dye-linked substrate called X-gal (5-bromo-4-chloro-3-indolyl-ß-D-galacto-pyranoside) into galactose and an insoluble blue pigment (4-chloro-3-brom-indigo), which allows the bacterial colonies to appear BLUE on an agar plate. Most plasmid vectors, including pUC19, carry a short segment of lacZ that contains coding information for the first 146 amino acids of B-galactosidase. The host E. coli strains (ie, DH5a, which is used in this experiment) contain the lacZAM15 deletion mutation. When the plasmid vector is taken up by the bacteria, a functional ß- galactosidase enzyme is produced, which can break down X-gal to create blue colonies. If, however, the plasmid has a cloned gene of interested in the Multiple Cloning Site (pHPU-4), this will disrupt lacZ on the plasmid. If there is no lacZ on the plasmid to interact with the mutated lacZ in E. coli, no B- galactosisdase will be produced. Therefore, if X-gal is in the agar media, there is no enzyme to break it down so the colonies will appear white: What gene from the lac operon was cloned into the plasmid? What enzyme does that gene encode?. What is the lactose analog that we use to mimic lactose? What is the dye-linked suhstrate? What color colonies will be produced if E. coli can produce LacZ when grown with the analog and substrate? Color Fig. 1A below.

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dye-linked substrate called X-gal (5-bromo-4-chloro-3-indolyl-ß-D-galacto-pyranoside) into galactose and an
insoluble blue pigment (4-chloro-3-brom-indigo), which allows the bacterial colonies to appear BLUE on an
agar plate.
Most plasmid vectors, including pUC19, carry a short segment of lacZ that contains coding information for the
first 146 amino acids of B-galactosidase. The host E. coli strains (ie, DH5¤, which is used in this experiment)
contain the lacZAM15 deletion mutation. When the plasmid vector is taken up by the bacteria, a functional B-
galactosidase enzyme is produced, which can break down X-gal to create blue colonies.
If, however, the plasmid has a cloned gene of interested in the Multiple Cloning Site (PHPU-4), this will disrupt
lacZ on the plasmid. If there is no lacZ on the plasmid to interact with the mutated lacZ in E. coli, no ß-
galactosisdase will be produced. Therefore, if X-gal is in the agar media, there is no enzyme to break it down so
the colonies will appear white:
What gene from the lac operon was cloned into the plasmid?
What enzyme does that gene encode?
What is the lactose analog that we use to mimic lactose?
What is the dye-linked suhstrate?
What color colonies will be produced if E. coli can produce LacZ when grown with the analog and substrate?
Color Fig. 1A below.
What color colonies will be produced if an insert is cloned into the lacZ gene on the plasmid?
Color Fig. 1B below.
Figure 1. Expected Results from Blue/White Screening. Color in the colonies (little
circles) as you would expect them to look after transformation and screening for blue/
White colonies. A, DH5¤ transformed with PUC19;B, DH5¤ transformed with PHPU4.
Transcribed Image Text:dye-linked substrate called X-gal (5-bromo-4-chloro-3-indolyl-ß-D-galacto-pyranoside) into galactose and an insoluble blue pigment (4-chloro-3-brom-indigo), which allows the bacterial colonies to appear BLUE on an agar plate. Most plasmid vectors, including pUC19, carry a short segment of lacZ that contains coding information for the first 146 amino acids of B-galactosidase. The host E. coli strains (ie, DH5¤, which is used in this experiment) contain the lacZAM15 deletion mutation. When the plasmid vector is taken up by the bacteria, a functional B- galactosidase enzyme is produced, which can break down X-gal to create blue colonies. If, however, the plasmid has a cloned gene of interested in the Multiple Cloning Site (PHPU-4), this will disrupt lacZ on the plasmid. If there is no lacZ on the plasmid to interact with the mutated lacZ in E. coli, no ß- galactosisdase will be produced. Therefore, if X-gal is in the agar media, there is no enzyme to break it down so the colonies will appear white: What gene from the lac operon was cloned into the plasmid? What enzyme does that gene encode? What is the lactose analog that we use to mimic lactose? What is the dye-linked suhstrate? What color colonies will be produced if E. coli can produce LacZ when grown with the analog and substrate? Color Fig. 1A below. What color colonies will be produced if an insert is cloned into the lacZ gene on the plasmid? Color Fig. 1B below. Figure 1. Expected Results from Blue/White Screening. Color in the colonies (little circles) as you would expect them to look after transformation and screening for blue/ White colonies. A, DH5¤ transformed with PUC19;B, DH5¤ transformed with PHPU4.
A. Read the following section to review what you learned about plasmids, transformation and antibiotic
selection (which antibiotic?)
Plasmids and Recombinant DNA Technology
A plasmid is a circular piece of extra-chromosomal DNA (between 2000-10,000 bp) that is normally found in
bacteria. In nature, the plasmid will often contain a gene that encodes a protein that allows the bacteria to be
resistant to antibiotics, or a protein that allows the bacteria to cause an infection. Plasmids were discovered by
researchers in the late sixties, and it was quickly realized that they could be used to amplify a gene of interest to
create recombinant DNA. The gene of interest is inserted into the plasmid at restriction endonuclease sites. The
plasmid can then be used as a vector to shuttle DNA to a different host/bacteria.
