A Polysaccharide Utilization Locus from an Uncultured Bacteroidetes Phylotype Suggests Ecological Adaptation and Substrate Versatility

ABSTRACT Recent metagenomic analyses have identified uncultured bacteria that are abundant in the rumen of herbivores and that possess putative biomass-converting enzyme systems. Here we investigate the saccharolytic capabilities of a polysaccharide utilization locus (PUL) that has been reconstructed from an uncultured Bacteroidetes phylotype (SRM-1) that dominates the rumen microbiome of Arctic reindeer. Characterization of the three PUL-encoded outer membrane glycoside hydrolases was performed using chromogenic substrates for initial screening, followed by detailed analyses of products generated from selected substrates, using high-pressure anion-exchange chromatography with electrochemical detection. Two glycoside hydrolase family 5 (GH5) endoglucanases (GH5_g and GH5_h) demonstrated activity against β-glucans, xylans, and xyloglucan, whereas GH5_h and the third enzyme, GH26_i, were active on several mannan substrates. Synergy experiments examining different combinations of the three enzymes demonstrated limited activity enhancement on individual substrates. Binding analysis of a SusE-positioned lipoprotein revealed an affinity toward β-glucans and, to a lesser extent, mannan, but unlike the two SusD-like lipoproteins previously characterized from the same PUL, binding to cellulose was not observed. Overall, these activities and binding specificities correlated well with the glycan content of the reindeer rumen, which was determined using comprehensive microarray polymer profiling and showed an abundance of various hemicellulose glycans. The substrate versatility of this single PUL putatively expands our perceptions regarding PUL machineries, which so far have demonstrated gene organization that suggests one cognate PUL for each substrate type. The presence of a PUL that possesses saccharolytic activity against a mixture of abundantly available polysaccharides supports the dominance of SRM-1 in the Svalbard reindeer rumen microbiome.

[1]  J. Gordon,et al.  Starch catabolism by a prominent human gut symbiont is directed by the recognition of amylose helices. , 2008, Structure.

[2]  H. Gilbert,et al.  Understanding How the Complex Molecular Architecture of Mannan-degrading Hydrolases Contributes to Plant Cell Wall Degradation* , 2013, The Journal of Biological Chemistry.

[3]  H. Gilbert,et al.  The modular architecture of Cellvibrio japonicus mannanases in glycoside hydrolase families 5 and 26 points to differences in their role in mannan degradation. , 2003, The Biochemical journal.

[4]  J Kirby,et al.  Dockerin-like sequences in cellulases and xylanases from the rumen cellulolytic bacterium Ruminococcus flavefaciens. , 1997, FEMS microbiology letters.

[5]  T. Scheffer,et al.  Taxonomic metagenome sequence assignment with structured output models , 2011, Nature Methods.

[6]  A. Mackenzie,et al.  Do Rumen Bacteroidetes Utilize an Alternative Mechanism for Cellulose Degradation? , 2014, mBio.

[7]  A. S. Blix,et al.  Seasonal changes in the ruminal microflora of the high-arctic Svalbard reindeer (Rangifer tarandus platyrhynchus) , 1985, Applied and environmental microbiology.

[8]  L. Ten,et al.  Development of a plate technique for screening of polysaccharide-degrading microorganisms by using a mixture of insoluble chromogenic substrates. , 2004, Journal of microbiological methods.

[9]  A. Travis,et al.  16S rDNA library-based analysis of ruminal bacterial diversity , 2004, Antonie van Leeuwenhoek.

[10]  S. Tringe,et al.  Metagenomic Discovery of Biomass-Degrading Genes and Genomes from Cow Rumen , 2011, Science.

[11]  Eric C. Martens,et al.  Complex Glycan Catabolism by the Human Gut Microbiota: The Bacteroidetes Sus-like Paradigm , 2009, The Journal of Biological Chemistry.

[12]  Dmitry A Rodionov,et al.  New Substrates for Tonb-dependent Transport: Do We Only See the 'tip of the Iceberg'? , 2022 .

[13]  A. Boraston,et al.  Bacteria of the human gut microbiome catabolize red seaweed glycans with carbohydrate-active enzyme updates from extrinsic microbes , 2012, Proceedings of the National Academy of Sciences.

