Skip to main content

Phylogenetic analyses suggest multiple changes of substrate specificity within the Glycosyl hydrolase 20 family



Beta-N-acetylhexosaminidases belonging to the glycosyl hydrolase 20 (GH20) family are involved in the removal of terminal β-glycosidacally linked N-acetylhexosamine residues. These enzymes, widely distributed in microorganisms, animals and plants, are involved in many important physiological and pathological processes, such as cell structural integrity, energy storage, pathogen defence, viral penetration, cellular signalling, fertilization, development of carcinomas, inflammatory events and lysosomal storage diseases. Nevertheless, only limited analyses of phylogenetic relationships between GH20 genes have been performed until now.


Careful phylogenetic analyses of 233 inferred protein sequences from eukaryotes and prokaryotes reveal a complex history for the GH20 family. In bacteria, multiple gene duplications and lineage specific gene loss (and/or horizontal gene transfer) are required to explain the observed taxonomic distribution. The last common ancestor of extant eukaryotes is likely to have possessed at least one GH20 family member. At least one gene duplication before the divergence of animals, plants and fungi as well as other lineage specific duplication events have given rise to multiple paralogous subfamilies in eukaryotes. Phylogenetic analyses also suggest that a second, divergent subfamily of GH20 family genes present in animals derive from an independent prokaryotic source. Our data suggest multiple convergent changes of functional roles of GH20 family members in eukaryotes.


This study represents the first detailed evolutionary analysis of the glycosyl hydrolase GH20 family. Mapping of data concerning physiological function of GH20 family members onto the phylogenetic tree reveals that apparently convergent and highly lineage specific changes in substrate specificity have occurred in multiple GH20 subfamilies.


Carbohydrates are involved in many biological functions including maintenance of cell structural integrity, energy storage, pathogen defence, viral penetration, cellular signalling and fertilization. Enzymes specifically responsible for carbohydrate hydrolysis have been classified in 111 families of glycosyl hydrolases (GH) on the basis of amino acid sequence similarity [1, 2]. Hexosaminidases belong to families GH3, GH20 and GH84 [2]. Among these, family 20 is of particular interest, and includes β-N-acetylhexosaminidases (β-hexosaminidase) (EC, enzymes that hydrolyze non-reducing terminal β-1,4 linked N-acetylglucosamine (GlcNAc) or β-N-acetylgalactosamine (GalNAc) residues of oligosaccharides and their conjugates, bacterial chitobiases (EC and lacto-N-biasidase (EC Crystal structures are known for numerous β-N-acetylhexosaminidases including the bacterial enzymes from Serratia marcescens [3] and Streptomyces plicatus [4], and the α- and β-chains of human lysosomal enzymes. The catalytic domain is an α/βTIM-barrel with the active site at the centre of the barrel complex [57].

In mammals, there are two major β-N-acetylhexosaminidase isoforms, named HEXA and HEXB, which reside in lysosomes and participate in the degradation of glycoproteins, glycolipids and glycosaminoglycans. HEXA is a heterodimer of subunits α (encoded by the gene HEXA) and β (encoded by the gene HEXB), whereas HEXB is a homodimer of β subunits. The subunits arose via a gene duplication event and the primary sequences are approximately 60% identical [8, 9]. In particular, mutations in human HEXA and HEXB genes cause Tay-Sachs and Sandhoff, fatal neurodegenerative diseases, respectively [10, 11]. Recent data suggest that lysosomal exoglycosidases along with many other factors may participate in the progression of development of tumor cells [12]. The potential involvement of a β-N-acetylhexosaminidase in fertilization in hamster [13] and human [14] has been also hypothesized.

Beta-hexosaminidases are also widely distributed in Insects. Several studies have led to the identification, molecular cloning and purification of β-N-acetylhexosaminidases in Lepidoptera like Manduca sexta [15], Spodoptera frugiperda [16], Bombyx mori [17], Trichoplusia ni [18], Diptera like Drosophila melanogaster [19, 20] and Aedes aegypti [21] and more recently in the coleopteran Tribolium Castaneum [22]. The β-hexosaminidase activity of insects is of particular interest because of the role this glycosidase plays in the alteration of the structures of N-glycans generated in the cells [16, 2224] and in the chitin degradation processes [16, 22, 24, 25]. Chitin, found in the cuticle of the integument and peritrophic membrane of the midgut, is a linear polymer of β-1,4 linked N-acetylglucosamine. Chitin degradation is catalyzed by chitinolytic enzymes in two successive steps: chitinase (EC hydrolizes chitin into oligosaccharides of GlcNAc, then β-N-acetylhexosaminidase further degrades the oligomers into monomers. Because of the important role of chitin, β-N-acetylhexosaminidase is considered to be a potential target for insect control agents such as biopesticides [26, 27]. Recently, the presence in the plasma membrane of spermatozoa of Drosophila melanogaster of two β-N-acetylhexosaminidases potentially involved in sperm-egg interactions has been demonstrated [20, 28].

In crustaceans, β-N-acetylhexosaminidase has been shown to be important in the degradation of chitin forming the exoskeleton. Beta-N-acetylhexosaminidases have been purified and characterized in different species, such as Euphausia superba [29] and Scylla serrata [30].

In the ascidian Phallusia mammillata a β-N-acetylhexosaminidase present in the plasma membrane of spermatozoa might have a role in the primary binding between gametes [31].

In addition, an important function of a β-N-acetylhexosaminidase has been postulated in the anaerobic parasitic protozoan Entamoeba histolytica, the causative agent of infectious amoebiosis. Two β-N-acetylhexosaminidases have been identified, cloned and characterized. These enzymes are most probably involved in the destruction of glycoconjugates of the extracellular matrix components to pass basement membranes [32].

Hexosaminidase genes are also distributed among fungi and bacteria and the enzyme family plays an important physiological role in the natural recycling of chitin, a structural component of cell wall [33, 34]. The molecular cloning of β-N-acetylhexosaminidases has been reported for several bacteria, such as Alteromonas sp. Strain O-7 [35], Alteromonas sp. Strain 10S-24 [36], Serratia marcescens [3], Vibrio harveyi [37], Vibrio vulnificus [38]Enterobacter sp. Strain G1 [39], Cellulomonoas fimi [40] and several fungi, such as Trichoderma harzianum [41], Trichoderma atroviride [42], Aspergillus oryzae [43], Aspergillus nidulans [44] and Candida albicans [45]. Beta-N-acetylhexosaminidase is an emerging target for the design of fungicides. In fact, several chitinolytic bacteria and fungi have been shown to be powerful biological control agents protecting for example plants against pathogens [41, 4648].

Plant β-hexosaminidases have been detected in a variety of tissues including seeds and leaves [49, 50]. In particular, high levels of β-N acetylhexosaminidase activity have been detected in germinating seeds [50] suggesting a role in the storage of glycoproteins [51]. A function in defence processes has also been proposed, since several of the purified β-N-acetylhexosaminidases could be chitin-degrading enzymes [27, 50]. More recently β-hexosaminidases of Arabidopsis thaliana have been cloned and characterized at the molecular level [52].

Despite the increasing number of hexosaminidase homologs that have been identified in different species, only restricted analyses of phylogenetic relationships between glycosyl hydrolases of the GH20 family have been conducted [3, 16, 22, 24, 31, 40, 53]. Because of their important roles in several biological processes, we have undertaken a more comprehensive analysis of the evolutionary history of the GH20 family. In this study we have identified, analyzed and characterized β-N-acetylhexosaminidases from prokaryotes and eukaryotes. We show that while the GH20 family is widely distributed among eubacteria, the observed taxonomic distribution is best explained by a combination of gene duplications and horizontal gene transfer events. Likewise, the limited occurrence of the family in archaebacteria is probably the result of lateral transfer from eubacteria. We trace gene duplication events both at basal and lineage-specific levels within eukaryotes and demonstrate that while the most widely studied GH20 family members derive from a single ancestral eukaryotic gene, a second subfamily of more divergent sequences present in at least the majority of metazoans was likely acquired from an independent prokaryotic source. Finally, we describe the patterns of conservation of protein features in numerous β-N-acetylhexosaminidase subfamilies and relate these features to the current understanding of GH20 family function, an important exercise given apparent convergence of physiological function of non-orthologous GH20 enzymes in eukaryotes.

Results and discussion

Beta-hexosaminidase sequences

The β-hexosaminidase sequences in our study were recovered from numerous organisms, including prokaryotic and eukaryotic species. Extensive similarity searches of the CAZy, Pfam and Swiss-Prot databases resulted in the identification of around 300 complete prokaryotic or eukaryotic β-hexosaminidase/β-hexosaminidase-like gene sequences encoding products belonging to the GH20 family (Table 1 and see additional file 1, 2, 3). Partial prokaryotic β-hexosaminidase sequences or those derived from whole genome shotgun (WGS) sequences that could not be reliably reassembled have not been used in this work. Vertebrate and non-vertebrate sequences show pairwise amino acid identity ranging from 20 to 40%, whereas identity is between 45% and 90% within mammals and from 20% to 75% between the members of the two insect orders examined here (Lepidoptera and Diptera).

