High cellulolytic potential of the Ktedonobacteria lineage revealed by genome-wide analysis of CAZymes

J Biosci Bioeng. 2021 Jun;131(6):622-630. doi: 10.1016/j.jbiosc.2021.01.008. Epub 2021 Mar 4.

Abstract

Traditionally, filamentous fungi and actinomycetes are well-known cellulolytic microorganisms that have been utilized in the commercial production of cellulase enzyme cocktails for industrial-scale degradation of plant biomass. Noticeably, the Ktedonobacteria lineage (phylum Chloroflexi) with actinomycetes-like morphology was identified and exhibited diverse carbohydrate utilization or degradation abilities. In this study, we performed genome-wide profiling of carbohydrate-active enzymes (CAZymes) in the filamentous Ktedonobacteria lineage. Numerous CAZymes (153-290 CAZymes, representing 63-131 glycoside hydrolases (GHs) per genome), including complex mixtures of endo- and exo-cellulases, were predicted in 15 available Ktedonobacteria genomes. Of note, 4-28 CAZymes were predicted to be extracellular enzymes, whereas 3-29 CAZymes were appended with carbohydrate-binding modules (CBMs) that may promote their binding to insoluble carbohydrate substrates. This number far exceeded other Chloroflexi lineages and were comparable to the cellulolytic actinomycetes. Six multi-modular extracellular GHs were cloned from the thermophilic Thermosporothrix hazakensis SK20-1T strain and heterologously expressed. The putative endo-glucanases of ThazG5-1, ThazG9, and ThazG12 exhibited strong cellulolytic activity, whereas the putative exo-glucanases ThazG6 and ThazG48 formed weak but observable halos on carboxymethyl cellulose plates, indicating their potential biotechnological application. The purified recombinant ThazG12 had near-neutral pH (optimal 6.0), high thermostability (60°C), and broad specificity against soluble and insoluble polysaccharide substrates. It also represented described a novel thermostable bacterial β-1,4-glucanase in the GH12 family. Together, this research revealed the underestimated cellulolytic potential of the Ktedonobacteria lineage and highlighted its potential biotechnological utility as a promising microbial resource for the discovery of industrially useful cellulases.

Keywords: Carbohydrate-active enzymes; Cellulases; Cellulolytic bacteria; Chloroflexi; Ktedonobacteria; Thermosporothrix hazakensis; Thermostable endo-β-1,4-glucanase.

MeSH terms

  • Bacteria / metabolism
  • Carbohydrate Metabolism / genetics*
  • Cellulases / genetics*
  • Cellulases / metabolism
  • Cellulose / metabolism*
  • Chloroflexi* / classification
  • Chloroflexi* / enzymology
  • Chloroflexi* / genetics
  • Chloroflexi* / metabolism
  • Chromosome Mapping
  • Fungi / metabolism
  • Gene Expression Regulation, Bacterial
  • Genome, Bacterial
  • Glycoside Hydrolases / genetics
  • Glycoside Hydrolases / metabolism
  • Metabolic Engineering
  • Organisms, Genetically Modified
  • Plants / metabolism
  • Polysaccharides / metabolism

Substances

  • Polysaccharides
  • Cellulose
  • Cellulases
  • Glycoside Hydrolases

Supplementary concepts

  • Thermosporothrix hazakensis