The Process of DNA Replication
The first step in DNA replication is to ‘unzip’ the double helix structure of the DNA? molecule.
This is carried out by an enzyme called helicase which breaks the hydrogen bonds holding the complementary bases of DNA together (A with T, C with G).
The separation of the two single strands of DNA creates a ‘Y’ shape called a replication ‘fork’. The two separated strands will act as templates for making the new strands of DNA.
DNA polymerase? binds to the leading strand and then ‘walks’ along it, adding new complementary? nucleotide? bases (A, C, G and T) to the strand of DNA in the 5’ to 3’ direction
Once all of the bases are matched up (A with T, C with G), an enzyme called exonuclease strips away the primer(s). The gaps where the primer(s) were are then filled by yet more complementary nucleotides. The new strand is proofread to make sure there are no mistakes in the new DNA sequence.
Finally, an enzyme called DNA ligase? seals up the sequence of DNA into two continuous double strands. The result of DNA replication is two DNA molecules consisting of one new and one old chain of nucleotides. This is why DNA replication is described as semi-conservative, half of the chain is part of the original DNA molecule, half is brand new.
Following replication the new DNA automatically winds up into a double helix.