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Selectable markers

The document discusses the selection and separation of recombinant transformants from non-transformants using antibiotic resistance genes and insertional inactivation. It highlights the challenges of the process, including contamination and time consumption, as well as the use of chromogenic substrates for identifying successful transformations. Additionally, it explains the role of the B-galactosidase enzyme as a reporter for phenotypic expression in recombinant plasmids.

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0% found this document useful (0 votes)
8 views

Selectable markers

The document discusses the selection and separation of recombinant transformants from non-transformants using antibiotic resistance genes and insertional inactivation. It highlights the challenges of the process, including contamination and time consumption, as well as the use of chromogenic substrates for identifying successful transformations. Additionally, it explains the role of the B-galactosidase enzyme as a reporter for phenotypic expression in recombinant plasmids.

Uploaded by

sgurdarshan386
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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[VII) Selection Transformant

of. from non transformant ;


recombinant
separation of, transformant from non-recombinant
transformant.

NT :

Non-transformant
NRT
=

Non-Recombinant transformant
RT =

Recombinant transformant

Insertional Inactivation : Inactivation of selectable marker gene


due to insertion of foreign DNA.


M-RNA
~
2 Protein In need see

↓ I

Phenotypic Expression . No Phenotypic expression

(a) Using two antibiotic resistance genes =>


pBR322 .

Non-Recombinant Bartl
Recombinant Plasmid
Plasmid gene of
tetR BamHI ampr interest
ampR ampe S
.

fetR tetS

·
o ·- NT

·00
·> -
NRT

he · -> RT

O ⑨
NT lack ampR gene ,
hence, Ampicilia will be added
eliminated .
get
S

·
O
O
O Parent Plate .

⑨ [ o

?
o
·
(

Replica plating on culture


medium containing tetracycle
RT's lack tetR due Y

to insertional inactivation
T
eliminated in
&
get O
retracycline containing [ in
medium ⑨
·
.

from parent plate.


RT's isolated and used for further
are
process .

Drawback
-

It is a cumbersome process because it is difficult


to attain accuracy a prevent contamination during
replica plating.
-
Also , maintaining two cultures is time
consuming.
(d) Selection by one lack gene and 1 antibiotic resistance
gene
-

pUC8 .

Lactose (chromogenic
ri ~ lac
z
gene
Subtrate) .

-
B-galactosidase
Glucose + Galactose
(x gal) = blue
NR-plasmid
-

.
Recombinant Plasmid-Produce Transparent/
white colonies

-- > NT
· - RT NT get eliminated
-
NRT X-amps
... &
- ·
& :
&
incubated in E
-
- -
> · Y
G -
M
-
ampicilin w
&
-
G &
-
chromogenic lactose & ·
- - &
medium
i
/ &
& E
NRT cells
W
1 RT-
blue
appear form while
colonied due to
insertional inactivation
of functional lat 2
gene
B-Galactosidase >
-
called Reporter Enzyme .

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