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1.
Int J Biol Macromol ; 163: 1471-1479, 2020 Nov 15.
Article in English | MEDLINE | ID: mdl-32763401

ABSTRACT

Flavobacteriia are important degraders in the marine carbon cycle, due to their ability to efficiently degrade complex algal polysaccharides. A novel exo-(α-1,3)-3,6-anhydro-D-galactosidase activity was recently discovered from a marine Flavobacteriia (Zobellia galactanivorans DsijT) on red algal carrageenan oligosaccharides. The enzyme activity is encoded by a gene found in the first described carrageenan-specific polysaccharide utilization locus (CarPUL) that codes for a family 129 glycoside hydrolase (GH129). The GH129 family is a CAZy family that is strictly partitioned into two niche-based clades: clade 1 contains human host bacterial enzymes and clade 2 contains marine bacterial enzymes. Clade 2 includes the GH129 exo-(α-1,3)-3,6-anhydro-D-galactosidase from Z. galactanivorans (ZgGH129). Despite the discovery of the unique activity for ZgGH129, finer details on the natural substrate specificity for this enzyme are lacking. Examination of enzyme activity on natural carrageenan oligomers using mass spectrometry demonstrated that ZgGH129 hydrolyses terminal 3,6-anhydro-D-galactose from unsulfated non-reducing end neo-ß-carrabiose motifs. Due to the lack of chromogenic substrates to examine exo-(α-1,3)-3,6-anhydro-D-galactosidase activity, a novel substrate was synthesised to facilitate the first kinetic characterisation of an exo-(α-1,3)-3,6-anhydro-D-galactosidase, allowing determination of pH and temperature optimums and Michaelis-Menten steady state kinetic data.


Subject(s)
Carrageenan/metabolism , Flavobacteriaceae/metabolism , Galactosidases/metabolism , Oligosaccharides/metabolism , Polysaccharides/metabolism , Bacterial Proteins/metabolism , Chromogenic Compounds , Glycoside Hydrolases/metabolism , Humans , Substrate Specificity
2.
Nat Commun ; 8(1): 1685, 2017 11 22.
Article in English | MEDLINE | ID: mdl-29162826

ABSTRACT

Macroalgae contribute substantially to primary production in coastal ecosystems. Their biomass, mainly consisting of polysaccharides, is cycled into the environment by marine heterotrophic bacteria using largely uncharacterized mechanisms. Here we describe the complete catabolic pathway for carrageenans, major cell wall polysaccharides of red macroalgae, in the marine heterotrophic bacterium Zobellia galactanivorans. Carrageenan catabolism relies on a multifaceted carrageenan-induced regulon, including a non-canonical polysaccharide utilization locus (PUL) and genes distal to the PUL, including a susCD-like pair. The carrageenan utilization system is well conserved in marine Bacteroidetes but modified in other phyla of marine heterotrophic bacteria. The core system is completed by additional functions that might be assumed by non-orthologous genes in different species. This complex genetic structure may be the result of multiple evolutionary events including gene duplications and horizontal gene transfers. These results allow for an extension on the definition of bacterial PUL-mediated polysaccharide digestion.


Subject(s)
Carrageenan/metabolism , Flavobacteriaceae/genetics , Flavobacteriaceae/metabolism , Regulon , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Bacteroidetes/genetics , Bacteroidetes/metabolism , Crystallography, X-Ray , Evolution, Molecular , Galactosidases/chemistry , Galactosidases/genetics , Galactosidases/metabolism , Genes, Bacterial , Metabolic Networks and Pathways/genetics , Models, Molecular , Multigene Family , Phylogeny , Protein Conformation , RNA, Bacterial/genetics , Sequence Analysis, RNA , Species Specificity
3.
Front Microbiol ; 5: 498, 2014.
Article in English | MEDLINE | ID: mdl-25324833

