Comparative Analysis of Glycoside Hydrolases Activities from Phylogenetically Diverse Marine Bacteria of the Genus Arenibacter

A total of 16 marine strains belonging to the genus Arenibacter, recovered from diverse microbial communities associated with various marine habitats and collected from different locations, were evaluated in degradation of natural polysaccharides and chromogenic glycosides. Most strains were affiliated with five recognized species, and some presented three new species within the genus Arenibacter. No strains contained enzymes depolymerizing polysaccharides, but synthesized a wide spectrum of glycosidases. Highly active β-N-acetylglucosaminidases and α-N-acetylgalactosaminidases were the main glycosidases for all Arenibacter. The genes, encoding two new members of glycoside hydrolyses (GH) families, 20 and 109, were isolated and characterized from the genomes of Arenibacter latericius. Molecular genetic analysis using glycosidase-specific primers shows the absence of GH27 and GH36 genes. A sequence comparison with functionally-characterized GH20 and GH109 enzymes shows that both sequences are closest to the enzymes of chitinolytic bacteria Vibrio furnissii and Cellulomonas fimi of marine and terrestrial origin, as well as human pathogen Elisabethkingia meningoseptica and simbionts Akkermansia muciniphila, gut and non-gut Bacteroides, respectively. These results revealed that the genus Arenibacter is a highly taxonomic diverse group of microorganisms, which can participate in degradation of natural polymers in marine environments depending on their niche and habitat adaptations. They are new prospective candidates for biotechnological applications due to their production of unique glycosidases.

crustaceans, insects and in the cell walls of fungi [13]. β-N-Acetyglucosaminidases, isolated from terrestrial microorganisms, have been applied to the preparation of a wide range of biologically and pharmaceutically significant compounds [13]. In addition, β-N-acetyglucosaminidases have been employed for the analysis of complex sugar chains in glycoproteins and glycopeptides, and their application as biocontrol agents, particularly against fungal pathogens of plants, has been found [17].
Arenibacters attracted our attention due to their ability to produce unique glycosidases such as α-N-acetylgalactosaminidase isolated from A. latericius KMM 426 T [25]. It has rare substrate specificity and is able to inactivate serological activity of human A red blood cells, efficiently removing terminal immunodominant α-1,3-linked N-acetylgalactosamine from group A structure antigen at neutral pH. The enzyme is continued to be of great interest in the medical, structural and biotechnology investigations.
The aim of this paper is characteristic of glycoside hydrolases profiles of phylogenetically diverse marine bacteria of the genus Arenibacter isolated from different marine environments and selection of the most prospective strains for biotechnological application.

