L1-3 Flashcards

(48 cards)

1
Q

What are the six main categories of microbes?

A

Bacteria, Archaea, Fungi, Algae, Protozoa, Viruses

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2
Q

Which microbes are considered acellular?

A

Viruses

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3
Q

What distinguishes prokaryotes from eukaryotes?

A

Prokaryotes lack a nucleus and internal organelles, while eukaryotes have both.

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4
Q

What are the three domains in the Universal Phylogenetic Tree?

A

Bacteria, Archaea, and Eukarya

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5
Q

Which microbe is a common single-celled fungus?

A

Saccharomyces cerevisiae (budding yeast)

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6
Q

What is a distinguishing feature of Archaea?

A

They often inhabit extreme environments and have unique metabolic activities.

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7
Q

What staining method is used to classify bacteria by cell wall?

A

Gram staining

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8
Q

What is the size range of typical microbial cells?

A

1–10 µm for most, but can range from 0.5 µm to 750 µm

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9
Q

What gene is commonly used to classify bacterial diversity?

A

16S rRNA gene

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10
Q

What is binary fission?

A

A method of asexual reproduction where one cell divides into two identical daughter cells.

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11
Q

What is vertical gene transfer?

A

The transmission of genetic material from parent to offspring.

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12
Q

What are the three mechanisms of horizontal gene transfer?

A

Transformation, Conjugation, Transduction

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13
Q

What is transformation in bacteria?

A

Uptake and integration of free DNA into the bacterial chromosome. DNA cell must be competent
Includes Naked DNA
Transposons
plasmids

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14
Q

What is conjugation?

A

DNA transfer between bacteria via a pilus= bacterial mating , often involving plasmids, conjugative transporons
and intergrons .

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15
Q

What is transduction?

A

Transfer of bacterial DNA by a bacteriophage.
transduction can involve movement of phage DNA and host
cell DNA
Generalised transduction
(random DNA encapsulation)
Specialised transduction
(lysogenic integrated phage,
specific encapsulation of adjacent DNA

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16
Q

What experiment proved DNA is the material of transformation?

A

Avery-MacLeod-McCarty experiment using DNase

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17
Q

Why is horizontal gene transfer important?

A

It introduces genetic diversity and contributes to antibiotic resistance.

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18
Q

What is generation time?

A

The time required for a microbial population to double.

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19
Q

What are the five phases of microbial population growth?

A

Lag- adjustment of cell metabolism to new conditions,
Exponential- cell
growth at max.
rate possible in
the medium
chosen
, Deceleration- limiting supply of
one nutrient or
accumulation of
toxic metabolites, Stationary- no net growth,
at least one nutrient
depleted - possible growth
at expense of cell death
and lysis;
, Death- decline of viable
cells due to exhaustion of
energy or accumulation of
toxic byproducts.
5

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20
Q

What affects bacterial growth rate?

A

Species, nutrients, temperature, pH, and osmolarity

21
Q

What is optical density (OD650)?

A

A light scattering method to estimate bacterial growth

22
Q

What is the specific growth rate (μ)?

A

The rate of increase in cell number per unit time during exponential phase

23
Q

What is a chemostat?

A

A continuous culture system where fresh medium is constantly added and culture removed

24
Q

How do weak acids act as preservatives?

A

They lower intracellular pH by diffusing into cells and dissociating

25
What are halophiles?
Microbes that thrive in high salt concentrations
26
What is the maximum specific growth rate (μmax)?
The steepest slope on a semi-log plot of bacterial growth
27
Are all microscopic organisms unicellular?
No, some microbes form multicellular complexes visible to the naked eye.
28
What is the role of fungi in nature?
They are decomposers, recycling nutrients from dead matter.
29
What is a lichen?
A symbiotic organism formed by algae and fungi.
30
What defines a protozoan?
Single-celled, eukaryotic, often predatory or parasitic microbes.
31
What are extremophiles?
Microbes, mostly archaea, that thrive in extreme conditions like high temperature or salinity.
32
Why is 16S rRNA used in classification?
It is highly conserved and useful for differentiating bacterial species.
33
What is budding in microbial reproduction?
Asexual reproduction where the daughter cell grows from the parent cell’s surface.
34
What is multiple fission?
A single cell divides into many daughter cells simultaneously.
35
What is a plasmid?
A small, circular DNA molecule separate from chromosomal DNA in bacteria.
36
Why are plasmids important?
They often carry antibiotic resistance or virulence genes.
37
What did the Lederberg and Tatum experiment show?
Genetic recombination occurs in bacteria through conjugation.
38
What is the lag phase of bacterial growth?
The adjustment period where cells adapt to new conditions without dividing.
39
Why plot bacterial growth on semi-log paper?
To produce a straight line during exponential growth for easier analysis.
40
What is diaminopimelic acid used for?
Estimating bacterial biomass as a component of peptidoglycan.
41
Why is aseptic technique important?
To maintain pure cultures by preventing contamination.
42
What is a roll tube used for?
Culturing anaerobic bacteria in oxygen-free environments.
43
What does OD650 = 1.6 indicate in E. coli culture?
Around 2 × 10⁹ cells per mL in the culture.
44
What is a limiting nutrient in a chemostat?
The specific nutrient whose availability controls microbial growth.
45
What are optimal conditions for mesophiles?
Moderate temperatures, typically around 39°C.
46
describe prokayotic cell division
p rokaryotes have circular chromosomes. *DNA synthesis starts at a single origin of replication, opening up the DNA helix *Chromosome replication -replication ‘bubble’ moves around chromosome in two directions - bidirectional replication * DNA copied exactly *In rapidly growing cells new replication forks start before cell divides * Bacteria often have plasmids = smaller circles of DNA
47
what are the two forms of strep pneumoniae
Exist in two forms - ‘S’ smooth colonies; virulent - ‘R’ rough; avirulent * ‘S’ smooth pneumococci produce a polysaccharide capsule that helps defend bacterium from host immune responses → bacterial infections and even death ‘R’ ‘S’
48
what are methods for measurements of growth
direct counts: microscope/ haemocytometer – viable counts: serially dilute, plate, count colonies – light scattering : spectrophotometer + cuvette – cell molecules: dry weight, DNA, protein