Table 1 Eukaryotic β-hexosaminidase proteins belonging to the Glycosyl hydrolase family 20 used in Figure 4.

Protein features and conserved

We observed hydrophobic sequences predicted to be a signal peptide with potential cleavage sites in the N-terminal regions of all metazoan β-hexosaminidases (not shown), except Hex3_Dm, Hex3_Dp, Hex2_Ag, that have a putative signal-anchor domain [20, 24]. Moreover, SOSUI and HMMTOP analyses identified one or two putative transmembrane helices in all sequences, but these predictions have a low degree of confidence. Although β-hexosaminidases are typically soluble lysosomal proteins, they have been also found in body fluids in mammals [5458], in insects [20, 5961] and in plants [52]. The presence of β-hexosaminidases in an extracellular compartment is not surprising. It is in fact known that lysosomal hydrolases can be released through constitutive secretion or through lysosomal exocytosis [57, 62, 63]. Furthermore, β-N-acetylhexosaminidases are present as intrinsic proteins of the plasma membrane in insects [20, 24], in ascidians [31], in plants [52], in vertebrates, including man [13, 14, 64] as well as in a variety of human somatic cells [65, 66]. Thus, it could be hypothesized that the membrane-associated β-N-acetylhexosaminidase might be generated by a deficient cleavage of the signal peptide sequence, as demonstrated for other transmembrane proteins that are also present as soluble enzymes [20, 6770]. If the signal peptide were not cleaved, the enzyme would be a type II plasma membrane protein with an anchor sequence, as demonstrated in a few human sperm and fruit fly proteins [14, 20, 28, 70].

A multiple alignment of representative β-hexosaminidase protein sequences is shown in Figure 1. Amino acids belonging to six of the eight motifs known to be a signature for GH20 family are highly conserved (SPRINTS database; [71]), while amino acids in the first and fifth motifs are much less conserved. In particular we observe greater difference in β-hexosaminidase protein sequences of the dipteran species, while β-hexosaminidase of the lepidopteran Spodoptera frugiperda is very similar to mammalian β-hexosaminidases – as previously indicated [16]. Residues involved in substrate binding (Asp196, Asp208, Arg211, Asp354, Tyr450, Glu491 – human HEXB numbering) and the triad aspartate (Asp240), histidine (His294), glutamate (Glu355) – known to be the amino acids involved in catalysis in human HEXB- are completely conserved [5, 6]. Six cysteine residues (Cys91-Cys137, Cys309-Cys360 and Cys534-Cys551 – human HEXB numbering) form three disulfide bonds in human HEXB [72] and the third disulfide bond has been demonstrated to be important for enzymatic activity [73]. Only the cysteine residues involved in the second disulfide bond are fully conserved – suggesting that the disulfide bonds cannot be considered a conserved feature of all β-hexosaminidases. The tyrosine-456 and alanine-543 of β-chain in human HEXB play an important role in dimerization since they form hydrophobic interactions with the isoleucine-454, tyrosine-492 and threonine-496 of the second β-subunit [5]. As shown in Figure 1, tyrosine-456 is conserved in ascidians, nematodes and fish, while in fungi, insects and in the slime mould Dictyostelium it is replaced by different amino acid residues. Conversely, only in Caenorhabditis and Dictyostelium is the alanine residue not conserved. Although dimerization is considered a prerequisite for the formation of catalytically active enzymes in metazoans, our observations do not preclude that the enzymes dimerize and are active, as recently demonstrated in insects [16, 20].

Figure 1

Multiple sequence alignments of representative β-hexosaminidase proteins. The sequences were aligned with Muscle [87]. The eight motifs known to be a signature for GH20 family are shaded in grey. Residues involved in substrate binding are blue and shaded in grey. The solid arrowheads indicated the amino acid residues that form the catalytic triad in human HEXB [5, 6]. Tyrosine and alanine residues that play an important role in dimerization of two subunits in human HEXB [5] are white in black background. Cysteines involved in the formation of disulfide bonds in human HEXB [72] are red.

Figure 2 shows the multiple alignments of several eukaryotic β-hexosaminidases that have been defined as members of glycoside hydrolase family 20 in the CAZy and NCBI databases, but which do not show extensive global sequence similarity to other GH20 family members. DIALIGN found only a conserved region (seven amino acids) containing the glutamate residue that is involved in the catalytic mechanism of hexosaminidase [53]. We have recovered additional eukaryotic and prokaryotic β-hexosaminidase sequences (See additional file 2, 3) that appear to be homologs of these sequences. MEME, a tool to discover conserved motifs in a set of unaligned protein sequences (See Methods), detected the presence of conserved regions different from those known to be distinctive of β-hexosaminidases of GH20 (Figure 2). However, further research will be necessary to clarify the biochemical and functional role of these highly conserved regions.

Figure 2

Multiple sequence alignments of representative eukaryotic divergent GH20 sequence proteins. Sequences were aligned with version Muscle [87]. Conserved motifs detected by MEME analysis are shaded in grey. Sequences containing the glutamate residue (E) known to be involved in the catalysis are red [5, 6]. Hex2_Ce: C. elegans [GenBank: AAA96105.3]; Hex3_Ce: C. elegans [GenBank: CAI06053.1]; Hex4_Ce: C. elegans [GenBank: CAO72177.1]; Hex5_Ce: C. elegans [GenBank: CAA22078.2]; Hex4_Dm: D. melanogaster [GenBank: NP_650689.1]; Hex4_Dp: D. pseudoobscura [GenBank XP_001359965.1]; Hex2_Aa: A. aegypti [GenBank: XP_001649003.1]; Hex2_Dr: D. rerio [GenBank: NP_001070635.1]; Hex3_Mm: M. musculus [GenBank: BAE32455.1]; Hex3_Hs: H. sapiens [GenBank: BAB85072.1].

Four gene products from C. elegans [GenBank: AAA96105.3, CAI06053.1, CAO72177.1, CAA22078.2] belong to this subfamily of GH20 and it has been recently demonstrated that they show β-hexosaminidase activity [53]. However, no data were presented on other amino acids involved in substrate binding and catalysis except the glutamate residue [5, 6]. Further experiments are necessary to determine the enzyme activity of the probable orthologs to these C. elegans genes – which show most similarity to divergent GH20 proteins from low G+C gram positive bacteria, planctomycetes and a single crenarcheote (Thermofilum pendens) (See additional file 2, 3).

Conservation and evolution of gene structure

Figure 3 and Additional file 4 show the lengths of introns and exons of a representative sample of the β-hexosaminidase genes examined in this study, obtained with Exalign [74]. Within the vertebrate Hex1 and Hex2 subfamilies, the numbers and lengths of exons are remarkably conserved, together with intron phase. Vertebrate Hex1 and Hex2 isoforms are universally encoded by 14 exons. Among sampled species, only Gallus gallus shows a small degree of exon slippage of exons 4, 5 and 6 (which might be due to misannotations), while different lengths of initial and terminal exons (which include UTR sequences) are not unexpected. It is interesting that one of the β-hexosaminidase genes identified (Hex2_Ci) on the genome of the ascidian C. intestinalis has also conserved the size of several exons corresponding to vertebrate exons 2, 6, 7, 8,11, 12 and 13, consistent with this structure representing an ancestral chordate layout. Genes from more basal organisms (arthropods and nematodes) show a more variable structure in terms of intron number and position; no significant similarities with vertebrate genes were noted at the level of gene structure. Unsurprisingly, we observe similar gene structures also between pairs of Drosophila species, such as D. melanogaster and D. pseudoobscura, both in number or size of exons and in intron phase. On the other hand, in the nematode C. elegans only two β-hexosaminidases [GenBank: AAA91263.1, AAA96105.3] are encoded by 10 exons, while the other three β-hexosaminidases [GenBank: CAI06053.1, CAO72177.1, CAA22078.2] show a more variable structure in terms of exon number and position and intron phase (data not shown).

Figure 3

Exon and intron patterns of representative genes of metazoan β-hexosaminidases of GH20 family. Exon and intron patterns of representative genes of metazoan β-hexosaminidase of GH20 family, used in this study and drawn to scale relative to the number of nucleotides presenting each region (see additional file). Exons are represented with a rectangle, and homologous exons are depicted by a similar fill pattern. Gray filled rectangles represent non homologous exons in the ascidian C. intestinalis. Introns are depicted by a line between exons.

Phylogenetic Analyses of β-hexosaminidase Sequences

Given the high degree of sequence divergence and indications of extensive saturation of substitutions at the nucleotide level (not shown), all phylogenetic analyses were performed on inferred full length amino acid sequences exhibiting overall co-linearity. Two separate datasets were prepared in order to maximize the number of unambiguously aligned amino acid residues used in phylogenetic analyses. The first set contained only eukaryote sequences showing overall co-linearity of alignment (76 sequences, 274 amino acid positions), the second included a the majority of eukaryote and prokaryote sequences – with only representatives of groups of highly similar sequences from closely related organisms removed to reduce the computational complexity of analysis of the large resulting dataset (233 sequences, 223 amino acid positions) – see materials and methods. A Bayesian phylogeny of the prokaryote and eukaryote dataset is shown in Figure 4, where the tree is rooted arbitrarily.

