Lecture 10 Flashcards

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1
Q

What two methods to measure the cell growth?

A

Cell mass or cell number

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2
Q

What indicates a microbial growth?

A

A growth in cell mass or cell number,

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3
Q

Define microbial growth.

A

An increase in volume and in mass, then divides.

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4
Q

What does microbial growth usually indicates?

A

Cell multiplication.

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5
Q

Explain how to measure cells by the Dry weight determination.

A

A collection of cells is made from a measured volume of the broth culture. Then you dry the cells overnights in an over of 90 degrees celsius then weight the dried cells.

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6
Q

By what qualificative measure is the cells reported?

A

x mg/mL.

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7
Q

True of false, the Dry weight determination method distinguishes between living and dead cells.

A

False, they do not distinguish the difference.

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8
Q

Explain the carbon, nitrogen, proteins content determinations for weighing cells.

A

This method states that with the increase of these elements, the cell mass increases.

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9
Q

True or False. The carbon, nitrogen, protein content determination does not determine the dead to living cells?

A

True.

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10
Q

Describe the turbidity measurement method.

A

This is the preferred method as it’s easily performed. As growth occurs, so does the turbidity of the broth (becomes opaque). The liquid is transferred to a cuvette where it’s placed in a spectrophotometer and reading is obtained. This method does not distinguishes living to dead cells.

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11
Q

Define the measurement of cell mass to cell number.

A

Cell mass measurement mesures the group and cell count is individual cells.

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12
Q

Define the measurement of the cell number using the direct microscope count method.

A

The cells are counted using a microscope and a special slide known as a counting chamber. This method does not differentiates living to dead cells.

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13
Q

Define the Coulter counter method for cell number count.

A

This is an electronic counter that counts cells that are suspended in liquid. This method does not differentiates living to dead cells.

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14
Q

Define the plate count method for cell number count.

A

This method is primarily based on assumptions that each cell deposited on or in the agar medium multiplies from one visible colony.

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15
Q

As the pour plate method for cell number count, what if you have 1 mL of a suspension containing 100 bacteria / mL is plated out. How many colonies should you expect?

A

100 colonies to develop.

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16
Q

Define “plated out”.

A

The addition of the inoculum to the agar medium and districting it over the surface or throughout the agar.

17
Q

Define confluent growth.

A

Also know as confluent lawn, it’s a covering of growth or colonies spread across the plate, making it difficult to differentiate the cells due to the lack of separation.

18
Q

If you have a suspension containing 2,500,000 bacteria / mL that is plated out, should you expect 2,500,000 colonies? Elaborate.

A

No, the confluent growth would occur. You could use other means to measure the growth.

19
Q

What means of measurement would be most suitable to measure large numbers of expected colony growths.

A

Making suitable dilutions of the suspended and plating out these dilutions.

20
Q

What does TNTC signify?

A

Too numerous to count.

21
Q

When given a bacterial culture ans asked to determine the number of visible cell/ mL, what should be the first step to follow?

A

Prepare a series of ten-fold dilutions.

22
Q

What frequency should the plating be done at?

A

Triplicate.

23
Q

True or false. You will need to apply aseptic technique to not contaminate and decrees the count.

A

False. Aseptic techniques are use to AVOID inflating the count due to contaminates.

24
Q

Plates containing between how many colonies should be used in determining the cell count.

A

30-300

25
Q

True or False. The number of viable bacteria /mL is determined with a specific formula.

A

True.

26
Q

Why do we name this method the viable count?

A

Because it’s capable of detecting the cells that are capable of growth on the plating medium under incubation conditions.

27
Q

Name three count errors.

A

1-pipette errors
2-counting errors
3-uneven distribution of the cells on the agar.

28
Q

What is the percentage of discrepancies acceptable for errors in count.

A

10 % is acceptable.

29
Q

Why do we say that the viable counting method gives a minimum estimate of the viable cells? Name 2.

A

1-Some organisms occur in clusters and do not break up during the procedure.
2-If 2 or more cells are close together and do not break up- a colony develops.

30
Q

True or false. Only cells that can grow on the plating medium can be accounted for and not all cultures will permit the growth of all species of bacteria.

A

True.

31
Q

How do you collect data for bacterial growth such expressed in a graphic?

A

By inoculating bacteria in a suitable medium and measuring the broth at different time periods.

32
Q

Describe a graphic curve when the viable count method is employed?

A

A upward slope, plateau and a slope (resembling a mountain).

33
Q

Describe a graphic curve when turbidity is used.

A

A upward slope that goes up and plateau and a straight line.

34
Q

Express the 4 phases of a typical growth curve when the cells are plotted as a function of time.

A

1-lag phase
2-logarithmic growth (exponential) also called the log phase
3-maximum stationary phase
4-death phase

35
Q

Explain the following statement with 2 supportive explanations. Microbial populations do not grow exponentially, at high rates, for very long. Growth is usually limited by one of these.

A

1-Exaustion of nutrients

2-the accumulation of toxic products of metabolism.

36
Q

To say the development of microbial population is self-limited is true or false?

A

True