ABSTRACT

A remarkable example of biological engineering is the capability of some marine animals to take advantage of photosynthesis by hosting symbiotic algae. This capacity, referred to as photosymbiosis, is based on structural and functional complexes that involve two distantly unrelated organisms. These stable photosymbiotic associations between metazoans and photosynthetic protists play fundamental roles in marine ecology as exemplified by reef communities and their vulnerability to global changes threats. Here we introduce a photosymbiotic tidal acoel flatworm, Symsagittifera roscoffensis, and its obligatory green algal photosymbiont, Tetraselmis convolutae (Lack of the algal partner invariably results in acoel lethality emphasizing the mandatory nature of the photosymbiotic algae for the animal's survival). Together they form a composite photosymbiotic unit, which can be reared in controlled conditions that provide easy access to key life-cycle events ranging from early embryogenesis through the induction of photosymbiosis in aposymbiotic juveniles to the emergence of a functional "solar-powered" mature stage. Since it is possible to grow both algae and host under precisely controlled culture conditions, it is now possible to design a range of new experimental protocols that address the mechanisms and evolution of photosymbiosis. S. roscoffensis thus represents an emerging model system with experimental advantages that complement those of other photosymbiotic species, in particular corals. The basal taxonomic position of S. roscoffensis (and acoels in general) also makes it a relevant model for evolutionary studies of development, stem cell biology and regeneration. Finally, it's autotrophic lifestyle and lack of calcification make S. roscoffensis a favorable system to study the role of symbiosis in the response of marine organisms to climate change (e.g., ocean warming and acidification). In this article we summarize the state of knowledge of the biology of S. roscoffensis and its algal partner from studies dating back over a century, and provide an overview of ongoing research efforts that take advantage of this unique system.

4.
J Biol Chem ; 288(10): 6957-67, 2013 Mar 08.
Article in English | MEDLINE | ID: mdl-23288852

ABSTRACT

Neuroglobins, previously thought to be restricted to vertebrate neurons, were detected in the brain of a photosymbiotic acoel, Symsagittifera roscoffensis, and in neurosensory cells of the jellyfish Clytia hemisphaerica. For the neuroglobin of S. roscoffensis, a member of a lineage that originated either at the base of the bilateria or of the deuterostome clade, we report the ligand binding properties, crystal structure at 2.3 Å, and brain immunocytochemical pattern. We also describe in situ hybridizations of two neuroglobins specifically expressed in differentiating nematocytes (neurosensory cells) and in statocytes (ciliated mechanosensory cells) of C. hemisphaerica, a member of the early branching animal phylum cnidaria. In silico searches using these neuroglobins as queries revealed the presence of previously unidentified neuroglobin-like sequences in most metazoan lineages. Because neural systems are almost ubiquitous in metazoa, the constitutive expression of neuroglobin-like proteins strongly supports the notion of an intimate association of neuroglobins with the evolution of animal neural systems and hints at the preservation of a vitally important function. Neuroglobins were probably recruited in the first protoneurons in early metazoans from globin precursors. Neuroglobins were identified in choanoflagellates, sponges, and placozoans and were conserved during nervous system evolution. Because the origin of neuroglobins predates the other metazoan globins, it is likely that neuroglobin gene duplication followed by co-option and subfunctionalization led to the emergence of globin families in protostomes and deuterostomes (i.e. convergent evolution).


Subject(s)
Globins/metabolism , Nerve Tissue Proteins/metabolism , Nervous System/metabolism , Protein Precursors/metabolism , Amino Acid Sequence , Animals , Crystallography, X-Ray , Evolution, Molecular , Gene Expression Profiling , Genetic Variation , Globins/chemistry , Globins/genetics , Hydrozoa/genetics , Hydrozoa/metabolism , In Situ Hybridization , Models, Molecular , Molecular Sequence Data , Nerve Tissue Proteins/chemistry , Nerve Tissue Proteins/genetics , Nervous System/cytology , Neuroglobin , Oxygen/chemistry , Oxygen/metabolism , Phylogeny , Platyhelminths/genetics , Platyhelminths/metabolism , Protein Binding , Protein Precursors/genetics , Protein Structure, Secondary , Protein Structure, Tertiary , Sequence Homology, Amino Acid
5.
J Biol Chem ; 287(36): 30571-84, 2012 Aug 31.
Article in English | MEDLINE | ID: mdl-22778272

