A novel pullulanase from a fungus Hypocrea jecorina QM9414: Production and biochemical characterization

Orhan N., Kiymaz N., PEKSEL A.

INDIAN JOURNAL OF BIOCHEMISTRY & BIOPHYSICS, vol.51, no.2, pp.149-155, 2014 (SCI-Expanded) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 51 Issue: 2
  • Publication Date: 2014
  • Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Page Numbers: pp.149-155
  • Keywords: Hypocrea jecorina QM92114, Culture conditions, Induction, Type II pullulanase, Purification, STARCH, AMYLOPULLULANASE, INDUCTION, ENZYMES, ACID
  • Yıldız Technical University Affiliated: Yes


Pullulanase production from a fungus Hypocrea jecorina QM9414 that produces native extracellular hydrolases having industrial applications was carried out in a shaking flask culture containing 0.5% amylopectin at a pH of 6.50 at 30 C. The enzyme was purified 11-fold by ammonium sulfate fractionation, anion-exchange and gel-filtration chromatographies with a yield of 10.12% and a specific activity of 1.36 +/- 0.14 U/mg protein. The molecular mass of pullulanase was estimated to be 130.56 kDa by PAGE and SDS-PAGE, indicating that the native enzyme was a monomer. The optimum pH and temperature for purified enzyme was 6.5 and between 35 degrees-65 degrees C, respectively. The Km values for amylopectin, starch and pullulan as substrates were 10.7, 15.5 and 38.4 mg/mL, respectively. The V-max values were found to be 3.32, 3.32 and 3.82 Delta A/min for amylopectin, starch and pullulan, respectively. The enzyme was stable at 40-70 degrees C for 30 min, but lost about 33% of its activity at 80 degrees C and about 43% of activity at 90 degrees C and 100 degrees C for the same incubation period. Pullulanase activity was stimulated by CoCl2, NiCl2, KI, NaCl, MgCl2, and LiSO4. The enzyme was slightly inhibited by urea, CaCl2 and beta-mercaptoethanol. The enyzmatic characteristics, substrate specificity and the products of hydrolysis indicated that the enzyme was similar to those of type II pullulanases.