432515250219pertemuan Vi Dan Vii Introduction of Dna Into Living Cell-1

Introduction of DNA into Living Cell
By Kusdianawati,S.Pt.,M.Si. dan Nurul Izzati,S.Si.,M.Sc.

Introduction of DNA into Living Cell
 Introduction of DNA into bacterial cells
a. Transformation
b. Transfection
 Introduction of DNA into non-bacterial cells

a. Protoplasts
b. Microinjection
c. Biolistics
I. Transformation
1. Preparation of competent E. coli cells
 Possibly CaCl2 causes the DNA to precipitate onto the

outside of the cells, or perhaps the salt is responsible for some
kind of change in the cell wall that improves DNA binding.
 In any case, soaking in CaCl2 affects only DNA binding, and
not the actual uptake into the cell. When DNA is added to
treated cells, it remains attached to the cell exterior, and is not
at this stage transported into the cytoplasm
CaCl2 Method
Delivering the Vector
 Combine the plasmid and host cell
 Hope for the best
2. Selection for transformed cells
 Selecting cells that contain pBR322 plasmids by

plating onto agar medium containing ampicillin
and/or tetracycline.
2. Selection for transformed cells
 Phenotypic expression. Incubation at 37°C for 1 hour before

plating out improves the survival of the transformants on
selective medium, because the bacteria have had time to begin
synthesis of the antibiotic resistance enzymes.
3. Identification of recombinants
 Insertional inactivation
(a) The normal, nonrecombinant vector molecule carries a gene
whose product confers a selectable or identifiable characteristic
on the host cell
(b) This gene is disrupted when new DNA is inserted into the
vector; as a result the recombinant host does not display the
relevant characteristic
3a. Recombinant selection with pBR322
 A map of pBR322 showing

the positions :
a. The ampicillin resistance
(ampR ) and tetracycline
resistance (tetR ) genes
b. The origin of replication
(ori)
c. Some of the most
important restriction sites
 pBR322 has several unique restriction sites. for example, BamHI cuts pBR322 at
just one position, within the cluster of genes that code for resistance to
tetracycline.
 A recombinant pBR322 molecule, one that carries an extra piece of DNA in the
BamHI site, is no longer able to confer tetracycline resistance on its host, as one
of the necessary genes is now disrupted by the inserted DNA.
 Cells containing this recombinant pBR322 molecule are still resistant to ampicillin,
but sensitive to tetracycline (ampRtetS ).
3b. Recombinant selection with pUC8
 A map of pUC8 showing the positions :

a. The ampicillin resistance (ampR ) and Lac Z genes
b. The origin of replication (ori)
c. Some of the most important restriction sites
3b. Recombinant selection with pUC8
 Most modern plasmid vectors
therefore make use of a
different system. An
 example is pUC8 (Figure 5.9a),
which carries the ampicillin
resistance gene and a gene
 called lacZ′, which codes for part
of the enzyme b-galactosidase.
Cloning with pUC8
 involves insertional inactivation
of the lacZ′ gene, with
recombinants identified because
 of their inability to synthesize
b-galactosidase (Figure 5.9b).
II. Transfection
 Transfection is equivalent to transformation, the only
difference being that phage DNA rather than a plasmid is
involved
 Just as with a plasmid, the purified phage DNA, or
recombinant phage molecule, is mixed with competent
E.coli cells and DNA uptake induced by heat shock
 Transfection is the standard method for introducing the
doublestranded RF form of an M13 cloning vector into
E. coli.
Introduction of DNA into non-bacterial
cells
 Protoplasts generally take up DNA quite readily, but transformation

can be stimulated by special techniques such as electroporation,
during which the cells are subjected to a short electrical pulse,
thought to induce the transient formation of pores in the cell
membrane, through which DNA molecules are able to enter the cell.
 After transformation the protoplasts are washed to remove the
degradative enzymes and the cell wall spontaneously re-forms.
Microinjection
 The first of these is microinjection, which makes use of a

very fine pipette to inject DNA molecules directly into the
nucleus of the cells to be transformed
 This technique was initially applied to animal cells but has
subsequently been successful with plant cells
Biolistics
 The second method involves bombardment of the cells with high

velocity microprojectiles, usually particles of gold or tungsten that
have been coated with DNA.
 These microprojectiles are fired at the cells from a particle gun.
 This unusual technique is termed biolistics and has been used with
a number of different types of cell.
Jagung (Zea mays L.)
Jagung yang sudah dimasukkan gen

penyandi protoksin dari bakteri
Bacillus thuringiensis sehingga jagung
ini tahan terhadap serangan hama
berupa serangga yang biasa
menyerang tanaman jagung seperti
penggerek buah
Padi (Oryza saliva) Golden Rice

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Introduction of DNA into Living Cell

By Kusdianawati,S.Pt.,M.Si. dan Nurul Izzati,S.Si.,M.Sc.

 Introduction of DNA into non-bacterial cells

 Possibly CaCl2 causes the DNA to precipitate onto the

 Selecting cells that contain pBR322 plasmids by

 Phenotypic expression. Incubation at 37°C for 1 hour before

 A map of pBR322 showing

 A map of pUC8 showing the positions :

 Protoplasts generally take up DNA quite readily, but transformation

 The first of these is microinjection, which makes use of a

 The second method involves bombardment of the cells with high

Jagung yang sudah dimasukkan gen

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