Cloning and characterization of β-agarase AgaYT from Flammeovirga yaeyamensis strain YT

J Biosci Bioeng. 2011 Sep;112(3):225-32. doi: 10.1016/j.jbiosc.2011.05.016. Epub 2011 Jun 28.

Abstract

A bacterium with potent agar-degrading capability was isolated from the surface of a red algae, Gracilaria tenuistipitata. Based on phenotypic characteristics, 16S rDNA gene sequence and a phylogenetic analysis, this bacterium was identified and named as Flammeovirga yaeyamensis strain YT. PCR using homology-based degenerate primers was employed to clone any agarase gene belonging to GH16 family encoded in F. yaeyamensis strain YT. The resolved 1512 nucleotides revealed that the cloned gene, namely AgaYT, encodes a protein of 503 amino acids comprising a signal peptide, a glycosyl hydrolase catalytic module and a C-terminal domain with an unknown function. The recombinant protein r-AgaYT is an endo-type β-agarase hydrolyzing agarose to yield neoagarobiose and neoagarotetraose as the main hydrolytic products. The specific activity of r-AgaYT was determined about 178.6 U mg(-1) at 40°C and pH 8.0.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacteria / enzymology*
  • Bacteria / genetics
  • Base Sequence
  • Cloning, Molecular
  • Disaccharides / metabolism
  • Enzyme Stability
  • Galactosides / metabolism
  • Glycoside Hydrolases / chemistry*
  • Glycoside Hydrolases / genetics*
  • Glycoside Hydrolases / metabolism
  • Humans
  • Molecular Sequence Data
  • Oligosaccharides / metabolism
  • Phylogeny
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Sepharose / metabolism
  • Sequence Alignment

Substances

  • Disaccharides
  • Galactosides
  • Oligosaccharides
  • Recombinant Proteins
  • neoagarotetraose
  • neoagarobiose
  • Sepharose
  • Glycoside Hydrolases
  • agarase