Suppose you wanted to study genes controlling thestructure of bacterial cell surfaces. You decide tostart by isolating bacterial mutants resistant to infection by a bacteriophage that binds to the cellsurface. The selection procedure is simple: Spreadcells from a culture of sensitive bacteria on a petriplate, expose them to a high concentration ofphages, and pick the bacterial colonies that grow.To set up the selection you could (1) spread cellsfrom a single liquid culture of sensitive bacteria onmany different plates and pick every resistant colony; or (2) start many different cultures, eachgrown from a single colony of sensitive bacteria,spread one plate from each culture, and then pick asingle mutant from each plate. Which methodwould ensure that you are isolating many independent mutations?
Suppose you wanted to study genes controlling the
structure of bacterial cell surfaces. You decide to
start by isolating bacterial mutants resistant to infection by a bacteriophage that binds to the cell
surface. The selection procedure is simple: Spread
cells from a culture of sensitive bacteria on a petri
plate, expose them to a high concentration of
phages, and pick the bacterial colonies that grow.
To set up the selection you could (1) spread cells
from a single liquid culture of sensitive bacteria on
many different plates and pick every resistant colony; or (2) start many different cultures, each
grown from a single colony of sensitive bacteria,
spread one plate from each culture, and then pick a
single mutant from each plate. Which method
would ensure that you are isolating many independent mutations?
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