Microbiology Flashcards

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1
Q

Prokaryotes def:-

A

Organism group which contains bacteria and fungi, have no membrane-bound nucleus, no double membraned organelles and have circular DNA.

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2
Q

Archaebacteria:1

A

Bacteria which thrive in extreme environments.

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3
Q

3 archaebacteria sub-divisions:-

A
  • Methanogenic
  • halophilic
  • thermoacidophilic
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4
Q

Methanogenic archaebacteria:-

A

Inhabit anaerobic habitats and give off methane as metabolic product. Are responsible for cattle intestinal gases.

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5
Q

Halophilic archaebacteria:-

A

Live in v. salty conditions. Grow in salt concs about 10 times that of sea water.

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6
Q

Thermoacidophilic archaebacteria:-

A

Can live in hot acidic springs where temps may exceed 100oC and pH may be as low as 2.

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7
Q

Eubacteria:-

A

Make up remaining bacteria and are found in all but the most extreme environments.

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8
Q

Photoautotrophs:-

A

Use light energy for nutrition.

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9
Q

Chemoautotrophs:-

A

Use chemical energy for nutrition.

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10
Q

Cyanobacteria:-

A

Photoautotrophs which photosynthesise in a similar way to plants and algae:- co2 +h2o ->(light) carbohydrate + O2

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11
Q

4 main bacterial cell shapes:-

A
  • cocci
  • bacilli
  • spirilla
  • vibrios
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12
Q

Cocci:-

A

Singular = coccus

Spherical shape. Come single, in bunches and in chains.

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13
Q

Bacilli:-

A

Singular = bacillus.
Rod shaped e.g salmonella, e.coli.
Come as single and in chains.

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14
Q

Spirilla:-

A

Singular= spirochaete

Spiral shaped sometimes w/tail.

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15
Q

Vibrios:-

A

Comma shaped. Sometimes w/ tail.

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16
Q

Bacteria cell wall vs eukaryotic:-

A

Peptidoglyxan vs cellulose.

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17
Q

Bacterial vs eukaryotic DNA structure:-

A

Single circular strand vs chromosomes (linear)

18
Q

Bacterial vs eukaryotic aerobic resp site:-

A

Mesosome vs mitochondria

19
Q

Bacterial vs eukaryotic ribosome size:-

A

70s vs 80s

20
Q

Peptidoglycan:-

A

Polysaccharide with amino acid side chains. Long straight chains w/ cross linking between molecules:- provides strength, maintains shape and protects against osmotic lysis. NAM and NAG.

21
Q

Bioassay:-

A

Using living organisms to test the effectiveness of a treatment.

22
Q

Gram staining process:-

A

Heat fixed bacterial smears stained with crystal violet solution then washed in ethanol, then flooded w/ safranin (counter-stain = red)

23
Q

Gram staining observations:-

A

Ethanol decolourises gram neg bac whereas gram pos remains violet. Gram pos have thick peptidoglycan walls which bind w/ cv stain. G neg have thin walls containing lipid and polysaccharides, lipid dissolved by ethanol so colour not retained- red colour from safranin.

24
Q

Gram staining medical application:-

A

G+ can be controllwd quickly by penicillin or penicillin-like antibiotics.
G- are usually controlled more quickly by diff antibiotic type e.g streptomycin.

25
Q

Requirements of bacteria in culture- nutrient media (liquid culture):-

A
  • glucose- energy source, C source for biosynth.
  • PO4^- for cell membranes and ATP/DNA/RNA.
  • H2O
  • Nitrogen:- ammonium, amino acids, NO3^-, urea.
26
Q

Bacteria in culture requirements conditions:-

A
  • suitable temp- microorg dependent (20-40oC, in labs 25oC to avoid human pathogenic bac).
  • pH:- slightly alkaline for bac, pH 7.5.
27
Q

Obligate aerobes:-

A

Require oxygen for growth.

28
Q

•obligate anaerobes:-

A

Can only survive in absence of oxygen, as oxygen inhibits growth and metabolism.

29
Q

Facultative anaerobes:-

A

Grow better in O2 press, but can slowly grow without.

30
Q

Binary fission:-

A

Bacterial growth:- mitosis, asexual reprod.

31
Q

Gram+ vs gram neg cell wall:-

A

Pos has thick peptidoglycan layer above phospholipid bilayer, neg has thin layer between inner and outer membranes.

32
Q

Methods for counting/quantifying microorganism pop size:-

A
  • Haemocytometer.

* turbidity:-cloudiness of culture, measured w/colourimeter, low transmission of light = high pop.

33
Q

Total count:-

A

All cells living or dead.

34
Q

Viable count:-

A

Only living cells, use serial dilution

35
Q

Serial dilution:-

A

Assume that 1 colony is produced by 1 bacteria. Repeatedly add 1cm^3 of current culture dilution to 9cm^3 of steeile medium and spread 1cm^3 on sterile agar plate until colony no. is just right..

36
Q

Calculating no of bacteria in 1cm^3:-

A

Count no present and multiply by dilution factor.

37
Q

Why is penicillin more effective in gram pos?

A

Inhibits peptidoglycan cross-linkage formation in bac cell wall.

38
Q

Aseptic technique for bioassay:-

A

B4, wipe bench w/ disinf and wash hands. Flame culture bottle neck. Use sterile equipment. Immediately replace lid of petri dish after lifting. Sterilise forceps in bunsen flame.

39
Q

Bacterial growth curve exponential/log phase:-

A
  • rapid cell div.
  • no limiting factors.
  • cell prod greater than cell death.
40
Q

Bacterial growth curve stationary:-

A
  • pop constant.

* production equal to death.

41
Q

Bacterial growth curve death phase

A
  • pop decreases.
  • death>div rate
  • lack of nutrients/O2/increase in toxic by-products.