May 26, 2015

Unraveling DNA Replication through Meselson and Stahl's Experiment

Genetic Material Replication

A crucial characteristic of genetic material is its ability to undergo replication. The DNA model proposed by Watson and Crick immediately hinted at a replication mechanism based on complementary base pairing. During replication, each original DNA strand from the parent molecule serves as a template for the creation of a new strand in the daughter molecule.

This process of DNA replication is termed semi-conservative replication because each daughter molecule retains one of the original strands. The replication process involves the following steps:

Unwinding: The parental DNA strands are unwound and separated, breaking the weak hydrogen bonds between the paired bases. The enzyme helicase is responsible for this unwinding.

Complementary Base Pairing: New complementary nucleotides, available within the nucleus, are precisely positioned through complementary base pairing.

Joining: Complementary nucleotides link together to form new strands. Each daughter DNA molecule consists of one original strand and one newly synthesized strand. The enzyme complex DNA polymerase facilitates both complementary base pairing and strand joining.


Semiconservative replication of DNA (simplified)

Meselson and Stahl's DNA Replication Experiment

The concept of semi-conservative replication was empirically validated by Matthew Meselson and Franklin Stahl at the California Institute of Technology in 1958. They employed centrifugation to separate particles from the suspending fluid within tubes. Meselson and Stahl exploited the principle that DNA molecules with varying densities could be separated through centrifugation. DNA containing heavy nitrogen (15N), with an atomic weight of 15, is the densest, while DNA containing light nitrogen (14N, with an atomic weight of 14) is the least dense. Hybrid DNA molecules, with one heavy and one light strand, exhibit intermediate density.

The experimental procedure involved growing bacteria in a medium containing 15N to ensure the presence of exclusively heavy DNA molecules. The bacteria were then transitioned to a medium containing 14N. After one division, the cells contained only hybrid DNA molecules. Following two divisions, the DNA molecules split into halves – half light and half hybrid. These results precisely matched the expectations for semi-conservative DNA replication.

Meselson and Stahl's DNA Replication Experiment

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