[14]  C. Forsberg,et al.  Cel9D, an Atypical 1,4-β-d-Glucan Glucohydrolase from Fibrobacter succinogenes: Characteristics, Catalytic Residues, and Synergistic Interactions with Other Cellulases , 2008, Journal of bacteriology.

[15]  B. Henrissat,et al.  Evolution, substrate specificity and subfamily classification of glycoside hydrolase family 5 (GH5) , 2012, BMC Evolutionary Biology.

[16]  M. Fields,et al.  A Prevotella ruminicola B14 Operon Encoding Extracellular Polysaccharide Hydrolases , 1997, Current Microbiology.

[17]  P. D. de Jong,et al.  Ligation-independent cloning of PCR products (LIC-PCR). , 1990, Nucleic acids research.

[18]  Bernard Henrissat,et al.  Effects of Diet on Resource Utilization by a Model Human Gut Microbiota Containing Bacteroides cellulosilyticus WH2, a Symbiont with an Extensive Glycobiome , 2013, PLoS biology.

[19]  R. Mackie,et al.  Transcriptomic Analyses of Xylan Degradation by Prevotella bryantii and Insights into Energy Acquisition by Xylanolytic Bacteroidetes* , 2010, The Journal of Biological Chemistry.

[20]  Antony Bacic,et al.  High-throughput mapping of cell-wall polymers within and between plants using novel microarrays. , 2007, The Plant journal : for cell and molecular biology.

[21]  P. B. Pope,et al.  Metagenomics of the Svalbard Reindeer Rumen Microbiome Reveals Abundance of Polysaccharide Utilization Loci , 2012, PloS one.

[22]  A. Bacic,et al.  Glycan profiling of plant cell wall polymers using microarrays. , 2012, Journal of visualized experiments : JoVE.

[23]  J.-F. Cheng,et al.  Adaptation to herbivory by the Tammar wallaby includes bacterial and glycoside hydrolase profiles different from other herbivores , 2010, Proceedings of the National Academy of Sciences.

[24]  H. Brumer,et al.  A discrete genetic locus confers xyloglucan metabolism in select human gut Bacteroidetes , 2014, Nature.

[25]  J. Deisenhofer,et al.  TonB-dependent receptors-structural perspectives. , 2002, Biochimica et biophysica acta.

[26]  Zoë A Popper,et al.  Primary cell wall composition of bryophytes and charophytes. , 2003, Annals of botany.

[27]  T. Wood Preparation of crystalline, amorphous, and dyed cellulase substrates , 1988 .

[28]  J. Vogel Unique aspects of the grass cell wall. , 2008, Current opinion in plant biology.

[29]  R. Langvatn,et al.  Forage chemistry and fermentation chambers in Svalbard reindeer (Rangifer tarandus platyrhynchus) , 1999 .

[30]  M. Morrison,et al.  Analysis of the bovine rumen microbiome reveals a diversity of Sus-like polysaccharide utilization loci from the bacterial phylum Bacteroidetes , 2014, Journal of Industrial Microbiology & Biotechnology.

[31]  E. Martens,et al.  How glycan metabolism shapes the human gut microbiota , 2012, Nature Reviews Microbiology.

[32]  G. L. Miller Use of Dinitrosalicylic Acid Reagent for Determination of Reducing Sugar , 1959 .

[33]  Ümit V. Çatalyürek,et al.  Metagenomic Insights into the Carbohydrate-Active Enzymes Carried by the Microorganisms Adhering to Solid Digesta in the Rumen of Cows , 2013, PloS one.

[34]  Bernard Henrissat,et al.  Recognition and Degradation of Plant Cell Wall Polysaccharides by Two Human Gut Symbionts , 2011, PLoS biology.

[35]  J. Sonnenburg,et al.  Specificity of Polysaccharide Use in Intestinal Bacteroides Species Determines Diet-Induced Microbiota Alterations , 2010, Cell.

[36]  H. Gilbert,et al.  Cloning and sequencing of the celA gene encoding endoglucanase A of Butyrivibrio fibrisolvens strain A46. , 1990, Journal of general microbiology.

[37]  A. Mackenzie,et al.  Two SusD-Like Proteins Encoded within a Polysaccharide Utilization Locus of an Uncultured Ruminant Bacteroidetes Phylotype Bind Strongly to Cellulose , 2012, Applied and Environmental Microbiology.