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Article

Characterization of the Specific Mode of Action of a Chitin Deacetylase and Separation of the Partially Acetylated Chitosan Oligosaccharides

by
Xian-Yu Zhu
1,2,
Yong Zhao
1,
Huai-Dong Zhang
1,3,
Wen-Xia Wang
1,
Hai-Hua Cong
2 and
Heng Yin
1,*
1
Liaoning Provincial Key Laboratory of Carbohydrates, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China
2
College of Food Science and Engineering, Dalian Ocean University, Dalian 116023, China
3
Engineering Research Center of Industrial Microbiology, Ministry of Education; College of Life Sciences, Fujian Normal University, Fuzhou 350117, China
*
Author to whom correspondence should be addressed.
Mar. Drugs 2019, 17(2), 74; https://doi.org/10.3390/md17020074
Submission received: 19 December 2018 / Revised: 15 January 2019 / Accepted: 16 January 2019 / Published: 22 January 2019
(This article belongs to the Special Issue Marine Enzymes: Sources, Biochemistry and Bioprocesses for Marine Biotechnology)
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Versions Notes

Abstract

:
Partially acetylated chitosan oligosaccharides (COS), which consists of N-acetylglucosamine (GlcNAc) and glucosamine (GlcN) residues, is a structurally complex biopolymer with a variety of biological activities. Therefore, it is challenging to elucidate acetylation patterns and the molecular structure-function relationship of COS. Herein, the detailed deacetylation pattern of chitin deacetylase from Saccharomyces cerevisiae, ScCDA2, was studied. Which solves the randomization of acetylation patterns during COS produced by chemical. ScCDA2 also exhibits about 8% and 20% deacetylation activity on crystalline chitin and colloid chitin, respectively. Besides, a method for separating and detecting partially acetylated chitosan oligosaccharides by high performance liquid chromatography and electrospray ionization mass spectrometry (HPLC-ESI-MS) system has been developed, which is fast and convenient, and can be monitored online. Mass spectrometry sequencing revealed that ScCDA2 produced COS with specific acetylation patterns of DAAA, ADAA, AADA, DDAA, DADA, ADDA and DDDA, respectively. ScCDA2 does not deacetylate the GlcNAc unit that is closest to the reducing end of the oligomer furthermore ScCDA2 has a multiple-attack deacetylation mechanism on chitin oligosaccharides. This specific mode of action significantly enriches the existing limited library of chitin deacetylase deacetylation patterns. This fully defined COS may be used in the study of COS structure and function.

1. Introduction

Chitin, which consists of β-1,4-linked N-acetyl-d-glucosamine residues, is the main component of crustacean shells, such as shrimp, crab and shellfish [1,2]. Chitin, a renewable raw material whose annual production is about 1011 tons, is the second most abundant natural biopolymer after cellulose [3,4]. As a new type of functional material, chitin has attracted wide attention in various fields [5]. However, it is insoluble in water and most organic solvents, this property severely restricts its development and application [3]. On the other hand, chitosan, the deacetylation product of chitin, is soluble in dilute acid solution and has been widely used in agriculture, biomedicine, environmental science and other fields, as a plant inducer, biodegradable hydrogel and sewage treatment agent in antitumor drugs and in other green products [2,6,7,8,9,10]. Chitooligosaccharide (COS), the hydrolytic product of chitosan, has broader biological activities, such as immunological, antitumor, antioxidant and antibacterial activity [11,12,13]. Due to its water-soluble ability and broad biological activity, COS has attracted more attention than chitosan. The biological activity of COS are believed to be strongly dependent on the degree of polymerization (DP), the degree of acetylation (DA) and the pattern of acetylation (PA) [14]. Vander et al. reported that COS with different degrees of deacetylation is involved in the induction of phenylalanine ammonia lyase and peroxidase activities, both of which must be activated for lignin biosynthesis [15]. It has previously been observed that the specific recognition of the N-acetyl moiety allows AtCERKl to distinguish chitin and chitosan, which then activate plant immune receptors and elicit a plant immune response [16].
In order to investigate the specific biological activity of COS in a particular acetylation pattern, COS with a completely known structure is required. However, chitosan and COS produced by chemical methods usually exhibit a randomized pattern of acetylation, making them difficult to control and predict their biological activity [17]. Moreover, chitosan produced by chemical methods requires high energy consumption and causes environmental pollution [1]. In contrast, chitin deacetylase (CDA, E.C. 3.5.1.41) is able to hydrolyse the N-acetamido groups of N-acetyl-d-glucosamine residues in chitin, chitin oligosaccharides, chitosan and chitosan oligosaccharides under mild conditions by a specific mode of action. Previous studies have identified CDAs from bacteria, fungi and insects, such as Bacillus thuringiensis [18], Bacillus amyloliquefaciens [19], Colletotrichum gloeosporioides [20] Mucor rouxii [21] Aspergillus nidulans [22] Saccharomyces cerevisiae [23] Bombyx mori [24], Drosophila melanogaster [25], Encephalitozoon cuniculi [26], Mamestra configurata [27]. Although some CDAs have been reported, the deacetylation patterns of deacetylases are poorly understood. CDA from different sources can modify their substrates in different ways: Some being specific for a single position [28], others show showing multiple-attack [29,30]. In addition, COS with specific deacetylation patterns can be produced by enzymatic deacetylation of chitin oligomers, but the diversity is limited by the available CDA.
Two genes encoding chitin deacetylases (CDA1 and CDA2) have been identified in Saccharomyces cerevisiae in previous reports. And these genes have been proved to be involved in the formation of the ascospores wall of Saccharomyces cerevisiae [31]. However, it is very interesting that the deletion of each gene will result in activity decrease of CDA, and the functions of the two genes cannot be replaced by each other [31]. Therefore, the deacetylation mechanisms of these two different chitin deacetylases may be different. However, detailed deacetylation mechanisms of chitin deacetylase from Saccharomyces cerevisiae have not been reported so far.
In this study, the chitin deacetylase (CDA2) from Saccharomyces cerevisiae (ScCDA2) with a specific mode of action has been characterized and a fast, convenient and online monitoring method has been developed that can be used to separate and detect partially acetylated chitosan oligosaccharides. Mass spectrometry sequencing showed that ScCDA2 can hydrolyze N-acetamido groups rather than the reducing ends of chitin oligosaccharides, producing fully defined chitosan oligosaccharides by a multiple attack mode of action. Furthermore, ScCDA2 is able to remove about 8% and 20% of the acetyl groups from crystalline chitin and colloidal chitin.

