The figure provided portrays the integration of Lambda phage into a host chromosome at the att site, located between the gal+ and bio+ genes. This prophage may disintegrate from the host carrying with it host genes, such as gal+ and/or bio+ and go on to ransduce another host bacterium. How would one determine if a gal- host bacterium's phenotype was changed from gal- to gal+? To clarify, the minus version cannot utilize galactose as a carbon source for growth because it does not produce galactase, the

Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
Section: Chapter Questions
Problem 1RQ: The correct sequence of levels forming the structural hierarchy is A. (a) organ, organ system,...
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2
3
inte
tion of Lormhda.
ne att si
ucated betwee de
ne
att sites
and go
ns
one
te n
vacter
aged
ot utilize
doot
ractose ato
la t
don s
gal*
uc
Integration to
form prophage
om
SOward
cor coct some cro
on!
ni imple ex
2
3
bio*
gal*
14. The figure provided portrays the integration of Lambda phage into a host chromosome at the att site, located between the gal+
and bio+ genes. This prophage may disintegrate from the host carrying with it host genes, such as gal+ and/or bio+ and go on to
transduce another host bacterium. How would one determine if a gal- host bacterium's phenotype was changed from gal- to gal+?
To clarify, the minus version cannot utilize galactose as a carbon source for growth because it does not produce galactase, the
enzyme that hydrolyzes galactose into monomeric sugars. There is a straight forward answer/solution to this – do not concoct
some crazy solution! Think simple experiment.
Transcribed Image Text:2 3 inte tion of Lormhda. ne att si ucated betwee de ne att sites and go ns one te n vacter aged ot utilize doot ractose ato la t don s gal* uc Integration to form prophage om SOward cor coct some cro on! ni imple ex 2 3 bio* gal* 14. The figure provided portrays the integration of Lambda phage into a host chromosome at the att site, located between the gal+ and bio+ genes. This prophage may disintegrate from the host carrying with it host genes, such as gal+ and/or bio+ and go on to transduce another host bacterium. How would one determine if a gal- host bacterium's phenotype was changed from gal- to gal+? To clarify, the minus version cannot utilize galactose as a carbon source for growth because it does not produce galactase, the enzyme that hydrolyzes galactose into monomeric sugars. There is a straight forward answer/solution to this – do not concoct some crazy solution! Think simple experiment.
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