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Literature summary extracted from

  • Chen, W.; Yu, H.; Ye, L.
    Comparative study on different expression hosts for alkaline phytase engineered in Escherichia coli (2016), Appl. Biochem. Biotechnol., 179, 997-1010 .
    View publication on PubMed

Cloned(Commentary)

EC Number Cloned (Comment) Organism
3.1.3.8 gene phy168, recombinant expression of wild-type and mutant enzymes in Bacillus subtilis strain WB800N, Escherichia coli TOP10 cells or strain BL21, and Pichia pastoris strain GS115, subcloning in Escherichia coli, evaluation of the best expression systems, overview. High glycosylation degree of the proteins when expressed in Pichia pastoris strain GS115, when the expression host is changed from Escherichia coli to Pichia pastoris, deglycosylation is conducted. The enzyme expressed in Pichia pastoris is secreted. Wild-type enzyme and the mutants D24G, D24G/K70R/K111E/N121S secreted by Pichia pastoris show decreased thermostability compared with those expressed in Escherichia coli, correspondingly. This reduction in residual activity might be ascribed to the N-glycosylation of phy168 in Pichia pastoris Bacillus subtilis

Protein Variants

EC Number Protein Variants Comment Organism
3.1.3.8 D24G site-directed mutagenesis, the Bacillus subtilis-expressed variant D24G shows 62.7, 68.3, and 17.9% higher specific activity than those expressed in Escherichia coli at pH 7.0, 60°C, pH 7.0, 37°C, and pH 4.5, 37°C, respectively. The specific activity of the Escherichia coli-expressed D24G at pH 7.0 and 37°C is improved by 40.3 % as compared with that of the wild-type, while the improvement is 91.9% in Bacillus subtilis and 82.2% in Pichia pastoris, respectively. Overall, the mutant's activity is increased compared to the wild-type Bacillus subtilis
3.1.3.8 D24G/K70R/K111E/N121S site-directed mutagenesis, the Bacillus subtilis-expressed variant D24G/K70R/K111E/N121S shows 54.1, 42.6, and 10.8% higher specific activity than those expressed in Escherichia coli at pH 7.0, 60°C, pH 7.0, 37°C, and pH 4.5, 37°C, respectively. Overall, the mutant's activity is significantly increased compared to the wild-type Bacillus subtilis
3.1.3.8 K265E site-directed mutagenesis, the mutant shows similar activity compared to wild-type Bacillus subtilis
3.1.3.8 additional information the specific activities of the Bacillus subtilis-expressed phy168 proteins are mostly higher than those of the corresponding phy168 enzymes expressed in Escherichia coli. The activties of wild-type and mutant enzymes vary dependent on conditions and expression system, overview Bacillus subtilis
3.1.3.8 S51A site-directed mutagenesis. Overall, the mutant's activity is increased compared to the wild-type Bacillus subtilis
3.1.3.8 S51A/K265E site-directed mutagenesis, overall, the mutant's activity is increased compared to the wild-type Bacillus subtilis

Natural Substrates/ Products (Substrates)

EC Number Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
3.1.3.8 myo-inositol hexakisphosphate + H2O Bacillus subtilis
-
1D-myo-inositol 1,2,4,5,6-pentakisphosphate + phosphate
-
?
3.1.3.8 myo-inositol hexakisphosphate + H2O Bacillus subtilis 168
-
1D-myo-inositol 1,2,4,5,6-pentakisphosphate + phosphate
-
?

Organism

EC Number Organism UniProt Comment Textmining
3.1.3.8 Bacillus subtilis P42094
-
-
3.1.3.8 Bacillus subtilis 168 P42094
-
-

Posttranslational Modification

EC Number Posttranslational Modification Comment Organism
3.1.3.8 glycoprotein two potential N-glycosylated sites within the Asn-Xaa-Ser/Thr sequence are found in the phy168 phytase. High glycosylation degree of the proteins when expressed in Pichia pastoris strain GS115 Bacillus subtilis

Specific Activity [micromol/min/mg]

EC Number Specific Activity Minimum [µmol/min/mg] Specific Activity Maximum [µmol/min/mg] Comment Organism
3.1.3.8 19.7
-
purified recombinant enzyme mutant D24G/K70R/K111E/N121S, expressed in Escherichia coli, pH 7.0, 60°C Bacillus subtilis
3.1.3.8 22.7
-
purified recombinant enzyme mutant D24G/K70R/K111E/N121S, expressed in Pichia pastoris, pH 7.0, 60°C Bacillus subtilis
3.1.3.8 30.4
-
purified recombinant enzyme mutant D24G/K70R/K111E/N121S, expressed in Bacillus subtilis, pH 7.0, 60°C Bacillus subtilis

Substrates and Products (Substrate)

EC Number Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
3.1.3.8 myo-inositol hexakisphosphate + H2O
-
Bacillus subtilis 1D-myo-inositol 1,2,4,5,6-pentakisphosphate + phosphate
-
?
3.1.3.8 myo-inositol hexakisphosphate + H2O
-
Bacillus subtilis 168 1D-myo-inositol 1,2,4,5,6-pentakisphosphate + phosphate
-
?

Subunits

EC Number Subunits Comment Organism
3.1.3.8 ? x * 45000, Pichia pastoris-expressed Phy168 after deglycosylation, SDS-PAGE Bacillus subtilis

Synonyms

EC Number Synonyms Comment Organism
3.1.3.8 phy168
-
Bacillus subtilis

Temperature Optimum [°C]

EC Number Temperature Optimum [°C] Temperature Optimum Maximum [°C] Comment Organism
3.1.3.8 60
-
recombinant wild-type enzyme Bacillus subtilis

Temperature Range [°C]

EC Number Temperature Minimum [°C] Temperature Maximum [°C] Comment Organism
3.1.3.8 additional information
-
the highest activities of wild-type and D24G expressed in Pichia pastoris are achieved at 50°C and 55°C, decreased by 10°C and 5°C compared to those expressed in Escherichia coli, respectively. Temperature profiles of the mutants expressed in Pichia pastoris and Bacillus subtilis, overview Bacillus subtilis

Temperature Stability [°C]

EC Number Temperature Stability Minimum [°C] Temperature Stability Maximum [°C] Comment Organism
3.1.3.8 additional information
-
temperature profiles of the mutants expressed in Pichia pastoris and Bacillus subtilis Bacillus subtilis
3.1.3.8 80
-
pH 7.0, 37°C, 70% activity remains for the purified recombinant enzyme mutant expressed from Bacillus subtilis, 25% activity remains for the purified recombinant enzyme mutant expressed from Pichia pastoris, and 50% activity remains for the purified recombinant enzyme mutant expressed from Escherichia coli Bacillus subtilis

pH Optimum

EC Number pH Optimum Minimum pH Optimum Maximum Comment Organism
3.1.3.8 7
-
recombinant wild-type enzyme Bacillus subtilis