Analysis of Glycosidase Activities of the Arenibacter Isolates
None of the extracts Arenibacter isolates had effect on polysaccharides used in this study at pH 5.2 or at pH 7.3 (Section 3.4.-"Enzymatic Assays"). However, under physiological conditions (pH 7.3) for the bacteria growth they synthesized a wide range of glycosidases. The values of the specific activity of intracellular glycosidases of the strains measured under standard conditions are listed in Table 3. All isolates synthesized β-N-aсetylglucosaminidases, α-N-aсetylgalactosaminidases, α-fucosidases and α-mannosidases, but the enzymes demonstrated different levels of a specific activity. It should be noted that none of the representatives of A. certesii, A. palladensis and A. troitsensis possessed significant α-xylosidase and β-galactosidase activities under conditions studied.
Highly active β-N-acetylglucosaminidases were found to be the main glycosidase for all Arenibacter strains irrespective of the isolation sources and geographic locations ( Table 3). The differences were observed only among the level of the enzyme expression. Highest activity of β-N-acetyglucosaminidase was observed in Arenibacter certesii KMM 3941 T , isolated from a green alga Ulva fenestrata. An equally high level of β-N-acetylglucosaminidase activity was found in A. latericius KMM 3522 and KMM 3557, isolated from a sea cucumber Apostichopus japonicus, as well as A. latericius KMM 3523, isolated from brown alga Chorda filum. In A. echinorum KMM 6047 from the sea urchin Strongylocentrotus intermedius and Arenibacter sp. KMM 6684 from brown algae Chorda filum the level of β-N-acetylglucosaminidase activity was slightly lower (Table 3). At the same time, all strains of phylogenetically closely related species A. troitsensis and A. palladensis were characterized by a lower level of activity of this enzyme than the above strains (Table 3).
Although little is known about chitin degradation in marine bacteria, it has been previously reported that Gammaproteobacteria of the genus Alteromonas and Vibrio possessed all kinds of chitinolytic enzymes [13,[26][27][28][29]. Surprisingly, no chitinases cleaving polymer to chitooligosacchrides as well as other polysaccharases were observed in any Arenibacter strains explored belonging to the phylum Bacteroidetes. However, the presence of β-N-acetyglucosaminidases, other key enzymes of chitinolytic complex in all strains, allow the suggestion that arenibacters can participate in the second step of chitin degradation, cleaving N-acetylglucosamine from non-reducing termini of chitooligosaccharides obtained after the action of endo-chitinases for other members of the microbial community on the insoluble chitin. Moreover, five strains, including KMM 426 T , KMM 3523, KMM 3941 T , KMM 6273 and KMM 6685, demonstrated the ability to oxidize N-acetylglucosamine, which can serve as a source of carbon and nitrogen (Table 2). α-N-Aсetylgalactosaminidase was glycosidase of the second level of activity in all Arenibacter strains. The ratio of β-N-aсetylglucosaminidases/α-N-aсetylgalactosaminidases activities were not above 10:1 for all strains studied (Table 3).
However, marine bacteria of the phylum Bacteroidetes, especially of genus Arenibacter, are the best producers of the enzyme [24]. A. latericius KMM 426 T have previously been shown to synthesize some molecular forms of α-N-atcetylgalactosaminidase. Previously, we isolated and characterized one of them as being biotechnologically important, as it removed serological activity of human A red blood cells [25].
Structural Characteristics of A. latericius α-N-acetylgalactosaminidase N-terminal sequence of the enzyme purified to homogeneity using the procedure previously described [25] was GAKYMGGFSAPKLDT. The molecular masses of the enzyme were 48 ± 2 and 94 ± 3 kDa, as determined by SDS-PAGE and analytical size, exclusion, fast performance, liquid chromatography, respectively. These results revealed that the enzyme is a homodimer protein in solution.

Molecular Genetic Analysis of Glycosidases
In this study, we employed a homology-based strategy to isolate genes of glycoside hydrolases from genomes of Arenibacter isolates. Several sets of oligonucleotide primers were designed based on the fully-characterized and putative genes of GH20 (Clan GH-K), GH27, GH36 (Clan GH-D) and GH109 enzymes from bacteria, fungi and eukaryotes recovered from the GenBank database. Evolutionary relationships were established between GH20, GH27 and GH36 proteins. Enzymes of the clans GH-D and GH-K share the most important functional characteristics, such as composition of the active center, anomeric configuration of cleaved glycosidic bonds, and retaining mechanism of the catalyzed reaction. Proteins of these clans have the same three-dimensional structure of catalytic domains as (β/α) 8 and common evolutionary origin of their genes [30]. However, only two PCR products, namely GH20 β-N-acetylglucosaminidase and GH109 α-N-acetylgalactosaminidase, were successfully amplified from the genomic DNA of Arenibacter strains. No genes of GH27 and GH36 proteins were found.
The PCR-products pattern with the set of GH20-specific oligonucleotides was found to reflect the different types of Arenibacter strains, corresponding to the 16S rRNA gene analysis results (Figure 1, right). The PCR resulted in three to six bands per sample. The major bands for all Arenibacter isolates with the length of about 750-800 bp were corresponded to the partial sequence of β-N-acetyglucosaminidase genes (Figure 1, right). The other bands bearing unidentified proteins suggest that there may be a large undiscovered metabolic capacity of Arenibacter.

