1.-Genetic-Engineering-rem
1.-Genetic-Engineering-rem
NegOr_Q3_GenBio2_SLKWeek1_v2
1
NegOr_Q3_GenBio2_SLKWeek1_v2
FOREWORD
NegOr_Q3_GenBio2_SLKWeek1_v2
2
OBJECTIVES
LEARNING COMPETENCIES
• Outline the processes involved in genetic engineering
(STEM_BIO11/12-IIIa-b-6)
NegOr_Q3_GenBio2_SLKWeek1_v2
3
Ma’am, why is it that Good question, Cardo!
the tomatoes do not The reason for that is
have the same size? the so-called
recombinant DNA.
I. WHAT HAPPENED
PRE-TEST
NegOr_Q3_GenBio2_SLKWeek1_v2
4
M_D_C_L AP_LIC_T_ON
4. It is a molecule which contains all information necessary
to build and maintain an organism.
D_O_YR_B_N_CL_IC A_C_D
5. Production of chemical compounds of commercial
importance
_ND_STRI_L A_PL_C_TI_N
6. It is a process using recombinant DNA technology to alter
the genetic makeup of an organism.
G_N_T_C ENG_N_ER_NG
7. It is the basic unit of heredity.
G_N_S
8. It produces copies of genes or segments of DNA.
G_N_ C_O_N_NG
DISCUSSION
5
Escherichia coli (E. coli) species. Following these successful pilot
experiments, in 1978 Cohen and colleagues progressed to transfer
an insulin synthesis gene into a plasmid of E. coli, with that producing
the first genetically modified organism (GMO). By 1982, this protocol
received full approval from national drug regulatory authorities,
notably the US Food and Drug Administration, thereby enabling the
economically viable mass production of human insulin, a hormone
that regulates blood sugar levels and is made naturally by beta cells
in the pancreas. This facilitated the widespread commercial
availability of insulin at a price affordable to patients with the
metabolic disorders’ types 1 and 2 diabetes mellitus, who either fail
to produce or to metabolize sufficient insulin.
What is recombinant
DNA?
NegOr_Q3_GenBio2_SLKWeek1_v2
6
Recombinant DNA
1. Distant hybridization
With the advancement of genetic engineering, it is now
possible to transfer genes between distantly related species. The
barriers of gene transfer between species or even genera have
been overcome. The desirable genes can be transferred even from
lower organisms to higher organisms through recombinant DNA
technology.
NegOr_Q3_GenBio2_SLKWeek1_v2
7
2. Development of transgenic plants
Genetically transformed plants which contain foreign genes
are called transgenic plants. Resistance to diseases, insects and
pests, herbicides, drought; metal toxicity tolerance; induction of
male sterility for plant breeding purpose; and improvement of
quality can be achieved through this recombinant DNA
technology. BT-cotton resistant to bollworms is a glaring example.
4. Development of C4 plants
Improvement in yield can be achieved by improving the
photosynthetic efficiency of crop plants. The photosynthetic rate
can be increased by conversion of C3 plants into C4 plants, which
can be achieved either through protoplasm fusion or recombinant
DNA technology. C4 plants have higher potential rate of biomass
production than C3 plants. Most C4 plants (sorghum, sugarcane,
maize, some grasses) are grown in tropical and subtropical zones.
1. Production of antibiotics
Penicillium and Streptomyces fungi are used for mass
production of famous antibiotics penicillin and streptomycin.
Genetically efficient strains of these fungi have been developed to
greatly increase the yield of these antibiotics.
8
structure from human insulin. As a result, it leads to allergic reactions
in about 5% patients. Human gene for insulin production has been
incorporated into bacterial DNA and such genetically engineered
bacteria are used for large-scale production of insulin.
3. Production of vaccines
Vaccines are now produced by transfer of antigen-coding genes
to disease-causing bacteria. Such antibodies provide protection
against the infection by the same bacteria or virus.
4. Production of interferon
Interferons are virus-induced proteins produced by
virusinfected cells. Interferons are antiviral in action and act as first
line of defense against viruses causing serious infections, including
breast cancer and lymph node malignancy. Natural interferon is
produced in very small quality from human blood cells. It is thus very
costly also. It is now possible to produce interferon by recombinant
DNA technology at a much cheaper rate.
5. Production of enzymes
Some useful enzymes can also be produced by recombinant
DNA technique. For instance, enzyme urokinase, which is used to
dissolve blood clots, has been produced by genetically engineered
microorganisms.
6. Gene therapy
Genetic engineering may one day enable the medical
scientists to replace the defective genes responsible for hereditary
diseases (e.g., hemophilia, phenylketonuria, alkaptonuria) with
normal genes. This new system of therapy is called gene therapy.
8. Diagnosis of disease
Recombinant DNA technology has provided a broad range
of tools to help physicians in the diagnosis of diseases. Most of these
involve the construction of probes: short segments of singlestranded
DNA attached to a radioactive or fluorescent marker. Such probes
NegOr_Q3_GenBio2_SLKWeek1_v2
9
are now used for the identification of infectious agents, for instance,
food poisoning Salmonella, pus-forming Staphylococcus, hepatitis
virus, HIV, etc. By testing the DNA of prospective genetic disorder
carrier parents, their genotype can be determined and their
chances of producing an afflicted child can be predicted.
Examples:
Cow, sheep, goat – therapeutic human proteins in their milk. Fish
like common carp, catfish, salmon and goldfish contain human
growth hormone (hGH).
What is genetic
engineering?
