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Since chitin is a highly abundant natural biopolymer, many attempts have been made to convert this insoluble polysaccharide into commercially valuable products using chitinases and β-N-acetylglucosaminidases (GlcNAcases). We have previously reported the structure and function of chitinase A from Vibrio harveyi 650. This study t reports the identification of two GlcNAcases from the same organism and their detailed functional characterization.
The genes encoding two new members of family-20 GlcNAcases were isolated from the genome of V. harveyi 650, cloned and expressed at a high level in E. coli. VhNag1 has a molecular mass of 89 kDa and an optimum pH of 7.5, whereas VhNag2 has a molecular mass of 73 kDa and an optimum pH of 7.0. The recombinant GlcNAcases were found to hydrolyze all the natural substrates, VhNag2 being ten-fold more active than VhNag1. Product analysis by TLC and quantitative HPLC suggested that VhNag2 degraded chitooligosaccharides in a sequential manner, its highest activity being with chitotetraose. Kinetic modeling of the enzymic reaction revealed that binding at subsites (-2) and (+4) had unfavorable (positive) binding free energy changes and that the binding pocket of VhNag2 contains four GlcNAc binding subsites, designated (-1),(+1),(+2), and (+3).
Two novel GlcNAcases were identified as exolytic enzymes that degraded chitin oligosaccharides, releasing GlcNAc as the end product. In living cells, these intracellular enzymes may work after endolytic chitinases to complete chitin degradation. The availability of the two GlcNAcases, together with the previously-reported chitinase A from the same organism, suggests that a systematic development of the chitin-degrading enzymes may provide a valuable tool in commercial chitin bioconversion.
Chitin is a β-1,4-linked homopolymer of N-acetylglucosamine (GlcNAc), which is found mainly in the exoskeleton of crustaceans, insects and in the cell walls of fungi. Chitin is one of the most abundant polymers in nature and its degradation derivatives are pharmaceutically valuable. for example, chitoligosaccharides can stimulate the immune system to respond to microbial infections and chitin monomers have been shown to act as anti-aging and anti-tumor agents, as well as to relieve the symptoms of osteoarthritis [1-6]. Complete degradation of chitin requires chitinases (EC 188.8.131.52) and β-N-acetylglucosaminidases (GlcNAcases) or chitobiases (EC 184.108.40.206), so such enzymes could potentially serve as biocatalysts in the production of chitin derivatives of desired sizes during the recycling of chitin biomass.
As well as functioning in chitin degradation by bacteria, GlcNAcases are also known to be key enzymes in the catabolism of glycoconjugates containing N-acetylglucosamine residues [7,8] and mutations of the gene encoding a human GlcNAcase homologue (HexA) cause a fatal genetic lipid storage disorder, known as Tay-Sachs disease . In the CAZy database (http://www.cazy.org), GlcNAcases are classified into glycosyl hydrolases family 3 (GH-3) or family 20 (GH-20), which differ in sequence and mode of enzyme action [10,11]. Family-3 GlcNAcases are thought to act by a standard retaining mechanism involving a covalent glycosyl-enzyme intermediate while family-20 enzymes employ a 'substrate-assisted' mechanism involving the transient formation of an oxazolinium ion intermediate [12-15]. Most of the GlcNAcases described hitherto belong to the GH-20 family. To date, only five bacterial GH-3 GlcNAcases have been characterized, including NagZ or ExoII from Vibrio furnissii , Nag3A from Clostridium paraputrificum M-2 , NagA from Streptomyces thermoviolaceus , and NagA and CbsA from Thermotoga maritima and T. neapolitana .
Vibrio harveyi, formerly known as V. carchariae, is a Gram-negative marine bacterium that causes luminous Vibriosis, a serious disease that affects commercially farmed fish and shellfish species [20,21]. We previously reported isolation of the gene encoding endochitinase A from Vibrio harveyi type strain 650 for functional and structural characterization [22,23]. In this study, we employed a homology-based strategy to isolate two GlcNAcase genes from the genome of the same Vibrio strain. Sequence analysis suggested that the resultant polypeptides were new members of the GH-20 family. Enzymic properties of the GlcNAcases expressed in E. coli were investigated. Their kinetic properties and identification of the subsites in the more active enzyme are discussed in further detail.