Band Pattern Analysis
According to the band pattern analysis, Arenibacter isolates were divided into 10 groups:

I.
A The results of the detailed taxonomic study showed that strains of the genus Arenibacter were phylogenetic and metabolic diverse organisms that were found in various marine microbial communities associated with seaweeds, invertebrates and sediments. Most of the isolates were affiliated with known species Arenibacter latericius, A. certesii, A. echinorum, A. palladensis and A. troitsensis. Three newly sequenced strains occupied distinct phylogenetic positions among the recognized Arenibacter species (Figure 1). Most of the strains explored belonged to the two separated phylogenetic clusters that formed by members of species A. troitsensis-A. paladensis-A. echinorum and A. certesii-A. latericius, respectively. Interestingly, despite significant phylogenetic distances, a novel strain KMM 6684, isolated from the Okhotsk Sea brown alga, and members of A. latericius, associated with holothurians from Sea of Japan, displayed similar glycosidase spectra and band patterns (Table 3, Figure 1). At the same time, four A. latericius strains having the comparable profiles of glycoside hydrolases (Table 3) were divided in to two groups according to the results of the band patterns. The first group incorporated isolates of holothurians KMM 3522 and KMM 3557, the next group included two other strains, KMM 426 T and KMM 3523, isolated from bottom sediment of South China Sea and brown alga of Okhotsk Sea, respectively (Figure 1). A. troitsensis and A. palladensis isolates were grouped together, which was in agreement with their taxonomic positions and glycosidase activity profiles (Figure 1; Table 3). However, A. troitsensis and A. palladensis, as well as A. latericius, band patterns were divided into two groups. Thus, glycosidase-encoding genes analysis using phylogenetic information was suggested to be suitable for providing a characterization of members of the genus Arenibacter in the natural microbial populations, their diversity prediction in the environmental samples and elucidation of their possible ecological role in the marine environment.

