Purification and biochemical characterization of a novel thermostable protease from the oyster mushroom Pleurotus sajor-caju strain CTM10057 with industrial interest

• Published in: BMC biotechnology 2019-07, Vol.19 (1), p.43-43, Article 43
• Main Authors: Omrane Benmrad, Maroua, Mechri, Sondes, Zaraî Jaouadi, Nadia, Ben Elhoul, Mouna, Rekik, Hatem, Sayadi, Sami, Bejar, Samir, Kechaou, Nabil, Jaouadi, Bassem
• Format: Article
• Language: English
• Subjects: Amino acids; Ammonium salts; Ammonium sulfate; Casein; Chromatography; Detergent formulations; Detergents; Detergents - chemistry; Electrophoresis; Enzyme Stability; Enzymes; Fungal Proteins - chemistry; Fungal Proteins - isolation & purification; Fungal Proteins - metabolism; Fungi; High performance liquid chromatography; Hot Temperature; Hydrogen-Ion Concentration; Hydrolysis; Industrial equipment; Industrial Microbiology - methods; Kinetics; Milk proteins; Molecular Weight; Mushrooms; Novels; Organic solvent; Oyster mushroom; Peptide synthesis; Peptides; Physiological aspects; Pleurotus - enzymology; Pleurotus sajor-caju; Polymerase chain reaction; Protease; Proteases; Proteins; Serine; Serine Proteases - chemistry; Serine Proteases - isolation & purification; Serine Proteases - metabolism; Substrate Specificity; Sulfates; Surface active agents; Thrombin
• ISSN: 1472-6750; 1472-6750
• DOI: 10.1186/s12896-019-0536-4

Proteases are hydrolytic enzymes that catalyze peptide linkage cleavage reactions at the level of proteins and peptides with different degrees of specificity. This group draws the attention of industry. More than one protease in three is a serine protease. Classically, they are active at neutral to alkaline pH. The serine proteases are researched for industrial uses, especially detergents. They are the most commercially available enzyme group in the world market. Overall, fungi produced extracellular proteases, easily separated from mycelium by filtration. A new basidiomycete fungus CTM10057, a hyperproducer of a novel protease (10,500 U/mL), was identified as Pleurotus sajor-caju (oyster mushroom). The enzyme, called SPPS, was purified to homogeneity by heat-treatment (80 °C for 20 min) followed by ammonium sulfate precipitation (35-55%)-dialysis, then UNO Q-6 FPLC ion-exchange chromatography and finally HPLC-ZORBAX PSM 300 HPSEC gel filtration chromatography, and submitted to biochemical characterization assays. The molecular mass was estimated to be 65 kDa by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), Native-PAGE, casein-zymography, and size exclusion by HPLC. A high homology with mushroom proteases was displayed by the first 26 amino-acid residues of the NH -terminal aminoacid sequence. Phenylmethanesulfonyl fluoride (PMSF) and diiodopropyl fluorophosphates (DFP) strongly inhibit SPPS, revealing that it is a member of the serine-proteases family. The pH and temperature optima were 9.5 and 70 °C, respectively. Interestingly, SPPS possesses the most elevated hydrolysis level and catalytic efficiency in comparison with SPTC, Flavourzyme® 500 L, and Thermolysin type X proteases. More remarkably, a high tolerance towards organic solvent tolerance was exhibited by SPPS, together with considerable detergent stability compared to the commercial proteases Thermolysin type X and Flavourzyme® 500 L, respectively. This proves the excellent proprieties characterizing SPPS, making it a potential candidate for industrial applications especially detergent formulations.