Cloning, sequence analysis and expression of a gene encoding an endoxylanase from Bacillus halodurans S7

MAMO G; DELGADO OD; MARTÍNEZ MA; MATTIASSON B; HATTI-KAUL R

Molecular Biotechnology

Humana Press Inc.

Año: 2006 p. 149 - 160

1559-0305

The gene encoding an alkaline active xylanase of Bacillus halodurans S7, containing an open reading frame of 1188 nucleotides encoding 396 amino acids, was cloned and expressed in Escherchia coli. On the basis of sequence similarity, possible –10 and –35, ribosome binding, and transcription terminator regions ere identified. Analysis of the deduced amino acid sequence revealed that the protein was a single domain enzyme belonging to family 10 and designated as xyn10A. The calculated molecular mass and isoelectric point (pI) of the mature peptide were 42.6 and 4.5 kDa, respectively. Xylanase activity expressed by the recombinant organism was detected in the cytoplasm, periplasm and the extracellular medium. In an 18-h old culture, about 39% of the xylanase was detected in the medium. The stability and activity profile of the recombinant xylanase was similar to the properties of the enzyme produced by the wild-type organism.