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Define and give examples of polysaccharides, triacylglycerols, nucleotides, and nucleosides. Explain how to name nucleosides.

Biology

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  1. Polysaccharides are complex carbohydrates formed by many monosaccharide units linked together.

    • Homopolysaccharides are composed of only one type of monosaccharide unit. Examples include starch, glycogen, and cellulose (all made of glucose units).
    • Heteropolysaccharides are composed of two or more different types of monosaccharide units. Examples include hyaluronic acid and heparin.
  2. TAG stands for Triacylglycerol (also known as triglyceride). It is a lipid molecule composed of a glycerol backbone esterified to three fatty acid molecules. TAGs serve as the primary form of energy storage in animals and plants.

  3. A nucleotide is the basic building block of nucleic acids (DNA and RNA). It consists of three components: a nitrogenous base (adenine, guanine, cytosine, thymine, or uracil), a pentose sugar (deoxyribose in DNA or ribose in RNA), and one or more phosphate groups.

  4. A nucleoside is a part of a nucleotide, consisting of a nitrogenous base covalently linked to a pentose sugar (deoxyribose or ribose), but without any phosphate groups.

  5. Naming Nucleosides: The nitrogenous base's name is modified.

    • For purine bases (Adenine, Guanine), the suffix "-osine" is added: Adenine becomes Adenosine, Guanine becomes Guanosine.
    • For pyrimidine bases (Cytosine, Thymine, Uracil), the suffix "-idine" is added: Cytosine becomes Cytidine, Thymine becomes Thymidine, Uracil becomes Uridine.

    Naming Nucleotides: Nucleotides are named by adding "monophosphate," "diphosphate," or "triphosphate" to the corresponding nucleoside name, indicating the number of phosphate groups attached.

    • Example: Adenine →\rightarrow Adenosine (nucleoside) →\rightarrow Adenosine monophosphate (AMP), Adenosine diphosphate (ADP), Adenosine triphosphate (ATP).
    • Similarly: Guanine →\rightarrow Guanosine →\rightarrow Guanosine monophosphate (GMP).
    • Cytosine →\rightarrow Cytidine →\rightarrow Cytidine monophosphate (CMP).
    • Thymine →\rightarrow Thymidine →\rightarrow Thymidine monophosphate (TMP).
    • Uracil →\rightarrow Uridine →\rightarrow Uridine monophosphate (UMP).
  6. A peptide bond is formed between two amino acids through a dehydration synthesis (or condensation) reaction. The carboxyl group (−COOH)(-\text{COOH}) of one amino acid reacts with the amino group (−NH2)(-\text{NH}_2) of another amino acid. A molecule of water is removed, and a covalent bond forms between the carbon atom of the carboxyl group and the nitrogen atom of the amino group, resulting in a −CO−NH−-\text{CO}-\text{NH}- linkage.

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