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BOTANY Higher Secondary Second Year - Textbooks Online

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Replication<br />

fork<br />

Super<br />

coil<br />

DNA<br />

polymerase<br />

RNA<br />

primer<br />

Fig. 3.9 Semiconservative method of replication of DNA<br />

their experiments on Escherichia coli using radioactive isotopes. The<br />

replication of chromosome in E. coli is completed in 40 minutes.<br />

During replication of DNA, the two complementary strand of DNA<br />

uncoil and separate from one end in a zipper like fashion. The enzyme<br />

helicase unwinds the two strands and as a result replication fork is formed.<br />

As the DNA unwinds, the part of the DNA that is found above the<br />

replication fork becomes supercoils. These are called positive supercoils.<br />

An enzyme called topoisomerase releases these supercoils. Based on<br />

separated DNA strands, new strands grow by the addition of nucleotides.<br />

DNA polymerase I, II and III are involved in this elongation. However,<br />

these enzymes are not capable of initiating DNA synthesis.<br />

For the synthesis of new DNA, two things are required. One is RNA<br />

primer and the enzyme primase. The DNA polymerase moves along the<br />

newly formed RNA primer nucleotides, which leads to the elongation of<br />

DNA. In the other strand, DNA is synthesized in small fragments called<br />

Okazaki fragments. These fragments are linked by the enzyme called<br />

135<br />

Topoisomerase<br />

Helicase<br />

Helix destabilising protein<br />

Primase<br />

RNA primer<br />

Okazaki fragments<br />

Ligase<br />

DNA polymerase

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