Erythorbic acid
Erythorbic acid is a stereoisomer of ascorbic acid. It is synthesized by a reaction between methyl 2-keto-D-gluconate and sodium methoxide. It can also be synthesized from sucrose or by strains of Penicillium that have been selected for this feature. It is denoted by E number E315, and is widely used as an antioxidant in processed foods.
Health effects
Clinical trials have been conducted to investigate aspects of the nutritional value of erythorbic acid. One such trial investigated the effects of erythorbic acid on vitamin C metabolism in young women; no effect on vitamin C uptake or clearance from the body was found.A later study found that erythorbic acid is a potent enhancer of nonheme-iron absorption, just like ascorbate. This is thought to be due to it exerting the same iron-reducing and iron-chelating activity as ascorbic acid. Neither of these reactions is mediated by an enzyme, which would confer some chiral selectivity. It is twice as effective as ascorbic acid in enhancing non-heme iron absorption. Americans are estimated to ingest 200 mg of erythorbic acid per day, making it a very important factor in understanding iron absorption.
Uses
Since the U.S. Food and Drug Administration banned the use of sulfites as a preservative in foods intended to be eaten fresh, the use of erythorbic acid as a food preservative has increased.It is also used as a preservative in cured meats and frozen vegetables. Much like ascorbic acid, it increases nitrosylation of the central iron atom of muscle myoglobin, resulting in the formation of reddish-brown nitrosomyoglobin and the characteristic pink color of nitrosohemochrome or nitrosyl-heme upon cooking. Again like ascorbic acid, it reduces the formation of nitrosamines.
History
It was first synthesized in 1933 by the German chemists Kurt Maurer and Bruno Schiedt.Production
Erythorbic acid is very easily produced by fermentation, being obtainable in just one step compared to ascorbic acid's two. A number of Penicillium naturally produce this chemical from glucose. This is the original process developed in the 1960s, but it has low volumetric efficiency and glucose yield compared to the modern method.Today the industrial process is quite similar to the Reichstein process used for ascorbic acid, only chirally flipped. Microbial fermentation first produces a 2-keto-sugar acid, e.g. by Pseudomonas fluorescens AR4 converting glucose to 2-keto-D-gluconate. Then chemical rearrangement produces the product.