Ch 4-5 Microbio Flashcards

1
Q

Distinguish between macronutrients and micronutrients, giving examples of each

A

-Macronutrients: CHONPS make up the bulk of all living cells (carbohydrates, lipids, proteins, nucleic acids)
—>Also include enzyme cofactors and signaling molecules like mg, fe, k, ca
-Micronutrients: needed for enzyme function but in small (trace) quantities (Co, cu, mn, mo, ni, zn)

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2
Q

Distinguish between heterotrophy and autotrophy

A

-Heterotrophs: rely on organic (C containing) compounds made by other organisms
-Autotrophs: make their own organic compounds from carbon dioxide

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3
Q

Distinguish between photoautotrophy and chemolithoautotrophy

A

-Photoautotrophs: use light energy to capture and fix CO2 into organic molecules
-Chemo: use eneergy from mineral oxidation to capture and fix CO2 into organic molecules (litho-rock)

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4
Q

Distinguish between photoheterotrophy and chemoheterotrophy

A

-Photoheterotrophs: like chemo but also uses light energy to obtain energy
-Chemoheterotrophs: beak down organic substances to obtain energy and build biomass (humans are this)

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5
Q

Define nitrogen fixation in terms of its chemical input and output

A

Takes nitrogen gas (plus hydrogen) and converts it ammonia and hydrogen

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6
Q

Discuss ways to import nutrients into a cell across the cell membrane(s)

A

Diffusion (passive, facilitated) and active transport

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7
Q

Define facilitated diffusion

A

Occurs when molecules diffuse through membrane-spanning protein channels or pores
–>requires channel or pores as gateways

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8
Q

Define coupled transport, symport, and antiport and describe what powers them

A

-Coupled transport: moves molecule up gradient. Gets energy by coupling the movement of that molecule to a different molecule (ion) typically moving down gradient
-Symport: both molecules are transported in same direction
-Antiport: actively transported molecule moves from the opposite direction of the driving ion

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9
Q

Define ABC transporter and their power sources

A

ATP binding cassette are very large family of energy driven transport system found in all 3 domains of life
–>use ATP to drive transport
–>2 types: Uptake (nutrients in) and Efflux (toxins/drugs out)

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10
Q

Define group translocation and how it works

A

Avoids uphill transport by chemically altering subtrate –> changed subtrate = starting subtrate not moving against concentration gradient any more
–> alteration requires energy

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11
Q

Define the function of a siderophore

A

Binds tightly to tiny amounts of soluble iron around and then imported into the cell

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12
Q

Give examples of molecules transported by the above pathways (active)

A

Glucose, amino acids, ions like Na and K

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13
Q

Describe the process of dilution streaking and its utility

A

A stick or loop carrying bacteria is spread across the agar surface, leaving cells behind

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14
Q

Describe how to make an agar Petri plate

A

A liquid culture or sample with bacteria is repeatedly diluted and spread on agar plates until single colonies are isolated

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15
Q

Describe a bacterial colony

A

A group of bacteria derived from the same mother cell

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16
Q

Describe how dilution plates enable bacteria to be counted

A

Ensures that there are enough spaces on the plate for each bacterial cell to grow into a distinct colony that can be counted individually

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17
Q

Define confluent growth

A

When cells or bacteria cover an entire surface area without gaps

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18
Q

Distinguish complex and synthetic media

A

-Complex: nutrient rich but poorly defined
-Synthetic: precisely defined ingredients

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19
Q

Define and distinguish selective and differential media

A

-Selective: favor the growth of one organism/strain over another
-Differential: highlight phenotypic differences between two species that may grow equally well on the medium

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20
Q

Describe a method to detect the presence of unculturable bacteria

A

Detect presence by extracting and sequencing DNA from the environment

21
Q

Describe and distinguish direct and indirect ways to count bacteria

A

-Direct: physically counted individual cells with a microscope
-Indirect: estimate bacterial populations based on measurable parameters (light scattering)

22
Q

Define planktonic growth

A

Growth as isolated cells, often happens in shaking liquid culture

23
Q

Define growth rate and its relationship to population size

A

-Growth rate: percentage change in a population over specific period of time (average change in population over time)
-Relates to population: positive growth rate = growing population.

24
Q

Define generation time/doubling time

A

Time required for the population to double

25
Q

Describe some of the culture conditions that can change generation time

A

Depends on the species and on the growth conditions (medium, temperature, shaking, etc.)

