Characterization of a Recombinant Thermostable Arylsulfatase from Deep-Sea Bacterium Flammeovirga pacifica

J Microbiol Biotechnol. 2015 Nov;25(11):1894-901. doi: 10.4014/jmb.1504.04028.

Abstract

A novel sulfatase gene, ary423 (1,536 bp ORF), encoding a protein of 511 amino acids with a calculated molecular mass of 56 kDa, was identified from Flammeovirga pacifica, which was isolated from deep-sea sediments of west Pacific Ocean. Amino acid sequence analysis revealed that Ary423 possessed a conserved C-X-A-X-R motif, which was recognized as the sulfatase signature. Phylogenetic analysis suggested that Ary423 belonged to arylsulfatases. After heterologous expression in Escherichia coli cells, the recombinant Ary423 was purified with a Ni(+) affinity column, and was shown to be highly active at a broad range of temperatures from 30° to 70°C, with maximum activity at 40°C. Furthermore, recombinant Ary423 retained more than 70% and 40% of its maximum activity after 12 h of incubation at 50°C and 60°C, respectively, exhibiting good thermostability at high temperatures. The optimal pH for Ary423 was determined to be 8.0 and the activity of Ary423 could be slightly enhanced by Mg(2+). The recombinant enzyme could hydrolyze sulfate ester bonds in pnitrophenyl sulfate (NPS) and Asparagus crude polysaccharides with a specific activity of 64.8 U/mg and 25.4 U/mg, respectively. These favorable properties could make Ary423 attractive for application in the desulfating process of agar production.

Keywords: Flammeovirga Pacifica; arylsulfatase; characterization; deep sea; thermostability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Arylsulfatases / chemistry
  • Arylsulfatases / genetics
  • Arylsulfatases / metabolism*
  • Bacteroidetes / enzymology*
  • Bacteroidetes / genetics
  • Bacteroidetes / isolation & purification
  • Chromatography, Affinity
  • Enzyme Activators / metabolism
  • Enzyme Stability
  • Escherichia coli / genetics
  • Escherichia coli / metabolism
  • Gene Expression
  • Geologic Sediments / microbiology*
  • Hydrogen-Ion Concentration
  • Hydrolysis
  • Magnesium / metabolism
  • Molecular Sequence Data
  • Molecular Weight
  • Nitrobenzenes / metabolism
  • Pacific Ocean
  • Phylogeny
  • Polysaccharides / metabolism
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism*
  • Sequence Homology, Amino Acid
  • Substrate Specificity
  • Temperature

Substances

  • Enzyme Activators
  • Nitrobenzenes
  • Polysaccharides
  • Recombinant Proteins
  • 4-nitrophenyl sulfate
  • Arylsulfatases
  • Magnesium