Lecture 10 Flashcards

1
Q

What two methods to measure the cell growth?

A

Cell mass or cell number

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

What indicates a microbial growth?

A

A growth in cell mass or cell number,

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

Define microbial growth.

A

An increase in volume and in mass, then divides.

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

What does microbial growth usually indicates?

A

Cell multiplication.

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

By what qualificative measure is the cells reported?

A

x mg/mL.

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

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

A

False, they do not distinguish the difference.

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

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

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

A

True.

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Define the measurement of cell mass to cell number.

A

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

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

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

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

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

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

25
True or False. The number of viable bacteria /mL is determined with a specific formula.
True.
26
Why do we name this method the viable count?
Because it's capable of detecting the cells that are capable of growth on the plating medium under incubation conditions.
27
Name three count errors.
1-pipette errors 2-counting errors 3-uneven distribution of the cells on the agar.
28
What is the percentage of discrepancies acceptable for errors in count.
10 % is acceptable.
29
Why do we say that the viable counting method gives a minimum estimate of the viable cells? Name 2.
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
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.
True.
31
How do you collect data for bacterial growth such expressed in a graphic?
By inoculating bacteria in a suitable medium and measuring the broth at different time periods.
32
Describe a graphic curve when the viable count method is employed?
A upward slope, plateau and a slope (resembling a mountain).
33
Describe a graphic curve when turbidity is used.
A upward slope that goes up and plateau and a straight line.
34
Express the 4 phases of a typical growth curve when the cells are plotted as a function of time.
1-lag phase 2-logarithmic growth (exponential) also called the log phase 3-maximum stationary phase 4-death phase
35
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.
1-Exaustion of nutrients | 2-the accumulation of toxic products of metabolism.
36
To say the development of microbial population is self-limited is true or false?
True