26
Q

Define batch culture and distinguish it from continuous culture

A

-Batch culture: in a closed system like a flask
-Continuous: fresh medium is constantly added and culture removed, so cells grow indefinately

27
Q

Define and order the 4 phases of bacterial growth in batch culture

A
  1. Lag: bacteria prepares cell machinery for growth (gearing up)
  2. Log: growth approximates an exponential curve (sprinting)
  3. Stationary: cells stop growing and shut down (stopping/break)
  4. Death: cells die with a “half life” similar to radioactive decay (negative exponential curve) (sleep/die)
28
Q

Describe some of the physiological changes that take place in different growth phases

A
  1. Lag: bacteria prepares cell machinery for growth
  2. Log: growth approximates an exponential curve
  3. Stationary: cells stop growing and shut down
  4. Death: cells die with a “half life” similar to radioactive decay (negative exponential curve)
29
Q

Define a biofilm and give an everyday example of a biofilm

A

Group of cells secretes a sticky extracellular matrix that encases the population of cells. Examples include dental plaque.

30
Q

Describe typical components of a bacterial extracellular matrix

A

Polysaccharides, proteins, and/or DNA

31
Q

Briefly describe the stages of biofilm formation

A
  1. Attachment to monolayer by flagella
  2. Microcolonies
  3. Exopolysaccharide production
  4. Mature biofilm
  5. Dissolution and dispersal
32
Q

Define endospore and mother cell

A

When species (i.e Bacillus and Clostridium genera) form endospores under starved conditions (survival cell)
–> form inside mother cell
–> complete formation results in mother cell dying

33
Q

Describe the characteristics of spores

A

-Dehydrated = resistant to all sorts of environmental insults
-Packed with small acid-soluble proteins (SASPs) to further protect their DNA

34
Q

Define extremophile

A

An organism that thrives in extreme environmental conditions, such as high salinity, temperature, or pressure

35
Q

Explain the relationship between growth rate and relative temperature

A

Growth rate increases with temperature up to an optimum, beyond which enzyme denature, slowing growth.
–> Below the optimum, enzymes work more slowly, and membranes lose fluidity

36
Q

Distinguish psychrophile, mesophile, thermophile, and hyperthermophile with respect to their growth temperature ranges

A

-Psychrophiles: 0-20 °C
-Mesophiles: 15-45°C
-Thermophiles: 40-80°C
-Hyperthermophiles: 65-121°C

37
Q

Define barophile/piezophile

A

Organisms adapted to grow at high pressure (>1,000 atm), often found in deep-sea environments

38
Q

Define osmotic pressure and why it is an issue for bacterial cells

A

-Pressure exerted by the movement of water across a membrane due to solute concentration differences.
-High osmotic pressure can cause cells to lose or gain water, impacting growth

39
Q

Define halophiles

A

-Organisms that require high salt concentrations (2-4 M NaCl) for growth
-Counteracts osmotic pressure by importing potassium or producing compatible solutes

40
Q

Distinguish between “philic” and “tolerant” species

A

-Philic: requires specific conditions for survival
-Tolerant: can survive but does not require extreme conditions

41
Q

Distinguish neutralophiles, acidophiles, and alkaliphiles with respec to their preferred growth pH

A

-Neutral: 5-8 pH
-Acid: 0-5 pH
-Alkali: 9-12 ph

42
Q

Describe how alkaliphiles deal with having few protons to establish a proton motive force

A

Use sodium gradients across membranes instead of protons to power processes, as protons are scarce in alkaline

43
Q

Distinguish strict anaerobes, strict aerobes, faculative microbes, and microaerophiles

A

-Strict aerobes: require oxygen for growth
-Microaerophiles: grow in low oxygen levels
-Strict anaerobes: die in presence of oxygen
-Facultative anaerobes: grow with or without oxygen
-Aerotolerant: doesn’t use oxygen but can tolerate it

44
Q

Distinguish among sterilization, disinfection, antisepsis, and sanitation with respect to controlling microbes

A

-Sterilization: kills all living organisms
-Disinfection: kills/removes pathogens from inanimate objects
-Antisepsis: kills/removes pathogens from living tissues
-Sanitation: reduces microbial populations to safe levels

45
Q

Define the parameters needed for effective sterilization via autoclaving

A

-Conditions: 121°C, 15 psi, >20 minutes
-Effective for sterilizing glassware, instruments, and media

46
Q

Distinguish physical and chemical agents for microbrial control and give at least 2 examples of each

A

-Physical Agents:
–>Autoclaving: High pressure and moist heat.
–>Filtration: Removes microbes using 0.2 µm filters.
Chemical Agents:
–>Ethanol: Damages proteins and membranes.
–>Chlorine: Oxidizes proteins and damages DNA.

47
Q

Distinguish among different methods of pasteurization

A

-LTLT (Low Temp, Long Time): 63°C for 30 min.
-HTST (High Temp, Short Time): 72°C for 15 sec.
-Both eliminate pathogens like Coxiella burnetii but do not kill spores.

48
Q

Define D-value

A

Time needed to reduce a microbial population by 90% under specific conditions

49
Q

Briefly describe phage therapy

A

-Use of bacteriophages (viruses targeting bacteria) to kill pathogenic bacteria
-Phages are narrow-spectrum and specific to certain bacterial species