Chitosanase Production from the Liquid Fermentation of Squid Pens Waste by Paenibacillus elgii

Chitosanases play a significant part in the hydrolysis of chitosan to form chitooligosaccharides (COS) that possess diverse biological activities. This study aimed to enhance the productivity of Paenibacillus elgii TKU051 chitosanase by fermentation from chitinous fishery wastes. The ideal parameters for achieving maximum chitosanase activity were determined: a squid pens powder amount of 5.278% (w/v), an initial pH value of 8.93, an incubation temperature of 38 °C, and an incubation duration of 5.73 days. The resulting chitosanase activity of the culture medium was 2.023 U/mL. A chitosanase with a molecular weight of 25 kDa was isolated from the culture medium of P. elgii TKU051 and was biochemically characterized. Liquid chromatography with tandem mass spectrometry analysis revealed that P. elgii TKU051 chitosanase exhibited a maximum amino acid identity of 43% with a chitosanase of Bacillus circulans belonging to the glycoside hydrolase (GH) family 46. P. elgii TKU051 chitosanase demonstrated optimal activity at pH 5.5 while displaying remarkable stability within the pH range of 5.0 to 9.0. The enzyme displayed maximum efficiency at 60 °C and demonstrated considerable stability at temperatures ≤40 °C. The presence of Mn2+ positively affected the activity of the enzyme, while the presence of Cu2+ had a negative effect. Thin-layer chromatography analysis demonstrated that P. elgii TKU051 chitosanase exhibited an endo-type cleavage pattern and hydrolyzed chitosan with 98% degree of deacetylation to yield (GlcN)2 and (GlcN)3. The enzymatic properties of P. elgii TKU051 chitosanase render it a promising candidate for application in the production of COS.


Introduction
Chitosan is a polysaccharide comprising glucosamine and N-acetylglucosamine units linked together by β-1,4-glycosidic bonds [1].This versatile compound is a promising non-toxic polymer with remarkable properties such as biocompatibility, antibacterial activity, biodegradability, film-forming ability, and others [2], making it useful for a wide range of applications, including food [3], cosmetics [4], biomedicine [5], agriculture [6], and environmental protection [7].However, due to its poor solubility at neutral pH values, chitosan has limited usage in the food and medicine industry [8].Recently, researchers have turned their attention to chitooligosaccharides (COS, the hydrolysis product of chitosan) because of their various biological activities, such as antioxidant, antidiabetic, antifungal, anti-inflammatory, antimicrobial, antitumor, and immuno-enhancing properties [8][9][10][11].As a result, COS is extensively applied in the domains of agriculture, food, biomedicine, and other related areas [12].COS can be obtained through chemical, physical, and enzymatic degradation techniques [8,13].Among these, the enzymatic approach offers several advantages, such as mild reaction conditions, high yields, good selectivity, controllability, reproducibility, and environment friendliness [13].Chitinase and chitosanase enzymes have high substrate specificity to chitosan, leading to their application in the production of COS.
Chitosanases (EC 3.2.1.132)are a class of enzymes that hydrolyze endo-β-1,4-glycosidic linkages in chitosan, forming COS with different degrees of polymerization (DP) [14].They are widely distributed in bacteria [15,16], fungi [17], viruses [18], and some plant tissues [19,20].Chitosanases are classified into six glycoside hydrolase (GH) families: GH 5, GH 7, GH 8, GH 46, GH 75, and GH 80 [21].Among them, GH 46, GH 75, and GH 80 are specific to chitosan hydrolysis; GH 46 chitosanases have been characterized most extensively compared with other chitosanases.The GH 46 chitosanases have a strong catalytic ability and are found mainly in bacteria [16].GH 46 chitosanases are endo-enzymes yielding COS (DP ≥ 2) [22]; this property could make them a potentially useful biotechnological tool for the green production of COS.Nevertheless, the high cost of enzyme production hinders the adoption of this method.This limitation can be overcome by lowering the enzyme production cost and potentially reducing the overall cost of COS production [8,23].
The cultivation parameters significantly impact the chitosanase productivity of microbial strains [17], with the cost of culture medium accounting for approximately 30-40% of the total enzyme production cost [23].Most microbial strains can be induced to synthesize chitosanase in media containing colloidal chitin or chitosan as the primary carbon source [17].However, the overall production cost may increase due to the cost and preparation process of colloidal chitin or chitosan, thus hindering the large-scale production of chitosanase.Hence, it is crucial to search for affordable substrates for the enzyme production and optimize the cultivation conditions to significantly reduce the cost [24].Fortunately, chitin and chitosan can be produced from chitinous fishery wastes through deproteinization and demineralization processes [25,26].This means that chitinous fishery wastes, such as shrimp heads, crab shells, and squid pens [27], can be used directly as a nutrient source for microbial fermentation to produce chitinolytic enzymes [9,28].One significant advantage of using fishery wastes is that they can serve as both carbon and nitrogen (C/N) sources and as enzyme inducers [27].
The genus Paenibacillus comprises endospore-forming and facultative anaerobic bacteria, formerly categorized as constituents of the Bacillus genus.Nevertheless, subsequent to a comprehensive comparative analysis of 16S ribosomal RNA sequences, the aforementioned bacteria were reclassified as a unique genus in 1993 [29].Several species in the genus of Paenibacillus have been reported to secrete different chitosanases [8,9,[30][31][32][33][34]. Kim et al. (2004) introduced Paenibacillus elgii as a novel species of the genus Paenibacillus [35].P. elgii, akin to many other Paenibacillus species, can generate the chitinolytic enzyme [31].Nonetheless, the production, characterization, and application of P. elgii chitosanase for COS preparation remain yet to be explored.In this study, P. elgii TKU051, a strain originally isolated from the soil of Tamkang University [26], was optimized for its chitosanase productivity in a shake-flask culture condition using chitinous fishery wastes as the unique C/N source.The study aimed to purify the P. elgii TKU051 chitosanase and characterize its biochemical properties.