The availability of the complete genome sequence allowed us to locate three open reading frames (ORFs), including VIBHAR_03430 (Swiss-Prot: A7MYY8), VIBHAR_06345 (Swiss-Prot: A7N8P3) and, VIBHAR_01265 (Swiss-Prot: A7N1G4) in the genome of V. harveyi type strain ATCC BAA-1116 BB120. These reading frames encode uncharacterized proteins with presumed GlcNAcase activity. In an attempt to isolate the genes that encode GlcNAcases in a closely-related organism, three sets of oligonucleotides were designed based on the above-mentioned ORFs. Two homologous DNAs were amplified by the oligonucleotides designed from the VIBHAR_03430 and VIBHAR_01265 ORFs, whereas the DNA fragment compatible with the VIBHAR_06345 ORF could not be amplified successfully. Hence, the first two DNA fragments (hereafter referred to as VhNag1 and VhNag2) were further cloned and expressed for functional characterization. Nucleotide sequence analysis showed that the VhNag1 full-length DNA contains 2,343 bp which encode a polypeptide of 88,849 Da, whereas the VhNag2 full-length DNA contains 1,926 bp, encoding a polypeptide of 73,143 Da. The pI values of VhNag1 and VhNag2 were calculated to be 4.9 and 5.4, respectively. The nucleotide and corresponding amino acid sequences of the newly-identified GlcNACases have been deposited in the GenBank/EMBL/DDBJ database with assigned accession numbers of HM175715 for VhNag1 and HM175716 for VhNag2. Although a BLAST search indicated high sequence similarity of VhNag1 and VhNag2 to GlcNAcases from other Vibrio species, most of these sequences turned out to be only hypothetical proteins with predicted GlcNAcase activity. Low sequence similarity with all GH-3 members (< 12%) suggested that neither of these enzymes belong to GH-3, but matches of up to 30% with previously studied GH-20 enzymes indicated that they are new GH-20 members. A sequence comparison with eleven functionally-characterized GH-20 enzymes (data not shown) shows that both VhNag sequences are closest to the α-chain of human GlcNAcase (HuHexA, 30% similarity) , followed by Serratia marcescens chitobiase (SmChb, 24%) . Fig. Fig.11 shows a sequence alignment of VhNag1 and VhNag2 with three selected GlcNAcases, including VhChb  (the only characterized GlcNAcase from V. harveyi), HuHexA and SmChb (which have the highest sequence similarities to the VhNag sequences). Since the structural details of SmChb are well studied, further sequence comparisons were with SmChb. As seen in Fig. Fig.1,1, a number of consensus residues are identified, a few of which may participate in the catalytic function of the Vibrio GlcNAcases. The most obvious of these are the acidic pairs Asp287-Glu288 (in VhNag1) or Asp437-Glu438 (in VhNag2) (Fig. (Fig.1,1, red asterisks) as they are completely aligned with Asp539-Glu540 of SmChb. These two residues were previously shown to be crucial for the catalytic function of SmChb, Glu540 acting as the catalytic residue [13,25]. Other residues found to be involved in binding the substrate in the enzyme-substrate complex of SmChb-diNAG include Asp346, Arg349, Asp378, Asp379, Trp616, Trp685, and Trp737. These residues are completely conserved among the GlcNAcase species (Fig. (Fig.1,1, blue dots).
The full-length VhNAg1 and VhNag2 DNAs were subsequently cloned into the pQE60 expression vector, which provides high-level expression in E. coli M15 of C-terminally (His)6-tagged polypeptides. The overall yields of the purified recombinant proteins obtained after Ni-NTA affinity chromatography were 5 - 10 mg/ml of bacterial culture. Fig. Fig.2A2A shows SDS-PAGE analysis, displaying a single band of VhNag1 migrating to slightly below the 96 kDa marker and VhNag2 closer 66 kDa. The molecular masses estimated from their mobilities are consistent with the theoretical masses of the enzymes (88,849 Da for VhNag1 and 73,143 Da for VhNag2). In peptide mass fingerprinting, 9 and 13 VhNag1 peptides unambiguously matched internal peptides of GlcNAcases from V. angustum and Photobacterium sp, respectively. For VhNag2, 20 and 21 peptides were identical with the internal peptides of V. parahaemolyticus and V. alginolyticus GlcNAcases (see additional file 1, Table S1). This peptide mass identification strongly indicates that the proteins expressed in E. coli are GlcNAcases.
