A plasmid, pUC18, contains the ampicillin-resistance gene, the origin of replication, and the B- gal gene, which codes for the B-galactosidase protein. This protein can break down the synthetic chemical X-gal, producing a blue product that stains the entire cell blue (but is harmless to the bacteria). At the beginning of the ß-gal gene there are several unique restriction sites (some of them are shown in the diagram below). You wish to clone a 1.0-kb Xbal fragment into the pUC18 plasmid, so you cut the plasmid with Xbal and, after removing the enzyme, mix the Xbal-cut plasmid with the 1.0-kb fragment, ligate, and transform competent bacteria. Pati EcoRI Xbal- B-gal R Amp ori Figure: pUC18 plasmid map (a) On what medium would you grow your transformed bacteria? (b) Do you expect the bacteria carrying plasmid pUC18 (without the insert) to be blue or white when grown in the presence of X-gal? Explain.

Human Anatomy & Physiology (11th Edition)
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Chapter1: The Human Body: An Orientation
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A plasmid, pUC18, contains the ampicillin-resistance gene, the origin of replication, and the ß -
gal gene, which codes for the B-galactosidase protein. This protein can break down the synthetic
chemical X-gal, producing a blue product that stains the entire cell blue (but is harmless to the
bacteria). At the beginning of the B-gal gene there are several unique restriction sites (some of
them are shown in the diagram below). You wish to clone a 1.0-kb Xbal fragment into the pUC18
plasmid, so you cut the plasmid with Xbal and, after removing the enzyme, mix the Xbal-cut
plasmid with the 1.0-kb fragment, ligate, and transform competent bacteria.
Pati
Xbal
EcoRI
B-gal
A
Amp
ori
Figure: pUC18 plasmid map
(a) On what medium would you grow your transformed bacteria?
(b) Do you expect the bacteria carrying plasmid pUC18 (without the insert) to be blue or white
when grown in the presence of X-gal? Explain.
Transcribed Image Text:A plasmid, pUC18, contains the ampicillin-resistance gene, the origin of replication, and the ß - gal gene, which codes for the B-galactosidase protein. This protein can break down the synthetic chemical X-gal, producing a blue product that stains the entire cell blue (but is harmless to the bacteria). At the beginning of the B-gal gene there are several unique restriction sites (some of them are shown in the diagram below). You wish to clone a 1.0-kb Xbal fragment into the pUC18 plasmid, so you cut the plasmid with Xbal and, after removing the enzyme, mix the Xbal-cut plasmid with the 1.0-kb fragment, ligate, and transform competent bacteria. Pati Xbal EcoRI B-gal A Amp ori Figure: pUC18 plasmid map (a) On what medium would you grow your transformed bacteria? (b) Do you expect the bacteria carrying plasmid pUC18 (without the insert) to be blue or white when grown in the presence of X-gal? Explain.
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