This enabled Hershey and Chase to track the location of the DNA and protein according to the radiation concentrations. Once tagged they were introduced and infected E. coli. They then used a blender to violently disturb the infected bacteria resulting in the shells of the protein to detach from their host. A centrifuge was used next in order to separate the bacterium from the phages and protein. After completion, the radiation concentrations of E. coli and the protein shells were measured. The results showed that there were large quantities of the phosphorus tracer only in the bacterial sample, demonstrating that DNA was transferred from the bacteriophage to the host organism. Further to this, despite the protein shells being detached while phage reproduction, the virus was copied in each of the host cells, suggesting that the protein shell was not required for the replication process following the initial insertion of genetic material (scarc,
This enabled Hershey and Chase to track the location of the DNA and protein according to the radiation concentrations. Once tagged they were introduced and infected E. coli. They then used a blender to violently disturb the infected bacteria resulting in the shells of the protein to detach from their host. A centrifuge was used next in order to separate the bacterium from the phages and protein. After completion, the radiation concentrations of E. coli and the protein shells were measured. The results showed that there were large quantities of the phosphorus tracer only in the bacterial sample, demonstrating that DNA was transferred from the bacteriophage to the host organism. Further to this, despite the protein shells being detached while phage reproduction, the virus was copied in each of the host cells, suggesting that the protein shell was not required for the replication process following the initial insertion of genetic material (scarc,