BTEC3301
Plant biotechnology is a process to produce a
genetically modified plant by removing
genetic information from an organism,
manipulating it in the laboratory and then
transferring it into a plant to change certain of
its characteristics .
Plant Biotechnology is a rapidly expanding field
within Biotechnology.
…INTRODUCTION
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It chiefly involves the introduction of foreign
genes into economically important plant
species, resulting in crop improvement and
the production of novel products in plants.
Today, biotechnology is being used as a tool
to give plants new traits that benefit
agricultural production, the environment, and
human nutrition and health.
…INTRODUCTION
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The goal of plant breeding is to combine
desirable traits from different varieties of
plants to produce plants of superior quality.
This approach to improving crop production
has been very successful over the years.
For example, it would be beneficial to cross a
tomato plant that bears sweeter fruit with one
that exhibits increased disease resistance.
…INTRODUCTION
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The red juicy tomatoes on shelves are results
of genetic engineering.
For hundreds of years plant breeders have
cross fertilised related plant, selecting
combinations from the offspring that provide
the plant with new characteristics beneficial
to men.
Today plant biotechnology encompasses two
major areas, plant tissues culture and plant
genetic engineering.
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A transgenic crop plant contains a gene or
genes which have been artificially inserted
instead of the plant acquiring them through
pollination.
The inserted gene sequence (known as the
transgene) may come from another unrelated
plant, or from a completely different species
..What are transgenic plants?
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Example transgenic Bt corn, for example,
which produces its own insecticide, contains
a gene from a bacterium.
Plants containing transgenes are often called
genetically modified or GM crops
Desirable genes may provide features such as
higher yield or improved quality, pest or
disease resistance, or tolerance to heat, cold
and drought.
…What are transgenic plants?
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Combining the best genes in one plant is a
long and difficult process, especially as
traditional plant breeding has been limited to
artificially crossing plants within the same
species or with closely related species to
bring different genes together.
Corn and soybean to resist pest in US are in
the forefront of Biotechnological revolution.
A. Selective Breeding
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This is usually done by crossing two
members of the same species which has
dominant alleles for particular genes such as
long life and quick metabolism in one
organism crossed with another organism
possessing genes for fast growth and high
yield.
….A. Selective Breeding
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Since both these organisms have dominant
genes for these desirable characteristics, when
they are crossed they will produce at least
some offspring that will show ALL of these
desirable characteristics.
When such a cross occurs, the offspring is
termed a hybrid
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B. Cloning:
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(Growing plant from a single cell)
 Cloning is the process of creating
an identical copy of an original.
 In plant cloning is done by tissue
culture methods.
Refer for more info on tissue culture:
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http://www.jmu.edu/biology/biofac/facfro/cloning/cloning3.htm
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C. Nature's way:
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Agrobacterium tumefaciens is a common soil
bacterium that causes crown gall disease by
transferring some of its DNA to the plant
host.
The transferred DNA (T-DNA) is stably
integrated into the plant genome, where its
expression leads to the synthesis of plant
hormones and thus to the tumorous growth of
the cells.
After discovering this process, scientists were
able to "disarm" the bacterium, put new genes
into it, and use the bacterium to harmlessly
insert the desired genes into the plant
genome
D. Cellular target practice:
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Many of the techniques used in plant biotechnology
can be grouped under the headings of Plant Tissue
Culture and Plant Genetic Engineering.
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One problem with working with plants is that
they have a cell wall - how do you get a
recombinant plasmid to cross that barrier?
The following are some of the techniques used:
 1.Microinjection of
single cells
2. Biolistic gene transfer
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D. Cellular target practice:
 In the "biolistic" (a cross
between biology and
ballistics )or "gene gun" method, microscopic gold
beads are coated with the gene of interest and shot
into the plant cell with a pulse of helium.
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Once inside the cell, the gene comes off the bead
and integrates into the cell's genome.
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D. Cellular target practice:
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http://www.Bio-Rad.com/images/gene_gun_delivery.gif
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D. Cellular target practice:
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Model from BioRad:
Biorad's Helios Gene Gun
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3.Electroporation of cells grown
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D. Cellular target practice:
without
a cell wall (protoplasts)
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Plant cells could be "electroporated" or
mixed with a gene and "shocked" with
a pulse of electricity, causing holes to
form in the cell through which the
DNA could flow.
The cell is subsequently able to repair
the holes and the gene becomes a part
of the plant genome.
4. Agrobacterium-mediated
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D. Cellular target practice:
transfer
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This process is called Agrobacterium mediated transformation. (Refer article
PN Achar 2000).
The process "disarm" the bacterium,
put new genes into it, and use the
bacterium to harmlessly insert the
desired genes into the plant genome.
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5. Protoplast Fusion (Plant
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tissue culture)
D. Cellular target practice:
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Plant tissue culture is the cultivation of
plant cells or tissues on specifically
formulated nutrient enriched media.
Under appropriate conditions, an
entire plant can be regenerated from
each single cell, permitting the rapid
production of many identical plants.
Plant Biotechnology
 Protoplast
is a cell without cell wall
Plant Biotechnology Techniques
Fusion (Plant are
tissue culture)
Protoplast
Protoplasts
capable of fusing; forms
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somatic hybrids of even genetically
incompatible plants
Hybrid protoplasts are then regenerated
by tissue culture into whole hybrid
plants .
Boccoflower is a hybrid between
broccoli and cauliflower. (Refer pg fig.6.2 in text
book)
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Plant Biotechnology Techniques
Protoplast Fusion (Plant tissue culture)
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6.
Leaf
Fragment
technique/
Leaf
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D. Cellular
target practice:
Disk
Method
For Agrobacterium Mediated
Transformation of Higher Plants:
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Culture leaf disc in genetically modified
Agrobacterium.
