBACTERIAL AGENTS SIDE EFFECTS Aminoglycosides renal (kidney) toxicity, ototoxicity (hearing loss), dizziness, nausea/vomiting, nystagmus Sulfonamides nausea/vomiting, diarrhea, anorexia, abdominal pain, rash, photosensitivity, headache, dizziness Tetracyclines nausea/vomiting, diarrhea, anorexia, abdominal pain, tooth discoloration in children < 8 years, liver toxicity Quinolones nausea/vomiting, diarrhea, abdominal pain, headache, lethargy, insomnia, photosensitivity (can be severe)