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How Do We Absorb Nucleic Acids?

Published in Human Digestion 2 mins read

We absorb nucleic acids (DNA and RNA) through digestion in the small intestine, facilitated by enzymes from both the pancreas and the small intestine itself.

Here's a breakdown of the process:

1. Digestion in the Small Intestine

  • Dietary nucleic acids, primarily DNA and RNA from the food we consume, enter the small intestine.
  • The breakdown begins with the action of pancreatic enzymes:
    • Ribonuclease: This enzyme targets and breaks down RNA molecules into smaller fragments.
    • Deoxyribonuclease: This enzyme targets and breaks down DNA molecules into smaller fragments.

2. Further Breakdown by Intestinal Enzymes

  • The smaller nucleic acid fragments produced by the pancreatic enzymes are further digested by enzymes present in the small intestine. These enzymes include:
    • Phosphatases: Remove phosphate groups.
    • Nucleosidases: Break down nucleosides into nitrogenous bases (adenine, guanine, cytosine, thymine, uracil) and pentose sugars (ribose or deoxyribose).
    • Phosphorylases: Break the bond between the nitrogenous base and the sugar.

3. Absorption of Components

  • The final products of nucleic acid digestion – nitrogenous bases, pentose sugars, and phosphate groups – are then absorbed by the cells lining the small intestine (enterocytes).
  • These components are absorbed via active transport mechanisms.
  • Once absorbed, they can be used by the body for nucleotide synthesis or catabolized for energy.

In summary, the absorption of nucleic acids is a multi-step enzymatic process within the small intestine, resulting in the absorption of nitrogenous bases, sugars, and phosphates that can be utilized by the body.

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