Figure 4

Bayesian Consensus tree of representive Eukaryote and Prokaryote GH20 protein sequences. The tree is rooted arbitrarily. Bayesian Posterior probabilities and Maximum-likelihood bootstrap proportions at important nodes are shown where above 0.5 or 50% respectively. All analyses were performed with the WAG amino acid substitution model and 1 invariable and 4 gamma distributed site rate categories.

The GH20 family does not appear to be distributed evenly among bacterial phyla. Indeed, the majority of available sequences are derived from the Proteobacteria, Actinobacteria, Firimcutes, the Bacteroidetes/Chlorobi (CFB) group and Acidobacteria. Our phylogenetic analyses recover several well-supported clades containing members of well-defined taxonomic groups. For example, beta-proteobacterial and the majority of the gamma proteobacterial sequences are recovered as a well-supported monophyletic group which has a moderately supported association with some alpha-proteobacterial sequences. However, other gamma- and alpha-proteobacteria fall in disparate positions in the tree while Actinobacteria also fall in at least two clusters. Analogously, the Bayesian analysis recovers disparate clades of sequences derived from members of the Bacteroidetes/Chlorobi. These data suggest either ancient gene duplications or multiple horizontal gene transfer events within bacteria. We note that both Bayesian posterior probability and, in particular, bootstrap support for deep level relationships between groups is consistently low, prohibiting strong inferences regarding the evolution of the gene family in prokaryotes. Indeed analysis of constrained tree topologies using the Shimodaira/Hasegawa test suggested that a variety of relationships between the well defined groups indicated in Figure 3 were not significantly worse explanations of the data than the Bayesian consensus tree (not shown). It is thus impossible to judge whether an ancient origin of the GH20 family in bacteria was followed by multiple gene duplications and lineage specific losses of paralogs or whether the GH20 family arose within a discrete bacterial phylum and that the observed current distribution is a result of extensive lateral transfer coupled with occasional gene duplication. Interestingly, a well supported clade consisting mainly of sequences derived from Firmicutes (herein the "Firmicute" clade) also includes several sequences from CFB group bacteria, members of the Chlamydia/Verrucomicrobia group, a single Actinobacterial sequence, several members of the Thermatogae, several Chloroflexi and the few Archaebacterial sequences identified in this study. Taken together with the discontinuous presence GH20 family genes in Archaebacteria, Thermatogae, Chlamydiae and other bacterial taxa (and their apparent absence from other major bacterial groups (eg. Cyanobacteria), we suggest that extensive horizontal gene transfer has played a significant role in generating the observed taxonomic distribution of GH20 family members in prokaryotes.

The eukaryotic sequences are recovered as two principal monophyletic groups, each with high bootstrap support and Bayesian posterior probability. The moderately-supported sister taxa to the first eukaryote clade (Eukaryote clade A (Figure 5) – which includes most of the sequences which have been subjected to functional analyses (see below)) is a paraphyletic assemblage of Acidobacterial and Proteobacterial species. While a second assemblage of divergent metazoan sequences (Eukaryote clade B – Figure 6) is recovered as a moderately supported sister to several CFB group proteins within the aforementioned "Firmicute" clade. Despite extensive constrained tree searches, we were unable to identify topologies portraying these two eukaryotic clades as a monophyletic group that were not excluded by the Shimodaira/Hasegawa test (not shown). While, the current data argue strongly for two acquisitions of GH20 family genes by eukaryotes (one in a common ancestor of plants, animals, fungi and mycetozoa, and another potentially in an early metazoan) the aforementioned considerations render speculation as to the nature of the prokaryote donors premature.

Figure 5

Bayesian Consensus tree of Eukaryote GH20 protein sequences (Clade A). Analyses were performed on 274 unambiguously aligned amino acid positions from eukaryotic sequences passing tests of compositional homogeneity. The tree is rooted in a way to minimize inferred gene duplication events and maximize accordance with current understanding of organismal phylogenetic relationships. Bayesian Posterior probabilities and Maximum-likelihood bootstrap proportions are shown where above 0.5 or 50% respectively. All analyses were performed with the WAG amino acid substitution model and 1 invariable and 4 gamma distributed site rate categories. Proteins known to exhibit exochitinase activity are in red, whereas proteins involved in the formation of paucimannosidic N-glycans are in blue.

Figure 6

Bayesian Consensus tree of Eukaryote GH20 protein sequences (Clade B). Experimental details as for Figure 4. Rooting is as inferred from the global analysis of GH20 sequences. Bayesian posterior probability and bootstrap support values are shown where over 0.5/50% respectively.

It is notable that sequences from the parasitic protist Trichomonas vaginalis are recovered within a well-supported clade of sequences from CFB group bacteria. Indeed, this case of probable prokaryote to eukaryote horizontal gene transfer was explicitly noted during the characterization of the genome of this parabasalid flagellate [75].

To better understand the evolution of the GH20 family within eukaryotes, we performed Bayesian – and maximum likelihood bootstrap – phylogenetic analyses of unambiguously aligned regions of inferred eukaryote clade A protein sequences (Figure 5). Vertebrate alpha and beta chains constitute monophyletic groups and are each others well supported sisters. The emergence of tunicate sequences as the monophyletic sister group of the vertebrate forms is consistent with a gene duplication in a common ancestor of vertebrates after the divergence of tunicates. Well-supported clusters of arthropod, nematode and schistosome sequences emerge basal to the tunicate clade.

A second, well-supported, cluster of arthropod sequences emerges in a distinct part of Eukaryote clade A (Figure 5). Indeed, the Bayesian analysis also recovers two clusters of plant, fungal and mycetozoan sequences – suggesting that a gene duplication event occurred in a common ancestor of plants, animals and fungi. However, it is not possible to position the root of the tree in such a way as to explain these multiple clusters with a single duplication event. We therefore investigated alternative hypotheses to explain the observed distribution of GH20 paralogs using constrained phylogenetic trees. We were unable to generate constrained topologies in which plant or arthropod sequences are monophyletic that were not statistically worse explanations of the data than the Bayesian topology according to the Shimodaira/Hasegawa (SH) test implemented in TREE-PUZZLE although all fungal sequences can be constrained as monophyletic as can mycetozoan (Entamoeba and Dictyostelium) sequences (which emerge close together in the bootstrap consensus tree). Several topologies describing plausible organismal relationships and invoking a single ancestral gene duplication in eukaryotes are not rejected by the SH test (See additional file 5) and the GH20 sequence data is thus compatible with current hypotheses of deep level organismal relationships within eukaryotes [76] and does not require invocation of eukaryote to eukaryote gene transfer as an explanation. While the monophyly, or otherwise, of fungal sequences cannot be established with confidence, the current data suggest that the observed diversity of arthropod and plant GH20 family genes result in part from ancient duplications that occurred before the divergence of plants and animals. However, subsequent "local" gene duplications have also occurred in both lineages. This phenomenon is particularly notable in plant clade I and in animal clade II – where successive gene duplications have given rise to Hexo1, Hexo2 and fused lobes (named fdl) genes.

Sequence similarity searches of the DOE Joint Genome Institute eukaryotic genome databases and other eukaryotic genome projects recover a large number of sequences that clearly derive from the GH20 family. Given the low quality of annotation and the widespread occurrence of potentially prokaryotic contaminants in such databases we have omitted such sequences from our phylogentic analyses. However, it is clear that the GH20 family is represented in all but a few major eukaryotic lineages. Taxa where complete or nearly complete genome sequences are available but where we were unable to recover traces of GH20 genes in at least one genome were restricted to divergent protists and unicellular organisms with secondarily reduced genomes: Diplomonads, Euglenozoa, Apicomplexa, and several Fungi (Saccharomyces, Schizosaccharomyces and Microsporidia).

Two acquisitions of GH20 family genes by eukaryotes?

The Eukaryote clade B sequences (Figure 6) while conserved between each other, are characterized by generally high levels of divergence from the "Firmicute" clade in which they are embedded. Sequence similarity searches of the JGI eukaryotic genome databases revealed convincing traces of clade B sequences on the genomes of the cnidarian Nematostella [JGI:82909, JGI:245803], the placozoan Trichoplax [JGI:23741, JGI:2986, JGI:2419, JGI:51551], the mollusk Lottia [JGI:140764, JGI:235755] and the annelid Capitella [JGI:235755]. Unfortunately all associated gene predictions were of rather low quality and either incomplete or including apparently un-detected introns (or highly divergent insertions) and lacking in supporting EST evidence. Accordingly they were not used in phylogenetic analyses. However, the presence of highly conserved potentially coding sequences in these genomes (and the absence of such traces in the genome of the choanoflagellate Monosiga and other protist, fungal and plant genomes) is of some considerable interest. Our data are consistent with the proposition of Gutternigg et al. [53] that eukayotes have obtained GH20 family members from at least two phylogenetically distinct sources. The apparent absence of clade B sequences from non-metazoan genomes suggests a lateral transfer event into a basal metazoan, although an earlier acquisition – and subsequent loss from plant, protist and fungal genomes – can not be excluded. The strong statistical support for the monophyly of the "Firmicute" clade in which these and other more divergent sequences are embedded (Figure 4), our failure to identify acceptable topologies in which Eukaryote clade A and B sequences represent sister groups and the apparent absence of excessively long branches in this clade (not shown) lead us to prefer the hypothesis that these sequences represent a truly monophyletic assemblage rather than a phylogenetic artifact resulting from independent accelerations in evolutionary rates and resulting "long-branch attraction" between unrelated sequences.

