Polysaccharide utilization loci and associated genes in marine Bacteroidetes - compositional diversity and ecological relevance

The synthesis of marine organic carbon compounds by photosynthetic macroalgae, microalgae (phytoplankton) and bacteria provide a basis for life in the ocean. In marine surface waters this primary production is largely dominated by microalgae and is especially pronounced during spring phytoplankton blooms. During and after these often diatom-dominated blooms, increased amounts of organic matter are released into the surrounding waters. Here, the organic matter, rich in polysaccharides, can trigger blooms of heterotrophic bacteria. Marine members of the Bacteroidetes are consistently found related to such bloom events. These bacteria are regularly detected as the first responders to thrive after phytoplankton spring blooms in temperate coastal regions and are often equipped with a variety of polysaccharide utilization gene clusters. These gene clusters, termed polysaccharide utilization loci (PULs), encode enzymes for the extracellular hydrolysis of polysaccharides and the subsequent uptake of oligosaccharides into the periplasm, where they are shielded from competing bacteria. This mechanism allows for rapid uptake and substrate hoarding, and thus could be one reason why Bacteroidetes are often seen as the first responders of the bacterioplankton community. The investigation of the so far largely unknown diversity and the ecological relevance of PULs in marine Bacteroidetes was the major goal of the work presented here. We could show that genomes of Bacteroidetes isolates from the North Sea, with free-living to micro- and macro-algae associated lifestyles, harboured a variety of these loci predicted to target in total 18 different substrate classes. Overall PUL repertoires of these isolates showed considerable intra-genus and inter-genus, variations suggesting that Bacteroidetes species harbour distinct glycan niches, independent of their phylogenetic relationships. By investigating the PUL repertoires of uncultured free-living Bacteroidetes during three consecutive years of spring phytoplankton blooms at the North Sea island of Helgoland, I could further reveal that the set of targeted substrates during these bloom events was dominated by only five of the substrate classes targeted by the isolates. These were the diatom storage polysaccharide laminarin, alpha-glucans, alginates, as well as substrates rich in alpha-mannans and sulfated xylans. In addition to this constrained set of substrate classes targeted by the free-living Bacteroidetes community, I could show that the species diversity during these blooms was limited and dominated by only 27 abundant and recurrent species that carried a limited number of abundant PULs. The majority of these PULs were targeting laminarin and alpha-glucan substrates, which were likely targeted during the entire time of the blooms. The less frequent PULs, targeting alpha-mannans and sulfated xylans, were predominantly detected during mid- and late- bloom phases, suggesting a relevance of these two substrate classes in the later phases of phytoplankton blooms. Overall these findings highlight the recurrence of a few specialized Bacteroidetes species and the environmental relevance of specific polysaccharide substrate classes during spring phytoplankton blooms. However, for some of these substrate classes the origin, structural details and their abundance during blooms are as yet largely unknown. To further shed light on the polysaccharide niches of abundant key-players, these findings can serve as a guide for future laboratory studies

