Genetic Engineering: Future Foods

by Food and Drug Administration (FDA)

Take a peek into the supermarket of the near future.

At first glance, products on display won't seem much different from those you are used to. Cucumbers. Peppers. Corn. They'll still be there. But amid all the produce and other kitchen staples, you're apt to find new versions of familiar foods — ones that are custom "built" to improve quality or remove unwanted traits. Insect-resistant apples, long-lasting raspberries, and potatoes that absorb less fat are among the more than 50 plant products under study now that are likely to reside soon on grocers' shelves.

These commodities will arrive courtesy of genetic engineering, a process that allows plant breeders to modify the genetic makeup of a plant species precisely and predictably, creating improved varieties faster and easier than can be done using more traditional plant-breeding techniques. Genetic engineering already is improving lives in areas such as disease diagnostics and treatments, but at the moment it is a fledgling economic force in the commercial food business.

Though genetic engineering promises better and more plentiful products, genetically engineered foods may encounter a few obstacles to widespread public acceptance. Some consumers, along with a few advocacy groups, have voiced concern about the safety and environmental impact of these new food products. Some urge an outright ban on any genetically engineered foods. Others support mandatory labeling that discloses the use of genetic engineering. Still others advocate more stringent testing of these products before marketing.

New Foods Safe

From the standpoint of the Food and Drug Administration, the important thing for consumers to know about these new foods is that they will be every bit as safe as the foods now on store shelves. All foods, whether traditionally bred or genetically engineered, must meet the provisions of the Federal Food, Drug, and Cosmetic Act.

To let both the public and companies know how these new foods would be regulated, FDA published a detailed statement in the May 29, 1992, Federal Register explaining how foods derived from new plant varieties — fruits, vegetables, grains, and their byproducts, such as vegetable oil — will be regulated under the act. The statement contains a thorough scientific discussion, complete with carefully designed flow charts, to help plant developers ensure food safety in genetically engineered products.

Present Situation

To understand how FDA will oversee the safety of these new foods, it helps to know how new foods reach supermarkets today. Each year, 10,000 to 20,000 new food products are introduced. In 1994, FDA expected only 100 to 150 genetically engineered foods to be introduced over the next five years. Early in 1997, 18 of these foods had been cleared by FDA, as well as by, the Environmental Protection Agency and U.S.Department of Agriculture.

Except for a handful of new "food additives" such as artificial sweeteners, which must receive premarket approval from FDA before entering the marketplace, most new foods are introduced under the "postmarket" authority of the Food, Drug, and Cosmetic Act. Under this authority, foods made up of proteins, fats and carbohydrates with a history of safe use in food can be sold once companies are satisfied the new product is safe without first getting FDA permission.

This system, which has been in place for more than 50 years, has resulted in one of the world's safest, most abundant, and cheapest food supplies. Should a problem arise with any of these products, FDA has powerful enforcement tools that enable the agency to seize a product as soon as a safety concern is identified.

To help assure the public that this system will work as well for genetically engineered foods as it has for the 30,000 products that can be found in the typical supermarket, FDA encourages firms to provide the agency with a summary of their assessment of the food's safety and nutritional makeup. Companies should discuss these results with agency scientists before marketing the food. "This will ensure that FDA remains abreast of developments achieved through this rapidly evolving technology," says Jim Maryanski, Ph.D., FDA's food biotechnology coordinator.

Labeling Issues

FDA has received many inquiries asking about the labeling of genetically engineered foods. Congress has provided FDA a limited basis on which to require labeling. Generally, for FDA to require labeling there must be something tangibly different about the food.

In general, this means most genetically engineered foods will not need special labeling because they will be similar to traditionally bred varieties. But there are exceptions, such as when a gene from a food that could cause an allergic reaction — peanuts, for example — is transferred into another food. In that case, FDA policy places the burden on the developer. "The food will have to be labeled so everyone will know it contains an allergen, unless the developer can show scientifically that the allergenicity has not been transferred," says Laura Tarantino, Ph.D., deputy director of FDA's Office of Premarket Approval. Fortunately, the products in front of us right now don't raise those issues."

FDA also will require labeling if a company uses genetic engineering techniques to change a food's composition significantly. For example, when one manufacturer modified canola to produce increased levels of lauric and myristic acids in the seed oil, FDA agreed that the common or usual name for this oil would be "laurate canola oil" in order to distinguish it from traditional canola oil.

About the Author

www.fda.gov
FDA is A United States government body that oversees medical devices, including contact lenses, intraocular lenses, excimer lasers and eyedrops. In the US, these products must be approved by the FDA before they can be marketed.