Evolution of substrate specificity in Eukaryote GH20 family members

The phylogenetic hypotheses presented here may be used to understand the evolution of GH20 family functionality in eukaryotes. While our phylogenetic reconstructions do not allow reliable rooting of the eukaryote tree or permit us to understand the evolutionary position of the more divergent GH20 isoforms, many clades and relationships are robustly supported. In this light it is informative to map functional data onto the trees. One of the most important differences between vertebrate and insects/worms/plants N-linked glycosylation is the presence of the paucimannosidic N-glycans structures in the second group. For example, the insect fdl genes are closely related to the Hexo1 and Hexo2 genes of insects. The fdl gene products are involved in the formation of paucimannosidic N-glycans [24, 53], while Hexo1 and Hexo2 gene products (as well as fungal GH20 proteins [34]) are believed to function as degradative enzymes (exochitinases) [24]. Plant clade II sequences also have an exochitinase-like function, as recently demonstrated in Arabidopsis thaliana [52]. In this light it can be seen as likely that the ancestral activity for the plant, fungal and insect clade II sequences was likely to be as an exochitinase and that the fdl gene products have undergone a change in substrate specificity towards N-glycans. The animal Clade I sequences have been shown to be involved in the degradation of oligosaccharide chains of glycoproteins and glycolipids [7, 77], although the proteins encoded by the lepidoptera Spodoptera frugiperda genes have been shown to be also responsible for the generation of paucimannosidic N-glycans [16, 78], and might potentially represent a second example of functional shift within insects. Plant clade I sequences have been demonstrated to participate in the biosynthesis of truncated N-linked oligosaccharides and degradation of chitooligosaccharides [52, 53]. Furthermore, the C. elegans hexosaminidase emerging in animal clade I likely has a role as a exochitinase [53] and may represent another example of a functional shift. We note that Drosophila species are not represented in clade I and speculate that their need for N-glycan-metabolizing β-hexosaminidases is fulfilled by the fdl gene product. Moreover, nematode and insect N-glycan hexosaminidases are membrane-bound proteins and are not localized in the lysosomes, while in plants the processing of N-glycans to paucimannosidic saccharides is in the vacuole [24]. An understanding of the functional roles of the Mycetozoan proteins which provide one with best candidates for the most ancient divergence in the eukaryote tree might be the key to understanding the nature of the ancestral enzyme activity. However, functional characterization of the slime mould Dictyostelium GH20 protein has not been published and biochemical data of the β-N-acetylglucosaminidases of Entamoeba histolytica do not allow strong inference as to the substrate specificity of these amoebozoan enzymes [79]. Furthermore, although we have observed high conservation of amino acids involved in substrate binding (see above), a crystal structure of a β-hexosaminidase involved in paucimannosidic N-glycans formation might provide precise information about the characteristics of active sites of β-hexosaminidases that display exochitinase activity. Despite the incompleteness of functional information, the phylogenetic tree presented in Figure 5 suggests that synthesis of paucimanosidic glycans is a derived characteristic that has evolved independently on at least 3 occasions. Finally, Gutternigg et al. [53] showed that two clade B C. elegans gene products [GenBank: AAA96105.3, CAI06053.1] are involved in the metabolism of paucimannosidic N-glycans, while other two nematode β-hexosaminidases have chitoligosaccharidase activity [GenBank: CAO72177.1; CAA22078.2]. The functional roles of the vertebrate sequences that appear to be most closely related to these divergent nematode genes (see above and additional file 3) remain obscure.


Our phylogenetic analyses of GH20 family proteins provides new insights into evolutionary relationships and the history of the protein family and represent the first such detailed study of the GH20 protein family. We show that eukaryote sequences derive from two independent gene acquisitions. The most widely studied group of genes was present in a common ancestor of plants animals and fungi and the ancestral sequence underwent at least one gene duplication event early in eukaryote evolution gaving rise to at least two paralogs that evolved differential functions as degradative enzymes or a processing activity involved in the synthesis of paucimannosidic N-linked oligosaccharides. Despite these ancient roles, members of both subfamilies of eukaryote clade A have undergone apparent functional shifts, typified by the FDL proteins of insects which appear to be derived from exochitinase-like ancestors but which now play a role in the metabolism of paucimannisodic N-glycans. Conversely, the C. elegans sequence represented in Figure 5 is derived from paucimannisodic glycan proccessing enzymes, but functions as an exochitinase [53]. Indeed, the mammalian isoforms also derived from paucimannosidic N-glycans proccessing enzymes, but exhibit specificity towards the more complex oligosaccharides present in mammal cells. It remains unclear whether these differences reflect differential substrate specificities, or are more related to physiological patterns of expression.

Our data lend strong support to the contention of Gutternigg et al. [53] that more divergent GH20 family members from C. elegans and other metazoa are likely to be derived from a separate acquisition from prokaryotes. While the physiological roles of these proteins have not yet been studied experimentally outside of nematodes, it is unlikely that they should be involved in the production of paucimannosidic N-glycans in mammals, and it is thus probable that additional important roles for GH20 members remain to be discovered in animals.


Sequence retrieval

All characterized and complete β-N-acetylhexosaminidases protein sequences belonging to the GH20 family were retrieved from CAZy [2], Pfam [80] and Swiss-Prot [81] databases. In order to retrieve all the other β-N-acetylhexosaminidase sequences available we performed PSI-BLAST searches of the protein database throughout all organisms at NCBI [82] and through translated BLAST searches (tBLASTn) against the full genomic sequences available at the UCSC genome browser [83], using Homo sapiens protein sequences HEXA [GenBank: AAB00965.1] and HEXB [GenBank: AAA52645.1], Arabidopsis thaliana β-N-acetylhexosaminidase-like protein [GenBank: AAM61367.1], Danio rerio Zgc:112084 protein [GenBank: AAH93192.1], Drosophila melanogaster protein sequences HEXO1 [GenBank: AAF47881.1], HEXO2 [GenBank: AAM48390.1] and FDL [GenBank: AAM29423.1], and Streptomyces plicatus β-N-acetylhexosaminidase protein [GenBank: AAC38798.3] as queries, respectively. Only complete and representative protein sequences were employed for subsequent evolutionary study and protein analysis. For proteins with possible splice variants the longest predicted isoforms were used. A total of 223 protein sequences distributed across Eubacteria, archaebacteria and eukaryotes, were selected for the analysis of protein features and phylogenetic study (Table 1 and See additional file 1, 2, 3). In this study, we denote β-N-acetylhexosaminidase proteins as Hex followed by Arabic number when two or more β-N-acetylhexosaminidase proteins have been identified in the same organism and the abbreviation of genus and species name (e.g. Bacteroides fragilis NCTC 9343 β-N-acetylhexosaminidase will be denoted as Hex1_Bfr).

Protein sequence analysis of β-N-acetylhexosaminidases

Beta-N-acetylhexosaminidase sequences were analyzed using SignalP 3.0 [84], with default options to predict signal peptide sequences; SOSUI [85] and HMMTOP [86] with default parameters for the prediction of transmembrane helices; SMART [87] to predict the domain architecture. Conserved motif analysis was performed by MEME program [88] using default settings.

Multiple sequence alignment and phylogenetic analysis

In order to maximize the number of unambiguously aligned sites used for phylogenetic analysis of eukaryote sequences, two separate datasets were prepared. The first set contained only eukaryote sequences which passed tests of compositional homogeneity implemented in TREE-PUZZLE [89] while the second included available prokaryote sequences (several clusters of extremely closely related sequences from taxonomically similar bacteria were excluded to reduce the computational burden of phylogenetic analyses).

In both cases, inferred protein sequences were aligned with the software Muscle [90] and alignments refined manually. Unambiguously aligned regions were identified using the program GBlocks [91]. The resulting datasets contained 233 sequences with 223 amino acid positions (prokaryote and eukaryote dataset) and 76 sequences with 274 amino acid positions (eukaryote-only dataset). The WAG amino acid substitution model [92] with gamma distributed site rates and an invariable site category was used in all phylogenetic analyses as the Prottest software [93] indicated that this model provided the best fit to the data. Phylogenetic trees were estimated within the Bayesian statistical framework using a parallelized version of the program MrBayes v3.1 [94] on a cluster of processors running the linux operating system (2000000 generations with trees sampled every 50 generations). The first 5000 trees generated were excluded as "burnin" for the MCMC chains (likelihood stabilization was determined graphically). The program SEQBOOT from the PHYLIP [95] package was used to generate 100 pseudoreplicate datasets, maximum-likelihood trees were estimated for each replicate using the program PHYML [96] and consensus trees were inferred using the program CONSENSE. Constrained trees were generated manually and evaluated according to the Shimodaira/Hasegawa test of alternative tree topologies [97] as implemented in TREE-PUZZLE.


