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CP BIOTECHNOLOGY 
CHAPTER 13
13.1 What is biotechnology? 
The use of organisms to 
perform practical tasks 
for humans
13.1 Biologists Manipulate DNA 
 Today, we mainly manipulate the genomes of 
organisms. 
 We called this act of manipulation DNA 
technology.
13.1 Bacteria – Commonly used in 
Biotechnology 
* because they can acquire 
new genes in many ways! 
1. Tunnel-like structure 
forms between 2 bacteria 
so DNA can be passed- 
Conjugation 
2. Transformation – 
bacteria can “take up” 
free floating DNA into 
their own DNA 
3. Viruses can carry 
bacterial genes from 
one bacteria to another-transduction.
13.1 Recombinant DNA 
Technology 
Definition - technology involving the combining 
of DNA and/or genes from different sources 
(even genes from different species). 
Uses of DNA technology: 
1. Make more nutritious crops (ex. Corn) 
2. Make medicine in large quantities 
3. Help us understand specifically how gene 
sequences work
13.2 Engineering Bacteria 
 Bacteria contain plasmids 
 Plasmids are small circular pieces of DNA 
separate from the bacterial chromosome. 
 Plasmids carry genes
13.2 Plasmids 
 Scientists can manipulate plasmids to make 
them useful to us and Bacteria can transfer 
plasmids!! 
 Example: 
1. Insert a gene to make a medicine into a 
plasmid 
2. Put the plasmid into bacteria 
3. When the bacteria reproduce they make many 
copies of the medicine!
Process of Making Recombinant 
Bacterial Cell 
Process of Making Recombinant 
Bacterial Cell
13.2 How Do They Do It??? 
1. 1. Cut 
 1.  1. 2.  Use rreessttrriiccttiioonn eennzzyymmeess to cut 
the desired DNA/gene out of a 
larger chromosome 
1. Paste 
 Put the desired DNA/gene fragment 
into a plasmid 
1. Put the plasmid into a 
bacterium 
2. As the bacterium reproduces 
it makes many copies of the 
desired gene!! (Page 270 
Case Study) 
Restriction 
Enzyme=scisso 
rs 
Restriction 
Enzyme=scisso 
rs
13.2 
Genomic Library & Nucleic Acid 
Probes 
 Genomic Library: the 
complete collection of cloned 
DNA fragments from an 
organism 
 Nucleic Acid Probe: 
complimentary nucleotides 
labeled with a radioactive 
isotope used to “tag” single 
strand of a DNA sequence of 
choice.
13.2 FYI: Useful Products Using Genetic 
Engineering 
1. Bacteria make chemicals that clean up hazardous 
spills and toxic waste sites 
2. Bacteria are mass-producing useful chemicals like 
pesticides and therapeutic drugs 
3. Pigs & Cattle make human insulin hormone in their 
milk for people with diabetes 
4. Recombinant DNA technology is used to develop 
Vaccines – Hepatitis B (viral proteins are massed 
produced in yeast cells then used in vaccines)
1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd 
OOrrggaanniissmmss 
 A ggeenneettiiccaallllyy mmooddiiffiieedd oorrggaanniissmm ((GGMMOO)) is any 
organism that has acquired any genes 
artificially. 
 If a species is called TTRRAANNSSGGEENNIICC if it has 
foreign genetic material from a different 
species.
1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd 
PPllaannttss
Do you eat genetically modified 
organisms? 
YES NO
JJuusstt aa ffeeww……GGMMOO FFOOOODDSS 
Honey 
 Cotton 
 Tomatoes 
Corn 
 Vegetable Oil 
 Peas 
 Potatoes
Warm-Up - In Groups… 
 ½ the class will use their books to compile a 
list of postive or good reasons/outcomes of 
using genetically modified organisms (plants 
and animals) 
 ½ the class will use their books to make a list 
of negative or unwanted reasons to use 
genetically modified organisms.