2. Results and Discussion

2.1. Bioinformatic Analysis and Expression of ScCDA2

CDA belongs to the carbohydrate esterase family 4 (CE4) according to the classification of the CAZY database (www.cazy.org) [32]. The presence of divalent metal ions, such as Zn2+, Ca2+ and Co2+, have been proved to increase the catalytic activity and stability of the CDAs [30]. The Colletotrichum lindemuthianum’s CDA crystal structure indicates that there is a zinc-binding triad (His-His-Asp) around Zn2+ [33].
The sequence of ScCDA2 aligned with deacetylase sequences from marine Arthrobacter (ArCE4A, 34%) [34], Streptomyces lividans (SlCE4, 33%) [35] and Streptococcus pneumoniae (SpPgdA, 29%) [36] (Figure 1) [37]. The structure-based sequence alignments of ArCE4A, SlCE4 and SpPgdA showed different levels of sequence identities according to their source from different genera and enabled identification the key residues that may contribute to catalysis function, including active site residues (Asp102, His250) and zinc-binding residues (Asp103, His149, His153) (Figure 1). Asp103, His149 and His153 form a zinc-binding triplet (His-His-Asp) around Zn2+, which is similar to chitin deacetylase from Colletotrichum lindemuthianum [33], although the CDA sequence from C. lindemuthianum only has a 30% similarity to ScCDA2. The full-length open reading frame encoding the N-acetylglucosamine deacetylase sequence from Saccharomyces cerevisiae was successfully cloned and transformed into Pichia pastoris X-33 for highly efficient secretion expression (Figure 2). The molecular weight of ScCDA2, which was digested by N-glycosidase F (PNGase F), decreased by about 10 kDa. PNGase F is an amidase working by cleaving between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides from N-linked glycoproteins and glycopeptides. This results in a deaminated protein or peptide and a free glycan [38,39]. Therefore, there are N-glycosylation post-translational modifications in ScCDA2. Glycosylation is one of the most common post-translational modifications of proteins in fungi. It plays an important role in protein activity, thermal stability, proteolytic resistance, folding and secretion [40]. Mass spectrometry showed that ScCDA2 have N-glycosylation post-translational modification at positions Asn 181, Asn 199 and Asn 203 (Figure S5).

2.2. Homology Modeling and Substrate Binding Specificity of ScCDA2

The crystal structures of several CDAs have already been determined, while CDA/substrate complex structure determination is less well defined and the interaction between the enzyme and the substrate is poorly understood. To study the characteristics of ScCDA2 and chitin molecule interactions, we performed molecular docking to understand the binding mechanism of ScCDA2. Homology modelling of ScCDA2 (Figure 3A) revealed that the secondary structure consists of a conserved (α/β)8 folded barrel structure and six loops. The model was further evaluated for protein geometry by SAVES. Evaluation report shows that 97.3% residues in additional allowed regions and 85.57% of the residues have averaged 3D-1D score ≥0.2, and the quality factor is 91.2214, indicating that the structure quality was acceptable (Figure S1). The docking results (Figure 3B) show that chitin lies in the substrate-binding pocket which is surrounded by six loops, His250, Asp102, Asp103, His149 and His153. Asp103, His149 and His153 form a coordinate bond with Zn2+, and the metal ion serves as a Lewis acid to assist the water affinity attack on the carbon atom on the amide bond. The adjacent His250 and Asp102 play a catalytic role through protonation, and the common action of these amino acids leads to the cleaving of the acetyl group. In addition, the structural superposition of ArCE4A (PDB ID: 5LFZ), SLCE4 (PDB ID: 2CC0), SpPgdA (PDB ID: 2C1G) and model of ScCDA2 reveal that there are six conserved loop domains in ScCDA2 (Figure 3C).

