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Cloning, Expression, and Characterization of a GHF 11 Xylanase from Alteromonas Macleodii HY35 in Escherichia Coli

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Specialty Microbiology
Date 2022 Aug 14
PMID 35965062
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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 CHNOS. 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.

Citing Articles

Improving the Catalytic Properties of Xylanase from Alteromones Macleadii H35 Through Sequence Analysis.

Cui C, Xu J, Wu J, Wang N, Zhang Z, Zhou C Appl Biochem Biotechnol. 2024; 196(11):7736-7746.

PMID: 38538873 DOI: 10.1007/s12010-024-04936-0.