  1. 1.

    Henrissat B, Davies G: Structural and sequence-based classification of glycoside hydrolases. Curr Opin Struct Biol. 1997, 7: 637-644. 10.1016/S0959-440X(97)80072-3.

    CAS  Article  PubMed  Google Scholar 

  2. 2.

    Coutinho PM, Henrissat B: Carbohydrate-active enzymes: an integrated database approach. Recent Advances in Carbohydrate Bioengineering. Edited by: Gilbert HJ, Davies G, Henrissat B, Svensson B. 1999, Cambridge, The Royal Society of Chemistry, 3-12. []

    Google Scholar 

  3. 3.

    Tews I, Vincentelli R, Vorgias CE: N-Acetylglucosaminidase (chitobiase) from Serratia marcescens: gene sequence, and protein production and purification in Escherichia coli. Gene. 1996, 170: 63-67. 10.1016/0378-1119(95)00848-9.

    CAS  Article  PubMed  Google Scholar 

  4. 4.

    Williams SJ, Mark BL, Vocadlo DJ, James MN, Withers SG: Aspartate 313 in the Streptomyces plicatus hexosaminidase plays a critical role in substrate-assisted catalysis by orienting the 2-acetamido group and stabilizing the transition state. J Biol Chem. 2002, 277: 40055-40065. 10.1074/jbc.M206481200.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Maier T, Strater N, Schuette CG, Klingenstein R, Sandhoff K, Saenger W: The X-ray crystal structure of human beta-hexosaminidase B provides new insights into Sandhoff disease. J Mol Biol. 2003, 328: 669-681. 10.1016/S0022-2836(03)00311-5.

    CAS  Article  PubMed  Google Scholar 

  6. 6.

    Mark BL, Mahuran DJ, Cherney MM, Zhao D, Knapp S, James MN: Crystal structure of human beta-hexosaminidase B: understanding the molecular basis of Sandhoff and Tay-Sachs disease. J Mol Biol. 2003, 327: 1093-1109. 10.1016/S0022-2836(03)00216-X.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  7. 7.

    Lemieux MJ, Mark BL, Cherney MM, Withers SG, Mahuran DJ, James MN: Crystallographic structure of human beta-hexosaminidase A: interpretation of Tay-Sachs mutations and loss of GM2 ganglioside hydrolysis. J Mol Biol. 2006, 359: 913-929. 10.1016/j.jmb.2006.04.004.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  8. 8.

    Korneluk RG, Mahuran DJ, Neote K, Klavins MH, O'Dowd BF, Tropak M, Willard HF, Anderson MJ, Lowden JA, Gravel RA: Isolation of cDNA clones coding for the alpha-subunit of human beta-hexosaminidase. Extensive homology between the alpha- and beta-subunits and studies on Tay-Sachs disease. J Biol Chem. 1986, 261: 8407-8413.

    CAS  PubMed  Google Scholar 

  9. 9.

    Proia RL: Gene encoding the human beta-hexosaminidase beta chain: extensive homology of intron placement in the alpha- and beta-chain genes. Proc Natl Acad Sci USA. 1988, 85: 1883-1887. 10.1073/pnas.85.6.1883.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  10. 10.

    Gravel RA, Triggs-Raine BL, Mahuran DJ: Biochemistry and genetics of Tay-Sachs disease. Can J Neurol Sci. 1991, 18: 419-423.

    CAS  PubMed  Google Scholar 

  11. 11.

    Mahuran DJ: Biochemical consequences of mutations causing the GM2 gangliosidoses. Biochim Biophys Acta. 1999, 1455: 105-38.

    CAS  Article  PubMed  Google Scholar 

  12. 12.

    Wielgat P, Walczuk U, Szajda S, Bien M, Zimnoch L, Mariak Z, Zwierz K: Activity of lysosomal exoglycosidases in human gliomas. J Neurooncol. 2006, 80: 243-249. 10.1007/s11060-006-9188-z.

    CAS  Article  PubMed  Google Scholar 

  13. 13.

    Zitta K, Wertheimer EV, Miranda PV: Sperm N-acetylglucosaminidase is involved in primary binding to the zona pellucida. Mol Hum Reprod. 2006, 12: 557-563. 10.1093/molehr/gal059.

    CAS  Article  PubMed  Google Scholar 

  14. 14.

    Martinez SL, Menendez Helman RJ, Zitta KS, Brandelli A, Miranda PV: Characterization of human sperm N-acetylglucosaminidase. Int J Androl. 2008, 31: 315-324. 10.1111/j.1365-2605.2007.00766.x.

    CAS  Article  Google Scholar 

  15. 15.

    Zen KC, Choi HK, Krishnamachary N, Muthukrishnan S, Kramer KJ: Cloning, expression, and hormonal regulation of an insect beta-N-acetylglucosaminidase gene. Insect Biochem Mol Biol. 1996, 26: 435-444. 10.1016/0965-1748(95)00111-5.

    CAS  Article  PubMed  Google Scholar 

  16. 16.

    Tomiya N, Narang S, Park J, Abdul-Rahman B, Choi O, Singh S, Hiratake J, Sakata K, Betenbaugh MJ, Palter KB, Lee YC: Purification, characterization, and cloning of a Spodoptera frugiperda Sf9 beta-N-acetylhexosaminidase that hydrolyzes terminal N-acetylglucosamine on the N-glycan core. J Biol Chem. 2006, 81: 19545-19560. 10.1074/jbc.M603312200.

    Article  Google Scholar 

  17. 17.

    Nagamatsu Y, Yanagisawa I, Kimoto M, Okamoto E, Koga D: Purification of a chitooligosaccharidolytic beta-N-acetylglucosaminidase from Bombyx mori larvae during metamorphosis and the nucleotide sequence of its cDNA. Biosci Biotechnol Biochem. 1995, 59: 219-225.

    CAS  Article  PubMed  Google Scholar 

  18. 18.

    van Die I, van Tetering A, Bakker H, Eijnden van den DH, Joziasse DH: Glycosylation in lepidopteran insect cells: identification of a beta 1-->4-N-acetylgalactosaminyltransferase involved in the synthesis of complex-type oligosaccharide chains. Glycobiology. 1996, 6: 157-64. 10.1093/glycob/6.2.157.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Sommer U, Spindler KD: Physical properties of beta-N-acetyl-D-glucosaminidase and beta-N-acetyl-D-hexosaminidase from Drosophila Kc-cells. Arch Insect Biochem Physiol. 1991, 18: 45-53. 10.1002/arch.940180105.

    CAS  Article  PubMed  Google Scholar 

  20. 20.

    Cattaneo F, Pasini ME, Intra J, Matsumoto M, Briani F, Hoshi M, Perotti ME: Identification and expression analysis of Drosophila melanogaster genes encoding beta-hexosaminidases of the sperm plasma membrane. Glycobiology. 2006, 16: 786-800. 10.1093/glycob/cwl007.

    CAS  Article  PubMed  Google Scholar 

  21. 21.

    Filho BP, Lemos FJ, Secundino NF, Páscoa V, Pereira ST, Pimenta PF: Presence of chitinase and beta-N-acetylglucosaminidase in the Aedes aegypti: a chitinolytic system involving peritrophic matrix formation and degradation. Insect Biochem Mol Biol. 2002, 32: 1723-1729. 10.1016/S0965-1748(02)00112-1.

    CAS  Article  PubMed  Google Scholar 

  22. 22.

    Hogenkamp DG, Arakane Y, Kramer KJ, Muthukrishnan S, Beeman RW: Characterization and expression of the β-N-acetylhexosaminidase gene family of Tribolium castaneum. Insect Biochem Mol Biol. 2008, 38: 478-489. 10.1016/j.ibmb.2007.08.002.

    CAS  Article  PubMed  Google Scholar 

  23. 23.

    Altmann F, Schwihla H, Staudacher E, Glossl J, Marz L: Insect cells contain an unusual, membrane-bound beta-N-acetylglucosaminidase probably involved in the processing of protein N-glycans. J Biol Chem. 1995, 270: 17344-17349. 10.1074/jbc.270.29.17344.

    CAS  Article  PubMed  Google Scholar 

  24. 24.

    Leonard R, Rendic D, Rabouille C, Wilson IB, Preat T, Altmann F: The Drosophila fused lobes gene encodes an N-acetylglucosaminidase involved in N-glycan processing. J Biol Chem. 2006, 281: 4867-4875. 10.1074/jbc.M511023200.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Fukamizo T, Kramer KJ, Mueller DD, Schaefer J, Garbow J, Jacob GS: Analysis of chitin structure by nuclear magnetic resonance spectroscopy and chitinolytic enzyme digestion. Arch Biochem Biophys. 1986, 249: 15-26. 10.1016/0003-9861(86)90555-2.

    CAS  Article  PubMed  Google Scholar 

  26. 26.

    Zen KC, Choi HK, Krishnamachary N, Muthukrishnan S, Kramer KJ: Cloning, expression, and hormonal regulation of an insect beta-N-acetylglucosaminidase gene. Insect Biochem Mol Biol. 1996, 26: 435-444. 10.1016/0965-1748(95)00111-5.