Genetic engineering
10
• It involves the direct manipulation of one or more genes. Most
Source: https://www.slideshare.net/mobile/dineshbhati5209000/genetically-modified-organisms34236637
NegOr_Q3_GenBio2_SLKWeek1_v2
11
Five Basic Processes in Genetic Engineering
Backcross
Breeding
NegOr_Q3_GenBio2_SLKWeek1_v2
12
Step 2: Gene cloning
The second step of the genetic engineering process is gene
cloning. During DNA extraction, all of the DNA from the organism is
extracted at once. Scientists use gene cloning to separate the
single gene of interest from the rest of the genes extracted and
make thousands of copies of it.
Since plants have millions of cells, it would be impossible to insert a copy of the
transgene into every cell. Therefore, tissue culture is used to propagate masses
of undifferentiated plant cells called callus. These are the cells to which the new
transgene will be added.
The new gene is inserted into some of the cells using various techniques. Some
of the more common methods include the gene gun, agrobacterium,
microfibers, and electroporation.
The main goal of each of these methods is to transport the new gene(s) and
deliver them into the nucleus of a cell without killing it.
Transformed plant cells are then regenerated into
transgenic plants. The transgenic plants are grown to
maturity in greenhouses, and the seed they produce,
which has inherited the transgene, is collected. The
genetic engineer's job is now complete. He/she will
hand the transgenic seeds over to a plant breeder
who is responsible for the final step.
NegOr_Q3_GenBio2_SLKWeek1_v2
13
Step 5 : Backcross breeding (e.g., engineered crop) Transgenic
plants are crossed with elite breeding lines using traditional plant
breeding methods to combine the desired traits of elite parents
and the transgene into a single line. The offspring are repeatedly
crossed back to the elite line to obtain a high-yielding transgenic
line. The result will be a plant with a yield potential close to current
hybrids that expresses the trait encoded by the new transgene.
(Source:
http://passel-
test.unl.edu/beta/pages/informationmodule.php?idinformationmodule=957879329&topicorder=3&maxto=9&minto=1
I. Gene design
II. Transformation
III. DNA extraction
IV. Backcross breeding
NegOr_Q3_GenBio2_SLKWeek1_v2
14
V. Gene cloning
1. __________
2. __________
3. __________ 4. __________
5. __________
2. DNA extraction
B. Extraction of DNA from a
3. Recombinant DNA
donor organism
4. Gene cloning
C. Gene insertion into vector 5.
Agricultural application
6. Genetic engineering
D. Combination of two DNA
7. Gene design
molecules form new genetic
8. Medicinal application combination
NegOr_Q3_GenBio2_SLKWeek1_v2
15
F. Production of
antibiotics,
hormones, and vaccines
J. Production of
chemical compounds
NegOr_Q3_GenBio2_SLKWeek1_v2
16
REFERENCES
https://medcraveonline.com/JABB/application-of-
recombinantdna-technology-genetically-modified-
organisms-to-theadvancement-of-agriculture-medicine-
bioremediation-andbiotechnology-industries.html
https://www.biologydiscussion.com/dna/recombinant-
dnatechnology/applications-of-recombinant-dna-
technology-3applications/15650
https://www.tandfonline.com/doi/abs/10.1080/0020723800873741
9#:~:text=Genetic%20engineering%20is%20accomplished%2
0in,vector%20in%20an%20appropriate%20host
http://www.fao.org/3/Y4955E/y4955e06.htm
https://www.genome.gov/genetics-glossary/Genetic-Engineering
http://agbiosafety.unl.edu/education/summary.htm
https://www.news-medical.net/life-sciences/What-is-
Recombinant-DNA.aspx
https://www.investopedia.com/terms/g/genetic-engineering.asp
NegOr_Q3_GenBio2_SLKWeek1_v2
17
DEPARTMENT OF EDUCATION
SCHOOLS DIVISION OF NEGROS ORIENTAL
ROSELA R. ABIERA
Education Program Supervisor – (LRMS)
ARNOLD R. JUNGCO
PSDS – Division Science Coordinator
MARICEL S. RASID
Librarian II (LRMDS)
ELMAR L. CABRERA
PDO II (LRMDS)
RUSSEL C. CADAY
Writer
ALPHA QA TEAM
LIEZEL A. AGOR
MA. OFELIA I. BUSCATO
ANDRE ARIEL B. CADIVIDA
THOMAS JOGIE U. TOLEDO
BETA QA TEAM
LIEZEL A. BESAS
JOAN B. VALENCIA
LIELIN A. DE LA ZERNA
PETER PAUL A. PATRON
THOMAS JOGIE U. TOLEDO
DISCLAIMER
The information, activities and assessments used in this material are designed to provide
accessible learning modality to the teachers and learners of the Division of Negros Oriental. The
contents of this module are carefully researched, chosen, and evaluated to comply with the set
learning competencies. The wri ters and evaluator were clearly instructed to give credits to
information and illustrations used to substantiate this material. All content is subject to copyright
and may not be reproduced in any form without expressed written consent from the division.
NegOr_Q3_GenBio2_SLKWeek1_v2
18
ABOUT THE AUTHOR
RUSSEL C. CADAY finished his Bachelor’s Degree in
Secondary Education major in Biological Sciences at Negros
Oriental State University, Bais Campus II in 2017. He is currently
pursuing his Master’s Degree in Education major in General
Science at Central Philippine State University , San Carlos
Campus. Currently , he is a teacher I at Owacan Provincial
Community High School of Jimalalud District in the Division of
Negros Oriental.
NegOr_Q3_GenBio2_SLKWeek1_v2
19