WorksheetsBiotechnology
Total questions: 77
Worksheet time: 1hrs 1mins
ATG TGA CAG
An individual’s code determines the number of times the restriction enzymes will cut and the number and size of DNA pieces that will result.
True
False
What is a palindrome?
Sticky end
Blunt end
A sequence that reads the same forwards and backwards
A sequence that is complementary to the other
Which RE's from above make blunt cuts?
Alul
HaeIII
BamHI
HindIII
EcorRI
Which RE's from above make sticky cuts?
Alul
HaeIII
BamHI
HindIII
EcorRI
How many fragments resulted from the cut above?
1
2
3
4
"bp" stands for...
Blood Pressure
Base Pair
Body Pressure
Body Pair
How many bp's make up each fragment?
11
14
7
22
28
How many restriction sites appear in the picture?
1
2
3
4
Is the restriction site above en example of a palindrome?
Yes
No
1. If the recognition sequence of the restriction enzyme HindIII is AAGCTT, then how many covalent bonds will be broken by the enzyme in the following DNA molecule?
1
2
3
4
A technique for making millions of copies of a specific region of DNA.
DNA ligase
restriction enzymes
gel electrophoresis
polymerase chain reaction
From where does Taq polymerase come?
Bacteria that live in hydrothermal vents/hot springs.
Cambodia
The rain forest
The CDC
If the primer sequence is TCG, what section of DNA will it anneal?
AGC
CAT
GAC
ATC
What is the function of DNA Polymerase?
attach primers to target sequence
separate the DNA
attach nucleotides to the target sequence
separate the fragments according to size
How is Fast PCR able to run at such a shorter time frame
Lower the temperature of Denaturation
raises the temperature for annealing so that it and extension can happen almost simultaneously
Shortens the time frame of denatureation
all of the answers are correct
If two double-stranded DNA molecules are used at the beginning of a polymerase chain reaction (PCR) process, how many double-stranded DNA molecules can be obtained after two cycles?
2
4
8
32
Which is the correct order for the PCR process
denaturation, elongation, annealing
annealing, elongation, denaturation
denaturation, annealing, elongation
annealing, denaturation, elongation
This is the process of reading the entire DNA for an organism, identifying the order of the bases
Cloning
Gel Electrophoresis
Genetic Engineering
DNA Sequencing
small segment of DNA or RNA that binds to a specific DNA sequence and allows DNA polymerase to begin copying the strand
terminator base
plasmid
primer
SNP
This image shows
polymerase chain reaction
genetic engineering
DNA sequencing
gene mapping
This picture shows
DNA sequencing
GWAS
plasmid
CRISPR
This image shows
Synthetic Biology
CRISPR
GWAS
PCR
Who matches the crime scene DNA?
suspect #1
suspect #2
suspect #3
none of the suspects match the DNA
Who can be included as source of paternal DNA for this child?
male #1
male #2
neither male
What is the purpose of gel electrophoresis?
to make copies of the DNA so there is enough to test
to separate the DNA segments by size
to isolate the DNA from the cell
to pull out repeating regions of DNA
Which fragments would move the farthest in gel electrophoresis?
a 12 base pairs long fragment
a 54 base pairs long fragment
a 108 base pairs long fragment
This image shows a
electropherogram
gel electrophoresis
PCR
electrocardiogram
Which of the following is FALSE?
Humans share a large percentage of their DNA with other organisms and even plants, like bananas.
Much of the human genome is “junk” DNA, which codes for nothing at all.
All of the letter sequences in DNA code for the production of proteins.
Proteins are produced by combining amino acids according to the DNA sequence.
On an electropherogram, alleles are represented by...
peaks on a graph
letters like AA or Aa
blue dots on a test strip
band on an autorad
DNA can be degraded or destroyed by ...
moisture
heat
sunlight
all answers
First stage involved in gene cloning.
Amplification of the target gene
Insertion of the target gene
Polymerase Chain Reaction
Isolation of the target gene
The plasmids carrying the target gene (recombinant plasmids) must be introduced into a host cell through _____.
Cloning
insertion
Transformation
Isolation
Types of plasmids produced after insertion of the target gene into a vector.
Recombinant plasmids
Non-recombinant plasmids
Bacterial plasmids
Isolated plasmids
Which technology below would probably be the most important to a person who had diabetes and had to take insulin every day?
using recombinant DNA to produce human hormones from bacteria
testing parents for genetic disorders before they have children
engineering fruits and vegetables that resist insects and other pests
C. developing ways to identify criminals through DNA fingerprinting
How do scientists cut DNA into smaller strands?
restriction enzymes
scissors
ligase
agarose
In order to insert a human gene into plasmid, both must
code for the same gene product.
be cut by the same restriction enzyme.
originate from the same type of cell.
have identical sequences.
Which enzyme "glues" DNA fragments together during insertion?
restriction enzymes
DNA ligase
DNA polymerase
DNA helicase
Which of the following could be used as a vector for a human gene?
Bacterial Plasmid
Bacteria
A mitochondria
mRNA
The site where restriction enzymes cut are a called:
cut sites
restriction sites
recognition sites
cleave sites
Sticky ends are produced when the restriction enzyme cuts in a:
staggered manner
straight through the DNA
How many times do you want a restriction enzyme to cut a human genome in order to cut out the gene of interest to insert into a plasmid?
1 - through the gene
2 - on either side of the gene
3 - through the gene and on either side of the gene
Cell that receive recombinant DNA for cloning purpose
Host cell
plasmid
DNA target
Gene of interest
Which of the following is NOT a tool used in recombinant DNA technology?
Cloning vector
RNA polymerase
Target DNA
DNA ligase
What is recombinant DNA
DNA from 2 different organisms combined
DNA from 2 different ribosomes
DNA that is separated out from a vector
The following are the steps taken during the cloning process.
1. Transformation 2. Insertion 3. Isolation 4. Screening 5. Cut
3, 2, 5, 1, 4
3, 2, 5, 4, 1
3, 5, 2, 1, 4
3, 5, 2, 4, 1
Recombinant DNA technology involves a screening process. What is the purpose of screening process?
Isolate recombinant DNA from bacteria
Identify cell with target DNA to be cut by restriction enzyme
Identify bacteria with plasmid to be used as vector
Identify bacteria with recombinant plasmid
