Exploring and exploiting plant biomass degradation by Bacteroidetes
CAZymes are extremely diverse in activity and structure, and for some enzyme families only little is known to date. For example, certain carbohydrate esterases (CEs) combine multiple catalytic domains within one protein, resulting in multicatalytic enzyme architectures, and the properties of these have been little explored. In this thesis, I present biochemical data showcasing the existence of intramolecular synergy between the active domains of multicatalytic CEs (BoCE6-CE1). The observed intramolecular synergy facilitated more efficient degradation of xylan-rich biomass compared to non-multicatalytic CEs, giving a possible explanation as to why multicatalytic CEs exist in the genomes of Bacteroidetes species. Well-defined activity profiles of several here characterized CEs support the hypothesis that each catalytic domain fulfills an individual role during concerted plant biomass degradation, explaining why some PULs encode multiple CEs from the same enzyme family. Further, the investigated CEs cleaved xylan decorations and increased the activity of xylanase-mediated biomass degradation up to 20-fold (FjCE6-CE1). During the investigation of the CAZyme repertoire of different species I also identified a remarkably active and promiscuously acting acetyl xylan esterase (DmCE6A), as well as a rare enzyme architecture that may offer new insights into the multitude of interacting enzyme activities necessary to degrade plant biomass (BeCE15A-Rex8A).
PULs encode a plethora of CAZymes and have been shown to be vital for the glycan degradation abilities of Bacteroidetes species. However, the investigation of PULs is aggravated by their usually large size, which often limits the scope of genetic studies. In this thesis, I present a new method for the transfer of PULs between Bacteroidetes species, thus expanding the tools available for the identification and characterization of PULs and their components. The PUL transfer was demonstrated for a previously characterized mixed-linkage β-glucan utilization locus and conferred the ability to metabolize mixed-linkage β-glucan to the receptor strain.
polysaccharide utilization locus
plant biomass degradation
Chalmers, Biologi och bioteknik, Industriell bioteknik
Multimodular fused acetyl–feruloyl esterases from soil and gut Bacteroidetes improve xylanase depolymerization of recalcitrant biomass
Biotechnology for Biofuels,; Vol. 13(2020)
Artikel i vetenskaplig tidskrift
A polysaccharide utilization locus from the gut bacterium dysgonomonas mossii encodes functionally distinct carbohydrate esterases
Journal of Biological Chemistry,; Vol. 296(2021)
Artikel i vetenskaplig tidskrift
Kmezik C, Krska D, Mazurkewich S, Larsbrink J. Characterization of a novel multidomain CE15-GH8 enzyme encoded by a polysaccharide utilization locus in the human gut bacterium Bacteroides eggerthii
Kmezik C, Porter NT, Pope PB, Koropatkin NM, Martens E, Larsbrink J. Enabling metabolism of mixed-linkage β-glucan in Bacteroides thetaiotaomicron by transfer of a polysaccharide utilization locus using a new versatile method
With this thesis, I contribute to the understanding of multicatalytic CEs by demonstrating how their active domains complement each other in a synergistic manner. The biochemical characterization of various PUL encoded CEs also led to the identification of a highly active acetyl xylan esterase and a multicatalytic CE with a novel and rare enzyme architecture. The large size of PULs (often spanning tens of thousands of DNA basepairs) hampers genetic studies. In this thesis, I also present a new genetic tool, the pICKUP method, which allows for the transfer of PULs between Bacteroidetes species thus expanding the genetic toolbox available to conduct PUL research.
Overall, the work presented in this thesis contributes to our understanding of microbial plant biomass degradation and has implications for biorefinery applications and gut health.
Doktorsavhandlingar vid Chalmers tekniska högskola. Ny serie: 4999
Chalmers tekniska högskola
Opponent: Prof. Birte Svensson, Department of Biotechnology and Biomedicine, Technical University of Denmark, Denmark