Recombinant production and characterization of a metal ion-independent Lysophospholipase from a hyperthermophilic archaeon Pyrococcus abyssi DSM25543

Int J Biol Macromol. 2024 Feb;259(Pt 2):129345. doi: 10.1016/j.ijbiomac.2024.129345. Epub 2024 Jan 12.

Abstract

Genome sequence of Pyrococcus abyssi DSM25543 contains a coding sequence (PAB_RS01410) for α/β hydrolase (WP_010867387.1). Structural analysis revealed the presence of a consensus motif GXSXG and a highly conserved catalytic triad in the amino acid sequence of α/β hydrolase that were characteristic features of lysophospholipases. A putative lysophospholipase from P. abyssi with its potential applications in oil degumming and starch processing was heterologously produced in E. coli Rosetta (DE3) pLysS in soluble form followed by its purification and characterization. The recombinant enzyme was found to be active at temperature of 40-90 °C and pH 5.5-7.0. However, the enzyme exhibited its optimum activity at 65 °C and pH 6.5. None of the metal ions (Mn2+, Mg2+, Ni2+, Cu2+, Fe2+, Co2+, Zn2+ and Ca2+) being tested had stimulatory effect on lysophospholipase activity. Km and Vmax for hydrolysis of 4-nitrophenyl butyrate were calculated to be 1 ± 0.089 mM and 1637 ± 24.434 U/mg, respectively. It is the first report on the soluble production and characterization of recombinant lysophospholipase from P. abyssi which exhibits its lipolytic activity in the absence of divalent metal ions. Broad substrate specificity, activity and stability at elevated temperatures make recombinant lysophospholipase an ideal candidate for potential industrial applications.

Keywords: Characterization; Lysophospholipase; Metal ion-independency; P. abyssi.

MeSH terms

  • Archaea / metabolism
  • Cloning, Molecular
  • Escherichia coli / genetics
  • Ions / metabolism
  • Lysophospholipase* / chemistry
  • Metals / metabolism
  • Metals / pharmacology
  • Pyrococcus abyssi* / genetics
  • Pyrococcus abyssi* / metabolism
  • Recombinant Proteins / chemistry
  • Substrate Specificity

Substances

  • Lysophospholipase
  • Metals
  • Ions
  • Recombinant Proteins