2.3. Biochemical Characterization of ScCDA2

The investigation of substrate specificity could provide important information for the potential applications of deacetylase. Using a coupled enzyme assay measure the amount of acetate released has been reported to be successfully applied to quantitatively determine the deacetylation activity of a recombinant chitin deacetylase [14]. When determining activity and substrate specific, interestedly, ScCDA2 was observed that it is able to remove about 8% and 20% of the acetyl groups from crystalline chitin, alpha-chitin and beta-chitin (Figure 4). In addition, An (A = GlcNAc; n = 1, 2, 3, 4, 5 or 6) as substrates also have been measured (Figure S3). To promote the application of ScCDA2 in industry, more detailed physical and chemical properties characterization of CDA is essential. The optimal PH and metal ions of ScCDA2 are pH = 8.0 and 50 °C when A4 was used as a substrate (Figure S4). When Co2+ is present, ScCDA2 exhibits the maximum activity on A4. Despite the existence of a conserved zinc-binding triad in the ScCDA2, biochemical data (Figure S4C) and structure-based on sequence alignments (Figure 1) indicate that ScCDA2 as a metal-dependent metalloenzyme with a Co2+ dependence greater than Zn2+. The peptidoglycan deacetylase from Streptococcus pneumoniae also shows that the peptidoglycan deacetylase is more metal-dependent on Co2+ than Zn2+. Besides, the reported structures of two distinct acetylxylan esterases of CE4 from Streptomyces lividans and Clostridium thermocellum, in native and complex forms, show that the enzymes are sugar-specific and metal ion-dependent and possess a single metal (Zn2+) center however with a chemical preference for Co2+ [35].
Most of the reported CDAs show only minimal activity or no activity on chitin in vitro. For example, CDA from Cyclobacterium marinum has been reported to be able to convert acetylglucosamine to glucosamine only with the cooperation of chitinase [17]. However, ScCDA2 can release up to 20.33% of acetyl groups from colloid chitin, as well as 9.16% and 7.29% of acetyl groups from insoluble alpha-chitin and Betabeta-chitin (Figure 4). Previous reported CDAs have no activity or low activity on insoluble chitin, which may be due to poor accessibility of chitin substrates [41]. However, the charge distribution on the surface of ScCDA2 indicates that ScCDA2 has an excessive negative charge in the region that interacts with the longer substrate, which may lead to enhanced substrate accessibility of ScCDA2 to chitin (Figure S2).

2.4. Isolation and Identification of Partially Acetylated Chitooligosaccharides

Due to its special biological activity, partially acetylated chitosan oligosaccharides have attracted wide interest, and these potential activities are significantly correlated with the degree of polymerization and degree of acetylation of chitooligosaccharides [14,42]. However, the method of preparing and isolating high-purity chitooligosaccharides is time consuming and labor intensive, which severely limits the large-scale production of partially acetylated chitooligosaccharides [43]. Much research into the separation of chitosan oligosaccharides has so far limited to the separation and identification of chitosan oligosaccharides of different degrees of polymerization [44,45,46]. As far as we know, the method for isolation and identification of partially acetylated chitosan oligosaccharides with a degree of polymerization of four has not been reported.
We have separated and identified the partially acetylated chitosan oligosaccharides with a degree of polymerization of 4. Chitin oligomers were deacetylated with recombinant ScCDA2 to form partially acetylated chitosan oligosaccharides. Three different partially acetylated chitosan oligosaccharides (A1D3, A2D2, A1D3) were obtained. These partially acetylated chitosan oligosaccharides were separated and detected by HPLC-ESI-MS (Figure 5).

2.5. Partially Acetylated Chitooligosaccharides Production Processes

Exploring the partially acetylated chitooligosaccharides production process (simultaneously or in some order) is important to aid in understanding the action mode of CDA deacetylation. Therefore, the effects of enzyme concentration on the production process of partially acetylated COS have also been determined. As is shown in Figure 6, partially acetylated chitosan oligosaccharides (A1D3, A2D2, A1D3) are gradually produced according to the degree of deacetylation. With the amount of enzymes in the system increases, the types of enzyme reaction products gradually increase. From almost no product generation, to the production of the A3D1 and A2D2, the final substrate is completely consumed at the same time producing A1D3.

