1. A Novel Phytase Derived from an Acidic Peat-Soil Microbiome Showing High Stability under Acidic Plus Pepsin Conditions.
- Author
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Tan H, Wu X, Xie L, Huang Z, Peng W, and Gan B
- Subjects
- 6-Phytase chemistry, 6-Phytase isolation & purification, Acidobacteria enzymology, Acidobacteria genetics, Biochemistry, Enzyme Stability, Escherichia coli genetics, Escherichia coli metabolism, Gastric Juice enzymology, Gastrointestinal Agents, Gene Expression, Germany, Hydrogen-Ion Concentration, Metagenomics, Pepsin A metabolism, Recombinant Proteins chemistry, Recombinant Proteins genetics, Recombinant Proteins isolation & purification, Recombinant Proteins metabolism, Sequence Homology, Soil, Temperature, 6-Phytase genetics, 6-Phytase metabolism, Metagenome, Soil Microbiology
- Abstract
Four novel phytases of the histidine acid phosphatase family were identified in two publicly available metagenomic datasets of an acidic peat-soil microbiome in northeastern Bavaria, Germany. These enzymes have low similarity to all the reported phytases. They were overexpressed in Escherichia coli and purified. Catalytic efficacy in simulated gastric fluid was measured and compared among the four candidates. The phytase named rPhyPt4 was selected for its high activity. It is the first phytase identified from unculturable Acidobacteria. The phytase showed a longer half-life than all the gastric-stable phytases that have been reported to date, suggesting a strong resistance to low pH and pepsin. A wide pH profile was observed between pH 1.5 and 5.0. At the optimum pH (2.5) the activity was 2,790 μmol/min/mg at the physiological temperature of 37°C and 3,989 μmol/min/mg at the optimum temperature of 60°C. Due to the competent activity level as well as the high gastric stability, the phytase could be a potential candidate for practical use in livestock and poultry feeding., (© 2016 S. Karger AG, Basel.)
- Published
- 2016
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