GH20 β-N-acetylglucosaminidase of Arenibacter Isolates
Sequence analysis of the major 750 bp-length bands of Arenibacter isolates suggested that the resultant DNA fragments were new GH20 members (Figure 1, right). All Arenibacter strains demonstrated 99.9%-100% β-N-acetyglucosaminidase gene sequence homology to each other (data not shown).
As seen in Figure 2, several consensus residues identified may participate in the catalytic function of the Arenibacter β-N-acetyglucosaminidases. In accordance with sequence-based CAZy classification all well-characterized marine bacterial β-N-acetyglucosaminidases are related to the GH20 family of Clan GH-K and catalyzed the hydrolysis of O-glycoside bond with retention of anomeric configuration [33,34]. GH20 enzymes employ a "substrate-assisted" mechanism involving the transient formation of an oxazolinium ion intermediately required for action of the catalytic nucleophile/base-carbonyl oxygen of C-2 acetamido group of substrate and catalytic proton donor-Glu [35]. The GH20 enzymes show significant sequence homology to each other but differ in its substrate specificity. For example, Tsujibo et al. purified and characterized a transglycosylating GH20 enzyme from Alteromonas sp. strain O-7 which synthesized β-(1→6)-(GlcNAc) 2 , 2-acetamido-6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-2-deoxyglucopyranose from β-(1→4)-(GlcNAc) 2 [26]. At the same time, the active site of V. furnissii is of the second type of β-N-acetyglucosaminidase that contains three to five GlcNAc binding subsites, depending on the substrate specificity of individual enzymes [27]. ExoI of V. furnisii can act as a chitobiase, but only at non-physiological pH values (pH 5.8). It remains to be seen whether this large homology of the Arenibacter β-N-acetyglucosaminidase and the aligned V. furnissi ExoI, V. harveyi chitobiase, P. gingivalis and C. fimi enzymes will extend to the whole protein. Figure 2. Alignment of a partial A. latericius β-N-acetyglucosaminidase (BGLC) amino acid sequence with other characterized GH20 family β-hexosaminidases: Vibrio furnissii ExoI, HEX1_VIBFU (P96155), Vibrio harveyi chitobiase (A7N8P3), Porphyromonas gingivalis β-hexosaminidase, HEXA_PORGI (P49008), and Cellulomonas fimi β-hexosaminidase, HEX20_CELFI (AF478459). Identical residues are indicated by black and similar residues by darkly grey and lightly grey. The acidic pair important for enzyme catalysis is in bold font.
Phylogenetic analysis showed that α-N-acetylgalactosaminidase of marine bacterium Arenibacter latericius KMM 426 T belongs to GH109 enzymes and was most closely related to the predicted protein structures of Akkermansia muciniphila, an inhabitant of the human intestinal tract, affiliated with the phylum Verrucomicrobia, and marine gammaproteobacterium Shewanella pealeana (Figure 3).
GH109 enzyme, isolated from a clinical strain Elizabethkingia meningoseptica (formerly [Flavobacterium] meningosepticum), which is also the representative of the phylum Bacteroidetes, evolutionarily distant from the α-N-acetylgalactosaminidase of Arenibacter latericius, though descended from the same ancestor. Both enzymes have a common ancestor with the oxidoreductases that perform very different functions and have high homology with GH109 enzymes. GH109 α-N-acetylgalactosaminidase catalyzes the hydrolysis of O-glycoside bond with retention of anomeric configuration and reveals a catalytic mechanism involving NAD + , unusual for the classic glycoside hydrolases, proposed by Koshland [39]. GH109 α-N-acetylgalactosaminidase of Elizabethkingia meningoseptica is capable to efficient removal of A antigens at neutral pH with low consumption of recombinant enzymes.
According to BLAST search results, the highest gene sequence similarity of A. latericius α-N-acetylgalactosaminidase was found with the predicted proteins from the other marine Bacteroidetes: Zobellia galactanivorans, Maribacter sp. and Muricauda ruestringensis (69%-83% identity, 82%-92% homology) (data not shown). It is an interesting fact that this list was followed by the human symbiotic gut colonizer, Akkermansia muciniphila, breaking down extracellular polymeric substrates, including mucin [40]. However, A. latericius is an aerobic marine bacterium found in a wide variety of environments including sediments, animals and alga. This suggests that Arenibacter can be a marine host associate, as well as attach to solid surfaces and form biofilms. The wide spectrum of glycoside hydrolyses can play a role in facilitating detachment and dispersion of Arenibacter cells for successful colonization of new surfaces. It is within the realm of possibility that Arenibacter lifestyle includes participation in degradation of the remains of other organisms such as chitin or plant biopolymers, making them important organisms in carbon recycling. Indeed, it has been previously reported that marine planktonic Flavobacteria (dominated by Polaribacter) have been defined to attach to, and to degrade, diverse complex algal organic material and then make labile compounds available to Alphaproteobacteria and Gammaproteobacteria [41]. It is evident that many of the Arenibacter multienzyme complex features are niche and are habitat adaptations that facilitate depolymerization of complex polysaccharides in the marine environment. Arenibacter can be responsible for producing natural unique glycosides useful for biotechnology and human medicine.

Strains Isolation and Purification
The strains were isolated from bottom sediments; the green algae Acrosiphonia sonderi and Ulva fenestrata, the brown algae Chorda filum, the sea urchin Strongylocentrotus intermedius and the holothurian Apostichopus japonicus collected in Troitsa Bay, Gulf of Peter the Great, the Sea of Japan (Table 1). For strains isolation, 0.1 mL bottom sediment suspension or tissue homogenates were transferred onto marine agar 2216 (Difco) plates. After primary isolation and purification, strains were cultivated at 28 C on the same medium and stored at −80 °C in marine broth (Difco) supplemented with 20% (v/v) glycerol.