2.6. Specific Mode of Action of ScCDA2 on A4

The partially acetylated chitooligosaccharide derivatized with a reducing amine showed molecular weights of 1005.96 Da (A3D1), 963.82 Da (A2D2) and 921.80 Da (A1D3) in MALDI-TOF mass spectrometry (Figure 7).
Then, by applying MALDI-TOF-MS analysis in MS2 mode, we were able to identify and analyze ScCDA2’s partially acetylated products and determine specific acetylation pattern of partially acetylated chitooligosaccharides. As is shown in Figure 8, the A4 is first deacetylated to DAAA, ADAA and AADA (Figure 8A), followed by further deacetylation products to the intermediate product DDAA, DADA and ADDA (Figure 8B). Finally, the end product DDDA was obtained, due to the third deacetylation (Figure 8C). Therefore, deacetylation occurred mainly at the non-reducing end, and the acetyl at the reducing end was always present. No matter how we prolonged the reaction time or increased the concentration of the enzyme, the acetyl group at the reducing end could not be removed. After comparing the intermediate and end products generated by the deacetylation of the chitin tetramer, we found that the deacetylation occurred at any position except for the reducing end, indicating that ScCDA2 has a multiple attack mechanism like ClCDA and SpPgdA [33,36]. However, ScCDA2 cannot deacetylate at the reducing end to form completely deacetylated COS (DDDD). Therefore, the deacetylation pattern of ScCDA2 is significantly different from the reported CDA derived from C. lindemuthianum, Mucor rouxii, Aspergillus nidulans, Vibrio cholera, Puccinia graminis, etc [14,29,30,41,47]. A “subsite-capping model” has been proposed to explain the differentiation of the deacetylation process and product patterns of CDA [30]. This subsite-capping model states that the position and dynamics of loops play an important role in substrate preference and regioselectivity of deacetylation. So, the difference in the deacetylation mode of ScCDA2 may be due to the loop length, position and dynamic effects [47].

3. Materials and Methods

3.1. Materials

Escherichia coli TOP10, plasmid pPICZαA, T4 DNA ligase and DNA polymerase were purchased from Takara Biotechnology (Dalian). Pichia pastoris X-33 was stored in our laboratory. Beta-chitin was purchased from Sigma (St. Louis, MO, USA). Alpha-chitin was purchased from Seikagaku (Tokyo, Japan) [33]. Colloidal chitin was prepared according to the previously reported method [48]. AMAC, chitin oligosaccharides (GlcNAc) n (n = 2–6, dimers to hexamers (A2 to A6; A, GlcNAc)) were purchased from Sigma-Aldrich (Munich, Germany). Unless otherwise noted, all reagents were analytical grade. Acetate release was measured using an acetate kit from R-Biopharm (Darmstadt, Germany) [14].

3.2. Cloning, Expression and Purification of ScCDA2

The cda2 gene from Saccharomyces cerevisiae S288c (GenBank: NP_013411.1) was amplified with upstream primer ScCDA2-F:(5′-CATGCCATGGGAAGCTAATAGGGAAGATTTA-3′) and downstream primer: ScCDA2-R (5′-CCGCTCGAGGGACAAGAATTCTTTTATGTAATC-3′). The target gene was digested and then ligated into a pPICZαA expression vector containing the N-terminal hexa histidine fusion tag coding region.
The cda2 gene was recombined into a Pichia pastoris X-33 chromosome. Then the recombinant Pichia pastoris X-33 was induced by 0.5% methanol for 4 days, and methanol was added in batches every 24 h. The culture supernatant was collected by centrifugation at 8000× g, 4 °C for 20 min. The crude enzyme from the supernatant was concentrated using a 10 kDa ultrafiltration membrane. Then, the concentrated supernatant was purified by Ni-NTA Sepharose excel column (GE Healthcare). The pre-equilibrated buffer was subjected to Ni-NTA with buffer containing 20 mM PBS, pH 7.4, 300 mM NaCl and then washed with 50 mM PBS, pH 7.4, 300 mM NaCl, 20 mM imidazole. Finally, the target protein, eluted with 20 mM PBS, pH 7.4, 300 mM NaCl, 250 mM imidazole was obtained. Protein concentration was determined by using the Pierce™ BCA Protein Assay Kit (Thermo Fisher Scientific).

