Chapter 5 - Microbial Growth and Control. Flashcards

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1
Q

What is growth in Microbiology?

A

An increase in the number of cells.

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2
Q

What is binary fission?

A

Cell division by whereby a cell grows by intercalary growth to twice its minimum size and then divides to form two cells. As well as the fact that 2 cells have arisen from 1.

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3
Q

What is the generation time?

A

The time required for a cell population to double. Also called doubling time.

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4
Q

What are some of the factors that generation time depends on?

A

Nutritional and Genetic factors as well as temperature; different species have different requirements and generation times.

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5
Q

What are FtsZ proteins

A

proteins essential for cell division.

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6
Q

What is FtsZ?

A

A protein that forms a ring along the mid-cell division plane to initiate cell division. Just as Tubulin is an important cell division protein in eukaryotes.

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7
Q

What is a Divisome?

A

A complex of proteins that direct cell division processes in bacteria.

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8
Q

How does the formation of the divisome occur and what is the outcome of this process?

A

1) FtsZ molecules polymerize to form the ring, attracting other divisome proteins FtsA and ZipA. 2) ZIpA- an anchor that connects to the FtsZ ring and stabilizes it. 3)FtsA connects the FtsZ ring to the cytoplasmic membrane and recruit more divisome proteins such as FtsL-needed for peptidoglycan synthesis forming the divisome. The divisome orchestrates the synthesis of new cytoplasmic membrane and cell material called the division septum.

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9
Q

DNA replicates before the FtsZ ring forms because the ring forms between the duplicated nucleotide and effectively block the formation of the FtsZ ring. (T/F)

A

True

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10
Q

How do the Min proteins guide the FtsZ to the midpoint for cell division?

A

The proteins MinC,MinD, and MinE all interact with FtsZ to guide it to the midpoint. 1) MinD forms a spiral structure in the inner surface of the cytoplasmic membrane to localize MinC. 2) MinD spiral oscillates along the axis preventing FtsZ from forming. 3) MinE oscillates from side to side pushing MinA and MinC aside leaving the center with the least concentration and the most permissive site for the ftsZ to bind. As a result the Min proteins ensure that the divisome forms only at the cells’ center.

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11
Q

How does the 2 daughter cells form?

A

As elongation continues and septum formation begins. As the cell constricts the FtsZ ring depolymerizes, triggering the inward growth of the wall materials to form the septum and seal off the 2 daughter cells. FtsZ also hydrolyzes GTP to fuel the process of polymerizing and depolymerizing.

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12
Q

How does Genome Replication Keep up with fast growing cells?

A

Genome replication keeps up with fast growing cells because they are able to contain multiple replication forks where the new round of replication begins before the old one has been completed.

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13
Q

What is the major shape determining factor in bacteria?

A

MreB-a protein that forms the cytoskeleton of the in bacteria and some archea.

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14
Q

how does MreB define a cells shape?

A

It is thought that MreB localizes the synthesis of new cell wall to specific locations along the axis of the cell during growth. This allows the cell to wall to form at several points rather from a single location at the FtsZ site outward. By rotating the within the cell cylinder and imitating cell wall synthesis in such a way that a rod shaped cell only elongates along its long axis.

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15
Q

What protein in addition to the MreB is thought to be associated with the curved shape of Calobacter?

A

The curved morphology is thought to be due in part to the protein crescentin; this protein organizes itself into 10nm wide filaments that localize the concave face of the cell.

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16
Q

what proteins in eukaryotes are related to those of the MreB protein and Cresentin?

A

IN eukaryotes MreB is thought to be related to actin-forms microfilaments, Tubulin-microtublues, and FtsZ proteins. Cresentin is thought to be related to the protein to keratin proteins that make up the intermediate filaments of the eukaryotic cells.

17
Q

How does peptidoglycan synthesis occur?

A

Bactoprenol transports peptidoglycan precursors across the membrane interior by rendering them hydrophobic. Once in the periplasm, reacts with enzymes transglycosylases that insert cell wall precursors into the growing point of the cell wall and catalyze glycosidic bond formation. Then the new cell wall material is added to small gaps in the peptidoglycan created by the enzymes autolysins and spliced to the new tetra peptide its, then followed by Transpeptidation.

18
Q

What is Transpeptidation?

A

The formation of peptide bonds between the short peptides present in peptidoglycan, the cell wall of the bacteria.

19
Q

What is the exponential growth?

A

Growth of the microbial population in which the cell number doubles within a fixed time period.

20
Q

How is the fixed relationship between initial cell and the exponential growth represented in a mathematical equation?

A

N=No^2n; where N is the final cell number, and No is the initial cell number, and n is the number of generations during the period of exponential growth.

21
Q

What is a Batch Culture?

A

A closed-system microbial culture of fixed volume.

22
Q

What are the 5 phases of the growth cycle?

A

The lag phase, exponential phase, stationary phase, and the death phase?

23
Q

What is the Lag phase and when can they be observed?

A

The lag phase is a period of time before growth of the cells begin. and can be seen when a microbial culture is inoculated into a medium,when transferred from old medium with depleted nutrient to the new rich media or vise versa, and when a few live cells that have been damaged but not killed by some stressors such as extreme temperatures,radiation or chemicals.

24
Q

What is the exponential phase and what influences this phase.

A

The exponential phase is when the population doubles at regular intervals for a brief or extended period of time depending on the available resources and influenced by factors such as environmental- temp,composition of culture medium; and genetic characteristics specific to the organism.

25
Q

What causes the stationary and death phases of the cell cycle?

A

It is when the exponential growth ceases due to depleted essential nutrients or because the waste products accumulate.

26
Q

What is the stationary phase?

A

There is no net increase or decrease in the cell number and thus the growth rate of the population is zero. This occurs because some cells in the population grow while others die known as cryptic growth.

27
Q

What is the death phase?

A

When the number of living cells begin to deplete and the and this occurs at an exponential rate and occurs at a much slower rate and may remain in a culture for several months or years.

28
Q

What is a continuous culture?

A

Which is an open system where fresh medium is added at a constant rate while an equal volume of spent culture medium is removed at the same rate.

29
Q

What is a chemostat?

A

A chemostat is a device that controls both the growth rate and the cell density can be controlled independently.

30
Q

What are the 2 factors that control the growth rate and cell densities respectively?

A

1) the dilution rate, which is the rate at which fresh medium is pumped in and spent medium is removed; and 2) the concentration of a limiting nutrient.

31
Q

What are the 2 common measures of cell growth?

A

Cell counts and turbidity

32
Q

What is a viable cell?

A

A cell that is alive and able to divide and reproduce.

33
Q

What is a viable count?

A

A measurement of the concentration of live cells in a microbial population.

34
Q

What is a plate count?

A

A viable counting method in which the number of colonies on a plate is used as a measure of cell number.

35
Q

What are 2 ways of performing a plate count and how do they differ?

A

the 2 ways are the pour-method and the spread plate method. IN the pour method the microbial sample is pipetted into a sterile plate, then the sterile medium is added to the plate solidified and then incubated. In the spread plate method the microbial sample is pipetted onto an agar plate using a sterile glass spreader and then incubated.

36
Q

What are some of the errors that can occur in plate counting ?

A

plating inconsistencies such as inaccurate pipetting of a liquid sample, insufficient mixing, heat intolerance.

37
Q

What is the equation used to calculate the generation time?

A

g=t/n; Where g; is the generation time, t; is the time, and n; is the number of generations.