
Term 2 - Week 1 - 11ADV - DNA Technology (L1)
Presentation
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Biology
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11th Grade
•
Practice Problem
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Easy
Standards-aligned
Kirsten Feather
Used 13+ times
FREE Resource
17 Slides • 8 Questions
1
DNA Technology
Lesson 1
2
Week 1:
3.1.1 Differentiate, using examples, between genetic engineering and biotechnology
3.1.2 Summarize the roles of DNA tools (Include: restriction enzymes and gel
electrophoresis)
3.1.3 Interpret data collected from the process of gel electrophoresis
3.1.4 Sequence, using diagrams and models, how recombinant DNA is made and
manipulated
3.1.5 Explain the role of plasmids and DNA ligase in recombinant DNA technology
Week 2:
3.1.6 Describe in steps, using a diagram, the process of gene cloning
3.1.7 Describe in steps, using a diagram, the process of DNA sequencing
3.1.8 Detail, using a diagram, the steps of PCR
3.1.9 Analyze the application of biotechnology (transgenic organisms) in plants,
animals, and bacteria
Lab 10: The Missing Restaurant Owner
Lab 11: Quick Investigation: Model Restriction Enzymes
Learning outcomes – KPI’s
3
WEEK 1 – Class work
Quizizz and
GOFORMATIVE
4
Focus Question
What is the difference between
genetic engineering and
biotechnology?
MENTIMETER
5
New Vocabulary
genetic engineering
genome
transformation
restriction enzyme
DNA ligase
cloning
gel electrophoresis
polymerase chain reaction
recombinant DNA
transgenic organism
plasmid
6
Review Vocabulary
DNA: the genetic material of all organisms,
composed of two complementary chains of
nucleotides wound in a double helix
7
8
Genetic Engineering
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By about 1970, researchers had discovered
the structure of DNA and determined the
central dogma that information flowed from
DNA to RNA to proteins.
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However, scientists did not know much about
the function of individual genes.
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The situation changed when scientists began
using genetic engineering, technology that
involves manipulating the DNA of one
organism in order to insert exogenous DNA
(the DNA of another organism).
3.1.1 Differentiate, using examples, between genetic engineering and biotechnology
9
DNA Tools
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Genetic engineering can be used to increase or
decrease the expression of specific genes in
selected organisms. It has many applications
from human health to agriculture.
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An organism’s genome is the total DNA present
in the nucleus of each cell.
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In order to study a specific gene, DNA tools can
be used to manipulate DNA and to isolate genes
from the rest of the genome.
3.1.2 Summarize the roles of DNA tools (Include: restriction enzymes and gel electrophoresis)
10
DNA Tools
Restriction Enzymes
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Restriction enzymes are proteins that recognize
and bind to specific DNA sequences and cleave
the DNA within that sequence.
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Restriction enzymes are used as powerful tools
for isolating specific genes or regions of the
genome.
11
DNA Tools
EcoRI
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EcoRI is a restriction
enzyme that specifically
cuts DNA containing the
sequence GAATTC.
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Sticky ends are single
stranded DNA sequences
at the end of fragments.
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They can be joined
together with
complementary sticky
ends.
12
13
Multiple Choice
Which of the following is a protein that acts as DNA scissors?
plasmid
ligase
restriction enzyme
protein expression
14
DNA Tools
Gel Electrophoresis
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In gel electrophoresis, an electric current is used
to separate DNA fragments according to the size
of the fragments.
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When an electric current is applied, the DNA
fragments move toward the positive end of the
gel.
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The unique pattern created based on the size of
the DNA fragments can be compared to known
DNA fragments for identification.
3.1.3 Interpret data collected from the process of gel electrophoresis
15
16
Multiple Choice
Gel electrophoresis enables scientists to
separate DNA fragments.
count the genes in DNA
combine DNA fragments
insert DNA in cells
17
Multiple Choice
Based on these results whose blood was found in the blood stain at the crime scene?
Bob
John
Sue
Lisa
18
Recombinant DNA Technology
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DNA fragments from different sources can be
combined to make new DNA molecules.
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The newly generated DNA molecules with DNA
from different sources is called recombinant DNA.
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Recombinant DNA is placed into bacterial cells for
study via a vector.
3.1.4 Sequence, using diagrams and models, how recombinant DNA is made and manipulated
19
Recombinant DNA Technology
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Common vectors include viruses and plasmids.
Plasmids are small, circular, double-stranded DNA
molecules that occur naturally in bacteria and
yeasts.
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DNA ligase, a cellular repair enzyme, attaches the
recombinant DNA to the plasmid.
3.1.5 Explain the role of plasmids and DNA ligase in recombinant DNA technology
20
Multiple Choice
Which of the following is a circular piece of DNA from bacteria that can hold a foreign gene?
plasmid
ligase
restriction enzyme
protein expression
21
Multiple Choice
When human DNA is inserted in bacterial DNA to create insulin it is called
viral DNA
bacterial DNA
recombinant DNA
transcribed DNA
22
Recombinant DNA Technology
23
Draw
Label the diagrams missing labels
24
Multiple Choice
Which of the following tools or processes is NOT involved in genetic engineering?
restriction enzymes
the human genome
gene cloning
DNA sequencing
25
Poll
Rate your level of understanding and ability to answer all questions on DNA technology
1 - no understanding at all
2 - I sort of understand
3 - I still need to practice these concepts
4 - I have full understanding of this topic
DNA Technology
Lesson 1
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