3.3. ScCDA2 Activity Assay and Biochemistry Properties

The purified ScCDA2 was studied to determine its enzymatic properties and deacetylation patterns. The colloidal chitin (water-soluble chitin), colloidal chitin and chitin oligomers dimers to hexamers (A2 to A6) were used as substrates [14]. The reaction mixture for ScCDA2 enzyme activity assay containing 20 mM Tris-HCl buffer (pH8.0), including 1 mM CoCl2, 0.5 mg/mL substrate and 0.75 μM purified soluble protein (ScCDA2) or distilled water as a control was incubated at 37 °C for 30 min. The reaction was terminated by the addition of 10 µL 5% formic acid [14]. Determination of CDA activity by measuring the amount of acetate released by a coupled enzyme assay using an acetate assay kit [14]. The total reaction volume of the coupled enzyme reaction was 266 μL, which was measured spectrophotometrically at 340 nm [14].
In order to determine the optimum pH of ScCDA2, protein in different buffers (final concentration 20 mM) was incubated at 37 °C for 30 min at the pH range of 4.0 to 10.0, in either sodium citrate disodium hydrogen phosphate buffer (pH 3.0–5.0), sodium phosphate dibasic sodium dihydrogen phosphate buffer (pH 6.0–7.0), Tris-HCl buffer (pH 8.0) or sodium carbonate sodium bicarbonate buffer (pH 9.0–10.0). The optimum temperature was determined in the 20 mM Tris-HCl buffer, at the optimum pH of 8.0, and each protein solution was incubated at 37 °C, 50 °C and 65 °C for 60 min. Subsequently, the remaining enzyme activity was measured using standard activity assays. The effects of different metal ions on enzyme activity were verified by adding 1 mM of different metal ion solutions (NaCl, NH4Cl, BaCl2, CoCl2, MnCl2, ZnCl2, CuCl2, MgCl2 and FeCl3) to the reaction mixtures [17].

3.4. Identification of ScCDA2 Products by MALDI-TOF-MS

To determine the effect of different enzyme concentrations on the enzyme reaction products, four concentration gradients (0.25 μM, 0.5 μM, 0.75 μM, 1 μM) were prepared under 20 mM pH = 8.0 Tris-HCl. MS spectra were obtained using an Ultraflex™ ToF/ToF mass spectrometer (Bruker Daltonik GmbH, Bremen, Germany) to analyze the degree of acetylation, as previously described [49].

3.5. Preparation of Partially Acetylated COS

To analysis the deacetylation pattern of ScCDA2, 20 mM Tris-HCl buffer (pH8.0), including 1 mM CoCl2, 0.5 mg/mL substrate and 0.75 μM purified soluble protein (ScCDA2) was incubated at 37 °C for 30 min. Then, 50 μL of the sample was injected into an X-Amide (4.6 mm × 250 mm) column for separation. The column was eluted with 0.3% formic acid and 50 mM ammonium formate buffer at a flow rate of 2 mL/min. The separated sample was analyzed by electrospray ionization mass spectrometry (ESI-MS).

3.6. Acetylation Pattern Analysis of COS

Reductive amine derivatisation of partially acetylated COS was performed as previously described [50]. In brief, 0.5 mg of the partially acetylated product was dissolved in 10 μL of 0.1 mol/L solution of 2-aminoacridone (AMAC) in acetic acid/DMSO (v/v, 3/17) and stirred manually for 30 s; then 10 μL of 1 M sodium cyanoborohydride solution was added and stirred for a further 30 s. The mixture was heated at 90 °C for 30 min, cooled to −20 °C and then completely freeze-dried. The dried sample was dissolved in 200 μL of methanol/water (v/v, 50/50) solution and sufficiently centrifuged at 12,000× g, 4 °C for 10 min. Then the supernatant was immediately analyzed by mass spectrometry or stored at −20 °C for one month. The method of mass spectrometry to detect the results of reductive amine derivatization was the same as the method of mass spectrometry detection of the enzyme reaction product mentioned previously [51]. MS2 spectra were used to analyze the acetylation pattern of COS [52].

3.7. Homology Modelling and Molecular Docking

YASARA software (version 14.12.2) was used to build the homology model of ScCDA2 with three crystal structures (PDB ID: 5LFZ, 2CC0 and 2C1G) as templates, the similarity between ScCDA2 and templates is 34%, 33%, 29%, respectively [53], which are highly homologous to ScCDA2, based on BLAST results using. The 3D structural model was visualized using VMD software (version 1.9.3, University of Illinois; Urbana–Champaign, IL, USA) [54]. The model was further evaluated for protein geometry by SAVES (http://services.mbi.ucla.edu/SAVES/), PROCHECK, ERRAT and VERIFY3D [55]. The chitin molecule structure was acquired from the zinc database (http://zinc.docking.org/). Molecular docking was performed using LeDock software (http://www.lephar.com/) with default parameters [56]. The dimensions of the binding box were set as 10 Å around the active site. The docking center was set at the Zn2+. The number of binding poses of the ligand was 100. Finally, the docking pose that fulfilled the catalytic criteria was chosen as the initial conformation for analysis.

