Step 1: Understanding the Concept:
Analytical ultracentrifugation using a CsCl density gradient separates DNA based on its buoyant density (\(\rho\)).
The density of DNA is influenced by its base composition because G-C base pairs are held together by three hydrogen bonds, packing more tightly and having a higher density than A-T base pairs, which are held by two hydrogen bonds.
Step 2: Detailed Explanation:
The empirical equation relating the buoyant density of double-stranded DNA to its base composition in a cesium chloride gradient is:
\[ \rho = 66 + 0.098 X_{G+C} \]
In this linear equation:
- \(\rho\) represents the buoyant density of the DNA in \(\text{g/cm}^3\).
- \(66\) is the buoyant density of a theoretical DNA containing only A-T base pairs.
- \(X_{G+C}\) represents the mole fraction of G+C base pairs in the DNA molecule, which ranges from \(0\) to \(1\).
As the proportion of G+C base pairs in the DNA increases, its buoyant density increases linearly.
Measuring the buoyant density allows researchers to determine the overall G-C content of a genomic DNA sample.
Step 3: Final Answer:
In the buoyant density equation, \(X_{G+C}\) denotes the mole fraction of G+C content.