<p>In the present study, characterization of bacterial isolate from fermented foods based on the morphology, biochemical, and molecular analysis identified <i>Lactiplantibacillus plantarum</i>. The bacterium was tested for its ability to degrade monocrotophos (MCP) at a concentration of 1000&#xa0;ppm. The dephosphorylation potential of this bacterial enzyme against organophosphate substrates including MCP was analyzed. The <i>Lactiplantibacillus plantarum</i> phosphatase showed optimal activity at 40&#xa0;°C and 6 pH. The Michaelis–Menten constant was found to be 238.14&#xa0;µM while Vmax is 357.14&#xa0;µmol/min.ml for MCP as a substrate. The enzyme activity was enhanced by metal ions such as Mn<sup>2+</sup>, Mg<sup>2+</sup>, and Ca<sup>2+</sup> and inhibited by K<sup>+</sup>, Zn<sup>2+</sup>, and Fe<sup>2+</sup> ions. Plant growth promotion assays of <i>Lp. plantarum</i> exhibited characteristic traits including phosphate solubilization, cellulase, catalase, and xylanase activities. The degradation of MCP was confirmed based on the presence of acetamide and trimethyl phosphate as intermediate metabolites, confirmed by FTIR and GC–MS analysis. Thus, <i>L. plantarum</i>&#xa0;is a suitable candidate for phosphate solubilization, plant growth promotion, and bio-fertilizer application.</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

Lactiplantibacillus plantarum as a sustainable solution for monocrotophos degradation and plant growth enhancement

  • Archana Kumari,
  • Chiranjit Ghosh,
  • N. Kannan,
  • S. Balaji

摘要

In the present study, characterization of bacterial isolate from fermented foods based on the morphology, biochemical, and molecular analysis identified Lactiplantibacillus plantarum. The bacterium was tested for its ability to degrade monocrotophos (MCP) at a concentration of 1000 ppm. The dephosphorylation potential of this bacterial enzyme against organophosphate substrates including MCP was analyzed. The Lactiplantibacillus plantarum phosphatase showed optimal activity at 40 °C and 6 pH. The Michaelis–Menten constant was found to be 238.14 µM while Vmax is 357.14 µmol/min.ml for MCP as a substrate. The enzyme activity was enhanced by metal ions such as Mn2+, Mg2+, and Ca2+ and inhibited by K+, Zn2+, and Fe2+ ions. Plant growth promotion assays of Lp. plantarum exhibited characteristic traits including phosphate solubilization, cellulase, catalase, and xylanase activities. The degradation of MCP was confirmed based on the presence of acetamide and trimethyl phosphate as intermediate metabolites, confirmed by FTIR and GC–MS analysis. Thus, L. plantarum is a suitable candidate for phosphate solubilization, plant growth promotion, and bio-fertilizer application.