Now showing1 - 2 of 2
- Some of the metrics are blocked by yourconsent settings
Item type:Publication, Access status: without files , Characterization of a new, recombinant thermo-active subtilisin-like serine protease derived from Shewanella arctica(2015-06); ; ; ; Proteases represent the commercially most relevant enzyme family with applications in the chemical, cosmetic and pharmaceutical industry. For the personal care industry, both cold-active and thermo-active protease variants are of particular interest for detergent formulation. We have identified a gene sequence encoding a putative subtilisin-like serine protease in a gene library of the psychrophilic bacterium Shewanella arctica (DSM 16509, JCM 14208). The recombinant protein (67 kDa, 644 amino acids) product was flanked by 4.4 kDa (38 a.a.) signal sequence. Initial in-silico sequence analysis and protein modelling revealed the dominant alpha helical structural features embedding the catalytic residues Asp-180, His-213 and Ser-364, which form the canonical catalytic triad of subtilisin-like serine proteases. Further, in the N-terminal region a subtilisin-N domain was detected between residues Asp-55 and Thr-135. Phylogenetic analysis indicated that this enzyme can be classified as subtilisin-like serine protease with 73% amino acids identity to its closest characterized relative, the putative protease of Pseudoaltermonas sp. This is the first report of a detailed biochemical characterization of Shewanella spp. derived protease activity. The recombinant protein (28.18 mg/L), termed SaP, was purified to homogeneity from a crude E. coli lysate with an activity of 0.52 U/mg. Surprisingly, although derived from psychrophilic bacteria, SaP is active over a very broad temperature (T = 0-80 °C) and pH (pH 6-10) range, with optimal proteolytic activity at 60 °C and pH 8. The unique enzyme displayed an activity half-life of 45 h and 1.5 h at 40 °C and 70 °C, respectively. The specific activity of SaP (Kcat/Km: 71.14 s-1 M-1) toward the model substrate casein is comparable to other prokaryotic serine proteases. The enzyme activity was not affected by various metal ions or non-specific protease inhibitors, which positions SaP for industrial application operating over a broad temperature range, such as household detergent formulations.Publicationtype: Journal Article88 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Access status: without files , Cloning, expression and characterization of the recombinant cold-active type-I pullulanase from Shewanella arctica(2015-06); ; ; ; An activity-based screening approach led to the identification of a novel glycoside hydrolase family-13 pullulanase gene (pul13A) from a psychrophilic bacterium. The recombinant enzyme exhibited a deduced peptide sequence of 1440 amino acid residues and was produced in a heterologous host in Escherichia coli. Purification from inclusion bodies was achieved by a six-step dialysis protocol enabling mild refolding of the urea-denaturated protein followed by affinity- and size-exclusion chromatography under native conditions. Pul13A is a type-I pullulanase, which is capable of hydrolysing α-1,6-glycosidic bonds in pullulan to produce maltotriose, while maltose and intermediate oligosaccharides are produced from soluble starch and amylopectin. The recombinant enzyme exhibited typical properties of cold-adapted proteins including low thermostability at elevated temperatures. It showed a temperature optimum at 35°C, while at 10°C residual activity (25%) remained. The optimal pH was in the range of 6.0-7.0, with Pul13A being stable at neutral and basic pH, but not in the acidic range. Catalytic activity was increased in the presence of divalent cations calcium and cobalt and both metal ions were also able to restore catalytic activity of EDTA-chelated enzyme samples. Pul13A represents the first type-I pullulanase from a psychrophile that has been produced in recombinant form. Moreover, its favourable enzymatic properties make this enzyme a potential candidate for industrial applications such as starch degradation for ethanol based biofuel production.Publicationtype: Journal Article46