Isomers are molecules that have the same chemical constituents in different physical arrangements. Some terpenoid isomers have very different aromas and are important food seasonings. A batch of carrot top pesto led to an exploration of intriguing terpenoid isomers in the mint, carrot, and lemon families.
“Oh, c’mon. Try it,” my husband admonished me with a smile. “If anyone would be excited about doing something with them, I should think it would be you.”
The “them” in question were carrot tops, the prolific pile of lacy greens still attached to the carrots we bought at the farmer’s market. I have known for years that carrot tops are edible and have occasionally investigated recipes for them, but that was the extent of my efforts to turn them into food. My excuse is that I harbored niggling doubts that carrot tops would taste good. Edible does not, after all, imply delicious. My husband had thrown down the gauntlet, though, by challenging my integrity as a vegetable enthusiast. I took a long look at the beautiful foliage on the counter.
“Fine,” I responded, sounding, I am sure, resigned. “I’ll make a pesto with them.”
Carrot tops, it turns out, make a superb pesto. I have the passion of a convert about it, and not just because my carrot tops will forevermore meet a fate suitable to their bountiful vitality. The pesto I made combined botanical ingredients from two plant families whose flavors highlight the fascinating chemistry of structural and stereo isomers. Continue reading
Posted in Flavor, herbs, Recipes, Uncategorized, Vegetables
Tagged ajwain, Apiaceae, carrot, carvacrol, carvone, Jeanne L. D. Osnas, Lamiaceae, oregano, pesto, recipe, terpene, thyme, thymol
The Cooks Illustrated recipe masters recently added nutmeg and orange zest to a pepper-crusted steak to replace two flavorful terpenes, pinene and limonene, lost from black pepper when simmered in oil. In doing so they take advantage of convergent evolution of terpenoids, the most diverse group of chemical products produced by plants. Nutmeg and orange zest, though, were hardly their only options.
The terpene swap
Black pepper growing (photo by L. Osnas)
To develop satisfying crunch, the Cooks Illustrated recipe for pepper-crusted beef tenderloin requires a prodigious quantity of coarsely ground black pepper (Piper nigrum; family Piperaceae). If applied to the meat raw, however, in the recipe authors’ view, this heap of pepper generates an unwelcome amount of spicy heat. To mellow it, the recipe authors recommend simmering the pepper in oil and straining it out of the oil before adding it to the dry rub. The hot oil draws out the alkaloid piperine, which makes black pepper taste hot, from the cracked black pepper fruits (peppercorns).
To their dismay, however, the recipe authors discovered that the hot oil also removes flavorful compounds from the cracked pepper, in particular the terpenes pinene and limonene. To rectify this flavor problem, the recipe authors added pinene-rich nutmeg (Myristica fragrans; Myristicaceae) and limonene-rich orange (Citrus x sinensis; Rutaceae) zest to the dry rub, along with the simmered black pepper. In doing so they take advantage of widespread and diverse array of terpenoids in the plant kingdom. Continue reading