Morphological, Biochemical, and Physiological Characterization
The physiological, morphological and biochemical properties of the strains were studied using the standard methods. Gram-staining was performed as recommended by Smibert et al. [42]. Oxidative or fermentative utilization of glucose was determined on the Hugh-Leifson medium modified for marine bacteria [43]. Catalase activity was tested by addition of 3 % (v/v) H 2 O 2 solution to a bacterial colony and observation for the appearance of gas. Oxidase activity was determined by using tetramethyl-p-phenylenediamine. Degradation of agar, starch, casein, gelatin, chitin, Tweens 20, 40 and 80, DNA and urea, growth at different pH values and production of acid from carbohydrates, nitrate reduction, production of hydrogen sulphide, acetoin (Voges-Proskauer reaction) and indole, and presence of alkaline phosphatase activity were tested according to standard methods [42]. The temperature range for growth was assessed on MA. Tolerance to NaCl was assessed in medium containing 5 g Bacto Peptone (Difco), 2 g Bacto Yeast Extract (Difco), 1 g glucose, 0.02 g KH 2 PO 4 and 0.05 g MgSO 4 · 7H 2 O per liter of distilled water with 0, 0.5, 1.0, 1.5, 2.0, 2.5, 3, 4, 5, 6, 8, 10 and 12% (w/v) of NaCl. Carbon source utilization was tested (i) using commercial API 20E (bioMé rieux) identification strip following the instructions of the manufacturer, and (ii) using a medium that contained 0.2 g NaNO 3 , 0.2 g NH 4 Cl, 0.05 g Yeast Extract (Difco) and 0.4% (w/v) carbon source per liter of artificial seawater as described by Suzuki et al. [44].
For mol% G + C determination, DNA was isolated following the method of Marmur [45] and the DNA G + C content was determined by the thermal denaturation method [46].

Antimicrobial Activity
To order to determine antimicrobial activity of the isolates, the following test organisms were used: Bacillus subtilis ATCC 6633 T , Enterococcus faecium LMG 11423 T and Staphylococcus aureus ATCC 21027 T as the Gram-positive strains, Escherichia coli 3254, Pseudomonas aeruginosa ATCC 27853 T and Vibrio parahaemolyticus CIP 75.2 T as the Gram-negative strains, and Candida albicans KMM 455 as the yeast strain. All strains were grown on tryptic soy agar (TSA) plates with adding of NaCl (15 g/L) at 37 °С. The agar plates were inoculated by using overnight cultures of each test strain with approximately 10 9 cells per milliliter (100 μL for the bacterial strains and 200 μL for the yeast strain). The Arenibacter isolates were grown as a lawn on MA at 28 °C for 24 h. Plugs 10 mm in diameter were cut out with a chokbore and placed with the bacterial side down onto test strains agar plates. After incubation at 30 °С for 24 h, antimicrobial activity was evaluated by measuring the inhibition zones (in mm) around the agar plugs.