Distribution and Function of marine Bacteroidetes

Members of the phylum Bacteroidetes play a pivotal role in degrading organic matter and appear everywhere in marine and freshwater systems, from coastal to open ocean, from polar to equatorial, from surface waters down to the deep sea as well as in association with aggregates and with phytoplankton blooms. The studies described in this thesis elaborate on the distribution and function of marine Bacteroidetes. Specifically their association with spring phytoplankton blooms, substrate association by direct surface attachment and their genetic capability of degrading high molecular weight organic matter and in particular polysaccharides were examined. The Bacteroidetes distribution and community structure were analyzed at a temporal scale, by investigating the responses of distinct bacteroidetal clades during and after spring phytoplankton blooms of four consecutive years at the coastal station Helgoland Roads. It could be shown by automated microscopic cell counting that shortly after the chlorophyll a maximum concentration Bacteroidetes increased to more than 50% of the total bacterioplankton community during spring seasons. The Bacteroidetes community comprised only a few dominant genera, which accounted together for more than half of the Bacteroidetes. Each year a distinct succession pattern of the clades Ulvibacter, Formosa A, and Polaribacter was observed with relative abundances of single clades with up to 20%. Furthermore, members of the Bacteroidetes inhabited not only the free-living fraction, but they were also found attached to diatoms. Although a quantification of attached Bacteroidetes was difficult, qualitative observations were made. For example members of this phylum attach frequently to the diatom Chaetoceros spp., which is commonly blooming in spring at Helgoland Roads. The clades Polaribacter and Formosa A were identified as dominating among those Chaetoceros-associated Bacteroidetes. In contrast, Ulvibacter was not found attached to Chaetoceros, but to Asterionella spp., another diatom genus occurring in spring blooms. Since members of Bacteroidetes are the first in responding to algal blooms and attached even to distinct diatom species, we investigated their genetic potential to degrade algal derived organic matter. In particular we searched for the presence of polysaccharide utilization loci (PULs) in fosmids retrieved from two contrasting provinces of the North Atlantic Ocean. In total 14 PULs were identified, six on fosmids from the northern station and eight on fosmids from the southern station. Among those PULs one seems to be involved in xylan degradation and four were identified as potential laminarin degradation PULs. Interestingly, GHs were identified which had been assumed to be unique among terrestrial Flavobacteria, suggesting a higher capability of open ocean Bacteroidetes clades for organic matter degradation than previously anticipated

Exploring and exploiting plant biomass degradation by Bacteroidetes

Bacteroidetes bacteria have evolved to become excellent biomass degraders. They achieved this by applying carbohydrate-active enzymes (CAZymes) and organizing genes connected to the degradation of specific polysaccharides into discrete gene cassettes, so-called polysaccharide utilization loci (PULs). Consequently, CAZymes and PULs may hold the potential to improve biomass valorization processes in biorefineries and to advance our understanding of human and livestock gut health.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

Proteiniphilum saccharofermentans str. M3/6T isolated from a laboratory biogas reactor is versatile in polysaccharide and oligopeptide utilization as deduced from genome-based metabolic reconstructions

Proteiniphilum saccharofermentans str. M3/6T is a recently described species within the family Porphyromonadaceae (phylum Bacteroidetes), which was isolated from a mesophilic laboratory-scale biogas reactor. The genome of the strain was completely sequenced and manually annotated to reconstruct its metabolic potential regarding biomass degradation and fermentation pathways. The P. saccharofermentans str. M3/6T genome consists of a 4,414,963 bp chromosome featuring an average GC-content of 43.63%. Genome analyses revealed that the strain possesses 3396 protein-coding sequences. Among them are 158 genes assigned to the carbohydrate-active-enzyme families as defined by the CAZy database, including 116 genes encoding glycosyl hydrolases (GHs) involved in pectin, arabinogalactan, hemicellulose (arabinan, xylan, mannan, β-glucans), starch, fructan and chitin degradation. The strain also features several transporter genes, some of which are located in polysaccharide utilization loci (PUL). PUL gene products are involved in glycan binding, transport and utilization at the cell surface. In the genome of strain M3/6T, 64 PUL are present and most of them in association with genes encoding carbohydrate-active enzymes. Accordingly, the strain was predicted to metabolize several sugars yielding carbon dioxide, hydrogen, acetate, formate, propionate and isovalerate as end-products of the fermentation process. Moreover, P. saccharofermentans str. M3/6T encodes extracellular and intracellular proteases and transporters predicted to be involved in protein and oligopeptide degradation. Comparative analyses between P. saccharofermentans str. M3/6T and its closest described relative P. acetatigenes str. DSM 18083T indicate that both strains share a similar metabolism regarding decomposition of complex carbohydrates and fermentation of sugars. © 2018 The Author