Both of the purified GlcNAcases were active against pNP-GlcNAc, but VhNag2 was found to be much more active than VhNag1. We suspect that the full-length VhNag1 is expressed as a pro-enzyme, which requires proteolytic processing to attain its full activity. The hydrolysis of pNP-GlcNAc by VhNag1 and VhNag2 was determined as a function of time (additional file 2, Fig. S1). VhNag2 activity was significantly greater than that of VhNag1 over the entire course of reaction. In the reaction progress curves, the activity of both enzymes was constant for up to 15 min, and then began to decrease at longer incubation times. Therefore, the reaction time was set to 10 min to ensure that initial velocities were measured in subsequent kinetic experiments.
The effect of pH on GlcNAcase activity was examined with pNP-GlcNAc as substrate. The pH activity profiles of VhNag1 and VhNag2 were typical bell-shaped curves as seen for most glycosyl hydrolases. Fig. Fig.2B2B shows enzymic activity decreasing at low and high pH values. The maximal activity of VhNag1 was at pH 7.5 and of VhNag2 at pH 7.0. When specific hydrolytic activity was determined with various substrates (Fig. (Fig.3),3), pNP-GlcNAc was found to be the most effective. While VhNag2 could hydrolyze all the three pNP-glycosides (although pNP-GlcNAc2 and pNP-Glucose were respectively hydrolyzed 300-fold and 700-fold less efficiently than pNP-GlcNAc), VhNag1 was only active with pNP-GlcNAc. Both enzymes could hydrolyze chitooligosaccharides (GlcNAc2-6) and colloidal chitin with VhNag2 being at least ten-times more active than VhNag1. Of the natural glycosides, chitotetraose was the best substrate and chitotriose the second best. In contrast, chitobiose, chitopentaose and chitohexaose were only fair substrates, and insoluble (colloidal) chitin was the poorest of all (Fig. (Fig.33).
The kinetic parameters of the hydrolytic activity of the two GlcNAcases were further assessed. As shown in Table Table1,1, kcat/Km with pNP-GlcNAc was 11-fold greater for VhNag2 than for VhNag1. It was noted throughout this study that VhNag1 was tended to undergo rapid and progressive loss of GlcNAcase activity. Although several attempts were made to obtain the kinetic values of this higher-Mr enzyme, the data acquired with VhNag1 could not be evaluated precisely, and we decided not to present it in this study. In accordance with our earlier demonstration (see Fig. Fig.3),3), VhNag2 had the lowest Km and highest kcat, yielding overall kcat/Km of 4,935 M-1s-1 towards pNP-GlcNAc. When natural substrates were compared, VhNag2 had the greatest catalytic activity with GlcNAc4 (kcat/Km 304 M-1s-1), followed by GlcNAc3 (228 M-1s-1), GlcNAc5 (181 M-1s-1), GlcNAc6 (166 M-1s-1), and GlcNAc2 (56 M-1s-1). Overall, kcat/Km of VhNag2 with pNP-GlcNAc is 88-fold greater than with GlcNAc2 (the poorest glycoside substrate) and 16-fold greater than with GlcNAc4 (the best glycoside substrate). In general, the glycosidic bond of pNP-GlcNAc is more easily cleaved than that of GlcNAc-GlcNAc, because of the higher electron-withdrawing capacity of p-nitrophenyl moiety. However, the rate of hydrolysis of p-nitrophenyl glycoside depends on the affinity to the enzyme used. For example, Keyhani & Roseman  showed that Vibrio furnssii β-GlcNAcidase (exoI) hydrolyzed pNP-GlcNAc about 5-fold faster than GlcNAc2, but 1.4 fold slower than GlcNAc3-6, whereas Kubota et al.  reported that Streptomyces thermoviolacacus NagC could hydrolyze pNP-GlcNAc and GlcNAc2 at equal rates. On the other hand, its activity with the pNP substrate was between 2- to 3.5-fold greater than with GlcNAc3-5.
