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  Home > JCE Print > Journal of Chemical Education > Issues > 2008  > February  >
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JCE Featured Molecules
Molecular Models of Lycopene and Other Carotenoids
William F. Coleman
Department of Chemistry, Wellesley College, Wellesley, MA 02481
Cover
February 2008
Vol. 85 No. 2
p. 320

Full Text
Over the past decade or so the phrase “emerging research suggests” has entered the argot of advertising, and that phrase has been applied to this month’s Featured Molecule, lycopene, particularly with regard to potential health benefits of tomatoes. The paper by Jie Zhu, Mingjie Zhang, and Qingwei Liu (1) describes an extraction and purification of lycopene from tomato paste using an emulsion rather than the traditional solvent-based extraction.

Figure 1

lycopene: a bright red carotenoid pigment found in tomatoes and other red fruits

Lycopene is a member of the family of molecules called carotenoids, the most familiar of which is beta-carotene. This family of natural products includes more than 500 members that have been isolated and whose structures have been determined. Professor Hanspeter Pfander’s research group at the University of Bern maintains a Web site with a significant amount of information on carotenoid structure, synthesis, and activity (2).

Structurally one can think of carotenoids as consisting of three segments, a relatively rigid conjugated central portion with end groups. The end groups are, in general, flexible with respect to rotation about the bond connecting them to the central portion. For example, in beta-carotene, the dependence of total energy on the dihedral angle shown in Figure 1, displays a very broad range of essentially isoenergetic conformations (Figure 2). The energies shown in Figure 2 were calculated at the PM3 level using Hyperchem 7.5 (3). Calculations at the HF/631-G(d,p) level, with many fewer data points, show a similar trend.

Figure 1

Figure 1. The dihedral angle of beta-carotene.

 

Figure 1

Figure 2. Dependence of total energy on the dihedral angle of beta-carotene (shown in Figure 1).

Many of the health benefits derived from various carotenoids are attributed to their antioxidant activities. Carotenoids react with singlet-oxygen in a physical, diffusion-controlled, quenching process that results in ground state triplet-oxygen and, following a non-radiative relaxation, ground state carotenoid. Of the various carotenoids that have been studied, lycopene and beta-carotene show the greatest quenching rate constants (4).

The carotenoids provide us with countless explorations by students and teachers looking for connections between fundamental chemical concepts and real-world applications. Structure, reactivity, chemical synthesis, biosynthesis, and stereochemistry are just a few of the concepts involved in understanding the manifest important roles that these molecules play.

Literature Cited

  1. Zhu, Jie; Zhang, Mingjie; Liu; Qingwei. J. Chem. Educ. 2008, 85, 256–257.
  2. Pfander Group (accessed Dec 2007).
  3. HyperChem (accessed Dec 2007; HyperChem is a registered product of Hypercube, Inc.).
  4. Cantrell A.; McGarvey, D. J.; Truscott, T. G.; Rancan, F.; Böhm, F. Arch Biochem Biophys. 2003, Apr 1; 412 (1), 47–54.
Supplement
Find Molecular Models of Lycopene and Other Carotenoids in the JCE Digital Library.
More Information
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Citation
Coleman, William F. J. Chem. Educ. 2008, 85, 320.
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Keywords
Computer-Based Learning; First-Year Undergraduate / General; Food Science; Hands-On Learning / Manipulatives; High School / Introductory Chemistry; Upper-Division Undergraduate
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History
Created:
Last Updated:
1/4/2008
1/9/2008
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