Characterization and gene cloning of a novel beta-mannanase from alkaliphilic Bacillus sp. N16-5

Extremophiles. 2004 Dec;8(6):447-54. doi: 10.1007/s00792-004-0405-4. Epub 2004 Aug 14.

Abstract

An alkaline beta-mannanase was purified to homogeneity from a culture broth of alkaliphilic Bacillus sp. N16-5. The enzyme had optimum activity at pH 9.5 and 70 degrees C. It was composed of a single polypeptide chain with a molecular weight of 55 kDa deduced from SDS-PAGE, and its isoelectric point was around pH 4.3. The enzyme efficiently hydrolyzed galactomannan and glucomannan, producing a series of oligosaccharides and monosaccharides. The beta-mannanase gene (manA) contained an open reading frame (ORF) of 1,479 bp, encoding a 32-amino acids signal peptide, and a mature protein of 461 amino acids, with a calculated molecular mass of 50,743 Da. Strain N16-5 ManA, deduced from the manA ORF, exhibited relatively high amino acid similarity to the members of the glycosyl hydrolase family 5. The eight conserved active-site amino acids in family 5 glycosyl hydrolase were found in the deduced amino acid sequence of strain N16-5 ManA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Bacillus / classification
  • Bacillus / enzymology*
  • Bacillus / genetics*
  • Base Sequence
  • Catalytic Domain / genetics
  • Cloning, Molecular
  • Conserved Sequence
  • DNA, Bacterial / genetics
  • Enzyme Stability
  • Genes, Bacterial
  • Hydrogen-Ion Concentration
  • Kinetics
  • Metals
  • Molecular Sequence Data
  • Molecular Weight
  • Open Reading Frames
  • Sequence Homology, Amino Acid
  • Substrate Specificity
  • Temperature
  • beta-Mannosidase / chemistry
  • beta-Mannosidase / genetics*
  • beta-Mannosidase / metabolism*

Substances

  • DNA, Bacterial
  • Metals
  • beta-Mannosidase