Degradation patterns of chitooligosaccharides by VhNag2 were analyzed by TLC (Fig. (Fig.4).4). The most significant result obtained from TLC analysis is that VhNag2 acted exolytically, yielding GlcNAc as the end product from all chitin oligomers. Additionally, GlcNAc3 and GlcNAc4 were degraded rapidly and almost completely within 10 min (Fig. (Fig.4B4B and and4C),4C), whilst the reaction of GlcNAc5 was not complete until 1 h of incubation (Fig. (Fig.4D).4D). The degradation of GlcNAc2 (Fig. (Fig.4A)4A) and GlcNAc6 (Fig. (Fig.4E)4E) was even slower, complete hydrolysis of these two substrates being attained only after 2 h of incubation.
The time course of chitin oligosaccharide hydrolysis by VhNag2 was further investigated by quantitative HPLC. Fig. Fig.5A5A shows GlcNAc2 hydrolysis, showing a rapid increase of the resultant product (GlcNAc) with increasing reaction time. Fig. Fig.5B5B and Fig. Fig.5C5C show GlcNAc3 and GlcNAc4 hydrolysis. In agreement with the TLC results, GlcNAc3 and GlcNAc4 were consumed more rapidly than GlcNAc2 (Fig. (Fig.5A),5A), GlcNAc5 (Fig. (Fig.5D)5D) and GlcNAc6 (Fig. (Fig.5E).5E). At the end of recording (180 min), no substrate was left from the digestion of GlcNAc3 and GlcNAc4, whereas substantial amounts of the other substrates remained. All substrates were hydrolyzed exolytically, so that GlcNAcn was degraded to GlcNAcn-1 + GlcNAc. The intermediate products, such as GlcNAcn-1 and GlcNAcn-2, were further degraded to the final product GlcNAc. Fig. Fig.5F5F shows the overall rates of hydrolysis to be in the order: GlcNAc4 GlcNAc3 > GlcNAc5 > GlcNAc6 > GlcNAc2. The substrate-size dependence of the reaction rate can be confirmed from the reaction time-course of extensive hydrolysis of GlcNAc6 over a longer period of incubation (1,500 min (25 h), the upper right panel of Fig. Fig.6);6); that is, chitin pentamer and dimer accumulated during the course of the reaction, whereas tetramer and trimer were generated only transiently before being hydrolyzed instantaneously by the enzyme. Of the natural glycosides, GlcNAc4 was found to be the best substrate for VhNag2. Similar results were reported for β-GlcNAcidase (exoI) from Vibrio furnssii . This enzyme showed its highest Vmax towards GlcNAc4, while the Vmax values decreased 1.1-fold with GlcNAc3 and 1.4-fold with GlcNAc2. Further sequence analysis suggested no putative signal peptide in the sequences of VhNAg1 and VhNag2. Therefore, the two enzymes are suggested to be non-secretory proteins that act intracellularly. In bacterial cells, the transport of chitin oligomers into the intracellular compartments for further degradation by these GlcNAcases could be achieved by specific membrane transporters. It has been proposed for V. furnissii that the uptake of short-chain chitooligosaccharides, such as GlcNAc3 and GlcNAc4, takes place through a chitooligosaccharide-specific channel known as chitoporin [29,30].
Kinetic modeling of the enzymic reaction was carried out based on the reaction scheme presented in Fig. Fig.7.7. To model the time-course of GlcNAc6 hydrolysis (shown in the upper panels of Fig. Fig.6),6), numerical calculations were conducted using the differential equation derived from the reaction scheme . At first, the binding free energy changes for the subsites from (-1) to (+4) were estimated roughly by repeating the calculations with various values of the free energy changes. Starting with initial guessed values, optimization of the free energy changes conducted by the modified Powell method  was employed using the cost function,
where e and c represent the experimental and calculated values, respectively, n is the number of GlcNAc units in the oligosaccharides, and i the reaction time.
