Antibiotics Flashcards
Antimicrobial Agents
- ________: Chemical agents applied to non-living objects with the objective of reducing the number of bacteria, NOT _________ them
- ________: Chemical agents applied to living skin or tissue with the objective of reducing the chance of infection
- _______: Naturally occurring and man-made organic compounds that are used to systematically inhibit or kill bacteria
- ________: General term for antiseptics or antibiotics that have a well-proven ability to inhibit or kill bacteria
- Disinfectants; killing
- Antiseptics
- Antibiotics
- Antibacterials
Antibiotics: Organic Compounds That Inhibit or Kill Microbes
- ________: Any substance produced by a microorganism that is antagonistic to the growth of other microbes in high dilution
- _______ ______ (1888-1973): First lab at Rutgers with a milestone site and was awarded the 1952 Nobel Prize for Physiology or Medicine for discovering __________
- Antibiotic
- Selman Waksman; streptomycin
General Characteristics of Antibiotics
- _______: Kill microbes
- ________: Inhibits growth
- Antibiotics are either ________ or _________, NEVER both
- ______ _______: Effective against both Gram Negative and Positive bacteria
- ______ ______ ______(___): Concentration at which the bacteria stop growing and can be measured using a series of tubes with varying [______] added in serial dilution. Is identified in the first tube where bacteria are no longer _________ and appears ________
- ______-_____ _______: Allows for using different [antibiotic] on different plates that can all be used on the same ______ plate. Measure antibiotic effectiveness by measuring the _____ of ______
- Bactericidal
- Bacteriostatic
- bactericidal; bacteriostatic
- Broad Spectrum
- Minimum Inhibitory Concentration (MIC)
- [antibiotic]; growing; clear
- Kirby-Bauer Method; agar; zone of inhibition
-_______ ______: Impacting and targeting the microorganism specifically without harming the host. Best bacterial target is the cell wall composed of ________
-Selective Toxicity; peptidoglycan
Classification of Antibiotics Based on Their Mechanism of Action
- ___________ of cell wall biosynthesis
- Disruption of _____ _______
- Inhibition of _____ _____ biosynthesis/DNA _________
- Inhibition of ________ synthesis, the ________ group of antibiotics
- Inhibition
- cell membranes
- nucleic acid; replication
- protein; largest
Inhibition of Cell Wall Biosynthesis: Cytoplasm Stage
- General Precursor: ____-_-_______ ____, the carrier for the compounds that serve as substrates
- The first 3 peptides are added to ___-_-_______ _____, then a dipeptide of -___--_______ is added
- ____-_-_______ is added forming a disaccharide-pentapeptide, this is the basic building block of ___________
- UDP-N-Acetylmuramic Acid
- UDP-N-Acetylmuramic Acid
- D-Alanyl-D-Alanine
- UDP-N-Acetylglucosamine; peptidoglycan
Inhibition of Cell Wall Biosynthesis: Cytoplasm Stage
Steps:
1. Addition of -_________, -______ ___, and ____-____ to UDP-N-Acetylmuramic Acid
2. Conversion of _-______ to _-______ which forms the dipeptide _-____--_____ that gets added
3. ____--________ gets added forming the disaccharide-pentapeptide
Antibiotics:
-__-_____ is inhibitory to peptidoglycan since it’s a structural analog of D-Alanine and prevents the addition of -___--______ so no peptidogylcan is synthesized
- L-Alanine; D-Glutamic Acid; meso-DAP
- L-Alanine; D-Alanine; D-Alanyl-D-Alanine
- UDP-N-Acetylglucosamine
- D-Cycloserine; D-Alanyl-D-Alanine
Inhibition of Cell Wall Biosynthesis: Membrane Stage
-The ________-________ complex is very water soluble and cannot cross the hydrophobic membrane on its own
-Addition of a _____ _____ to DAP (amino acid position ___)
-_____ ______: Greater than 50C long and are very large __________ hydrophobic molecules that carry the peptidoglycan precursor _______ the membrane, by attaching to the phosphates on ____-_-_______ ____ .
-Crossing the membrane results in the loss of 2 _________ from the _______-_______ complex, since they remain attached to the ______ _______ Carrier, will lose 1 _______ and then get ______ to be used again
Antibiotics:
-_______: Prevents the recycling of the lipid carrier inhibiting ________ synthesis in Gram Positive and Negative bacteria, but additionally prevents _________(___) biosynthesis in Gram Negative bacteria.
