Xylonic acid explained

Xylonic acid is the organic compound with the formula . It is an oxidized derivative of xylose. Xylonic acid is a colorless, water-soluble solid. Several isomers are known, all being classified as sugar acids, several of which can be obtained by oxidation of the corresponding pentoses. The C-2 epimer of xylonic acid is known as lyxonic acid.

Like other sugar acids, xylonic acid readily converts to a lactone (RN 15384-37-9) by dehydration. Lyxonic acid behaves similarly.

Genetically engineered Pseudomonas fragi converts D-xylose to D-xylonic acid. Decarboxylation of the xylonic acid by a strain of Escherichia coli give 1,2,4-butanetriol, which is of commercial interest.[1] [2]

References

  1. 10.1021/ja036391. 14570452 . 2003 . Niu . W. . Molefe . M. N. . Frost . J. W. . Microbial synthesis of the energetic material precursor 1,2,4-butanetriol . Journal of the American Chemical Society . 125 . 43 . 12998–12999 .
  2. 10.1186/s13068-020-01744-6. free . Engineering Microbial Pathways for Production of Bio-based Chemicals from Lignocellulosic Sugars: Current Status and Perspectives . 2020 . Francois . Jean Marie . Alkim . Ceren . Morin . Nicolas . Biotechnology for Biofuels . 13 . 118 . 32670405 . 7341569 .