Here’s what YOU think…
1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd PPllaannttss 
 Over 50% of soybean and corn crops were 
genetically modified in some way! 
 Most common genetic modifications: 
 Genes for herbicide resistance 
 Genes to resist insect and fungi pests
1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd 
AAnniimmaallss 
 Goals for GMO animals… 
 Produce mass quantities of hormones (insulin) 
 Get animals to market quicker (salmon) 
 Breed animals with better quality products (sheep 
wool) 
 FUN!! $$$$$$$
FFeeww mmoorree 
eexxaammpplleess……
1133..33 TThhee GGMMOO CCoonnttrroovveerrssyy 
Although studies to date have shown that eating 
genetically modified foods have no negative 
health affects…people continue to demand 
stricter regulations. 
MMaajjoorr CCoonncceerrnn:: 
GMO food can pose unknown health risk…request 
strict labeling laws 
**”ORGANIC CRAZE”**
1133..33 GGMMOO CCoonnttrroovveerrssyy
13.4 DNA Tech Has Many 
APpPCCpRlRic ooarr t PPiooonllyysmmeerraassee 
 PPCCRR oorr PPoollyymmeerraassee 
CChhaaiinn RReeaaccttiioonn 
technique can mass 
produce specific 
sequences of DNA 
without the use of living 
cells 
 Takes less time than 
use of living cells 
 Requires less amount 
of desired DNA 
initially 
 Used for cloning rare 
Thermocycler-machine 
used 
for PCR
1133..44 PPCCRR TTeecchhnniiqquuee 
“make a lot of DNA” from a small sample 
PPaaggee 227788 ffiigguurree 1133--1155
1133..44 GGeell EElleeccttrroopphhoorreessiiss 
 Used when you want to compare DNA from 
different sources. 
 Produces “banding patterns” which can be 
compared and analyzed.
13.4 Comparing DNA: How it 
works! (Pg 279) 
1.Different DNA 
samples are cut 
into “fragments” 
by restriction 
enzymes 
2.DNA “fragments” 
move through gel 
using electric current. 
2.DNA “fragments” 
move through gel 
using electric current. 
Smaller DNA 
fragments 
move further 
1.Different DNA 
samples are cut 
into “fragments” 
by restriction 
enzymes 
Each sample 
produces different 
banding patterns 
in the gel so they 
are easily 
compared 
Each sample 
produces different 
banding patterns 
in the gel so they 
are easily
13.4 Comparing DNA: Genetic 
Markers 
 Genetic Markers: 
are particular 
streches of DN that 
are variable among 
individuals. 
 Can be used to ID 
carriers of certain 
diseases
1133..44 CCoommppaarriinngg DDNNAA:: DDNNAA 
FFiinnggeerrpprriinntt 
 Just like every person has their own unique 
fingerprint…everyone has a unique banding 
pattern produced by their restriction fragments in 
gel electrophoresis. 
 97% of our DNA is “junk” or non-coding and is 
extremely different from any other persons “junk” 
DNA. 
 Forensics!!
1133..44 WWhhoo ccoommmmiitttteedd tthhee ccrriimmee?? 
Suspect # Bloodstain evidence from crime scene! 
1 2 3 4 5 6 7 
Using PCR and Gel 
Electrophoresis, a DNA 
fingerprint can be made 
from a single drop of 
blood or from a hair 
follicle. 
Using PCR and Gel 
Electrophoresis, a DNA 
fingerprint can be made 
from a single drop of 
blood or from a hair 
follicle. 
DNA is extracted from 
a small sample and 
multiple copies are 
made using PCR 
DNA is extracted from 
a small sample and 
multiple copies are 
made using PCR 
Gel Electrophoresis of 
unique genetic markers 
are compared 
Gel Electrophoresis of 
unique genetic markers 
are compared
13.5 SStteemm CCeellllss aanndd HHoommeeoottiicc GGeenneess 
 Stem cells – cells (early in 
development) that remain 
undifferentiated and have 
the potential to be any type 
of cell. 