The final iteration of the calculations yielded the values of the rate constants for glycosidic bond cleavage (k+1) for various chain lengths of GlcNAcn. The kcat values obtained were allocated to k+1 for individual oligosaccharide substrates (Table (Table1).1). The individual k+1 values were fixed in the modeling calculation. Since no evidence for transglycosylation was obtained from HPLC determination of the enzymic products, this process was not considered in the kinetic model. A much higher value of 50 s-1 was tentatively allocated to the rate constant for hydration k+2. Since VhNag2 splits off a monosaccharide from the non-reducing end of the substrate, indicating that subsite (-2) should be the most unfavorable for binding of the GlcNAc residue, we tentatively allocated a high positive value (+7.0 kcal/mol) to the binding free energy change at subsite (-2). Using the fixed values of k+1, k+2, and the binding free energy change of subsite (-2), the values of binding free energies of individual subsites from (-1) to (+4) were optimized on the basis of the experimental time-course (upper panels of Fig. Fig.6).6). As shown in lower panels of Fig. Fig.6,6, the calculated time-courses were satisfactorily fitted to the experimental ones, for both the early stage (left panels) and the later stage (right panels) of the reaction, yielding the binding free energy changes of the individual subsites as listed in Table Table22.
The TLC and kinetic data suggested that the catalytic pocket of VhNag2 probably contains a sequence of four favorable GlcNAc binding subsites, designated (-1)(+1)(+2)(+3). Such an implication is certainly supported by the binding free energy changes obtained by the kinetic modeling. As shown in Table Table2,2, a very high positive value +7.0 kcal/mol for subsite (-2) suggests that there is a large steric hindrance interfering with binding at this subsite. A less positive value of +0.9 kcal/mol of subsite (+4) suggests that the sugar residue binding to this subsite is moderately unfavorable, but still possible. Thus, GlcNAc4 binds to (-1) (+1), (+2), and (+3) more strongly than GlcNAc5 to (-1) (+1), (+2), (+3) and (+4). A low negative free energy change, -0.1 kcal/mol, was estimated for binding at subsite (+3). This is consistent with the fact that the GlcNAc3 binding affinity to the subsites (-1) (+1), and (+2) (Km = 441 μM) is somewhat weaker than that of the GlcNAc4 binding to (-1) (+1), (+2), and (+3) (Km = 329 μM). All of these results clearly indicate that an array of four GlcNAc binding subsites (-1)(+1)(+2)(+3) define the substrate affinity of VhNag2. It appears that the GlcNAcases reported to date possess two major types of substrate specificity. The first type has marked preference towards chitobiose, while the other type favours chitooligomers (GlcNAc3-6) over chitodimer. Examples of the former type are hyperthermophilic kodakaraensis KOD1 GlmATK , SmChb , and S. thermoviolacacus NagC . On the other hand, V. furnissii exoI , human di-N-acetylchitobiase , and VhNag2 (in this report) are among the other type. The active site of the second type of GlcNAcases has been demonstrated to contain three to five GlcNAc binding subsites, depending on the substrate specificity of individual enzymes. Multiple sugar-binding-site architecture is not uncommon, as has been demonstrated for other exo-glycosidases such as Aspergillus niger cellobiase , a GH-3 enzyme that degrades cellobioase and cello-oligosaccharides into glucose units. The catalytic center of this enzyme has been reported to contain up to five binding subsites. Also, structural studies of the active site of Bacillus halodurans C-125 REX , a GH-8 exo-oligoxylanase that hydrolyzes xylooligosaccharides to xylose from the reducing end, revealed three substrate binding subsites.
This study reports the isolation, cloning and recombinant expression of the genes encoding two intracellular GH-20 GlcNAcases from a marine bacterium, Vibrio harveyi type strain 650. Data obtained from TLC and quantitative HPLC suggested that the active GlcNAcase homolog (VhNag2) was an exolytic enzyme that degraded chitin oliogmers, releasing GlcNAc as the end product. Kinetic modeling suggested that the active site of VhNag2 comprises four GlcNAc binding subsites, (-1), (+1), (+2), (+3). Such subsite identification is strongly supported by kinetic data, which showed chitin tetramer as the most effective substrate for this enzyme.
V. harveyi type strain 650 was a marine isolate from Greek sea bass and was a gift from Professor Brian Austin, Heriot-Watt University, Edinburgh, United Kingdom. E. coli strain DH5α was used for routine cloning and plasmid preparations. pGEM®-T easy vector used for subcloning purpose was a product of Promega (Promega Pte Ltd, Singapore Science Park I, Singapore). The pQE 60 expression vector and E. coli type strain M15 (Qiagen, Valencia, CA, USA) were used for cloning and a high-level expression of recombinant GlcNAcases.