    CAS  Article  PubMed  Google Scholar 

  27. 27.

    Dowd PF, Johnson ET, Pinkerton TS: Oral toxicity of beta-N-acetyl hexosaminidase to insects. J Agric Food Chem. 2007, 55: 3421-3428. 10.1021/jf063562w.

    CAS  Article  PubMed  Google Scholar 

  28. 28.

    Cattaneo F, Ogiso M, Hoshi M, Perotti ME, Pasini ME: Purification and characterization of the plasma membrane glycosidases of Drosophila melanogaster spermatozoa. Insect Biochem Mol Biol. 2002, 32: 929-941. 10.1016/S0965-1748(02)00031-0.

    CAS  Article  PubMed  Google Scholar 

  29. 29.

    Peters G, Saborowski R, Mentlein R, Buchholz F: Isoforms of an N-acetyl-beta-D-glucosaminidase from the Antarctic krill, Euphausia superba: purification and antibody production. Comp Biochem Physiol B Biochem Mol Biol. 1998, 120: 743-751. 10.1016/S0305-0491(98)10073-1.

    CAS  Article  PubMed  Google Scholar 

  30. 30.

    Zhang JP, Chen QX, Wang Q, Xie JJ: Purification and some properties of beta-N-acetyl-D-glucosaminidase from viscera of green crab (Scylla serrata). Biochemistry (Mosc). 2006, 71 (Suppl 1): S55-59.

    CAS  Article  Google Scholar 

  31. 31.

    Koyanagi R, Honegger TG: Molecular cloning and sequence analysis of an ascidian egg beta-N-acetylhexosaminidase with a potential role in fertilization. Dev Growth Differ. 2003, 45: 209-218. 10.1046/j.1524-4725.2003.689.x.

    CAS  Article  PubMed  Google Scholar 

  32. 32.

    Riekenberg S, Flockenhaus B, Vahrmann A, Muller MC, Leippe M, Kiess M, Scholze H: The beta-N-acetylhexosaminidase of Entamoeba histolytica is composed of two homologous chains and has been localized to cytoplasmic granules. Mol Biochem Parasitol. 2004, 138: 217-225. 10.1016/j.molbiopara.2004.09.003.

    CAS  Article  PubMed  Google Scholar 

  33. 33.

    Bulawa CE: Genetics and molecular biology of chitin synthesis in fungi. Annu Rev Microbiol. 1993, 47: 505-534. 10.1146/annurev.mi.47.100193.002445.

    CAS  Article  PubMed  Google Scholar 

  34. 34.

    Ettrich R, Kopecký V, Hofbauerová K, Baumruk V, Novák P, Pompach P, Man P, Plíhal O, Kutý M, Kulik N, Sklenár J, Ryslavá H, Kren V, Bezouska K: Structure of the dimeric N-glycosylated form of fungal beta-N-acetylhexosaminidase revealed by computer modeling, vibrational spectroscopy, and biochemical studies. BMC Struct Biol. 2007, 7: 32-10.1186/1472-6807-7-32.

    PubMed Central  Article  PubMed  Google Scholar 

  35. 35.

    Tsujibo H, Miyamoto K, Yoshimura M, Takata M, Miyamoto J, Inamori Y: Molecular cloning of the gene encoding a novel beta-N-acetylhexosaminidase from a marine bacterium, Alteromonas sp. strain O-7, and characterization of the cloned enzyme. Biosci Biotechnol Biochem. 2002, 66: 471-475. 10.1271/bbb.66.471.

    CAS  Article  PubMed  Google Scholar 

  36. 36.

    Ueda M, Fujita Y, Kawaguchi T, Arai M: Cloning, nucleotide sequence and expression of the beta-N-acetylglucosaminidase gene from Aeromonas sp. no. 10S-24. J Biosci Bioeng. 2000, 89: 164-169. 10.1016/S1389-1723(00)88731-9.

    CAS  Article  PubMed  Google Scholar 

  37. 37.

    Soto-Gil RW, Zyskind JW: N,N'-diacetylchitobiase of Vibrio harveyi. Primary structure, processing, and evolutionary relationships. J Biol Chem. 1989, 264: 14778-14783.

    CAS  PubMed  Google Scholar 

  38. 38.

    Somerville CC, Colwell RR: Sequence analysis of the beta-N-acetylhexosaminidase gene of Vibrio vulnificus: evidence for a common evolutionary origin of hexosaminidases. Proc Natl Acad Sci USA. 1993, 90: 6751-6755. 10.1073/pnas.90.14.6751.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  39. 39.

    Matsuo Y, Kurita M, Park JK, Tanaka K, Nakagawa T, Kawamukai M, Matsuda H: Purification, characterization and gene analysis of N-acetylglucosaminidase from Enterobacter sp. G-1. Biosci Biotechnol Biochem. 1999, 63: 1261-1268. 10.1271/bbb.63.1261.

    CAS  Article  PubMed  Google Scholar 

  40. 40.

    Mayer C, Vocadlo DJ, Mah M, Rupitz K, Stoll D, Warren RA, Withers SG: Characterization of a beta-N-acetylhexosaminidase and a beta-N-acetylglucosaminidase/beta-glucosidase from Cellulomonas fimi. FEBS J. 2006, 273: 2929-2941. 10.1111/j.1742-4658.2006.05308.x.

    CAS  Article  PubMed  Google Scholar 

  41. 41.

    Lisboa De Marco J, Valadares-Inglis MC, Felix CR: Purification and characterization of an N-acetylglucosaminidase produced by a Trichoderma harzianum strain which controls Crinipellis perniciosa. Appl Microbiol Biotechnol. 2004, 64: 70-75. 10.1007/s00253-003-1490-5.

    CAS  Article  PubMed  Google Scholar 

  42. 42.

    Brunner K, Peterbauer CK, Mach RL, Lorito M, Zeilinger S, Kubicek CP: The Nag1 N-acetylglucosaminidase of Trichoderma atroviride is essential for chitinase induction by chitin and of major relevance to biocontrol. Curr Genet. 2003, 43: 289-295. 10.1007/s00294-003-0399-y.

    CAS  Article  PubMed  Google Scholar 

  43. 43.

    Matsuo I, Kim S, Yamamoto Y, Ajisaka K, Maruyama JI, Nakajima H, Kitamoto K: Cloning and overexpression of beta-N-acetylglucosaminidase encoding gene nagA from Aspergillus oryzae and enzyme-catalyzed synthesis of human milk oligosaccharide. Biosci Biotechnol Biochem. 2003, 67: 646-650. 10.1271/bbb.67.646.

    CAS  Article  PubMed  Google Scholar 

  44. 44.

    Kim S, Matsuo I, Ajisaka K, Nakajima H, Kitamoto K: Cloning and characterization of the nagA gene that encodes beta-N-acetylglucosaminidase from Aspergillus nidulans and its expression in Aspergillus oryzae. Biosci Biotechnol Biochem. 2002, 66: 2168-2175. 10.1271/bbb.66.2168.

    CAS  Article  PubMed  Google Scholar 

  45. 45.

    Cannon RD, Niimi K, Jenkinson HF, Shepherd MG: Molecular cloning and expression of the Candida albicans beta-N-acetylglucosaminidase (HEX1) gene. J Bacteriol. 1994, 176: 2640-2647.

    PubMed Central  CAS  PubMed  Google Scholar 

  46. 46.

    Horsch M, Mayer C, Sennhauser U, Rast DM: Beta-N-acetylhexosaminidase: a target for the design of antifungal agents. Pharmacol Ther. 1997, 76: 187-218. 10.1016/S0163-7258(97)00110-1.

    CAS  Article  PubMed  Google Scholar 

  47. 47.

    Cohen E: Chitin synthesis and inhibition: a revisit. Pest Manag Sci. 2001, 57: 946-950. 10.1002/ps.363.

    CAS  Article  PubMed  Google Scholar 

  48. 48.

    Seidl V, Druzhinina IS, Kubicek CP: A screening system for carbon sources enhancing beta-N-acetylglucosaminidase formation in Hypocrea atroviridis (Trichoderma atroviride). Microbiology. 2006, 152: 2003-2012. 10.1099/mic.0.28897-0.

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Barber MS, Ride JP: Purification and Properties of a wheat leaf N-acetyl-β-hexosaminidase. Plant Science. 1989, 60: 163-172. 10.1016/0168-9452(89)90162-3.

    CAS  Article  Google Scholar 

  50. 50.

    Oikawa A, Itoh E, Ishihara A, Iwamura H: Purification and characterization of beta-N-acetylhexosaminidase from maize seedlings. J Plant Physiol. 2003, 160: 991-999. 10.1078/0176-1617-01089.

    CAS  Article  PubMed  Google Scholar 

  51. 51.

    Harris N, Chrispeels M: Histochemical and Biochemical Observations on Storage Protein Metabolism and Protein Body Autolysis in Cotyledons of Germinating Mung Beans. Plant Physiol. 1975, 56: 292-299.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  52. 52.