 Homeotic Genes – genes 
that control development of 
specific locations in 
organisms.
Cloning 
 To make a clone: 
 A donor cell is fused with an 
egg cell 
 The fused cell begins to divide 
normally to form an embryo 
 Embryo is placed in uterus of 
foster mom 
 Clone is born
Cloning

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Applied biology chapter 13 biotechnology 2013 2

  • 2. 13.1 What is biotechnology? The use of organisms to perform practical tasks for humans
  • 3. 13.1 Biologists Manipulate DNA  Today, we mainly manipulate the genomes of organisms.  We called this act of manipulation DNA technology.
  • 4. 13.1 Bacteria – Commonly used in Biotechnology * because they can acquire new genes in many ways! 1. Tunnel-like structure forms between 2 bacteria so DNA can be passed- Conjugation 2. Transformation – bacteria can “take up” free floating DNA into their own DNA 3. Viruses can carry bacterial genes from one bacteria to another-transduction.
  • 5. 13.1 Recombinant DNA Technology Definition - technology involving the combining of DNA and/or genes from different sources (even genes from different species). Uses of DNA technology: 1. Make more nutritious crops (ex. Corn) 2. Make medicine in large quantities 3. Help us understand specifically how gene sequences work
  • 6. 13.2 Engineering Bacteria  Bacteria contain plasmids  Plasmids are small circular pieces of DNA separate from the bacterial chromosome.  Plasmids carry genes
  • 7. 13.2 Plasmids  Scientists can manipulate plasmids to make them useful to us and Bacteria can transfer plasmids!!  Example: 1. Insert a gene to make a medicine into a plasmid 2. Put the plasmid into bacteria 3. When the bacteria reproduce they make many copies of the medicine!
  • 8. Process of Making Recombinant Bacterial Cell Process of Making Recombinant Bacterial Cell
  • 9. 13.2 How Do They Do It??? 1. 1. Cut  1.  1. 2.  Use rreessttrriiccttiioonn eennzzyymmeess to cut the desired DNA/gene out of a larger chromosome 1. Paste  Put the desired DNA/gene fragment into a plasmid 1. Put the plasmid into a bacterium 2. As the bacterium reproduces it makes many copies of the desired gene!! (Page 270 Case Study) Restriction Enzyme=scisso rs Restriction Enzyme=scisso rs
  • 10. 13.2 Genomic Library & Nucleic Acid Probes  Genomic Library: the complete collection of cloned DNA fragments from an organism  Nucleic Acid Probe: complimentary nucleotides labeled with a radioactive isotope used to “tag” single strand of a DNA sequence of choice.
  • 11. 13.2 FYI: Useful Products Using Genetic Engineering 1. Bacteria make chemicals that clean up hazardous spills and toxic waste sites 2. Bacteria are mass-producing useful chemicals like pesticides and therapeutic drugs 3. Pigs & Cattle make human insulin hormone in their milk for people with diabetes 4. Recombinant DNA technology is used to develop Vaccines – Hepatitis B (viral proteins are massed produced in yeast cells then used in vaccines)
  • 12. 1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd OOrrggaanniissmmss  A ggeenneettiiccaallllyy mmooddiiffiieedd oorrggaanniissmm ((GGMMOO)) is any organism that has acquired any genes artificially.  If a species is called TTRRAANNSSGGEENNIICC if it has foreign genetic material from a different species.
  • 14. Do you eat genetically modified organisms? YES NO
  • 15. JJuusstt aa ffeeww……GGMMOO FFOOOODDSS Honey  Cotton  Tomatoes Corn  Vegetable Oil  Peas  Potatoes
  • 16. Warm-Up - In Groups…  ½ the class will use their books to compile a list of postive or good reasons/outcomes of using genetically modified organisms (plants and animals)  ½ the class will use their books to make a list of negative or unwanted reasons to use genetically modified organisms.
