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A novel glycoside hydrolase 43-like enzyme from Clostridium boliviensis is an endo-xylanase and a candidate for xylooligosaccharide production from different xylan substrates.
Salas-Veizaga, Daniel Martin; Rocabado-Villegas, Leonardo Roberto; Linares-Pastén, Javier A; Gudmundsdottir, Elisabet Eik; Hreggvidsson, Gudmundur Oli; Álvarez-Aliaga, María Teresa; Adlercreutz, Patrick; Nordberg Karlsson, Eva.
Affiliation
  • Salas-Veizaga DM; Division of Biotechnology, Department of Chemistry, Lund University, Lund, Sweden.
  • Rocabado-Villegas LR; Instituto de Investigaciones Fármaco Bioquímicas, Universidad Mayor de San Andrés, La Paz, Bolivia.
  • Linares-Pastén JA; Instituto de Investigaciones Fármaco Bioquímicas, Universidad Mayor de San Andrés, La Paz, Bolivia.
  • Gudmundsdottir EE; Division of Biotechnology, Department of Chemistry, Lund University, Lund, Sweden.
  • Hreggvidsson GO; Matis Ohf, Reykjavik, Iceland.
  • Álvarez-Aliaga MT; Matis Ohf, Reykjavik, Iceland.
  • Adlercreutz P; Instituto de Investigaciones Fármaco Bioquímicas, Universidad Mayor de San Andrés, La Paz, Bolivia.
  • Nordberg Karlsson E; Division of Biotechnology, Department of Chemistry, Lund University, Lund, Sweden.
Appl Environ Microbiol ; 90(4): e0222323, 2024 Apr 17.
Article in En | MEDLINE | ID: mdl-38497645
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, CbE1Xyn43-l, was produced in Escherichia coli. CbE1Xyn43-l (52.9 kDa) is a two-domain endo-ß-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. CbE1Xyn43-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. CbE1Xyn43-l also released xylobiose from pNPX2 with low turnover (kcat of 0.044 s-1) but was inactive on pNPX, 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, CbE1Xyn43-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-ß-xylanase of interest in the production of prebiotic xylooligosaccharides (XOs) from different xylan sources. CbE1Xyn43-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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligosaccharides / Xylans / Glucuronates / Glycoside Hydrolases Language: En Journal: Appl Environ Microbiol Year: 2024 Type: Article Affiliation country: Sweden

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oligosaccharides / Xylans / Glucuronates / Glycoside Hydrolases Language: En Journal: Appl Environ Microbiol Year: 2024 Type: Article Affiliation country: Sweden