Three sets of oligonucleotide primers were designed based on the three putative GlcNAce genes, designated VIBHAR_01265, VIBHAR_03430, VIBHAR_06345) from V. harveyi type strain ATCC BAA-1116 in the CAZy database. However, only two PCR products, namely VhNag1 and VhNag2, were successfully amplified from the genomic DNA of V. harveyi type strain 650. The oligonucleotides used for amplification of VhNag1 DNA are 5'-AGGATCCGGGCAGGGTAAAATC-3' for the forward primer and 5'-AGGAGATCTATCGGTTAAAGTGTGAAG-3' for the reverse primer. For VhNag2 DNA, 5'-AGGGATCCGAATACCGTGTTGATTTA-3' was used as the forward primer and 5'-AATAGATCTCTTCCACGGTTTACGGTA-3' for the reverse primer. The PCR products of expected sizes (2.3 kbp for VhNag1 and 1.9 kbp for VhNag2) were cloned in the pQE60 expression vector using BamH I and Bgl II cloning sites (sequences underlined) following the protocol supplied by the manufacturer.
The nucleotide sequences of VhNAg1 and VhNag2 were determined by automated double stranded DNA sequencing (Bio Service Unit, Thailand Science Park, Bangkok, Thailand). Ambiguous nucleotides were re-confirmed twice before submission to the Genbank database. The amino acid sequence alignment was constructed using ''CLUSTALW'' algorithm commercially available in Lasergene v.7 (DNASTAR, Inc., WI, USA) and displayed using the Genedoc program (http://www.psc.edu/biomed/genedoc/). The putative sequences of VhNag1 and VhNag2 were aligned with the previously published V. harveyi chitobiase  together with four bacterial and two human GlcNAcases of known structures.
The full-length VhNag1 and VhNag2 DNAs were cloned into pQE60 expression vector and expressed in E. coli M15 host as the C-terminally (His)6-tagged polypeptides. The cells were grown at 37°C in Luria Bertani (LB) medium containing 100 μg/ml ampicillin until the OD600 of the cell culture reached 0.6. Expression was induced by the addition of isopropyl thio-β-D-galactoside (IPTG) to a final concentration of 0.5 mM. After 18 h of induction at 20°C, the cell pellet was collected by centrifugation, re-suspended in lysis buffer (20 mM Tris-HCl buffer, pH 8.0, containing 150 mM NaCl, 1 mM phenylmethylsulphonyl fluoride (PMSF), and 1.0 μg/ml lysozyme), and then lysed on ice using a Sonopuls Ultrasonichomogenizer with a 6-mm-diameter probe (50% duty cycle; amplitude setting, 20%; total time, 30 s, 6-8 times). Unbroken cells were removed by centrifugation at 12,000 × g, 20 min at 4οC. The supernatant was immediately applied to a Ni-NTA agarose affinity column (1 × 10 cm) (QIAGEN GmbH, Hilden, Germany), and the chromatography was carried out under gravity at 4°C. The column was washed thoroughly with 5 mM imidazole, followed by 20 mM imidazole in equilibration buffer (20 mM Tris-HCl buffer, pH 8.0), and then 250 mM imidazole in the same buffer. Three eluted fractions (10 ml each) were collected and analyzed by 12% SDS-PAGE  to confirm purity. GlcNAcase fractions were pooled and then subjected to several rounds of membrane centrifugation using Vivaspin-20 ultrafiltration membrane concentrators (Mr 10,000 cut-off, Vivascience AG, Hannover, Germany) for complete removal of imidazole. The final concentration of the protein was determined by Bradford's method .
The purified VhNag1 and VhNag2 (2 μg) were applied in parallel onto a 12% SDS-PAGE gel, and stained with Coomassie blue R-250 after electrophoresis. After destaining, protein bands were subjected to in-gel digestion with trypsin (sequencing grade, Promega) using a standard protocol . The resultant peptides were analyzed by high resolution nanoESI/FTMS by the mass spectrometry facility located at the Max-Planck Institute for Molecular Physiology, Dortmund. Data bank searching was performed with ''Mascot search'' (http://www.matrixscience.com/) for peptide mass fingerprinting.
