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