Over-expression of a bacterial chitosanase gene in Yarrowia lipolytica and chitosan hydrolysis by the recombinant chitosanase

The bacterial strain OUC1 was found to be closely related to Pseudomonas sp. A-01. A chitosanase gene (chi) cloned from the marine bacterium Pseudomonas sp. OUC1 was over-expressed in Yarrowia lipolytica which is generally regarded as safe. After the expression vector carrying two copies of the chi gene was transformed into Y. lipolytica, the transformants obtained could secrete much more chitosanase (9.0 U/ml) than those (4.3 U/ml) transformed with the expression vector carrying one copy of the chi gene. The molecular mass of the recombinant chitosanase was 31.5 kDa. The optimal pH and temperature of the recombinant chitosanase were 6.0 and 50 °C, respectively. Mn2+ was found to greatly enhance its activity. Km and Vmax for chitosan were 6.77 mg/ml and 0.224 mg/ml min, respectively. Chitosan was actively hydrolyzed by the recombinant chitosanase into GluN2, GluN3, GluN4, GluN5 and GluN6.

Graphical abstractCell morphology of Yarrowia lipolyticaFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► The chitosanase gene from a marine bacterium was over-expressed in Y. lipolytica Po1h. ► The molecular mass of the purified chitosanase was 31.5 kDa. ► The optimal pH and temperature of the purified chitosanase were 6.0 and 50 °C, respectively. ► The activity of chitosanase was greatly stimulated in the presence of Mn2+. ► Chitosan could be actively converted into oligosaccharides.