Protein Assays
Protein concentration in bacterial biomass extracts was determined according to the Bradford [47] using bovine serum albumin (Sigma) as the standard. α-N-acetylgalactosaminidases was isolated, purified and identified according procedure described earlier [25]. The NH 2 -terminal amino acid sequence (15 a.a.) of the α-N-acetylgalactosaminidases was determined using a pulsed liquidphase protein sequencer (Procise 492; Applied Biosystems Foster City, CA, USA). Sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) was run essentially as described by the supplier of the electrophoresis equipment (Hoefer Scientific Instruments, San Francisco, CA, USA). The molecular mass of native α-N-acetylgalactosaminidases was estimated by gel filtration on a Superose 12 HR 10/30 column (Amersham Pharmacia) running fast protein liquid chromatograph (Acta, France) in 0.05 M Na + -phosphate, рН 7.3, 0.15 M NaCl at a flow of 0.4 mL/min at 8 °С and calibrated using gel filtration standard molecular weight markers (Sigma). The subunit molecular mass of the purified α-N-acetylgalactosaminidases was determined by 14% SDS-PAGE molecular-weight markers (Fermentas).
For bacterial extract preparation, the cells were separated from the culture medium by centrifugation at 3000 g. The bacterial biomass was frozen at −20 °C. The weighed portion of the frozen raw biomass was resuspended in 0.01 M Na + phosphate buffer solution, pH 7.3, on an ice bath up to concentration of 0.2 g/mL. The cells were homogenized by sonification at a frequency of 22 kHz and a current of 0.4 A three times for 20 s at intervals of 20 s. The cell suspension was incubated at 4 °C for 3 h; the homogenate was then centrifuged at 11,000 g for 30 min. The pellet was discarded; the protein concentration and glycosidase activities were determined in the extracts.
Glycosidase activity in bacterial extracts was measured as follows: 0.05 mL of the extract solution and 0.35 mL of p-nitrophenyl-glycoside solution (1 mg/mL) in 0.1 M Na + phosphate buffer, pH 7.3, was incubated for 5 to 120 min at 20 °C. The reaction was stopped by addition of 0.6 mL of 1 M Na 2 CO 3 . The initial reaction rate was determined from the linear segment of the A 400 time dependence. The substrate solution and extract solution in the same buffer with 1 M of Na 2 CO 3 served as the controls. The amount of released p-nitrophenol was determined spectrophotometrically by measuring OD at 400 nm (ε 400 = 18,300 mol -1 · cm -1 ). One unit of activity was defined as the amount of an enzyme that releases 1 μmol of p-nitrophenol per minute under the conditions used. Specific enzyme activity was estimated as units (U) per milligram protein.
The polysaccharide hydrolase and lyase activities were measured in 0.05 M Na + -phosphate buffer, pH 7.3, at 20 °C. The reaction was carried out alternatively in 0.05 M Na + -acetate buffer, рН 5.2, at 20 °C for 24 h. The reaction mixture contained 0.05 mL of 0.2 g/mL bacterial cell extracts and 0.2 mL of 0.1% corresponding substrate solution in 0.05 M Na + -phosphate or Na + -acetate buffer and 0.1 M NaCl, pH 7.3 and 5.2, respectively. The reaction was terminated by adding Nelson reagent. One unit of activity was defined as the quantity of reducing sugars released from substrate using corresponding monosaccharide as a standard Somogyi-Nelson method [48].

DNA Preparation and PCR Amplification
Genomic DNA was extracted from cultured marine bacteria using of commercial kit according to manufacturer's instruction (Fermentas). Fresh bacterial culture (200 μL) was used for DNA isolation and 20-50 μL of water was added for final DNA dissolving.
The oligonucleotide primers used for amplification of Arenibacter families GH 20, GH 27 and GH 36 genes were for the forward primers: Sets of oligonucleotides designed based on alignments of families GH20, GH27 and GH36 ORFs of closely related bacteria, fungi and eukaryotes in the GenBank database were: (1) and (5), (2) and (5), (3) and (5), (4) and (7), (4) and (8). PCR amplification was performed in a total volume of 20 μL mixture, containing 50 ng of chromosomal DNA, 2 μm primers, 1 mm each deoxyribonucleoside triphosphate, 5 U of Encyclo Polymerase. Samples were amplified for 35 cycles using the following program: initial denaturation at 95 °C for 2 min, denaturation at 95 °C for 15 s, annealing temperature (varying from 50 °C to 56 °C) for 15 s and elongation at 72 °C for 1.5 min.
The fully-length genes encoded GH109 α-N-acetylgalactosaminidases were amplified by the following oligonucleotides within the inserts in pET40 and TEV protease site for removal His-tags: 5′-TAACCATGGGTGGGGCTAAGTACATGGGCGGTTTTTCTGCT-3′ for the forward primer and 5′-TAAGTCGACACCCTGAAAATAAAGATTTTCGCTTACAATATCTAATGGTGCAGTGGT-3′ for the reverse primer. The forward oligonucleotide primer was designed on the base of the N-terminal amino acid sequence of Arenibacter latericius α-N-acetylgalactosaminidase.
PCR-products were purified with purification kit (Qiagen, USA) then cloned and sequenced. Amplified fragments were either cloned or directly sequenced using the automated PE/ABI 310 DNA sequencer and the PE/ABI-ABI PRISM BigDye Terminator cycle sequencing Ready Reaction Kit (PE Applied Biosystems). PCR products were identified using 1% agarose gel and visualization computer system (Herolab, Germany).

