Font size
WorksheetsRecombinant Bacteria and Transformation
Total questions: 45
Worksheet time: 26mins
Which of the following is NOT a tool used in genetic engineering?
plasmid
restriction enzyme
DNA helicase
DNA ligase
Which restriction enzyme listed below was isolated from E. coli bacteria?
EcoRI
HindIII
HaeII
SmaI
During insertion step,
The recombinant plasmid is inserted into a host cell
The gene of interest is inserted into a plasmid
The plasmid is inserted into the gene of interest
Antibiotic resistance gene
Process of gene transfer where a virus moves genetic material from one bacteria to another
conjugation
transdution
transformation
What is the blue circle toward the bottom of the prokaryote called?
(a)
What is the red stringy thing in the middle called?
(a)
Process of gene transfer where a virus die/bursts & another bacteria takes in the free-floating plasmids
conjugation
transduction
transformation
The process gene transfer where bacteria connect pili to exchange plasmids
conjugation
transformation
transduction
bla (beta-lactamase)
What does it mean for cells to be competent
They are made to be 'smart' through genetic engineering
Their cell walls are altered to allow DNA to pass more easily
They contain regular DNA and plasmid DNA
They contain a gene for resistance to ampicillin
What process increases the competency of cells?
calcium chloride and an ice bath
calcium chloride and heat shock
Luria broth (LB) and an ice bath
Luria broth (LB) and heat shock
Which is the correct sequence for the process of genetic transformation?
bacterial cells transferred to cold CaCl2 , plasma with foreign DNA added bacteria , cells heat shocked at 42oC , cells spread on agar petri dish , bacteria given time to grow on petri dish
bacterial cells transferred to cold CaCl2 , cells heat shocked at 42oC , plasma with foreign DNA added bacteria , bacteria given time to grow on petri dish , cells spread on agar petri dish
plasma with foreign DNA added bacteria , bacterial cells transferred to cold CaCl2 , cells spread on agar petri dish , bacteria given time to grow on petri dish , cells heat shocked at 42oC
Which one of these agar plates contains bacteria most like the original bacterial culture
+pGLO LB/amp
+pGLO LB/amp/ara
-pGLO LB/amp
-pGLO LB
Which one of these agar plates would there be no bacteria growth?
+pGLO LB/amp
+pGLO LB/amp/ara
-pGLO LB/amp
-pGLO LB
Which image is a plasmid?
The plasmids scientists use in a lab are MOST COMMONLY found in
plants
animals
archaea
bacteria
All plasmids have an origin of replication which is necessary for
DNA to be duplicated
DNA to be transcribed into RNA
DNA to be inserted easily
DNA to be cut open
All plasmids have a promoter region which is necessary for
DNA to be duplicated
DNA to be transcribed into RNA
DNA to be inserted easily
DNA to be cut open
When bacteria is able to take up DNA, it is considered
permeable
semi-permeable
competent
curated
This image is representing a successful bacterial transformation
True
False
Why are cells incubated at 42o C?
At 42o C, bacterial cells begin releasing DNA for other cells to take up
This is a good recovery temperature after heat shock
At 42o C, the membranes of bacterial cells begin to degrade, creating pores through which DNA can enter the cell
Ampicillin (antibiotic) is used in the plates to
isolate and select for only the bacteria that have been successfully transformed
give bacteria energy to grow
act as a trigger to turn on the expression of the gene of interest
give the bacteria a new trait (such as fluorescence or insulin production)
Arabinose is used in the plates to
isolate and select for only the bacteria that have been successfully transformed
give bacteria energy to grow
act as a trigger to turn on the expression of the gene of interest
give the bacteria a new trait (such as fluorescence or insulin production)
Describe the source of the fluorescence.
from jellyfish
from fireflies
from a plant
from the pGFP encoded by the plasmid
Cells that fluoresce under UV light prove successful transformation and are on the plate
without DNA and with ampicillin
with DNA and ampicillin
with DNA and without ampicillin
without DNA or ampicillin
In a plate with DNA and ampicillin plated with pGFP cells what would the results demonstrate?
transformation of cells resistant to ampicillin
transformation of cells not resistant to ampicillin
transformation of no cells
transformation of cells that are both sensitive and resistant to ampicillin
In a plate with DNA but without ampicillin plated with GFP cells what would the result demonstrate?
host bacterial cells are viable in the absence of ampicillin
no growth
untransformed and transformed cells are viable in the absence of ampicillin
transformation of cells resistant to ampicillin
In the plate with no DNA but with ampicillin what would the result be?
white colonies
no growth
smeared layer of cells
flourescent cells
In a plate with no DNA or ampicillin, there are no fluorescent cells visible, what does this demonstrate?
host bacterial cells are viable in the absence of ampicillin
host bacterial cells are sensitive to ampicillin
host bacterial cells are untransformed
host bacterial cells are resistant to ampicillin
What is pGFP?
A plasmid
A chromosome
A protein
The success of bacterial transformation is determined by:
Transformation efficiency
transformation success rate
standard deviation
gene expression ratio
