In this study, the xylanase gene from Cellulomonas flavigena KCTC 9104 was cloned into pPICZαB and expressed in Pichia pastoris X-33. An extracellular endo-1,4-β-xylanase was produced by novel engineered P. pastoris (rXynCf) and purified by Ni-NTA affinity column. Characterization of rXynCf was performed and results are as follows: 38kDa molecular weight, 55°C optimum temperature and optimum pH of 6. Under the conditions, the Km and V max of rXynCf were 3.6±0.08mg/mL and 4505±52μmol/minmg, respectively. rXynCf was applied in enzymatic hydrolysis process for sugars production from lignocellulosic biomass. Empty fruit bunch (EFB) was selected as a feedstock, and the total sugars conversion was found to be 3.8%, meanwhile the conversion by alkaline pretreatment improved approximately 16-fold (61.1%). In addition, rXynCf shows similar xylose conversion to commercial xylanase. Therefore, due to its properties, rXynCf has considerable potential in biorefinery applications.
- Cellulomonas flavigena
- Enzymatic hydrolysis
- Pichia pastoris
ASJC Scopus subject areas
- Applied Microbiology and Biotechnology