Bacterial Genetics Flashcards

1
Q

What is genomics?

A

The study of genomes and DNA/RNA, genome replication, gene expression, genetic variation and distribution

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2
Q

What are the two main components of the bacterial genome?

A

Chromosome and mobile genetic elements (like plasmids or prophages)

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3
Q

What is a plasmid?

A

Autonomously replicating circular DNA

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4
Q

What is a Prophage?

A

Viruses integrated into the chromosome

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5
Q

What can you do from a whole genome sequence?

A

Predict cell function. You can identify patterns and homologous to known genes and motifs

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6
Q

Where are the most differences between different strains of genomes found?

A

In the MGE

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7
Q

What is a single nucleotide polymorphism?

A

Error in DNA replication

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8
Q

What do many Mobile Genetic Elements encode?

A

Virulence, antimicrobial resistance or host specific genes

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9
Q

What can acquisition of MGEs lead to?

A

New bacterial variants with enhanced virulence or resistance or host range

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10
Q

What are the three major pathways for the MGEs to move between bacteria?

A

Bacterial transformation, transduction and conjugation

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11
Q

How does bacterial transformation work?

A

Bacteria dies and releases the viral DNA into the environment. The recipient cell takes up that DNA up from the environment

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12
Q

How does bacterial transduction work?

A

Bacteria is either infected with a virus, or the virus in the genome is popped out (usually under stressful conditions)

Bacteria then undergoes the lytic pathway and lysed releasing the virus

Virus then binds to a new bacteria and injects their genes into the recipient

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13
Q

How does bacterial conjugation work?

A

Plasmids encode for the conjugation ability. Two bacteria come into contact with one another and make a pore between the two that allows the plasmid to move across to the other bacteria

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14
Q

What is a lytic pathway in bacterial genomics?

A

When a virus starts to dictate what happens in the bacteria, so it makes lots of copies of itself

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15
Q

Give some features of mobile genetic elements

A
  • autonomously replicating circular DNA - not essential to the host bacteria - easy to manipulate
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16
Q

What size are mobile genomic elements?

A

2 kb to >100 kb

17
Q

What is the restriction site on a plasmid?

A

Where you can add DNA

18
Q

What is generalised transduction?

A

Temperate bacteriophages accidentally packages host bacterial DNA or plasmids into long phage particles and delivers it to new bacteria

19
Q

Can all DNA transfer into any bacteria?

A

No

20
Q

What does the restriction modification enzyme do?

A

Binds to a specific sequence on the DNA and digests it

21
Q

How many subunits do restriction modification enzymes have?

A

3

22
Q

How do bacteria protect themselves from self digestion?

A

Makes a copy of the restriction modification enzyme without the enzyme bit, which methylates that bit of DNA, marking it as ‘self’

23
Q

What are some environmental triggers for bacteria?

A

Nutrients, oxygen, iron, temperature, bacterial pheromones, mammalian cells / hormones

24
Q

What are bacterial pheromones used for?

A

How the bacteria speak to each other

25
Q

Where are many bacterial virulence factors soley expressed?

A

In Vivo or in conditions mimicking those found in Vivo

26
Q

Where is ‘in vivo ‘?

A

In the host(the body)

27
Q

What can you do in transcriptional genomics?

A

Change the conditions depending on what you’re interested in

28
Q

What are the steps in transcriptional genomics?

A
  • grow bacteria in conditions of interest - extract bacteria - extract bacterial mRNA - convert mRNA to DNA - sequence the DNA and quantitate the numbers of transcripts of each genes
29
Q

Why do we manipulate bacterial genomes?

A

To make tools for industrial production of proteins and for studying bacteria or gene function

30
Q

What is the first step in cloning?

A

Cut two different pieces of DNA using a restriction enzyme, leaving matching sticky ends on both . Mix the two together and use lipase to seal the join

31
Q

What are the most common cloning vectors?

A

Plasmids

32
Q

What is a cloning region?

A

Target site for multiple restriction enzymes

33
Q

Can any DNA be cloned?

A

Yes

34
Q

How do you check which clones have worked correctly?

A

Culture the cells in conditions where only the gene you’ve taken up could grow (add the antibiotic if you’ve added an antibiotic resistant gene)

35
Q

How do you construct a knockout (5)?

A

1- clone virulence gene into ‘suicide vector’ plasmid
2- clone antibiotic resistance marker into the gene to disrupt it
3- transform into a bacterial cell
4- Recombination via RecA protein (rare)
5- place onto agar with antibiotic and select for the rare isolate that has the resistance marker

36
Q

What is CRISPR?

A

Genetic manipulation of eukaryotes

37
Q

What does CRISPR stand for?

A
Clustered
Regularly
Interspaced
Short
Palindromic
Repeats
38
Q

What is a knockout?

A

When one of the organisms genes are made inoperative (knocked out)