Cloning, Expression, and Characterization of a GHF 11 Xylanase from Alteromonas macleodii HY35 in Escherichia coli

J Gen Appl Microbiol. 2022 Nov 10;68(3):134-142. doi: 10.2323/jgam.2021.10.003. Epub 2022 Aug 15.

Abstract

A xylanase gene xynZT-1 from Alteromonas macleodii HY35 was cloned and expressed in Escherichia coli (E. coli). The sequencing results showed that the ORF of xynZT-1 was 831 bp. The xylanase DNA sequence encoded a 29 amino acids (aa) signal peptide and a 247-aa mature peptide. The XynZT-1 has been a calculated molecular weight (MW) of 27.93 kDa, isoelectric point (pI) of 5.11 and the formula C1266H1829N327O384S5. The amino acid sequence of the xynZT-1 had a high similarity with that of glycosyl hydrolase family 11 (GHF11) reported from other microorganisms. The DNA sequence encoding mature peptide was subcloned into pET-28a(+) expression vector. The resulted plasmid pET-28a-xynZT-1 was transformed into E. coli BL21(DE3), and the recombinant strain BL21(DE3)/xynZT-1 was obtained. The optimum temperature and pH of the recombinant XynZT-1 were 45 ℃ and 5.0, respectively.

Keywords: Alteromonas macleodii HY35; enzymatic properties; expression; glycosyl hydrolase family11; xylanase.

MeSH terms

  • Cloning, Molecular
  • Enzyme Stability
  • Escherichia coli* / genetics
  • Escherichia coli* / metabolism
  • Peptides* / genetics
  • Peptides* / metabolism
  • Recombinant Proteins / metabolism

Substances

  • Peptides
  • Recombinant Proteins

Supplementary concepts

  • Alteromonas macleodii