Soil bacterium Agrobacterium tumefaciens causes
crown gall disease in plants.
This disease is characterized by the formation of
tumors on plants after infection of wound sites by
the bacterium.
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The
crown gall cells gain two genetic properties
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not possessed
bytechnique
normal plant cells.
6. Leaf Fragment
These are the ability to grow in culture in the
absence of externally added hormones, and the
production of unusual compounds called opines.
These opines are used by the bacterium as
sources of carbon and nitrogen. The bacterium
therefore creates a niche in the crown gall which
is favorable for growth.
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The
molecular basis for this disease was
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identified
in 1974technique
with the discovery of a 200 kb
6. Leaf Fragment
plasmid called the Ti plasmid (tumor inducing).
Removal of the plasmid leads to avirulence, and
re introduction restores virulence.
This Ti plasmid can be constructed with foreign
genes include antibiotic resistance markers,
genes for useful agronomic traits such as
herbicide tolerance, virus resistance, and insect
resistance.
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 The
significant
finding
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Techniques
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was that a 13 kb
Leaf the
Fragment
piece6. of
Titechnique
plasmid is transferred
into the genome of the recipient cell.
This piece of transferred DNA is called
the T DNA.
The transfer of this T DNA to plant cells
is the key step in using Agrobacterium
tumefaciens as an agent for directed
transformation and genetic modification
of higher plants.
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A
growing number of plant species have been
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6. Leaf Fragment
technique
successfully
transformed
with foreign genes
using such artificially constructed plasmid
vectors. .
The bacterial plasmid serves as an ideal
vehicle for transferring DNA. And this is
done by culturing leaf discs in medium
containing genetically modified
Agrobacterium.
Major limitation of this technique is that
Agrobacterium cannot infect monocotyledons
e.g. corn but can easily infect dicotyledons e.g.
potatoes, tomatoes, soybeans etc.
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 Refer pg
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138; fig 6.4
6. Leaf Fragmentof
technique
for regeneration
plants from leaf disc with the
aid of Agrobacterium tumefaciens.
Note:
 Gene gun an alternative method for inserting
gene instead of Agrobacterium!!!
 Assignment for next week: The gene Guns: Pg
140;fig.6.5
Plant Biotechnology
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Plant genetic engineering involves the
manipulation of genes at cellular and
molecular levels. Using techniques of plant
genetic engineering, it is now possible to
isolate genes of interest form one kind of
organism incorporating them into another,
thus resulting in the permanent change inn
the genetic make-up of the recipient.
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DNA in a cell chloroplast can also accept new
genes.
Plant can be transformed with new traits
using chloroplast DNA
Pollen DNA is separate from chloroplast
DNA hence, transformed chloroplast cannot
be released along with pollen DNA
Plant
Generally
ripe
Biotechnology
tomatoes are red and juicy;
Chloroplast
usuallyEngineering:
perish quickly if not refrigerated and
mushy….
 The FlavrSavrTM tomato (introduced in
1994by Calgene Inc.) can stay ripe for
weeks!!!! Without perishing quickly. Why?
 The Flavr Savr tomato is designed to ripen on
the vine, with minimal softening and
transported to consumers, a definite plus for
grocery stores.
Plant
Ripe
tomatoes
Biotechnology
produces the enzyme
Chloroplast
Engineering:
polyglacturonase(PG).
 The PG enzyme is responsible for the
breakdown pectin, a building block in cell
walls, which gives tomatoes their firmness.
 To slow down the softening process, the Flavr
Savr employs antisense technology to block
PG enzyme production.
 Antisense technology is a method of gene
silencing.
Antisense technology is a method of gene
silencing.
Chloroplast
Engineering:
 The first step in this process involved the
isolation of the PG gene from the tomato.
 The first step is to clone the antisense DNA
with the PG gene and insert this DNA into
the plasmid of an agrobacterium.
 The bacterium is introduced to plant cells
which transfers the gene of interest into plant
cells.
 The cells with the plasmid are grown by
adding specific hormones.
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Plant Biotechnology
The re-generated plants will express the
antisense
DNA and when the mRNA is made
Chloroplast
Engineering:
through the process of transcription the sense
mRNA will bind to the anti-sense mRNA.
This interferes with protein production (PG
enzyme in tomato).
 Antisense is being developed for potatoes to
resist bruising.
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Refer fig 6.7:The Flavr SavrTM tomato.
DNA
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Summary of Antisense mechanism:
Summary of Antisense
mechanism:
How enzyme is made? PRODUCE
What Happens When A
Cloned Antisense DNA Is
Added To The Original
DNA?
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Plant Biotechnology Techniques
Summary of Antisense mechanism:
Plant Biotechnology
Plant Biotechnology Techniques
Summary of Antisense mechanism:
DNA
How enzyme is made?
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Plant Biotechnology Techniques
Summary of Antisense mechanism:
When A Cloned
Antisense DNA Is Added
To The Original DNA:
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http://www.biores-irl.ie/biozone/plants.html
http://search.yahoo.com/search?p=Selective+breeding
&ei=UTF-8&fr=FP-tab-web-t&fl=0&x=wrt
http://www.colorado.edu/che/BioProcess%20Engineer
ing/Lecture%208/protoplastfusion.htm
http://www.inform.umd.edu/genetics/leafdisc.html
http://dragon.zoo.utoronto.ca/~jlmgmf/T0501D/methods.html for gene slicing
http://dragon.zoo.utoronto.ca/~jlmgmf/T0101A/Enzyme.html for Flavr Slavr
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Practical Applications of Genetic
Engineering in Plants
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Vaccine for plants