A simple procedure for preparing chitin oligomers through acetone precipitation after hydrolysis in concentrated hydrochloric acid

Carbohydr Polym. 2015 Nov 5:132:304-10. doi: 10.1016/j.carbpol.2015.05.082. Epub 2015 Jun 30.

Abstract

Chitin oligomers are of interest because of their numerous biologically relevant properties. To prepare chitin oligomers containing 4-6 GlcNAc units [(GlcNAc)4-6], α- and β-chitin were hydrolyzed with concentrated hydrochloric acid at 40 °C. The reactant was mixed with acetone to recover the acetone-insoluble material, and (GlcNAc)4-6 was efficiently recovered after subsequent water extraction. Composition analysis using gel permeation chromatography and MALDI-TOF mass spectrometry indicated that (GlcNAc)4-6 could be isolated from the acetone-insoluble material with recoveries of approximately 17% and 21% from the starting α-chitin and β-chitin, respectively. The acetone precipitation method is highly useful for recovering chitin oligomers from the acid hydrolysate of chitin. The changes in the molecular size and higher-order structure of chitin during the course of hydrolysis were also analyzed, and a model that explains the process of oligomer accumulation is proposed.

Keywords: Acetone precipitation; Acid hydrolysis; Chitin; Chitin oligomer; Water extraction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetone / chemistry*
  • Animals
  • Chemical Precipitation
  • Chitin / chemistry*
  • Decapodiformes / chemistry*
  • Hydrochloric Acid / chemistry*
  • Hydrolysis
  • Oligosaccharides / chemistry*
  • Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization

Substances

  • Oligosaccharides
  • Acetone
  • Chitin
  • N-acetylchitohexaose
  • Hydrochloric Acid