4. Conclusions

In this study, we firstly report the detailed deacetylation patterns of chitin deacetylase from Saccharomyces cerevisiae (ScCDA2). Fully defined chitooligosaccharides (DAAA, ADAA, AADA, DDAA, DADA, ADDA and DDDA) have been produced by ScCDA2 through multiple attack catalytic mechanisms. In addition, a fast, convenient and online monitoring method has been developed that can be used to separate and detect partially acetylated chitosan oligosaccharides. Enzymatic production of fully defined chitooligosaccharides and on-line monitoring and separation chitooligosaccharides, which solves the time-consuming and labor-intensive problem of isolating high purity chitooligosaccharides. This bio-enzymatic application could avoid the use of irritating chemicals and allows the production of functional chitosan and COS from crustacean waste chitin.

Supplementary Materials

The following are available online at https://www.mdpi.com/1660-3397/17/2/74/s1, Figure S1: The model was further evaluated for protein geometry by SAVES (A comprehensive measurement website for the quality of a protein structure). 97.3% Residues in additional allowed regions and 85.57% of the residues have averaged 3D-1D score ≥ 0.2, and the quality factor is 91.2214. Figure S2: Compare deacetylase charge distribution. These pictures show the surface charge distributions of chitin deacetylase from Saccharomyces cerevisiae (ScCDA2) and chitin deacetylase from Aspergillus Nidulans (AnCDA, PDB ID: 2Y8U) calculated using ABPS (The Adaptive Poisson-Boltzmann Solver to generate electrostatic surface displayed) in VMD. Red represents a negative charge and blue represents a positive charge. Figure S3: ScCDA2 substrate specificity on chitin oligomers. 0.5 mg/mL chitin oligomers as substrates were incubated with 0. 75 μM ScCDA2 at 37 °C for 30 min. The data represents the mean SD values of the results from three independent experiments. Figure S4: Effects of pH, temperature and metal ion on enzyme activity. (A) The optimum pH was determined by incubating the 0.75 µM ScCDA2 with A4 chitin oligomer (0.5 mg/mL) for 60 min at pH 3–11 in universal buffer. (B) To obtain the optimal temperature, the enzyme (075 µmol) was incubated for 60 min at different temperatures in 50 mM Tris-HCl buffer (pH 8.0) containing chitin oligomer mixture (0.5 mg/mL) as a substrate. (C) Relative activity with different metal cations. Proteins were incubated with 1 mm metallized cations, and activity was determined in 50 mM Tris-HCl buffer (pH 8.0) using 0.5 mg/mL A4 as a substrate. Figure S5: Spectra of N-glycosylation of ScCDA2. Mass spectrometry showed that ScCDA2 have N-glycosylation post-translational modification at Asn 181, Asn 199 and Asn 203.

Author Contributions

General concept and design of studies: H.Y. Experimental concept and data analysis: X.-Y.Z., Y.Z., Experimental conduct and manuscript writing: X.-Y.Z. Manuscript review: H.Y., H.-D.Z., W.-X.W. and H.-H.C. Page: 12. Manuscript finalization: H.Y.

Funding

This research was supported by National Natural Science Foundation of China: (31670803, 31770847), National Key Research and Development Project of China: (2017YFD0200902), and H.Y was supported by Dalian city Innovative Support Program for High-Level Talents (2015R010), CAS Youth Innovation Promotion Association (2015144).