PCR-Product and Sequence Analysis
The nucleotide sequences were edited using the software Chromas, Gene Runner and compared to published sequences in the NCBI GenBank using the nucleotide and protein BLAST and ClustalW2. Neighbor-joining (NJ) trees for 16S rRNA genes were generated from the corresponding matrix of nucleotide divergence between sequences using the program MEGA2 [52]. Confidence in the branching points was obtained with 1000 bootstrap replications. The sequence of Coenonia anatina LMG 1502-91 was used as outgroup for phylogenetic reconstruction. Pairwise sequence similarities were calculated by Ez-Taxon-e [53].
The phylogenetic tree was reconstructed using the protein maximum likelihood method implemented in the PHYLIP program (v3.6). Reliability for internal branch was assessed using the bootstrapping method (1000 bootstrap replicates). Graphical representation of the phylogenetic tree was performed with Drawtree from the PHYLIP package (v3.6) [37].
The resultant PCR-products obtained with the use of glycosidase-specific primers were analyzed by standard gel electrophoresis as band patterns. To reduce possible inter-sample PCR variation, all PCR reactions were run in triplicates and pooled together before loading on gel-electrophoresis and PCR amplification, and genomic DNA of E. coli was used as positive control, and PCR mixture without DNA template was used as negative control.

Conclusions
As a result of multifaceted research, we can draw the following conclusions. Marine bacteria of the genus Arenibacter are emerging as a recently discovered group of marine bacteria. The hydrolytic enzyme profiles of Arenibacter isolates include biotechnologically important β-N-aсetylheglucosaminidases, α-N-aсetylgalactosaminidases, α-fucosidases and α-mannosidases with the different levels of enzymatic activity. Molecular genetic analyses with use of the glycosidase-specific primers show the absence of classic GH27 and GH36 genes except for GH20 β-N-aсetylglucosaminidase. Although enzymatic characterization of the β-N-acetylglucosaminidase produced by Arenibacter strains has not been performed yet, there is a possibility to consider these enzymes as good tools for producing biologically active β-N-acetylglucosamine derivatives in the near future. α-N-Acetylgalactosaminidase of the Arenibacter latericius is classified as GH109 enzyme. This enzyme exhibits unusual structure and mechanism of action [25,36]. We hypothesize that many of these features may facilitate the beneficial adaptation plasticity of microorganisms in a constantly changing environment of an intertidal flat zone [1,4,5]. A high phylogenetically diversity and broad distribution in marine environments of members of the genus Arenibacter, in combination with their various glycoside hydrolase activities, have led to the notion that these microorganisms are specialists for degradation of natural carbohydrates. Moreover, the ability to produce multifarious glycosidases together with the absence of antimicrobial activities suggests that the enzymes play a major role in survival and successful competition of arenibacters in marine microbial communities. In summary, we have demonstrated that taxonomic diverse bacteria of the genus Arenibacter has a great potential in production of a wide spectrum of unique glycosidases, which are of special interest in biotechnology and medicine applications.