Polysaccharide degradation by the Bacteroidetes: mechanisms and nomenclature

The Bacteroidetes phylum is renowned for its ability to degrade a wide range of complex carbohydrates, a trait that has enabled its dominance in many diverse environments. The best studied species inhabit the human gut microbiome and use polysaccharide utilization loci (PULs), discrete genetic structures that encode proteins involved in the sensing, binding, deconstruction, and import of target glycans. In many environmental species, polysaccharide degradation is tightly coupled to the phylum-exclusive type IX secretion system (T9SS), which is used for the secretion of certain enzymes and is linked to gliding motility. In addition, within specific species these two adaptive systems (PULs and T9SS) are intertwined, with PUL-encoded enzymes being secreted by the T9SS. Here, we discuss the most noteworthy PUL and non-PUL mechanisms that confer specific and rapid polysaccharide degradation capabilities to the Bacteroidetes in a range of environments. We also acknowledge that the literature showcasing examples of PULs is rapidly expanding and developing a set of assumptions that can be hard to track back to original findings. Therefore, we present a simple universal description of conserved PUL functions and how they are determined, while proposing a common nomenclature describing PULs and their components, to simplify discussion and understanding of PUL systems

Characterization of a novel multidomain CE15-GH8 enzyme encoded by a polysaccharide utilization locus in the human gut bacterium Bacteroides eggerthii

Bacteroidetes are efficient degraders of complex carbohydrates, much thanks to their use of polysaccharide utilization loci (PULs). An integral part of PULs are highly specialized carbohydrate-active enzymes, sometimes composed of multiple linked domains with discrete functions—multicatalytic enzymes. We present the biochemical characterization of a multicatalytic enzyme from a large PUL encoded by the gut bacterium\ua0Bacteroides eggerthii. The enzyme,\ua0BeCE15A-Rex8A, has a rare and novel architecture, with an N-terminal carbohydrate esterase family 15 (CE15) domain and a C-terminal glycoside hydrolase family 8 (GH8) domain. The CE15 domain was identified as a glucuronoyl esterase (GE), though with relatively poor activity on GE model substrates, attributed to key amino acid substitutions in the active site compared to previously studied GEs. The GH8 domain was shown to be a reducing-end\ua0xylose-releasing\ua0exo-oligoxylanase (Rex), based on having activity on xylooligosaccharides but not on longer xylan chains. The full-length\ua0BeCE15A-Rex8A enzyme and the Rex domain were capable of boosting the activity of a commercially available GH11 xylanase on corn cob biomass. Our research adds to the understanding of multicatalytic enzyme architectures and showcases the potential of discovering novel and atypical carbohydrate-active enzymes from mining PULs

Dietary pectic glycans are degraded by coordinated enzyme pathways in human colonic Bacteroides.

The major nutrients available to human colonic Bacteroides species are glycans, exemplified by pectins, a network of covalently linked plant cell wall polysaccharides containing galacturonic acid (GalA). Metabolism of complex carbohydrates by the Bacteroides genus is orchestrated by polysaccharide utilization loci (PULs). In Bacteroides thetaiotaomicron, a human colonic bacterium, the PULs activated by different pectin domains have been identified; however, the mechanism by which these loci contribute to the degradation of these GalA-containing polysaccharides is poorly understood. Here we show that each PUL orchestrates the metabolism of specific pectin molecules, recruiting enzymes from two previously unknown glycoside hydrolase families. The apparatus that depolymerizes the backbone of rhamnogalacturonan-I is particularly complex. This system contains several glycoside hydrolases that trim the remnants of other pectin domains attached to rhamnogalacturonan-I, and nine enzymes that contribute to the degradation of the backbone that makes up a rhamnose-GalA repeating unit. The catalytic properties of the pectin-degrading enzymes are optimized to protect the glycan cues that activate the specific PULs ensuring a continuous supply of inducing molecules throughout growth. The contribution of Bacteroides spp. to metabolism of the pectic network is illustrated by cross-feeding between organisms.This work was supported in part by an Advanced Grant from the European Research Council (Grant No. 322820) awarded to H.J.G. and B.H. supporting A.S.L., D.N., A.C. and N.T., a Wellcome Trust Senior Investigator Award to H.J.G. (grant No. WT097907MA) that supported J.B. and E.C.L. a European Union Seventh Framework Initial Training Network Programme entitled the “WallTraC project” (Grant Agreement number 263916) awarded to M-C.R. and H.J.G, which supported X.Z. and J.S. The Biotechnology and Biological Research Council project ‘Ricefuel’ (grant numbers BB/K020358/1) awarded to H.J.G. supported A.L