ABSTRACT

Zobellia galactanivorans is an emerging model bacterium for the bioconversion of algal biomass. Notably, this marine Bacteroidetes possesses a complex agarolytic system comprising four ß-agarases and five ß-porphyranases, all belonging to the glycoside hydrolase family 16. Although ß-agarases are specific for the neutral agarobiose moieties, the recently discovered ß-porphyranases degrade the sulfated polymers found in various quantities in natural agars. Here, we report the biochemical and structural comparison of five ß-porphyranases and ß-agarases from Z. galactanivorans. The respective degradation patterns of two ß-porphyranases and three ß-agarases are analyzed by their action on defined hybrid oligosaccharides. In light of the high resolution crystal structures, the biochemical results allowed a detailed mapping of substrate specificities along the active site groove of the enzymes. Although PorA displays a strict requirement for C6-sulfate in the -2- and +1-binding subsites, PorB tolerates the presence of 3-6-anhydro-l-galactose in subsite -2. Both enzymes do not accept methylation of the galactose unit in the -1 subsite. The ß-agarase AgaD requires at least four consecutive agarose units (DP8) and is highly intolerant to modifications, whereas for AgaB oligosaccharides containing C6-sulfate groups at the -4, +1, and +3 positions are still degraded. Together with a transcriptional analysis of the expression of these enzymes, the structural and biochemical results allow proposition of a model scheme for the agarolytic system of Z. galactanivorans.


Subject(s)
Agar/chemistry , Bacterial Proteins/chemistry , Flavobacteriaceae/enzymology , Glycoside Hydrolases/chemistry , Models, Molecular , Crystallography, X-Ray , Protein Structure, Tertiary , Structure-Activity Relationship
7.
Nature ; 464(7290): 908-12, 2010 Apr 08.
Article in English | MEDLINE | ID: mdl-20376150

ABSTRACT

Gut microbes supply the human body with energy from dietary polysaccharides through carbohydrate active enzymes, or CAZymes, which are absent in the human genome. These enzymes target polysaccharides from terrestrial plants that dominated diet throughout human evolution. The array of CAZymes in gut microbes is highly diverse, exemplified by the human gut symbiont Bacteroides thetaiotaomicron, which contains 261 glycoside hydrolases and polysaccharide lyases, as well as 208 homologues of susC and susD-genes coding for two outer membrane proteins involved in starch utilization. A fundamental question that, to our knowledge, has yet to be addressed is how this diversity evolved by acquiring new genes from microbes living outside the gut. Here we characterize the first porphyranases from a member of the marine Bacteroidetes, Zobellia galactanivorans, active on the sulphated polysaccharide porphyran from marine red algae of the genus Porphyra. Furthermore, we show that genes coding for these porphyranases, agarases and associated proteins have been transferred to the gut bacterium Bacteroides plebeius isolated from Japanese individuals. Our comparative gut metagenome analyses show that porphyranases and agarases are frequent in the Japanese population and that they are absent in metagenome data from North American individuals. Seaweeds make an important contribution to the daily diet in Japan (14.2 g per person per day), and Porphyra spp. (nori) is the most important nutritional seaweed, traditionally used to prepare sushi. This indicates that seaweeds with associated marine bacteria may have been the route by which these novel CAZymes were acquired in human gut bacteria, and that contact with non-sterile food may be a general factor in CAZyme diversity in human gut microbes.


Subject(s)
Bacteroides/enzymology , Food Microbiology , Glycoside Hydrolases/metabolism , Intestines/microbiology , Marine Biology , Metagenome , Sepharose/analogs & derivatives , Adaptation, Physiological/physiology , Bacteroides/genetics , Biological Evolution , Crystallography, X-Ray , Cultural Diversity , Diet , Eukaryota/chemistry , Eukaryota/metabolism , Feces/enzymology , Feces/microbiology , Gene Transfer, Horizontal , Genome, Bacterial/genetics , Glycoside Hydrolases/chemistry , Glycoside Hydrolases/isolation & purification , Humans , Japan , Models, Molecular , North America , Phylogeny , Porphyra/chemistry , Porphyra/metabolism , Porphyra/microbiology , Protein Conformation , Sepharose/chemistry , Sepharose/metabolism , Substrate Specificity
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