Acknowledgments

The authors would like to thank L.H.W. for the MALDI-TOF-MS analyses.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Structure-based on sequence alignments between four chitin deacetylases (CDAs). The sequence of chitin deacetylase from Saccharomyces cerevisiae (ScCDA2) was aligned with ArCE4A sequences from a marine Arthrobacter species (PDB ID: 5LFZ), the SlCE4 sequence from Streptomyces lividans (PDB ID: 2CC0) and the SpPgdA sequence from Streptococcus pneumoniae (PDB ID: 2C1G). The conserved motifs are highlighted by a red background and the catalytic amino acids are marked with a yellow triangle. Amino acids capable of forming coordinate bonds with Zn2+ are marked with blue triangles. The symbol above the sequence represents the secondary structure, helices represent α-helices, and the arrow represents the beta fold.
Figure 1. Structure-based on sequence alignments between four chitin deacetylases (CDAs). The sequence of chitin deacetylase from Saccharomyces cerevisiae (ScCDA2) was aligned with ArCE4A sequences from a marine Arthrobacter species (PDB ID: 5LFZ), the SlCE4 sequence from Streptomyces lividans (PDB ID: 2CC0) and the SpPgdA sequence from Streptococcus pneumoniae (PDB ID: 2C1G). The conserved motifs are highlighted by a red background and the catalytic amino acids are marked with a yellow triangle. Amino acids capable of forming coordinate bonds with Zn2+ are marked with blue triangles. The symbol above the sequence represents the secondary structure, helices represent α-helices, and the arrow represents the beta fold.
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Figure 2. Analysis of molecular weight of ScCDA2 protein by 12% SDS-PAGE. (A) ScCDA2 crude enzyme; (B) purified ScCDA210 μM, 5 μM, 2.5 μM and 1.0 μM, marked as lanes 1, 2, 3 and 4, respectively; (C) PNGase F digestion confirmed that the enzyme is glycoprotein. Lane 1, ScCDA2 before being digested by PNGase F; lane 2, PNGase F; lane 3, ScCDA2 has been digested by PNGase F.
Figure 2. Analysis of molecular weight of ScCDA2 protein by 12% SDS-PAGE. (A) ScCDA2 crude enzyme; (B) purified ScCDA210 μM, 5 μM, 2.5 μM and 1.0 μM, marked as lanes 1, 2, 3 and 4, respectively; (C) PNGase F digestion confirmed that the enzyme is glycoprotein. Lane 1, ScCDA2 before being digested by PNGase F; lane 2, PNGase F; lane 3, ScCDA2 has been digested by PNGase F.
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Figure 3. Catalytic binding mode resulting from homologous modelling and molecular docking. (A) The stereo view of the overall structure of ScCDA2 (B) Highlights the binding pocket of ScCDA2 docked with GlcNAc. The pink sticks represent a catalytic amino acid, and the blue sticks represent the amino acid that forms a coordinate bond with Zn2+. The substrate GlcNAc is represented by a yellow stick. (C) Conservative loops were found through multiple structure superposition. The model of ScCDA2 was superposed with an ArCE4A structure from a marine Arthrobacter species (PDB ID: 5LFZ), a CE4 carbohydrate esterase structure from Streptomyces lividans (PDB ID: 2CC0) and an SpPgdA structure from Streptococcus pneumoniae (PDB ID: 2C1G). The conservative loops also have been marked.
Figure 3. Catalytic binding mode resulting from homologous modelling and molecular docking. (A) The stereo view of the overall structure of ScCDA2 (B) Highlights the binding pocket of ScCDA2 docked with GlcNAc. The pink sticks represent a catalytic amino acid, and the blue sticks represent the amino acid that forms a coordinate bond with Zn2+. The substrate GlcNAc is represented by a yellow stick. (C) Conservative loops were found through multiple structure superposition. The model of ScCDA2 was superposed with an ArCE4A structure from a marine Arthrobacter species (PDB ID: 5LFZ), a CE4 carbohydrate esterase structure from Streptomyces lividans (PDB ID: 2CC0) and an SpPgdA structure from Streptococcus pneumoniae (PDB ID: 2C1G). The conservative loops also have been marked.
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Figure 4. ScCDA2 substrate specificity on chitin. ScCDA2 activity on colloidal chitin, alpha-chitin and beta-chitin. 0.5 mg/mL substrates were incubated with 0. 75 μM ScCDA2 at 37 °C for 30 min. The data represent the mean SD values of the results from three independent experiments.
Figure 4. ScCDA2 substrate specificity on chitin. ScCDA2 activity on colloidal chitin, alpha-chitin and beta-chitin. 0.5 mg/mL substrates were incubated with 0. 75 μM ScCDA2 at 37 °C for 30 min. The data represent the mean SD values of the results from three independent experiments.
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Figure 5. HPLC-ESI-MS analysis of chitin tetramer (A4) treated with ScCDA2. (A) The target peak of the UHPLC-ESI chromatogram began to appear after 14 min, and the deacetylation peak was mainly concentrated between 20 and 26 min. (B) The m/z ratio in the MS spectrum corresponds to the mass of the substrate (A4; m/z 853.24), its mono-deacetylated products A3D1 (m/z 811.25), A2D2 (m/z 768.62) and A1D3 (m/z 727.13).