    Strasser R, Bondili JS, Schoberer J, Svoboda B, Liebminger E, Glossl J, Altmann F, Steinkellner H, Mach L: Enzymatic Properties and Subcellular Localization of Arabidopsis beta-N-acetylhexosaminidases. Plant Physiol. 2007, 145: 5-16. 10.1104/pp.107.101162.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  53. 53.

    Gutternigg M, Kretschmer-Lubich D, Paschinger K, Rendic D, Hader J, Geier P, Ranftl R, Jantsch V, Lochnit G, Wilson IB: Biosynthesis of truncated N-linked oligosaccharides results from non-orthologous hexosaminidase-mediated mechanisms in nematodes, plants and insects. J Biol Chem. 2007, 282: 27825-27840. 10.1074/jbc.M704235200.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  54. 54.

    Goi G, Fabi A, Lombardo A, Bairati C, Bovati L, Burlina AB, Agosti S, Serio C, Tettamanti G: The lysosomal beta-D-N-acetylglucosaminidase isozymes in human plasma during pregnancy: separation and quantification by a simple automated procedure. Clin Chim Acta. 1989, 179: 327-340. 10.1016/0009-8981(89)90096-X.

    CAS  Article  PubMed  Google Scholar 

  55. 55.

    Beccari T, Mancuso F, Costanzi E, Tassi C, Barone R, Fiumara A, Orlacchio A, Aisa MC, Orlacchio A: Beta-hexosaminidase, alpha-D-mannosidase, and beta-mannosidase expression in serum from patients with carbohydrate-deficient glycoprotein syndrome type I. Clin Chim Acta. 2000, 302: 125-132. 10.1016/S0009-8981(00)00360-0.

    CAS  Article  PubMed  Google Scholar 

  56. 56.

    Tulsiani DR: Glycan modifying enzymes in luminal fluid of rat epididymis: are they involved in altering sperm surface glycoproteins during maturation?. Microsc Res Tech. 2003, 61: 18-27. 10.1002/jemt.10313.

    CAS  Article  PubMed  Google Scholar 

  57. 57.

    Andersson SV, Edman MC, Bekmezian A, Holmberg J, Mircheff AK, Peter Gierow J: Characterization of beta-hexosaminidase secretion in rabbit lacrimal gland. Exp Eye Res. 2006, 83: 1081-1088. 10.1016/j.exer.2006.05.013.

    CAS  Article  PubMed  Google Scholar 

  58. 58.

    Balducci C, Pierguidi L, Persichetti E, Parnetti L, Sbaragli M, Tassi C, Orlacchio A, Calabresi P, Beccari T, Rossi A: Lysosomal hydrolases in cerebrospinal fluid from subjects with Parkinson's disease. Mov Disord. 2007, 22: 1481-1484. 10.1002/mds.21399.

    Article  PubMed  Google Scholar 

  59. 59.

    Kimura S: Insect haemolymph exo-beta-N-acetylglucosaminidase from Bombyx mori. Purification and properties. Biochim Biophys Acta. 1976, 446: 399-406.

    CAS  Article  PubMed  Google Scholar 

  60. 60.

    Marchini D, Bertini LF, Dallai R: B-N-acetylhexosaminidases in the secretion of the female reproductive accessory glands of Ceratitis capitata (Diptera). Insect Biochem. 1989, 19: 549-555. 10.1016/0020-1790(89)90020-6.

    CAS  Article  Google Scholar 

  61. 61.

    Del Pino FA, Brandelli A, Termignoni C, Gonzales JC, Henriques JA, Dewes H: Purification and characterization of beta-N-acetylhexosaminidase from bovine tick Boophilus microplus (Ixodide) larvae. Comp Biochem Physiol B Biochem Mol Biol. 1999, 123: 193-200. 10.1016/S0305-0491(99)00057-7.

    CAS  Article  PubMed  Google Scholar 

  62. 62.

    Mahuran D, Novak A, Lowden JA: The lysosomal hexosaminidase isozymes. Isozymes Curr Top Biol Med Res. 1985, 12: 229-288.

    CAS  PubMed  Google Scholar 

  63. 63.

    Journet A, Chapel A, Kieffer S, Roux F, Garin J: Proteomic analysis of human lysosomes: application to monocytic and breast cancer cells. Proteomics. 2002, 2: 1026-1040. 10.1002/1615-9861(200208)2:8<1026::AID-PROT1026>3.0.CO;2-I.

    CAS  Article  PubMed  Google Scholar 

  64. 64.

    Martinez ML, Martelotto L, Cabada MO: Purification and biological characterization of N-acetyl beta-D glucosaminidase from Bufo arenarum spermatozoa. Mol Reprod Dev. 2000, 57: 194-203. 10.1002/1098-2795(200010)57:2<194::AID-MRD11>3.0.CO;2-0.

    CAS  Article  PubMed  Google Scholar 

  65. 65.

    Mencarelli S, Cavalieri C, Magini A, Tancini B, Basso L, Lemansky P, Hasilik A, Li YT, Chigorno V, Orlacchio A, Emiliani C, Sonnino S: Identification of plasma membrane associated mature beta-hexosaminidase A, active towards GM2 ganglioside, in human fibroblasts. FEBS Lett. 2005, 579: 5501-5506. 10.1016/j.febslet.2005.08.081.

    CAS  Article  PubMed  Google Scholar 

  66. 66.

    Massaccesi L, Lombardo A, Venerando B, Tettamanti G, Goi G: Isoenzyme pattern and partial characterization of hexosaminidases in the membrane and cytosol of human erythrocytes. Clin Biochem. 2007, 40: 467-477. 10.1016/j.clinbiochem.2006.12.004.

    CAS  Article  PubMed  Google Scholar 

  67. 67.

    Gibson KR, Vanek PG, Kaloss WD, Collier GB, Connaughton JF, Angelichio M, Livi GP, Fleming PJ: Expression of dopamine beta-hydroxylase in Drosophila Schneider 2 cells. Evidence for a mechanism of membrane binding other than uncleaved signal peptide. J Biol Chem. 1993, 268: 9490-9495.

    CAS  PubMed  Google Scholar 

  68. 68.

    Fleisher B: CD26: a surface protease involved in T-cell activation. Immunol Today. 1984, 15: 180-183. 10.1016/0167-5699(94)90316-6.

    Article  Google Scholar 

  69. 69.

    Olivari S, Galli C, Alanen H, Ruddock L, Molinari M: A novel stress-induced EDEM variant regulating endoplasmic reticulum-associated glycoprotein degradation. J Biol Chem. 2005, 280: 2424-2428. 10.1074/jbc.C400534200.

    CAS  Article  PubMed  Google Scholar 

  70. 70.

    Intra J, Cenni F, Perotti ME: An alpha-L-fucosidase potentially involved in fertilization is present on Drosophila spermatozoa surface. Mol Reprod Dev. 2006, 73: 1149-1158. 10.1002/mrd.20425.

    CAS  Article  PubMed  Google Scholar 

  71. 71.

    Attwood TK, Bradley P, Flower DR, Gaulton A, Maudling N, Mitchell A, Moulton G, Nordle A, Paine K, Taylor P, Uddin A, Zygouri C: PRINTS and its automatic supplement, prePRINTS. Nucleic Acids Research. 2003, 31: 400-402. 10.1093/nar/gkg030. []

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  72. 72.

    Schuette CG, Weisgerber J, Sandhoff K: Complete analysis of the glycosylation and disulfide bond pattern of human beta-hexosaminidase B by MALDI-MS. Glycobiology. 2001, 11: 549-556. 10.1093/glycob/11.7.549.

    CAS  Article  PubMed  Google Scholar 

  73. 73.

    Kuroki Y, Itoh K, Nadaoka Y, Tanaka T, Sakuraba H: A novel missense mutation (C522Y) is present in the beta-hexosaminidase beta-subunit gene of a Japanese patient with infantile Sandhoff disease. Biochem Biophys Res Commun. 1995, 212: 564-571. 10.1006/bbrc.1995.2007.

    CAS  Article  PubMed  Google Scholar 

  74. 74.

    Pavesi G, Zambelli F, Caggese C, Pesole G: Exalign: a new method for comparative analysis of exon-intron gene structures. Nucleic Acids Res. 2008, 36 (8): e47-10.1093/nar/gkn153.

    PubMed Central  Article  PubMed  Google Scholar 

  75. 75.

    Carlton JM, Hirt RP, Silva JC, Delcher AL, Schatz M, Zhao Q, Wortman JR, Bidwell SL, Alsmark UC, Besteiro S, Sicheritz-Ponten T, Noel CJ, Dacks JB, Foster PG, Simillion C, Peer Van de Y, Miranda-Saavedra D, Barton GJ, Westrop GD, Müller S, Dessi D, Fiori PL, Ren Q, Paulsen I, Zhang H, Bastida-Corcuera FD, Simoes-Barbosa A, Brown MT, Hayes RD, Mukherjee M, Okumura CY, Schneider R, Smith AJ, Vanacova S, Villalvazo M, Haas BJ, Pertea M, Feldblyum TV, Utterback TR, Shu CL, Osoegawa K, de Jong PJ, Hrdy I, Horvathova L, Zubacova Z, Dolezal P, Malik SB, Logsdon JM, Henze K, Gupta A, Wang CC, Dunne RL, Upcroft JA, Upcroft P, White O, Salzberg SL, Tang P, Chiu CH, Lee YS, Embley TM, Coombs GH, Mottram JC, Tachezy J, Fraser-Liggett CM, Johnson PJ: Draft genome sequence of the sexually transmitted pathogen Trichomonas vaginalis. Science. 2007, 315 (5809): 207-12. 10.1126/science.1132894.

