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Purification and characterization of a novel tannase produced by Kluyveromyces marxianus using olive pomace as solid support, and its promising role in gallic acid production.
Mahmoud, Abeer E; Fathy, Shadia A; Rashad, Mona M; Ezz, Magda K; Mohammed, Amira T.
Affiliation
  • Mahmoud AE; Biochemistry Department, Division of Genetic Engineering and Biotechnology, National Research Centre, Dokki 12622, Giza, Egypt. Electronic address: ab_essam@yahoo.com.
  • Fathy SA; Biochemistry Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
  • Rashad MM; Biochemistry Department, Division of Genetic Engineering and Biotechnology, National Research Centre, Dokki 12622, Giza, Egypt.
  • Ezz MK; Biochemistry Department, Faculty of Science, Ain Shams University, Cairo, Egypt.
  • Mohammed AT; Biochemistry Department, Division of Genetic Engineering and Biotechnology, National Research Centre, Dokki 12622, Giza, Egypt.
Int J Biol Macromol ; 107(Pt B): 2342-2350, 2018 Feb.
Article in En | MEDLINE | ID: mdl-29055707
Tannase is considered one of the most important industrial enzymes that find great applications in various sectors. Production of tannases through solid state fermentation (SSF) using agro-industrial wastes is an eco-friendly and cheap technology. Tannase was produced by the yeast Kluyveromyces marxianus using olive pomace as a solid support under SSF. It was purified using ammonium sulfate fractional precipitation followed by Sephadex G-200 gel filtration resulting in 64.6% enzyme yield with 1026.12U/mg specific activity and 24.21 purification fold. Pure tannase had molecular weight of 65 KDa and 66.62 KDa by SDS-PAGE and gel filtration, respectively. It showed a maximal activity at 35°C having two different pH optima, one of which is acidic (4.5) and the other one is alkaline (8.5). The enzyme was stable in the acidic range of pH (4.0-5.5) for 30min, and thermostable within the temperature range 30-70°C. Using tannic acid, the enzyme had a Km value of 0.77mM and Vmax of 263.20µmolemin-1ml-1. The effect of different metal ions on enzymatic activity was evaluated. HPLC analysis data indicated that the purified enzyme could carry out 24.65% tannic acid conversion with 5.25 folds increase in gallic acid concentration within 30min only.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kluyveromyces / Carboxylic Ester Hydrolases / Gallic Acid Language: En Journal: Int J Biol Macromol Year: 2018 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kluyveromyces / Carboxylic Ester Hydrolases / Gallic Acid Language: En Journal: Int J Biol Macromol Year: 2018 Type: Article