  • 17. Here’s what YOU think…
  • 18. 1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd PPllaannttss  Over 50% of soybean and corn crops were genetically modified in some way!  Most common genetic modifications:  Genes for herbicide resistance  Genes to resist insect and fungi pests
  • 19. 1133..33 GGeenneettiiccaallllyy MMooddiiffiieedd AAnniimmaallss  Goals for GMO animals…  Produce mass quantities of hormones (insulin)  Get animals to market quicker (salmon)  Breed animals with better quality products (sheep wool)  FUN!! $$$$$$$
  • 21. 1133..33 TThhee GGMMOO CCoonnttrroovveerrssyy Although studies to date have shown that eating genetically modified foods have no negative health affects…people continue to demand stricter regulations. MMaajjoorr CCoonncceerrnn:: GMO food can pose unknown health risk…request strict labeling laws **”ORGANIC CRAZE”**
  • 23. 13.4 DNA Tech Has Many APpPCCpRlRic ooarr t PPiooonllyysmmeerraassee  PPCCRR oorr PPoollyymmeerraassee CChhaaiinn RReeaaccttiioonn technique can mass produce specific sequences of DNA without the use of living cells  Takes less time than use of living cells  Requires less amount of desired DNA initially  Used for cloning rare Thermocycler-machine used for PCR
  • 24. 1133..44 PPCCRR TTeecchhnniiqquuee “make a lot of DNA” from a small sample PPaaggee 227788 ffiigguurree 1133--1155
  • 25. 1133..44 GGeell EElleeccttrroopphhoorreessiiss  Used when you want to compare DNA from different sources.  Produces “banding patterns” which can be compared and analyzed.
  • 26. 13.4 Comparing DNA: How it works! (Pg 279) 1.Different DNA samples are cut into “fragments” by restriction enzymes 2.DNA “fragments” move through gel using electric current. 2.DNA “fragments” move through gel using electric current. Smaller DNA fragments move further 1.Different DNA samples are cut into “fragments” by restriction enzymes Each sample produces different banding patterns in the gel so they are easily compared Each sample produces different banding patterns in the gel so they are easily
  • 27. 13.4 Comparing DNA: Genetic Markers  Genetic Markers: are particular streches of DN that are variable among individuals.  Can be used to ID carriers of certain diseases
  • 28. 1133..44 CCoommppaarriinngg DDNNAA:: DDNNAA FFiinnggeerrpprriinntt  Just like every person has their own unique fingerprint…everyone has a unique banding pattern produced by their restriction fragments in gel electrophoresis.  97% of our DNA is “junk” or non-coding and is extremely different from any other persons “junk” DNA.  Forensics!!
  • 29. 1133..44 WWhhoo ccoommmmiitttteedd tthhee ccrriimmee?? Suspect # Bloodstain evidence from crime scene! 1 2 3 4 5 6 7 Using PCR and Gel Electrophoresis, a DNA fingerprint can be made from a single drop of blood or from a hair follicle. Using PCR and Gel Electrophoresis, a DNA fingerprint can be made from a single drop of blood or from a hair follicle. DNA is extracted from a small sample and multiple copies are made using PCR DNA is extracted from a small sample and multiple copies are made using PCR Gel Electrophoresis of unique genetic markers are compared Gel Electrophoresis of unique genetic markers are compared
  • 30. 13.5 SStteemm CCeellllss aanndd HHoommeeoottiicc GGeenneess  Stem cells – cells (early in development) that remain undifferentiated and have the potential to be any type of cell.  Homeotic Genes – genes that control development of specific locations in organisms.
  • 31. Cloning  To make a clone:  A donor cell is fused with an egg cell  The fused cell begins to divide normally to form an embryo  Embryo is placed in uterus of foster mom  Clone is born