ch2oh d-Glucosamine (f)

9. Separating Biomolecules In studying a particular biomolecule (a protein, nucleic acid, carbohydrate, or lipid) in the laboratory, the biochemist first needs to separate it from other biomolecules in the sample—that is, to purify it. Specific purification techniques are described later in the text. However, by looking at the monomeric subunits of a biomolecule, you should have some ideas about the characteristics of the molecule that would allow you to separate it from other molecules. For example, how would you separate (a) amino acids from fatty acids and (b) nucleotides from glucose?

10. Silicon-Based Life? Silicon is in the same group of the periodic table as carbon and, like carbon, can form up to four single bonds. Many science fiction stories have been based on the premise of silicon-based life. Is this realistic? What characteristics of silicon make it less well adapted than carbon as the central organizing element for life? To answer this question, consider what you have learned about carbon's bonding versatility, and refer to a beginning inorganic chemistry textbook for silicon's bonding properties.

11. Drug Action and Shape of Molecules Some years ago two drug companies marketed a drug under the trade names Dexedrine and Benzedrine. The structure of the drug is shown below.

The physical properties (C, H, and N analysis, melting point, solubility, etc.) of Dexedrine and Benzedrine were identical. The recommended oral dosage of Dexedrine (which is still available) was 5 mg/day, but the recommended dosage of Benzedrine (no longer available) was twice that. Apparently it required considerably more Benzedrine than Dexedrine to yield the same physiological response. Explain this apparent contradiction.

12. Components of Complex Biomolecules Figure 1-10 shows the major components of complex biomolecules. For each of the three important biomolecules below (shown in their ionized forms at physiological pH), identify the constituents.

(a) Guanosine triphosphate (GTP), an energy-rich nucleotide that serves as a precursor to RNA:

8. Drug Activity and Stereochemistry The quantitative differences in biological activity between the two enantiomers of a compound are sometimes quite large. For example, the d isomer of the drug isoproterenol, used to treat mild asthma, is 50 to 80 times more effective as a bronchodilator than the l isomer. Identify the chiral center in isoproterenol. Why do the two enantiomers have such radically different bioactivity?

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