Bacterial Metabolism & Growth Flashcards

1
Q

Microbial Metabolism - how it differs and is similar to eukaryotes

A
  • Have many of same pathways for synthesis of compounds and energy generation as eukaryotes
  • Do have a greater diversity of pathways
  • it is the enzyme systems that determine the substrates that can be utilised
  • substrates absorbed/transported from immediate enviro - they release extracellular enzymes to digest surrounding complex chemicals into smaller molecules that can be absorbed across cell membrane
    • many of their extracellular enzymes toxic to tissue
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Alternate substrates for Glycolysis

A
  • Many bacteria don’t use glucose
  • other substrates = other sugars (monosaccharides), disaccharides & polysaccharides, glyeral & fatty acids, proteins & aa
  • principle: alternative substrate is converted in fewest steps into intermediate in main pathways for glucose catabolism
    • often pyruvate or acetyle CoA
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Difference between Fermentation and Respiration

A

Respiration: uses an external electron acceptor to oxidize substrates completely to CO2
-i.e. molecule that is from external enviro.
Fermentation: final electron acceptor is internal by-product of catabolism (i.e. lactate)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Cellular Respiration - definition

A

-Is the flow of electrons through or w/in a membrane, from reduced coenzymes to an external electron acceptor usually accompanied by the generation of ATP (pumping of protons across membrane and back through ATPase)

  • coenzyems such as FAD and coenzyme Q involved
  • terminal e- acceptor Oxygen - reduced to water (in aerobic)
  • Alternate electron acceptors: nitrate, sulfate, methane
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Secretion of metabolites

  • effect
  • 3 examples
A
  • proteins and other cell metabolites actively secreted by variety of diff. secretory systems
  • Secretion of metabolites has important functions in pathogenicity

Secretion of enzymes such as;

  • Proteases
  • Nucleases
  • Phospholipases
  • some can cause important tissue damage
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

Why knowledge of bacterial metabolism import.?

-Selective & differential media

A
  • can make specific growth media that favours certain bacterium
    • can add substrate that is used by one

Selective media: particular substrates added that only particular bacteria

Differential media: components put into media that changes in response to by-products (i.e. pH indicator)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

Regulation of Metabolism

A

-Have similar systems to regulate production & activity of their enzymes

  1. Regulation of enzyme activity by feedback - product inhibition of enzymes allows rapid feedback - regulation via transcription is longer term control
  2. Regulation of enzyme production, 2 ways;
    i) Repression: excess end product interacts w/ repressor protein (that is always active) and become active - ceases production of that product
    ii) induction: repressor protein inactivated by substrate, which allows transcription & therefore enzyme production
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Two component regulatory system

A
  • Enables bacteria to respond to external enviro changes

- intracellular DNA binding proteins that regulate appropriate transcription

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Microbial Growth (2 types)

A
  • Either;
    1. Growth of individual cells by;
    i) Asymmetric budding
    ii) Binary fission (membrane folds and cell separates into 2 equal sized bits
  • Can be very quick
    2. Population growth: most significant for effects on other organisms
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Bacteria Cell growth & division (3 steps)

A
  1. DNA replication - starts at a point of origin on ds chromosome & proceeds in opposite directions for each strand
    - chromosome associated w/ cell membrane - so when cell begins to separate, two DNA dragged apart
    - is semi-conservative
  2. Cell elongation
  3. Cell division
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Population growth

-typical growth curve

A

-Large populations of microorganisms can overwhelm defence mechanism of a host
-Growth exponential
Typical growth curve:
1. Lag phase: cells alive, but population not increasing
-is a period of adjustment (may need to induce some genes)
2. Exponential Phase: cells growing and dividing at constant rate
-young cells usually most infective at this stage
3. Stationary Phase: population stops increase due to nutrient depletion, pH change, lack of O or build up of toxic compounds
4. Death/Decline stage: cell death > cell division - usually due to same factor that caused population to enter stationary phase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Rate of Growth

A

Measured by Mean Generation time (MGT)

-Depends on species, type of growth medium and enviro. conditions

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Continous culture

A
  • “chemostat” or fermentor
  • continous culture that continually supplies new substrates and removes end products
  • can be sustained for years
  • used when people want to study microbial evolution
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Measure measurement of growth (5)

A
  1. Total cell count: viable + dead
  2. Direct count: using a counting chamber - count every cell
  3. Viable cell count: miles and misra method, pour plate technique or filtration technique
  4. Electrical resistance
  5. Microbial mass (cell densities, wet weights, dry weights)
  6. Nitrogen determination: nitrogen content can be used to estimate amount of protein which therefore = bacterial numbers
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Methods to count colonies

  • miles & misra
  • Pour plate
  • Filtration
A
  • Miles and Misra: dilution of suspension, put small volume on agar plate, grow and count colonies
    - can work out number
  • Pour plate technique: bacterial dilutions suspended in molten agar - incubate, grow and count
  • Filtration technique: useful w/ small no. of bacteria in large volume of water
    • bacteria trapped on filter then filter incubated on plate
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Effect of Environment on Microbial growth

  • nutriends
  • temperature
  • pH
A
  • Nutrients: growth increases as more nutrients added to maximum growth rate (plateaus due to saturation of transport mechanisms)
  • Temperature: 37-41 degrees usu. optimum (body temp): growth increases w/ temp to certain point - then rapid drop off as organisms killed by heat
  • pH: optimum pH, outside this bacterial activity declines
17
Q

Effect of environment on Microbial growth

  • Salts, osmotic pressure
  • Gaseous environment (5 types of classes)
A
  • Salts, Osmotic pressure: most don’t handle well - halophiles grow well in high salt conc.
  • Gaseous environment:
    1. Obligate aerobes
    2. facultative anaerobes (grow w/out O, but can use it if it’s present)
    3. Aerotolerant anaerobes - anaerobes but can tolerate O for short periods
    4. Microaerophiles: require reduced O tensions, enriched w/ CO2
    5. Obligate anaerobes: can’t tolerate O at all
18
Q

Types of culture media

A
  • Solid media (agar): for initial isolation of bact. so individual colonies can be growth and identified
  • Liquid media (broths): for growth of large no. of microorganisms once isolated