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The Hershey-Chase Experiment
AIM
♦ In 1952, American biologists Alfred
Hershey and Martha Chase set out to
determine what composed the genetic
material of a bacteriophage.
♦ Their aim was to prove that DNA is the
genetic material being transferred from
parents to offsprings.
T2 Bacteriophage
♦ They are viruses which infect bacteria
♦ They consist of :
A protein head (genetic material)
Tail
♦ T2 infects the bacteria E.coli
Principle -
DNA contains phosphorous but no
sulphur.Protein contains sulphur but
hardly any phosphorous
Process -
♦Bacteriophage attach a
bacteriuminject genetic material
(DNA) into bacteriumsynthesis
of DNA replicate & protein coat
and tailform a new
bacteriophage
DNA is the genetic
♦Alfred Hershey and Martha
Chase discovered that DNA is
the genetic material of a phage
known as T2
Experiment
A. 1: Viral protein and DNA were
tagged with different radioactive
isotopes. Protein Tagging: T2 and E.
coli were grown in media with
radioactive sulfur (35S) which
incorporated only into the phage
protein. DNA Tagging: T2 and E.
coli were grown in media containing
radioactive phosphorus (32P) which
was incorporated only into the phage
DNA.
♦ 2: Protein-labeled and DNA-
labeled T2 phages were
allowed to infect separate
samples of nonradioactive E.
coli cells.
♦ 3: Cultures were agitated to
shake loose phages that
remained outside the bacterial
cells.
A.4: Mixtures were centrifuged
forcing the heavier bacterial
cells into a pellet on the bottom
of the tubes. The lighter viruses
remained in the supernatant.
♦5 : Radioactivity in the pellet
and supernatant was measured
and compared
Results:
♦In tubes with E. coli infected with
protein labeled T2, most of the
radioactivity was in the supernatant
with viruses.
♦In tubes with E. coli infected with
DNA-labeled T2, most of the
radioactivity was in the pellet with the
bacterial cells. When the bacteria
containing DNA-labeled phages were
returned to culture medium, the
bacteria released phage progeny which
contained 32P in their DNA.
Hershey and Chase found that
∀When bacteriophages containing 35
P
(radioactive), were allowed to
infect nonradioactive bacteria, all
the infected cells became
radioactive and, in fact, much of
the radioactivity was passed on to
the next generation of
bacteriophages.
Conclusions
A. Viral proteins remain outside
the host cell. Viral DNA is
injected into the host cell.
Injected DNA molecules cause
cells to produce additional
viruses with more viral DNA
and proteins. These data
provided evidence that nucleic
acids rather than proteins are
the hereditary material.
∀when the bacteria were infected
with bacteriophages labeled
with 35
S and then the virus coats
removed (by whirling them in
an electric blender), practically
no radioactivity could be
detected in the infected cells.
The hershey chase experiment

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The hershey chase experiment

  • 2. AIM ♦ In 1952, American biologists Alfred Hershey and Martha Chase set out to determine what composed the genetic material of a bacteriophage. ♦ Their aim was to prove that DNA is the genetic material being transferred from parents to offsprings.
  • 3. T2 Bacteriophage ♦ They are viruses which infect bacteria ♦ They consist of : A protein head (genetic material) Tail ♦ T2 infects the bacteria E.coli
  • 4. Principle - DNA contains phosphorous but no sulphur.Protein contains sulphur but hardly any phosphorous
  • 5.
  • 6. Process - ♦Bacteriophage attach a bacteriuminject genetic material (DNA) into bacteriumsynthesis of DNA replicate & protein coat and tailform a new bacteriophage
  • 7. DNA is the genetic ♦Alfred Hershey and Martha Chase discovered that DNA is the genetic material of a phage known as T2
  • 8. Experiment A. 1: Viral protein and DNA were tagged with different radioactive isotopes. Protein Tagging: T2 and E. coli were grown in media with radioactive sulfur (35S) which incorporated only into the phage protein. DNA Tagging: T2 and E. coli were grown in media containing radioactive phosphorus (32P) which was incorporated only into the phage DNA.
  • 9. ♦ 2: Protein-labeled and DNA- labeled T2 phages were allowed to infect separate samples of nonradioactive E. coli cells. ♦ 3: Cultures were agitated to shake loose phages that remained outside the bacterial cells.
  • 10. A.4: Mixtures were centrifuged forcing the heavier bacterial cells into a pellet on the bottom of the tubes. The lighter viruses remained in the supernatant. ♦5 : Radioactivity in the pellet and supernatant was measured and compared
  • 11. Results: ♦In tubes with E. coli infected with protein labeled T2, most of the radioactivity was in the supernatant with viruses. ♦In tubes with E. coli infected with DNA-labeled T2, most of the radioactivity was in the pellet with the bacterial cells. When the bacteria containing DNA-labeled phages were returned to culture medium, the bacteria released phage progeny which contained 32P in their DNA.
  • 12. Hershey and Chase found that ∀When bacteriophages containing 35 P (radioactive), were allowed to infect nonradioactive bacteria, all the infected cells became radioactive and, in fact, much of the radioactivity was passed on to the next generation of bacteriophages.
  • 13. Conclusions A. Viral proteins remain outside the host cell. Viral DNA is injected into the host cell. Injected DNA molecules cause cells to produce additional viruses with more viral DNA and proteins. These data provided evidence that nucleic acids rather than proteins are the hereditary material.
  • 14. ∀when the bacteria were infected with bacteriophages labeled with 35 S and then the virus coats removed (by whirling them in an electric blender), practically no radioactivity could be detected in the infected cells.