Enzymatic synthesis of an α-chitin-like substance via lysozyme-mediated transglycosylation

Carbohydr Res. 2012 Jan 10;347(1):16-22. doi: 10.1016/j.carres.2011.09.025. Epub 2011 Sep 29.

Abstract

The enzymatic synthesis of an α-chitin-like substance via a non-biosynthetic pathway has been achieved by transglycosylation in an aqueous system of the corresponding substrate, tri-N-acetylchitotriose [(GlcNAc)(3)] for lysozyme. A significant amount of water-insoluble product precipitated out from the reaction system. MALDI-TOFMS analysis showed that the resulting precipitate had a degree of polymerization (DP) of up to 15 from (GlcNAc)(3). Solid-state (13)C NMR analysis revealed that the resulting water-insoluble product is a chitin-like substance consisting of N-acetylglucosamine (GlcNAc) residues joined exclusively in a β-(1→4)-linked chain with stringent regio-/stereoselection. X-ray diffraction (XRD) measurement as well as (13)C NMR analysis showed that the crystal structure of synthetic product corresponds to α-chitin with a high degree of crystallinity. We propose that the multiple oligomers form an α-chitin-like substance as a result of self-assembly via oligomer-oligomer interaction when they precipitate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carbohydrate Sequence
  • Chemistry Techniques, Synthetic / methods*
  • Chitin / chemical synthesis*
  • Chitin / chemistry*
  • Glycosylation
  • Green Chemistry Technology / methods*
  • Micrococcus / enzymology
  • Molecular Sequence Data
  • Muramidase / metabolism*
  • Stereoisomerism
  • Substrate Specificity

Substances

  • Chitin
  • Muramidase