A novel glycoside hydrolase 43-like enzyme from Clostridium boliviensis is an endo-xylanase and a candidate for xylooligosaccharide production from different xylan substrates

Author:

Salas-Veizaga Daniel Martin12ORCID,Rocabado-Villegas Leonardo Roberto2ORCID,Linares-Pastén Javier A.1ORCID,Gudmundsdottir Elisabet Eik3ORCID,Hreggvidsson Gudmundur Oli3,Álvarez-Aliaga María Teresa2ORCID,Adlercreutz Patrick1ORCID,Nordberg Karlsson Eva1ORCID

Affiliation:

1. Division of Biotechnology, Department of Chemistry, Lund University, Lund, Sweden

2. Instituto de Investigaciones Fármaco Bioquímicas, Universidad Mayor de San Andrés, La Paz, Bolivia

3. Matis Ohf, Reykjavik, Iceland

Abstract

ABSTRACT An uncharacterized gene encoding a glycoside hydrolase family 43-like enzyme from Clostridium boliviensis strain E-1 was identified from genomic sequence data, and the encoded enzyme, CbE1 Xyn43-l, was produced in Escherichia coli. CbE1 Xyn43-l (52.9 kDa) is a two-domain endo-β-xylanase consisting of a C-terminal CBM6 and a GH43-like catalytic domain. The positions of the catalytic dyad conserved in GH43, the catalytic base (Asp74), and proton donor (Glu240) were identified in alignments including GH43-enzymes of known 3D-structure from different subfamilies. CbE1 Xyn43-l is active at pH 7.0–9.0, with optimum temperature at 65°C, and a more than 7 days’ half-life in irreversible deactivation studies at this temperature. The enzyme hydrolyzed birchwood xylan, quinoa stalks glucuronoarabinoxylan, and wheat arabinoxylan with xylotriose and xylotetraose as major hydrolysis products. CbE1 Xyn43-l also released xylobiose from p NPX 2 with low turnover ( k cat of 0.044 s −1 ) but was inactive on p NPX, showing that a degree of polymerization of three (DP3) was the smallest hydrolyzable substrate. Divalent ions affected the specific activity on xylan substrates, which dependent on the ion could be increased or decreased. In conclusion, CbE1 Xyn43-l from C. boliviensis strain E-1 is the first characterized member of a large group of homologous hypothetical proteins annotated as GH43-like and is a thermostable endo-xylanase, producing xylooligosaccharides of high DP (xylotriose and xylotetraose) producer. IMPORTANCE The genome of Clostridium boliviensis strain E-1 encodes a number of hypothetical enzymes, annotated as glycoside hydrolase-like but not classified in the Carbohydrate Active Enzyme Database (CAZy). A novel thermostable GH43-like enzyme is here characterized as an endo-β-xylanase of interest in the production of prebiotic xylooligosaccharides (XOs) from different xylan sources. CbE1 Xyn43-l is a two-domain enzyme composed of a catalytic GH43-l domain and a CBM6 domain, producing xylotriose as main XO product. The enzyme has homologs in many related Clostridium strains which may indicate a similar function and be a previously unknown type of endo-xylanase in this evolutionary lineage of microorganisms.

Funder

Swedish International Development Cooperation Agency

The World Academy of Sciences

Bioinnovation

The Swedish Foundation for Strategic Research

Horizon2020

Publisher

American Society for Microbiology

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