Lecture 6 Flashcards

1
Q

what happens in anaerobic jar?

A

chem rxn remove all O2, gen. H2 and CO2

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2
Q

what happen in candle jar?

A

5-10% cO2 after flame dies, some residual O2

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3
Q

candle jar good for:

A

neisseria (prefer lower O2, req. CO2)

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4
Q

how transport anaerobes?

A

anaerobic transport media

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5
Q

types of culture media

A

simple and complex

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6
Q

simple media good for:

A

grow bacteria have very basic nutr needs (eg. e. coli)

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7
Q

what’s in simple media?

A

glucose+few essential minerals (NaCl)

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8
Q

complex media good for:

A

bacteria that need pre-formed nutr for growth

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9
Q

what’s in complex media?

A

additional nutr like protein, CHO, minerals

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10
Q

best use simple or complex if not sure?

A

complex

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11
Q

why can’t some bacteria not be grown on lab culture media?

A

unusual enviro niche, unusual growth factors

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12
Q

this media has additives toxic to some org but not others

A

selective

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13
Q

examples of selective media

A

sabouraud agar

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14
Q

no inhibitors added to this media

A

differential media

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15
Q

type of differential media

A

blood agar (hemolytic vs nonhemolytic)

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16
Q

hemolytic has ____ around colonies

A

zone of clearing

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17
Q

diagnose ___ with blood agar

A

streptococcus

18
Q

both selective and differential

19
Q

how is MacConkey selective?

A

bile salts and crystal violet inhibit growth gram positive

20
Q

how is MacConkey differential?

A

lactose and pH indicator (lactose metabolized turn red, if not, stay white)

21
Q

chem substance either kill bacteria or prevent from growing

A

antibiotics

22
Q

how antibiotic diff from antiseptics and disinfectants?

A

selective action against bacteria

23
Q

who came up with concept of selective toxicity?

A

Paul Ehrlich

24
Q

Erhlich developed:

A

salvarsan (arsenic)–>syphilus

25
first of sulfa class of antibiotics
prontosil (leather dye)
26
who observed penicillin?
Fleming
27
most antibiotics are:
natural from soil microbes
28
dose which is toxic to host / dose requried kill bacteria is :
TI (therapeutic index)-->higher the better
29
Quinolones and Rifampin work against bacteria through this mechanism:
block DNA/RNA synth
30
inactivates DNA gyrase so no supercoiling:
quinolones
31
binds to RNA polymerase to block mRNA synth
Rifampin
32
how do antibiotics block protein synth?
bind to bacterial ribosome
33
sulfas affect bacteria thru this mechanism:
inhibition of metabolic paths
34
blocks synth of bacterial folic acid by acting as competitive inhibitor (similar to PABA structure)
sulfa
35
polymyxin B affect bacteria thru this mechanism:
disrupt bacterial cell mem by binding to phospholipid and inserting into membrane
36
why polymyxin B used only externally?
poor selective toxicity
37
beta-lactams affect bacteria thru this mechanism:
block PG synth (high TI!)-->bactericidal
38
these act at diff steps during PG synth:
non-beta-lactams (cycloserine, bacitracin, vancomycin)
39
why is static antibiotic + PG blocker antagonistic?
cuz PG blocker only act during PG synth, on cells metabolically active and dividing
40
using antibiotics in combo called:
antibiotic cocktails
41
sulfonamide+trimethoprim is ex. of:
synergism (act on diff parts of same biochem path)
42
synergism allows:
broader spectrum of action, less toxic, less likely resistance