GlcNAcase activity was determined spectrophotometrically using pNP-GlcNAc (Sigma-Aldrich Pte Ltd., The Capricorn, Singapore Science Park II, Singapore) as substrate or by a reducing sugar assay using GlcNAc2-6 (AMS Biotechnology (Europe) Ltd, Oxfordshire, UK) and colloidal chitin as substrates. For the pNP assay, a 100-μl assay mixture contained the protein sample (50 μg), 125 μM pNP-GlcNAc), and 0.065 M phosphate buffer, pH 7.0 The enzymic reaction was continued for 10 min at 37°C before being terminated by the addition of 100 μl 3 M Na2CO3. The amount of p-nitrophenol (pNP) released was determined spectrophotometrically at 405 nm in a microtiter plate reader (Applied Biosystems, Foster City, CA, USA). Molar concentrations of pNP were calculated from a calibration curve constructed with 0-20 nmol pNP. For the reducing sugar assay, the reaction mixture (100 μl) contained 250 μM GlcNAc2-6 in 0.1 M phosphate buffer, pH 7.0 and 200 μg enzyme or 500 μM pNP-glycoside in 0.1 M phosphate buffer, pH 7.0 and 100 μg enzyme. The reaction mixture was incubated at 37°C for 15 min in a Thermomixer comfort (Eppendorf AG, Hamburg, Germany), then heated at 100°C for 10 min. The entire reaction mixture was subjected to 3,5-dinitrosalicylic acid (DNS) assay following the protocol described by Miller . Release of the reducing sugars was detected spectrophotometrically at 540 nm and molar concentrations of the released sugars were estimated using a standard calibration curve of GlcNAc (0-500 nmol). For colloidal chitin, the reaction mixture (200 μl), containing 5% (w/v) colloidal chitin (prepared according to Hsu and Lockwood, 1975 ), 0.1 M phosphate buffer, pH 7.0, and 200 μg enzyme, was incubated at 37°C for 15 min. After centrifugation at 12,000 × g for 1 min to precipitate the remaining chitin, the product concentration in the supernatant (100 μl) was determined by DNS method as described for GlcNAc2-6.
A discontinuous assay was used to determine the pH profiles of VhNag1 and VhNag2. The reaction mixtures containing 500 μM pNP-GlcNAc were pre-incubated at 37°C for 5 min at different pH values ranging from 2.5 to 9.0 using the McIlvaine's sodium phosphate-citric acid - KCl buffer system , followed by addition of 1 μg VhNag1 or 0.5 μg VhNag2. After 10 min of incubation, the reactions were terminated with 100 μl of 3 M Na2CO3. The amounts of pNP released were estimated as described for the pNP assay.
Hydrolysis of chitooligosaccharides (GlcNAc2-6) by VhNag2 was carried out in a 20-μl reaction mixture, containing 0.1 M phosphate buffer, pH 7.0, 2.5 mM substrate and 5 μg purified enzyme. The reaction mixture was incubated at 30°C for 1, 5, 10, 15, 30 min, 3 h or 18 h, and the reaction terminated by boiling for 5 min. For product analysis, five 1-μl aliquots of each reaction mixture were applied to a silica TLC plate (7 × 10 cm), and then chromatographed three times (1 h each) in a mobile phase containing n-butanol:methanol:28% ammonia solution:H2O (10:8:4:2) (v/v), followed by spraying with aniline-diphenylamine reagent and baking at 180°C for 3 min. To determine the time course of chitin hydrolysis, the reaction was carried out in a 150-μl reaction mixture, containing 0.1 M phosphate buffer, pH 7.0, 20 mg colloidal chitin, and 50 μg purified enzyme. Subsequent reactions and determination of the reaction products were analyzed by TLC as described for chitooligosaccharide hydrolysis.
