(a) In 1928 Frederick Griffith, worked on Streptococcus pneumoniae (bacterium responsible for pneumonia).
When Streptococcus pneumoniae bacteria are grown on a culture plate, some produce smooth shiny colonies (S) while others produce rough colonies (R). This is because the S strain bacteria have a mucous (polysaccharide) coat, while R strain does not.
Mice infected with the S strain (virulent) die from pneumonia infection but mice infected with the R strain do not develop pneumonia.
S strain⟶Inject into mice⟶Mice dieR strain⟶Inject into mice⟶Mice live
Griffith was able to kill bacteria by heating them. observed that heat-killed S strain bacteria injected into: mice did not kill them.
S strain⟶Inject into mice⟶Mice die(heat - killed)S strain(heat-killed)+⟶Inject into mice⟶Mice dieR strain(live)
When he injected a mixture of heat-killed S and live R bacteria, the mice died. Moreover, he recovered living S bacteria from the dead mice. [2]
He concluded that the R strain bacteria had somehow been transformed by the heat-killed S strain bacteria and had become virulent. [1]
(b) Contribution of Macleod, Mc Carty and Avery : They purified biochemicals (proteins, DNA, RNA) from the heat killed S cells to see which ones could transform live R. cells into S cells. They discovered that DNA alone from S bacteria caused the bacteria to become transformed. They also discovered protein and RNA digesting enzymes did not affect transformation. Hence, they concluded that DNA is the hereditary material. [2]