Figure 5. HPLC-ESI-MS analysis of chitin tetramer (A4) treated with ScCDA2. (A) The target peak of the UHPLC-ESI chromatogram began to appear after 14 min, and the deacetylation peak was mainly concentrated between 20 and 26 min. (B) The m/z ratio in the MS spectrum corresponds to the mass of the substrate (A4; m/z 853.24), its mono-deacetylated products A3D1 (m/z 811.25), A2D2 (m/z 768.62) and A1D3 (m/z 727.13).
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Figure 6. Partially acetylated chitooligosaccharides production processes. To explore the production processes of partially acetylated chitooligosaccharides 0.25 μM, 0.5 μM, 0.75 μM and 1 μm enzymes were incubated with A4 in 20 mM Tris-Cl buffer (pH 8.0) for 30 min. Then determined by MALDI-TOF-MS.
Figure 6. Partially acetylated chitooligosaccharides production processes. To explore the production processes of partially acetylated chitooligosaccharides 0.25 μM, 0.5 μM, 0.75 μM and 1 μm enzymes were incubated with A4 in 20 mM Tris-Cl buffer (pH 8.0) for 30 min. Then determined by MALDI-TOF-MS.
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Figure 7. Analysis of partially acetylated COS by reductive amine derivatization with mass spectrometry. The reaction product generated after ScCDA2 treatment (GlcNAc)4 was labelled with AMAC and analyzed by MALDI-TOF-MS. (A). MS1 spectrum of A3D1 labelled with AMAC (m/z 1005.96). (B). MS1 spectrum of A2D2 labelled with AMAC m/z 963.82). (C). MS1 spectrum of A1D3 labelled with AMAC (m/z 921.80).
Figure 7. Analysis of partially acetylated COS by reductive amine derivatization with mass spectrometry. The reaction product generated after ScCDA2 treatment (GlcNAc)4 was labelled with AMAC and analyzed by MALDI-TOF-MS. (A). MS1 spectrum of A3D1 labelled with AMAC (m/z 1005.96). (B). MS1 spectrum of A2D2 labelled with AMAC m/z 963.82). (C). MS1 spectrum of A1D3 labelled with AMAC (m/z 921.80).
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Figure 8. MALDI-TOF-MS2 determines the acetylation pattern of partially acetylated COS. (A) The MS2 spectrum of A3D1 labelled with AMAC and the resulting ion fragments: A-amac, DA-amac, AA-amac, ADA-amac, DAA-amac, AAA-amac (m/z 438.15, 599.19, 641.20, 802.23, 844.24); so, the acetylation pattern of A3D1 is DAAA, ADAA and AADA. (B) MS2 spectrum of A2D2 labelled with AMAC and the resulting ion fragments: A-amac, DDA, DAD, ADD, DA-amac, AA-amac and ADA-amac, (m/z 438.16, 548.19, 599.22, 641.22, 802.29); so, the acetylation pattern of A2D2 is DDAA, ADDA and DADA. (C) MS2 spectrum of A1D3 labelled with AMAC, resulting in ion fragmentation of A-amac, DA-amac and DDA-amac (m/z 438.16, 599.21, 760.25); so, the acetylation pattern of A1D3 is DDDA. (D) The deacetylation process of ScCDA2 when A4 is used as a substrate.
Figure 8. MALDI-TOF-MS2 determines the acetylation pattern of partially acetylated COS. (A) The MS2 spectrum of A3D1 labelled with AMAC and the resulting ion fragments: A-amac, DA-amac, AA-amac, ADA-amac, DAA-amac, AAA-amac (m/z 438.15, 599.19, 641.20, 802.23, 844.24); so, the acetylation pattern of A3D1 is DAAA, ADAA and AADA. (B) MS2 spectrum of A2D2 labelled with AMAC and the resulting ion fragments: A-amac, DDA, DAD, ADD, DA-amac, AA-amac and ADA-amac, (m/z 438.16, 548.19, 599.22, 641.22, 802.29); so, the acetylation pattern of A2D2 is DDAA, ADDA and DADA. (C) MS2 spectrum of A1D3 labelled with AMAC, resulting in ion fragmentation of A-amac, DA-amac and DDA-amac (m/z 438.16, 599.21, 760.25); so, the acetylation pattern of A1D3 is DDDA. (D) The deacetylation process of ScCDA2 when A4 is used as a substrate.
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Zhu, X.-Y.; Zhao, Y.; Zhang, H.-D.; Wang, W.-X.; Cong, H.-H.; Yin, H. Characterization of the Specific Mode of Action of a Chitin Deacetylase and Separation of the Partially Acetylated Chitosan Oligosaccharides. Mar. Drugs 2019, 17, 74. https://doi.org/10.3390/md17020074

AMA Style

Zhu X-Y, Zhao Y, Zhang H-D, Wang W-X, Cong H-H, Yin H. Characterization of the Specific Mode of Action of a Chitin Deacetylase and Separation of the Partially Acetylated Chitosan Oligosaccharides. Marine Drugs. 2019; 17(2):74. https://doi.org/10.3390/md17020074

Chicago/Turabian Style

Zhu, Xian-Yu, Yong Zhao, Huai-Dong Zhang, Wen-Xia Wang, Hai-Hua Cong, and Heng Yin. 2019. "Characterization of the Specific Mode of Action of a Chitin Deacetylase and Separation of the Partially Acetylated Chitosan Oligosaccharides" Marine Drugs 17, no. 2: 74. https://doi.org/10.3390/md17020074

APA Style

Zhu, X. -Y., Zhao, Y., Zhang, H. -D., Wang, W. -X., Cong, H. -H., & Yin, H. (2019). Characterization of the Specific Mode of Action of a Chitin Deacetylase and Separation of the Partially Acetylated Chitosan Oligosaccharides. Marine Drugs, 17(2), 74. https://doi.org/10.3390/md17020074

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