A reaction mixture (100 μl) containing 1.25 mM chitin oligosaccharide (GlcNAc2-6), 38 μM VhNag2 and 0.2 M sodium phosphate buffer, pH 7.0 was incubated at 30°C. An aliquot of 12 μl was transferred to a new microfuge tube containing 12 μl 0.1 M NaOH after 5, 10, 15, 30, 60, 120 and 180 min, and the enzymic reaction was stopped by snap-freezing in liquid N2 and the mixture immediately stored at -20°C. To quantitatively determine the time-course of substrate degradation and product formation, 15-μl of the reaction mixture was applied to a gel-filtration column of TSK-GEL G2000PW (7.5 × 600 mm, Tosoh) connected with a Hitachi L-7000 HPLC system (Hitachi Koki Co., Ltd, Tokyo). Elution was conducted with distilled water at a flow rate of 0.3 ml/min, and the substrate and products were monitored by their absorption at 220 nm. Based on the peak areas obtained from the elution profiles, oligosaccharide concentrations were calculated using a standard curve obtained with authentic saccharide solutions, and then plotted against the reaction time to obtain the reaction time-course.
Kinetic parameters were determined using pNP-GlcNAc and chitooligosaccharides (GlcNAc2-6) by the reducing sugar assay as described above, with 0-500 μM of each substrate in the reaction mixture. The amounts of the reaction products were determined from a standard curve of GlcNAc (0-1.75 μmol). Kinetic parameter values were evaluated from three independent sets of data using the nonlinear regression function obtained from the GraphPad Prism v.5.0 (GraphPad Software Inc., San Diego, CA).
Kinetic modeling of the reaction time-course obtained by HPLC was carried out using the reaction model reported for the Coccidioides immitis family 18 chitinase . The model scheme is shown in Fig. Fig.7.7. Considering that the enzyme hydrolyzes the oligosaccharide substrate exolytically from the non-reducing end, VhNag2 was assumed to have a (-2)(-1)(+1)(+2)(+3)(+4)-type binding cleft, where subsite (-2) should have an unfavorable (positive) binding free energy change. By assuming rapid binding equilibrium, the concentrations of the ES-complexes formed through the individual binding modes (Cn,i, Bi,j, and Ai) were calculated from the binding constants, which were obtained from the binding free energy values of individual subsites occupied with the sugar residues assuming additivity. Details of the calculation method were described by Honda and Fukamizo .
GlcNAcn or NAG: β1-4 linked oligomers of N-acetylglucosamine residues where n = 1-6; GlcNAcase: β -N-acetyl-glucosaminidase; DNS: 3,5-dinitrosalicylic acid; pNP-GlcNAc: p-nitrophenyl-β-D-N-acetylglucosaminide; IPTG: isopropyl thio-β-D-galactoside; ORFs: open reading frames; PMSF: phenylmethylsulphonylfluoride; TLC: Thin Layer Chromatography.
WS initiated the research, was responsible for the theme setting, primer design and site-directed mutagenesis. She also carried out HPLC experiments, performed analysis and interpretation of the kinetic, TLC and HPLC data, and also prepared and finalized the manuscript. DC carried out genomic DNA isolation, cloning, recombinant expression, protein purification, TLC and kinetic experiments. MM performed the calculation of the rate constants and binding free energy changes. TF provided guidance on quantitative HPLC, theoretical analysis and deduction of the reaction scheme. He also edited and proofread the manuscript. All authors read and approved the final manuscript.
Table S1 Identification of V. harveyi GlcNAcases by mass spectrometry. Tryptic peptides of VhNag1 and VhNAg2 were resolved and detected by nano-HPLC/ESI-FTMS. Mascot search subsequently identified the resultant peptides of β-N-acetyl glucosaminidases from the NCBINr database.
Fig. S1 The reaction progress curve of VhNag1 and VhNag2 using pNP-GlCNAc as substrate. The reaction mixtures (200 μl) containing 250 μM pNP-GlcNAc, 10 μg VhNag1 or 5 μg VhNag2, and 0.1 M sodium phosphate buffer, pH 7.0 were incubated at 37°C for 5, 10, 15, 30, 45, 60 and 180 min. After the specified time the reaction was terminated by the addition of 100 μl 3 M Na2CO3. The release of pNP was determined as described in the main text.
This work was financially supported by Suranaree University of Technology (Grant no SUT1-102-52-24-08). We are grateful to P. Janning and A. Brockmeyer, Max Planck Institute of Molecular Physiology, Dortmund, for nano-HPLC/ESI-FTMS measurements and associated data interpretation.