Module 13 Flashcards

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1
Q

What are physical parameters that control growth? How does each physical parameter inhibit growth?

A

Temperature-denature the enzymes and proteins when too high; affects membrane fluidity; slows down enzyme activity when too cool
pH-proteins and enzymes denature at both; affects hydrogen bonding
Osmotic pressure-draws water out retarding growth; draws water in and cells swell and possibly burst

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2
Q

Describe the categories for prokaryotes for temp growth

A

Psychrophiles-cold loving
Psychotrophs-higher optimum
mesophiles-the most numerous group with moderate temp
thermophiles-heat loving
extreme thermophiles-archaea, hot springs and deep sea thermal vents

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3
Q

Describe the categories for prokaryotes for pH growth

A

Acidophiles- 0-5.5 pH

Neutrophiles- 5.5-8.0 pH

Alkalophile- 8.0-11.5 pH

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4
Q

Describe the categories for prokaryotes for osmotic pressure and growth

A

Hypotonic- water moves into the cell

Hypertonic- food preservation- causes plasmolysis, water moves out of the cell

Isotonic- no net gain or loss of water

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5
Q

What is the main difference between a halotolerant (facultative halophile) bacteria and an extreme (obligate) halophile?

A

extreme halophile
-In archaea (domain)
-High salt only 30-40%

Facultative halophile
-In bacteria (domain)
-Grow over a huge range- up to 15%

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6
Q

What is plasmolysis? Under what conditions does plasmolysis occur? Why does this condition inhibit the growth of a bacterium?

A

The shrinkage of the protoplasm away from the cell wall

Caused by the loss of water in the cell- due to being placed in hypertonic solution, exposed to increased salinity or chemicals

draws water out of the cell retarding growth

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7
Q

What elements are necessary for growth?

A

Carbon
-Backbone of all living matter (organic life)

Nitrogen
-14% dry weight of cell (protein and nucleic acid synthesis)

Oxygen and hydrogen
-Found in all components of cell

Sulfur and phosphorus
-4% dry weight of cell (cysteine and nucleic acid synthesis)

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8
Q

What is a trace element? Why are trace elements important to prokaryotes?

A

Small amounts of minerals

Important as cofactors for enzymes

Iron, copper, zinc

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9
Q

What are the 5 categories bacteria are divided into based upon the effects of oxygen on their growth? Be able to explain and recognize the growth pattern of each in a test tube.

A

Obligate aerobe
-Grow only in the presence of O2

Obligate anaerobe
-Killed by O2

Facultative anaerobe
-Organisms grow with or without the presence of O2 but prefer it

Aerotolerant anaerobe
-Don’t use O2 for growth, and not harmed either

Microaerophile
-Less than atmospheric concentrations of O2

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10
Q

What is the difference between a complex media and a chemically defined media? What is a fastidious bacterium? Which media will a fastidious bacterium grow on?

A

Chemically
-Know the exact amounts of every substance in the media
-Fastidious bacteria grow- require several different growth factors

Complex
-Composed of extracts which vary from batch to batch
-High in amino acids, vitamins, minerals

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11
Q

Where do you find anaerobic bacteria? How would you grow an anaerobic bacterium?

A

No oxygen or low oxygen environments

-Reducing media- deplete oxygen in the media
-Anaerobic jar
-Capnophiles- like CO2 environment

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12
Q

How does a selective media differ from a differential media? What is an enrichment culture? When would you use any of these three types of media?

A

Selective media- inhibits the growth of unwanted bacteria

Differential media- different types of bacteria will appear differently on the plate

Enrichment culture- designed to increase specific bacteria

—Allows for the isolation and identification of specific microorganisms from a mixed culture

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13
Q

What is binary fission? What is a generation time?

A

Type of asexual reproduction where a parent cell divides into two identical cells.

The time required for a cell to divide

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14
Q

Example problem: If you start with one bacterium that has a generation time of 15 minutes, how many bacteria will you have in 2 hours?

A

8 GT

1-2-4-8-16-32-64-128-256

256 bacteria

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15
Q

What does the growth curve of a bacterium look like? What does each phase of the graph represent (what is it called)? What is occurring at each phase?

A
  1. Lag phase
    -Little or no cell division
    -Period of synthesis
  2. Log phase
    -Exponential growth phase
    -Generation time reaches a constant
    -Cells most metabolically active
    -Most sensitive to antibiotics
  3. Stationary phase
    -Death=division
    -Constant number of cells
    -Run out of nutrients or pH changed
  4. Death phase
    -Death greater than division
    -No nutrients or extreme pH
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16
Q

How are scientists able to count bacteria? List and describe the techniques. When will each technique be useful?

A

1.Variable plate counts
Counts live cells
Serial dilutions done

  1. Filtration
    Only for a small number of cells
    Concentrate bacteria with a filter-> plate
    Used for coliforms (enteric bacteria from sewage)

3.Most probable number
Counting bacteria that don’t grow on their own using statistics
Dilute sample in nutrient broth-> to no cells
Used for bacteria that don’t grow in isolated colonies on plates
Statistical count

  1. Microscopy
    Direct counts-live and dead cells
    Petroff-Hausser counter used
  2. Turbidity- cloudiness
    Spectrophotometer- how uch light is absorbed or transmitted by the solution
    Indirect count
    Have to have a viable plate count or microscope count with it
  3. Metabolic activity- measure CO2 or acid released
  4. Dry weight
    Cells 70-80% water
    Have to know the number of cells or weight of one cell
17
Q

What is a biofilm? How are they important in health care?

A

Bacteria live in communities or groups which is surrounded by a matrix of polysaccharides with DNA and proteins- slime or hydrogel

1000 times more resistant to microbiocides
Most HAIs due to this
Research prevent formation of block quorum sensing

18
Q

What is quorum sensing?

A

The cell to cell chemical communication that allows communication- communication system of biofilms