Temperature Shifts for Extraction and Purification of Zygomycetes Chitosan with Dilute Sulfuric Acid
Artikel i vetenskaplig tidskrift, 2010

The temperature-dependent hydrolysis and solubility of chitosan in sulfuric acid solutions offer the possibility for chitosan extraction from zygomycetes mycelia and separation from other cellular ingredients with high purity and high recovery. In this study, Rhizomucor pusillus biomass was initially extracted with 0.5 M NaOH at 120 °C for 20 min, leaving an alkali insoluble material (AIM) rich in chitosan. Then, the AIM was subjected to two steps treatment with 72 mM sulfuric acid at (i) room temperature for 10 min followed by (ii) 120 °C for 45 min. During the first step, phosphate of the AIM was released into the acid solution and separated from the chitosan-rich residue by centrifugation. In the second step, the residual AIM was re-suspended in fresh 72 mM sulfuric acid, heated at 120 °C and hot filtered, whereby chitosan was extracted and separated from the hot alkali and acid insoluble material (HAAIM). The chitosan was recovered from the acid solution by precipitation at lowered temperature and raised pH to 8-10. The treatment resulted in 0.34 g chitosan and 0.16 g HAAIM from each gram AIM. At the start, the AIM contained at least 17% phosphate, whereas after the purification, the corresponding phosphate content of the obtained chitosan was just 1%. The purity of this chitosan was higher than 83%. The AIM subjected directly to the treatment with hot sulfuric acid (at 120 °C for 45 min) resulted in a chitosan with a phosphate impurity of 18.5%.

Rhizomucor pusillus

sulfuric acid

fungal chitosan

phosphate release

Författare

Akram Zamani Forooshani

Chalmers, Kemi- och bioteknik

Lars Edebo

Göteborgs universitet

Claes Niklasson

Chalmers, Kemi- och bioteknik, Kemisk reaktionsteknik

Mohammad Taherzadeh Esfahani

Högskolan i Borås

International Journal of Molecular Sciences

14220067 (eISSN)

Vol. 11 8 2976-2987

Ämneskategorier

Industriell bioteknik

Kemiteknik

Kemi

DOI

10.3390/ijms11082976

Mer information

Senast uppdaterat

2018-03-08