class #4- bacterial genetics Flashcards

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1
Q

what is a bacteriophage

A

a virus that parasitizes a bacterium by infecting it and reproducing inside it

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1
Q

what is the lytic cycle

A

-injection of phage dna
-replication & synthesis of new phage particles
-packaging of DNA into heads
-lysis
-infection (start again)

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2
Q

what is lysis

A

disintegration of cell by rupture of cell wall or membrane (killing)

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3
Q

what is the hershey heaven and the waring blender experiment

A

an experiment to prove dna is genetic material using s35 (radioactive sulfur) and p32 (radioactive phosphorus)

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4
Q

what was the role of s35 in hershey ex

A

to label protein

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5
Q

what was the role of p32 in hershey ex

A

to label the dna

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6
Q

what happened in the hershey ex

A
  1. let phage absorb to bacteria then put in blender
  2. separate phage from bacteria: s35 went with phage(virus) and p32 when with bacteria
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7
Q

how did the hershey experiment prove that dna was genetic material

A

p32 was detected in cells (was in dna) s35 was not detected in cells (was in protein)

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8
Q

what is a phage plaque

A

zone of lysed bacteria

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9
Q

what is a turbid plaque

A

created by a lysogenic phage

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10
Q

what is turbidity caused by

A

Caused by bacteria that have been infected and the phage has integrated into the genome

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11
Q

what is generalized transduction

A

The process by which phages can package any bacterial DNA (chromosomal or plasmid) and transfer it to another bacterium.

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12
Q

where does generalized transduction occur

A

during the lytic cycle

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13
Q

what happens during generalized transduction

A

host dna is degraded and bits are mistakenly packaged along with phage dna, host dna is now transferred to another host

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14
Q

is generalized transduction efficient

A

no, b/c only a single phage is getting packaged with dna from host

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15
Q

what is transformation

A

the uptake of naked dna.

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16
Q

what important experiment used transformation to show that DNA is genetic material?

A

Griffiths experiment (rats, s strain and r strains)

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17
Q

what are the most desperate ways to transform DNA

A

-biolistic transformation
-electroporation

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18
Q

what is naturally competent bacteria

A

bacteria that are naturally “competent” to take up DNA, they have structures & systems dedicated to taking up dna

19
Q

who is Joshua Lederberg

A

he coined the term “plasmids”, nobel prize for conjugation 1959

20
Q

what is conjugation

A

bacterial “sex”, where one bacterium transfers genetic material to another through direct contact

21
Q

what are self-transmissable plasmids

A

they encode machinery to iniate conjugation and transfer plasmid

22
Q

what is a mobilizable plasmid

A

can be transferred but need Tra functions supplied in trans

23
Q

role of donor and recipient in conjugation

A

donor- has plasmid
recipient - gets plasmid

24
Q

how is dna transferred in conjugation

A

rolling circle replication, direct contact between 2 bacteriums

25
Q

what is CRISPR

A

adaptive immunity for bacteria
Clustered Regularly Interspaced Short Palindromic Repeats

26
Q

what are CAS

A

CRISPR associated genes

27
Q

how does CRISPR work

A
  1. the array is transcribed
  2. Cas gene products process array
  3. crRNA has a piece that is bound by the Cas9
  4. crRNA-Cas9 complex can recognize specific DNA sequences
28
Q

what are transposons

A

DNA elements that ecode transposase,
they insert randomly

29
Q

role of transposase

A

they copy a short sequence of DNA and allows DNA to ‘jump’

30
Q

what is Barbara McClintock’s main contribution

A

she developed notion of gene regulation

31
Q

what is target duplication

A

it follows after insertion, duplicates a small genetic sequence

32
Q

what aids in duplicating a target sequence

A

transposase

33
Q

what is a promoter

A

A region of DNA upstream of a gene where relevant proteins bind to initiate transcription of that gene.

34
Q

what does a promoter drive

A

drives the expression of a single gene, or mulitple genes (co-expression)

35
Q

what is an operon

A

where genes that are co-expressed are found

36
Q

what is an activator

A

proteins that bind to DNA at sequence sites to promote RNA polymerase function

37
Q

who is Jacques Manod and what did he contribute

A

-founder of molecular bio
-worked out lac operon and trp operon

38
Q

what is a repressor

A

they block binding of RNA polymerase to promoter
their ability to bind DNA is often regulated by cofactors (sugars or other metabolites)

39
Q

in the lac operon, what is the uninduced state

A

lacl (repressor) binds to operator
no transcription

40
Q

what is a non-inducible mutant

A

lacZ, the Lacl repressor can no longer bind to lactose

41
Q

in the lac operon, what is the induced stat:

A

-the inducer (lactose) binds Lacl (repressor)
-and Lacl cannot bind to operator
-transcription of operon

42
Q

what is a constitutive mutant

A

when lacl: no repressor, no repression
and Oc: repressor binding site damaged, Lacl is made but cannot bind

43
Q

what is a cis mutation

A

cis-acting locus: a genetic region affecting the activity of genes on that same DNA molecule

44
Q

what is a trans mutation

A

trans-acting locus: encodes for a factor that can act else where