<p>This study reports the identification of a phosphatase-producing psychrotolerant bacterium, <i>Bacillus cereus</i> KR_O9, isolated from Arctic Krossfjorden sediments. The extracellular KR_O9 phosphatase was purified to homogeneity through acetone precipitation and ion exchange chromatography, achieving a specific activity of 12.51 U mg⁻<sup>1</sup>&#xa0;min⁻<sup>1</sup>, a 17.3-fold purification, and a 64.94% yield. The molecular mass of the enzyme was estimated as 37&#xa0;kDa by SDS-PAGE. <i>K</i><sub><i>m</i></sub><i>,</i> and <i>V</i><sub><i>max</i></sub> for KR_O9 phosphatase towards substrate <i>p-</i>NPP were determined as 0.033&#xa0;M L<sup>−1</sup>, 1.67&#xa0;mg<sup>−1</sup>&#xa0;min<sup>−1</sup>. The enzyme exhibited optimal activity at 40&#xa0;°C and pH 6.0, with stability up to ≤ 40&#xa0;°C and at pH levels ≤ 7.0, highlighting its thermolability and sensitivity to alkaline pH. At 10&#xa0;mM level, Cu<sup>2+</sup>, Hg<sup>2+</sup>, Co<sup>2+</sup>, Pb<sup>2+</sup>, urea, EDTA, and GSH significantly stimulated the enzyme, and Ca<sup>2+</sup>, Zn<sup>2+</sup>, Mn<sup>2+</sup>, SDS, and CTAB were, strong inhibitors. The kinetic efficiency, resilience to low to neutral pH, and tolerance to various metal ions, including heavy metals, underscore the potential of <i>B. cereus</i> KR_O9 phosphatase for bioremediation and biofertilizer applications, paving the way for industrial exploration.</p>

错误:搜索内容不能为空,请输入英文关键词
错误:关键词超出字数限制,请精简
高级检索

A psychrotolerant extracellular phosphatase from Krossfjorden sediment bacterium Bacillus cereus KR_O9: purification and functional characterization

  • E. S. Lisintta,
  • Annie George,
  • Sona Gafoor,
  • S. Vishnupriya,
  • Jesmi Yousuf,
  • Bhavya Kachiprath,
  • A. K. Valsa,
  • Ally C. Antony,
  • P. A. Aneesa,
  • A. A. Mohamed Hatha

摘要

This study reports the identification of a phosphatase-producing psychrotolerant bacterium, Bacillus cereus KR_O9, isolated from Arctic Krossfjorden sediments. The extracellular KR_O9 phosphatase was purified to homogeneity through acetone precipitation and ion exchange chromatography, achieving a specific activity of 12.51 U mg⁻1 min⁻1, a 17.3-fold purification, and a 64.94% yield. The molecular mass of the enzyme was estimated as 37 kDa by SDS-PAGE. Km, and Vmax for KR_O9 phosphatase towards substrate p-NPP were determined as 0.033 M L−1, 1.67 mg−1 min−1. The enzyme exhibited optimal activity at 40 °C and pH 6.0, with stability up to ≤ 40 °C and at pH levels ≤ 7.0, highlighting its thermolability and sensitivity to alkaline pH. At 10 mM level, Cu2+, Hg2+, Co2+, Pb2+, urea, EDTA, and GSH significantly stimulated the enzyme, and Ca2+, Zn2+, Mn2+, SDS, and CTAB were, strong inhibitors. The kinetic efficiency, resilience to low to neutral pH, and tolerance to various metal ions, including heavy metals, underscore the potential of B. cereus KR_O9 phosphatase for bioremediation and biofertilizer applications, paving the way for industrial exploration.