-________: Physically blocks the movement of the lipid carrier with the disaccharide-pentapeptide complex from crossing the membrane
- disaccharide-pentapeptide
- cross bridge; 3
- Isoprenoid Molecules; phosphorylated; across; UDP-N-Acetylmuramic Acid
- phosphates; disaccharide-pentapeptide; Isoprenoid Lipid; phosphate; recycled
- Bacitracin; peptidoglycan; Lipopolysaccharide (LPS)
- Vancomycin
Inhibition of Cell Wall Biosynthesis: Membrane Surface Stage
-A _____ strand must be opened for the disaccharide to be inserted
-The _____ ____ end must be free to be attached to a side chain on another _____ strand. This requires the removal of the terminal __-_______ by _________, AKA Penicillin Binding Protein (PBP)
Antibiotics:
-_______/________ ______: Structural analog of D-alanyl-D-Alanine and will bind to _______/PBPs preventing them from cross-linking ____ strands via amino acid _____-______. This ______ the peptidoglycan causing the cell to ______. Only effective against Gram _______ bacteria
- glycan
- cross bridge; glycan; D-Alanine; transpeptidases
- Penicillin/Penicillanic Acid; transpeptidases; glycan; cross-bridge; weakens; lyse; Positive
The Penicillin β-lactam Family of Antibiotics
-_____ ______(1881-1995) was awarded the 1945 Nobel Prize for Physiology or Medicine for his findings of penicillin
-Penicillin created a zone of inhibition on an agar plate streaked with _________ _____
-The __-_____ ring and the __-_____ bond (connects the _______ and Nitrogen in the ring) are essential to all __-_______ and allows them to act as _______ ______ to D-Alanyl-D-Alanine
-Can modify the __ groups to make the antibiotic more effective at protecting the __-_____ ring and __-____ bond from hydrolysis
Antibiotics:
-______ and _____ have a dihydrothiazine ring and 2 R groups
-_________: Has been modified to where it’s now degraded by acid so can no longer be taken orally
-_______: Modified penicillin with an Amino group attached that makes it now a _______ _______ antibiotic that can target both Gram Positive and Negative bacteria
- Alexander Fleming
- Staphylococcus aureus
- β-lactam; β-lactam; Carbonyl; β-lactams; structural analogs
- R; β-lactam; β-lactam
- Cephalosporins; Cephamycins
- Benzypenicillin
- Ampicillin; broad spectrum
Common Properties of Antibiotics the Inhibit Peptidoglycan Biosynthesis
- All are _________
- Only effective on actively ______ bacteria by inhibiting the _________ matrix
- Most ______/_____ _____ class of antibiotics
- bactericidal
- growing; peptidoglycan
- potent/selectively toxic
Antibiotics That Disrupt the Cell Membrane
-________: Alter permeability by insertion into the cell membrane through interactions with simple phospholipids, meaning they must too be _______. Are more effective against _______ and are considered bactericidal
-______: Alter permeability by insertion in cell membranes through interactions with sterols. Are more effective against ________ cells like _____ and _____.
Includes both _____ and _______ __
- Polymyxins; amphipathic; bacteria
- Polyenes; eukaryotic; fungi; yeast; Nystatin; Amphotericin B
Antibiotics that Inhibit Nucleic Acid Biosynthesis/DNA Replication
-________: Inhibit DNA replication by binding to and inhibiting DNA Gyrase. The _____ group.
______ binding to subunit A of DNA Gyrase:
-________ ___
-________
-________
-Both _____ and _____ have attached fluorine groups that makes them more effective and considered ____________
_______ binding to subunit B of DNA Gyrase:
-_______
- Quinolones; largest
- Quinolones
- Nalidixic Acid
- Ciprofloxacin
- Norfloxacin
- Ciprofloxacin; Norfloxacin; fluoroquinolones
- Quinolones
- Novobiocin
Antibiotics that Inhibit Nucleic Acid Biosynthesis/DNA Replication
- ___________: Inhibit DNA replication by producing free radicals and is very effective in _________ treatment since ROS are very effective at killing ________ bacteria
- __________: Inhibit transcription by binding to the B subunit of RNA Polymerase, _____/______ is an example
- ________: Inhibit the synthesis of tetrahydrofolic acid by inactivating enzymes in nucleic acid synthesis that form it. Selectively toxic since humans cannot synthesize ____ ____ (Vitamin B9 or M)
- Metronidazole; periodontal; anaerobic
- Rifamycins; Rifampicin/Rifampin
- Sulfonamides; folic acid
Antibiotics Effecting Protein Synthesis
30S Subunit Antibiotics
-________: Bind to the 30S and interfere with binding of tRNA to the ribosomal complex. Discovered by _____ ____ _____ (1872-1956), a total of __ R groups allows for many different derivates and is thought to have originated from _____
-_________: Bind to the 30S and cause the mRNA codon to be misread, interfering with the initiation complex of the 30S and 50S with mRNA.
50S Subunit Antibiotics:
-__________: Binds to the 50S and inhibits formation of peptide bonds
-________/________: Block the polypeptide E site on the 50S preventing the elongation of the polypeptide chain
- Tetracycline; Benjamin Minge Duggar; 4; beer
- Aminoglycosides
- Chloramphenicol
- Macrolides/Clindamycin