2.2.2 Antibiotics I Flashcards

1
Q

Compare and contrast the Gram positive and Gram negative cell structure

A

Gram POSITIVE = thick, outer layer of peptidoglycan, single cellular membrane

Gram NEGATIVE = thin layer of peptidoglycan, two membranes (outer and inner)

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2
Q

What are the two disaccharides that polymerize to make peptidoglycan?

A

N-acetyl glucosamine, and N-acetyl muramic acid

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3
Q

In Gram (+) bacteria, how many Glycine amino acids form “bridges” between glycan strands?

What is a functional consequence of this structure?

A

Five - these are called “pentapeptide bridges”.

This structure makes the bacterial cell wall thicker and more heavily cross-linked.

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4
Q

What is transpeptidation?

What amino acids are involved, and in what positions are they?

A

Transpeptidation is the cross-linking of peptides.

The COOH of D alanine of position 4 binds to NH2 side chain of amino acid 3 on opposing strand. Gram positives have an extra bridge of 5 glycine residues.

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5
Q

What enzymes catalyze transpeptidase cross-linking?

A

Transpeptidases and carboxypeptidases

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6
Q

What amino acids do transpeptidases and carboxypeptidases recognize?

A

They recognize D-alanine to D-alanine linkages

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7
Q

How are transpeptidases and carboxypeptidases inhibited by beta-lactam antibiotics (like penicillin)?

A

They can be competitively bound by these beta-lactam molecules because these molecules have a similar structure to the natural substrate (D-Ala to D-Ala).

This effectively stops bacterial cell wall synthesis.

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8
Q

What are penicillin-binding proteins (PBPs)?

A

PBPs are a group of proteins that are characterized by their affinity for and binding of penicillin. They are a normal constituent of many bacteria; the name simply reflects the way by which the protein was discovered!

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9
Q

Name four beta-lactam antibiotics

A
  1. Monobactam
  2. Penicillin
  3. Cephalosporin (or Cephamycin)
  4. Carbapenem
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10
Q

The bactericidal action of the beta-lactam antibiotics requires the following four steps:

A
  1. Association of the drug w/the bacteria.
  2. Penetration through the OUTER membrane and the PERIPLASMIC space (only Gm -).
  3. Interaction w/penicillin-binding proteins (PBPs) on the CYTOPLASMIC membrane.
  4. Activation of an autolysin that degrades the murein in the CELL WALL.
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11
Q

What two strategies to bacteria use to evade beta-lactam antibiotics?

A
  1. Produce a substance that inactivates the antibiotic (eg synthesis of beta-lactamase, which cleaves penicillin)
  2. Alter the target of the drug
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12
Q

Name three drugs that are resistant to cleavage by beta-lactamase

A
  1. Methicillin
  2. Oxacillin
  3. Nafcillin
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13
Q

How is methicillin is different from penicillin?

A

Methicillin is not bound and hydrolysed by penicillinase (even though it has a beta-lactam ring), meaning it can kill the bacteria, even if this enzyme is present

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14
Q

How does the mechanism of methicillin resistance differ from that of penicillin resistance?

A

Bacteria changed the target of drug interaction (done in two ways):

  1. Random mutations in PBP2, encoded by the mecA gene. mecA simply encodes for an alternative PBP.
  2. There is a higher frequency of transposons acquired during conjugation that jump into chromosome, conferring resistance.
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15
Q

If you have a bacteria that synthesizes beta-lactamase, what might be an effective treatment against it?

A

Use beta-lactamase inhibitors in conjunction with antibiotics.

Example: augmentin - a combined therapy with amoxicillin and clavulanic acid.

Amoxicillin is used to treat stomach ulcers and infections

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16
Q

What is the target recognized by vancomycin?

Describe the pathway that is inhibited as a result.

A

Binds to D-Ala D-Ala on MurNAc of the repeating disaccharides. Vancomycin sterically inhibits transglycosylation!

17
Q

How do bacteria develop vancomycin resistance?

A

By creating a change in the target molecule!

Some strains acquire genes via horizontal transfer to make (D-alanyl-D-serine) or (D-alanyl-D-lactate) instead.

This type of resistance is rare.

18
Q

Name two antibiotics that inhibit bacterial cell membranes.

A
  1. Polymyxin - an antibiotic produced by bacteria (used to create a niche against other bacteria). Polymyxin aggregates on the cell membrane and the lipid tail inserts into it. Polymyxin is a narrow spectrum antibiotic for gram negatives.
  2. Daptomycin - is similar to polymyxin, but for Gram (+).

Daptomycin has a cyclic amino acid structure which acts similarly to polymyxin.

Loss of the bacteria’s membrane potential and integrity leads to cell death.

Daptomycin is a good alternative to vancomycin for MRSA.