    PubMed Central  Article  PubMed  Google Scholar 

  76. 76.

    Baldauf SL: The deep roots of eukaryotes. Science. 2003, 300: 1703-1706. 10.1126/science.1085544.

    CAS  Article  PubMed  Google Scholar 

  77. 77.

    Aronson NN, Kuranda MJ: Lysosomal degradation of Asn-linked glycoproteins. FASEB J. 1989, 3 (14): 2615-2222.

    CAS  PubMed  Google Scholar 

  78. 78.

    Aumiller JJ, Hollister JR, Jarvis DL: Molecular cloning and functional characterization of beta-N-acetylglucosaminidase genes from Sf9 cells. Protein Expr Purif. 2006, 47 (2): 571-590. 10.1016/j.pep.2005.11.026.

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  79. 79.

    Werries E, Nebinger P, Franz A: Degradation of biogenic oligosaccharides by beta-N-acetyl-glucosaminidase secreted by Entamoeba histolytica. Mol Biochem Parasitol. 1983, 7 (2): 127-140. 10.1016/0166-6851(83)90040-3.

    CAS  Article  PubMed  Google Scholar 

  80. 80.

    Bateman A, Coin L, Durbin R, Finn RD, Hollich V, Griffiths-Jones S, Khanna A, Marshall M, Moxon S, Sonnhammer EL, Studholme DJ, Yeats C, Eddy SR: The Pfam protein families database. Nucleic Acids Res. 2004, 32: 138-141. 10.1093/nar/gkh121. []

    Article  Google Scholar 

  81. 81.

    Gasteiger E, Gattiker A, Hoogland C, Ivanyi I, Appel RD, Bairoch A: ExPASy: The proteomics server for in-depth protein knowledge and analysis. Nucleic Acids Res. 2003, 31: 3784-3788. 10.1093/nar/gkg563. []

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  82. 82.

    Wheeler DL, Barrett T, Benson DA, Bryant SH, Canese K, Chetvernin V, Church DM, DiCuccio M, Edgar R, Federhen S, Geer LY, Kapustin Y, Khovayko O, Landsman D, Lipman DJ, Madden TL, Maglott DR, Ostell J, Miller V, Pruitt KD, Schuler GD, Sequeira E, Sherry ST, Sirotkin K, Souvorov A, Starchenko G, Tatusov RL, Tatusova TA, Wagner L, Yaschenko E: Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. 2007, 35: 5-12. 10.1093/nar/gkl1031. []

    Article  Google Scholar 

  83. 83.

    Karolchik D, Baertsch R, Diekhans M, Furey TS, Hinrichs A, Lu YT, Roskin KM, Schwartz M, Sugnet CW, Thomas DJ, Weber RJ, Haussler D, Kent WJ: The UCSC Genome Browser Database. Nucleic Acids Res. 2003, 31: 51-54. 10.1093/nar/gkg129. []

    PubMed Central  CAS  Article  PubMed  Google Scholar 

  84. 84.

    Bendtsen JD, Nielsen H, von Heijne G, Brunak S: Improved prediction of signal peptides: SignalP 3.0. J Mol Biol. 2004, 340: 783-795. 10.1016/j.jmb.2004.05.028. []

    Article  PubMed  Google Scholar 

  85. 85.

    Hirokawa T, Boon-Chieng S, Mitaku S: SOSUI: classification and secondary structure prediction system for membrane proteins. Bioinformatics. 1998, 14: 378-379. 10.1093/bioinformatics/14.4.378. []

    CAS  Article  PubMed  Google Scholar 

  86. 86.

    Tusnady GE, Simon I: The HMMTOP transmembrane topology prediction server. Bioinformatics. 2001, 17: 849-850. 10.1093/bioinformatics/17.9.849. []

    CAS  Article  PubMed  Google Scholar 

  87. 87.

    Letunic I, Copley RR, Pils B, Pinkert S, Schultz J, Bork P: SMART 5: domains in the context of genomes and networks. Nucleic Acids Res. 2006, 34: 257-260. 10.1093/nar/gkj079. []

    Article  Google Scholar 

  88. 88.

    Grundy WN, Bailey TL, Elkan CP, Baker ME: Meta-MEME: motif-based hidden Markov models of protein families. Comput Appl Biosci. 1997, 13: 397-406. []

    CAS  PubMed  Google Scholar 

  89. 89.

    Schmidt HA, Strimmer K, Vingron M, von Haeseler A: TREE-PUZZLE: maximum likelihood phylogenetic analysis using quartets and parallel computing. Bioinformatics. 2002, 18: 502-504. 10.1093/bioinformatics/18.3.502.

    CAS  Article  PubMed  Google Scholar 

  90. 90.

    Edgar RC: MUSCLE: a multiple sequence alignment method with reduced time and space complexity. BMC Bioinformatics. 2004, 5: 113-10.1186/1471-2105-5-113.

    PubMed Central  Article  PubMed  Google Scholar 

  91. 91.

    Castresana J: Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis. Mol Biol Evol. 2000, 17: 540-552.

    CAS  Article  PubMed  Google Scholar 

  92. 92.

    Whelan S, Goldman N: A general empirical model of protein evolution derived from multiple protein families using a maximum-likelihood approach. Mol Biol Evol. 2001, 18: 691-699.

    CAS  Article  PubMed  Google Scholar 

  93. 93.

    Abascal F, Zardoya R, Posada D: ProtTest: selection of best-fit models of protein evolution. Bioinformatics. 2005, 21: 2104-2105. 10.1093/bioinformatics/bti263.

    CAS  Article  PubMed  Google Scholar 

  94. 94.

    Ronquist F, Huelsenbeck JP: MrBayes 3: Bayesian phylogenetic inference under mixed models. Bioinformatics. 2003, 19: 1572-1574. 10.1093/bioinformatics/btg180.

    CAS  Article  PubMed  Google Scholar 

  95. 95.

    Felsenstein J: PHYLIP (Phylogeny Inference Package) version 3.6. Distributed by the author. Department of Genome Sciences, University of Washington, Seattle. 2005

    Google Scholar 

  96. 96.

    Guindon S, Gascuel O: A simple, fast and accurate algorithm to estimate large phylogenies by maximum likelihood. Syst Biol. 2003, 52: 696-704. 10.1080/10635150390235520.

    Article  PubMed  Google Scholar 

  97. 97.

    Shimodaira H, Hasegawa M: Multiple comparisons of log-likelihoods with applications to phylogenetic inference. Mol Biol Evol. 1999, 16: 1114-1116.

    CAS  Article  Google Scholar 

Download references


This work was supported by PRIN grants from MIUR to D. Horner and G. Pavesi.

Author information



Corresponding author

Correspondence to Jari Intra.

Additional information

Authors' contributions

JI performed database searches, conducted data analysis, sequence alignment and drafted the manuscript. GP participated in data analysis and manuscript revision. DSH conducted comparative genome analysis and evolution, sequence alignment, phylogenetic analysis and drafted the manuscript. All authors read and approved the final manuscript.

Electronic supplementary material


Additional file 1: Eukaryotic GH20 protein sequences. All eukaryotic protein sequences of GH20 collected and used in this work. (TXT 43 KB)


Additional file 2: Prokaryotic GH20 protein sequences. All prokaryotic protein sequences of GH20 collected and used in this work. (TXT 88 KB)


Additional file 3: Divergent Eukaryotic GH20 protein sequences. Divergent eukaryotic protein sequences of GH20 collected and used in this work. (TXT 16 KB)


Additional file 4: Gene structure of metazoan β-hexosaminidases. Lengths of exons and introns of representative metazoan β-hexosaminidases. (DOC 119 KB)


Additional file 5: Alternative Hypotheses of relationships between major eukaryote GH20 clades. Schematic trees representing alternative hypotheses of relationships between major clades of eukaryotic GH20 family members. Hypotheses of relationships not excluded at the 5% confidence interval by the Shimodaira/Hasegawa test are depicted along with their log likelihoods, delta lnL and P-values. All analyses were performed with the WAG amino acid substitution model and 1 invariable and 4 gamma distributed site rate categories. (PDF 66 KB)

Authors’ original submitted files for images

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and Permissions

About this article

Cite this article

Intra, J., Pavesi, G. & Horner, D.S. Phylogenetic analyses suggest multiple changes of substrate specificity within the Glycosyl hydrolase 20 family. BMC Evol Biol 8, 214 (2008).

Download citation


  • Glycosyl Hydrolase
  • Gene Duplication Event
  • GH20 Family
  • Horizontal Gene Transfer Event
  • Intron Phase