Lecture 5 Flashcards

1
Q

Operon

A

A cluster of 2 or more genes that share an upstream control (regulatory) region and a termination sequence. Co-transcribe genes.

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2
Q

Trip Operon

A

Response to Environmental stimuli

E. coli can synthesize most molecules needed for growth

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3
Q

Repressible Operon

A

Something is added or accumulates (Trp) that turns off transcription

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4
Q

Inducible genes

A

Genes get “turned on” or activated when conditions change

Example:
E. coli prefers glucose but in glucose-free conditions, it can metabolize lactose
-but first, it needs to make genes that can metabolize lactose

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5
Q

Inducible Operon—Lac Operon

A

Default is off
-When lactose is added, it binds to repressor and pushes it off allow transcription to occur

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6
Q

Catabolism repression

A

Catabolite activator protein (CAP)

Two mechanisms:
-Lactose present, but no glucose
-Lactose present+glucose present

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7
Q

Inducible promoter

A

-E. coli prefers glucose
-when glucose is gone:
•lactose inactivates the repressor
•cAMP increases to activate transcription

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8
Q

Operon vs regulon

A

Regulon—when more than one Operon is under control of the same regulatory protein, the Operon are referred to as regulons

-Stress response
-Pathogenesis
-Phosphate deprivation
-Presence of maltose

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9
Q

Translation

A

Protein synthesis

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10
Q

sRNA

A

Small RNA

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11
Q

Mutation

A

Change in the DNA base sequence (nucleotides) of genome

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12
Q

Spontaneous mutation

A

Errors in DNA replication

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13
Q

Missense mutation

A

Change in amino acid

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14
Q

Nonsense mutation

A

Stop codon

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15
Q

Silent mutation

A

No amino acid change (wobble)

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16
Q

Frameshift mutation

A

Insertion or deletion of one or more nucleotide pairs

17
Q

Spontaneous mutation rate

A

1 error every 10^9 replicated base pairs=1 error in every 10^6 replicated genes

18
Q

Mutagens

A

Increase to 1 error in every 10^3 replicated gene

19
Q

Chemical mutagen examples

A

-Nitrous acid (HNO2)
-Nitrosamine (HN2O2)

20
Q

Physical mutagen examples

A

-UV light
•absorbed by DNA
-ionizing radiation
•causes breaks in DNA
•for cancer treatment + nuclear bombs
•nasty radiation

21
Q

Clastogens

A

-Lead to Genomic instability
Examples:
Acridine yellow, arsenic, benzene

22
Q

Three types of DNA repair

A
  1. SOS repair
  2. Photolyases
  3. Nucleotide excision repair
23
Q

SOS repair

A

Initiates regulon activity where over 40 genes are involved in different types of repair, growth arrest, & apoptosis.

24
Q

Photolyases

A

Separate thymine dimers

25
Nucleotide excision repair
Removes and replaces a single base
26
Positive (direct) selection
Detects mutant cells because they grow or appear different •Ames test
27
Negative (indirect) selection
Detects mutant cells because they do not grow •replica plating
28
Ames test
-for chemical mutagens -to see if more grow due to mutagen -test on media lacking histidine
29
Why eat liver extract in Ames test?
Because of enzymes and mimics metabolism of mutagens
30
Auxotroph
A mutant strain with a new nutritional requirement compared to parental/wildtype strain
31
Why are mutants (and mutagens) useful?
-make attenuated (less virulent) strains of microbes for vaccines -cancer treatment kills quickly diving cells
32
Replica plating
-identification of antibiotic resistant strains of bacteria -identification of auxotrophs
33
Vertical gene transfer
A parent cell divides through binary fission to make 2 daughter cells
34
Horizontal gene transfer
The transfer of genes between cells of the same generation
35
Horizontal transformation