There are many different kinds of plasmids commercially available. All of them contain:
1. a selectable marker (i.e., a gene that encodes for antibiotic resistance, color change, etc)
2. an origin of replication (which is used by the DNA making machinery in the bacteria as the starting
point to make a copy of the plasmid)
3. a multiple cloning site (MCS). The multiple cloning site has many restriction enzyme sites and is used to
insert the DNA of interest. The multiple cloning site is usually in the middle of a reporter gene like Lac
Z.
A commonly used plasmid that we will use in this lab is pUC19: (New England Biolabs)
Ind 91
Bam 51
HstAPI 179
BsmBI 2683
Ndel 183
Kasl - Narl - Sfol 235
Eco01091 2674
Aatll - Zral 2617
Bell 245
Fspl 256
Prul 276
Pvull 306
Hmrl 364
Boell 387
BeiVI 2542
Sspl 2501
Acll 2297,
lpol - EcoRI 396
Banll - Sacl - EcosSKI 402
lec651 - Kpnl 408
wal - BaoRI - Smal -
Хmnl 2294
lacza.
Begl 2215
MCS
Scal 2177-
Hamll 417
Nhal 423
Prul 2066
lecl - Hinell - Sall 429
BepMI - BfuAI 433
Avall 2059
PUC19
2,686 bp
BseDI 1935
Sphl 441
Acl 1924
HindllI 417
Fspl 1919
Pvull 628
Awall 1837
NmeI 1822
lgll 1813-
Bpml 1784
Bsrll 1779
Bsal 1766
Tril 641
BsaXI 659
BSPQI - Sapl 683
Til 781
AAIII - Peil 806
Doll 908
Bse 1753
Bmrl 1744
ori
Ahdl 1694
BeiVI 1015
BseYl 1110
AlwNI 1217
Bkell 1292
A. Which plasmid is used?
B. Which antibiotic was used?
B. Now read the section on Blue-White Screening to answer the following questions:
Blue-White Screening
The well-characterized bacterial lac operon contains a gene called lacZ that encodes for the enzyme B-
galactosidase. Expression of the lac operon is induced by lactose, and also by a lactose analogue, IPTG
(isopropyl B-D-1-thiogalactopyranoside). (To be completely accurate, IPTG binds and inactivates the lac operon
repressor, thereby allowing lac expression). When expressed, the B-galactosidase enzyme can break down a
Transcribed Image Text:A. Read the following section to review what you learned about plasmids, transformation and antibiotic selection (which antibiotic?) Plasmids and Recombinant DNA Technology A plasmid is a circular piece of extra-chromosomal DNA (between 2000-10,000 bp) that is normally found in bacteria. In nature, the plasmid will often contain a gene that encodes a protein that allows the bacteria to be resistant to antibiotics, or a protein that allows the bacteria to cause an infection. Plasmids were discovered by researchers in the late sixties, and it was quickly realized that they could be used to amplify a gene of interest to create recombinant DNA. The gene of interest is inserted into the plasmid at restriction endonuclease sites. The plasmid can then be used as a vector to shuttle DNA to a different host/bacteria. There are many different kinds of plasmids commercially available. All of them contain: 1. a selectable marker (i.e., a gene that encodes for antibiotic resistance, color change, etc) 2. an origin of replication (which is used by the DNA making machinery in the bacteria as the starting point to make a copy of the plasmid) 3. a multiple cloning site (MCS). The multiple cloning site has many restriction enzyme sites and is used to insert the DNA of interest. The multiple cloning site is usually in the middle of a reporter gene like Lac Z. A commonly used plasmid that we will use in this lab is pUC19: (New England Biolabs) Ind 91 Bam 51 HstAPI 179 BsmBI 2683 Ndel 183 Kasl - Narl - Sfol 235 Eco01091 2674 Aatll - Zral 2617 Bell 245 Fspl 256 Prul 276 Pvull 306 Hmrl 364 Boell 387 BeiVI 2542 Sspl 2501 Acll 2297, lpol - EcoRI 396 Banll - Sacl - EcosSKI 402 lec651 - Kpnl 408 wal - BaoRI - Smal - Хmnl 2294 lacza. Begl 2215 MCS Scal 2177- Hamll 417 Nhal 423 Prul 2066 lecl - Hinell - Sall 429 BepMI - BfuAI 433 Avall 2059 PUC19 2,686 bp BseDI 1935 Sphl 441 Acl 1924 HindllI 417 Fspl 1919 Pvull 628 Awall 1837 NmeI 1822 lgll 1813- Bpml 1784 Bsrll 1779 Bsal 1766 Tril 641 BsaXI 659 BSPQI - Sapl 683 Til 781 AAIII - Peil 806 Doll 908 Bse 1753 Bmrl 1744 ori Ahdl 1694 BeiVI 1015 BseYl 1110 AlwNI 1217 Bkell 1292 A. Which plasmid is used? B. Which antibiotic was used? B. Now read the section on Blue-White Screening to answer the following questions: Blue-White Screening The well-characterized bacterial lac operon contains a gene called lacZ that encodes for the enzyme B- galactosidase. Expression of the lac operon is induced by lactose, and also by a lactose analogue, IPTG (isopropyl B-D-1-thiogalactopyranoside). (To be completely accurate, IPTG binds and inactivates the lac operon repressor, thereby allowing lac expression). When expressed, the B-galactosidase enzyme can break down a
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