CAZymes in Maribacter dokdonensis 62–1 from the Patagonian shelf: genomics and physiology compared to related flavobacteria and a co-occurring Alteromonas strain

Carbohydrate-active enzymes (CAZymes) are an important feature of bacteria in productive marine systems such as continental shelves, where phytoplankton and macroalgae produce diverse polysaccharides. We herein describe Maribacter dokdonensis 62–1, a novel strain of this flavobacterial species, isolated from alginate-supplemented seawater collected at the Patagonian continental shelf. M. dokdonensis 62–1 harbors a diverse array of CAZymes in multiple polysaccharide utilization loci (PUL). Two PUL encoding polysaccharide lyases from families 6, 7, 12, and 17 allow substantial growth with alginate as sole carbon source, with simultaneous utilization of mannuronate and guluronate as demonstrated by HPLC. Furthermore, strain 62-1 harbors a mixed-feature PUL encoding both ulvan- and fucoidan-targeting CAZymes. Core-genome phylogeny and pangenome analysis revealed variable occurrence of these PUL in related Maribacter and Zobellia strains, indicating specialization to certain “polysaccharide niches.” Furthermore, lineage- and strain-specific genomic signatures for exopolysaccharide synthesis possibly mediate distinct strategies for surface attachment and host interaction. The wide detection of CAZyme homologs in algae-derived metagenomes suggests global occurrence in algal holobionts, supported by sharing multiple adaptive features with the hydrolytic model flavobacterium Zobellia galactanivorans. Comparison with Alteromonas sp. 76-1 isolated from the same seawater sample revealed that these co-occurring strains target similar polysaccharides but with different genomic repertoires, coincident with differing growth behavior on alginate that might mediate ecological specialization. Altogether, our study contributes to the perception of Maribacter as versatile flavobacterial polysaccharide degrader, with implications for biogeochemical cycles, niche specialization and bacteria-algae interactions in the oceans

Metagenomics of the Svalbard Reindeer Rumen Microbiome Reveals Abundance of Polysaccharide Utilization Loci

Lignocellulosic biomass remains a largely untapped source of renewable energy predominantly due to its recalcitrance and an incomplete understanding of how this is overcome in nature. We present here a compositional and comparative analysis of metagenomic data pertaining to a natural biomass-converting ecosystem adapted to austere arctic nutritional conditions, namely the rumen microbiome of Svalbard reindeer (Rangifer tarandus platyrhynchus). Community analysis showed that deeply-branched cellulolytic lineages affiliated to the Bacteroidetes and Firmicutes are dominant, whilst sequence binning methods facilitated the assemblage of metagenomic sequence for a dominant and novel Bacteroidales clade (SRM-1). Analysis of unassembled metagenomic sequence as well as metabolic reconstruction of SRM-1 revealed the presence of multiple polysaccharide utilization loci-like systems (PULs) as well as members of more than 20 glycoside hydrolase and other carbohydrate-active enzyme families targeting various polysaccharides including cellulose, xylan and pectin. Functional screening of cloned metagenome fragments revealed high cellulolytic activity and an abundance of PULs that are rich in endoglucanases (GH5) but devoid of other common enzymes thought to be involved in cellulose degradation. Combining these results with known and partly re-evaluated metagenomic data strongly indicates that much like the human distal gut, the digestive system of herbivores harbours high numbers of deeply branched and as-yet uncultured members of the Bacteroidetes that depend on PUL-like systems for plant biomass degradation