Materials
P. elgii TKU051 was the same strain as was used in our previous work [8].Macro-Prep CM and Macro-Prep High S were procured from Bio-Rad (Hercules, CA, USA).Chitosan with ≥75% degree of deacetylation (DDA) and Sephacryl S-200 gel were all obtained from Sigma Co. (St.Louis, MO, USA).High DDA chitosan (98%) was provided by the Microorganisms and Biochemistry Laboratory, Department of Chemistry, Tamkang University, New Taipei, Taiwan.The shrimp heads and shells, crab shells, and squid pens were obtained from Shin-Ma Frozen Food Co. (Su-Ao city, Taiwan).Other chemicals were of the highest purity obtainable.

Chitosanase Assay
The chitosanase activity was determined following a modified version of a previously established method [8].The chitosan hydrolysis reaction was conducted at pH 5.5, combining equal volumes of the substrate (0.1 mL of 1% w/v chitosan) and the sample (0.1 mL), with incubation at 60 • C for 30 min.Subsequently, the reaction mixture was mixed with 1.5 mL of the 3,5-dinitrosalicylic acid reagent and heated at 100 • C for 10 min.The absorbance of the developed color was measured at 515 nm on a spectrophotometer to determine the quantity of reducing sugar generated.Chitosanase activity was defined as the enzyme amount required to produce 1 µmol of reducing sugar per minute.

Production Condition Screening
To optimize the production conditions, a systematic screening approach was employed.Various factors potentially influencing chitosanase productivity were investigated using the one-factor-at-a-time (OFAT) method.These factors included the C/N source (crab shells powder, CSP; shrimp shells powder, SSP; shrimp heads powder, SHP; squid pens powder, SPP; colloidal chitin, CC), SPP concentration (0.5% to 6%), pH (5.6 to 9.6), temperature (28 • C to 40 • C), and incubation time (0 to 8 days).The initial conditions for the experiments were set as follows: 1% concentration for each C/N source, 0.1% KH 2 PO 4 , 0.05% MgSO 4 , pH 7.6, and a temperature of 37 • C. One at a time, each factor was varied, while the other factors were kept constant.The condition that resulted in the highest chitosanase activity was selected for further experimentation and optimization.

Production Optimization
Following the preliminary results from the OFAT experiments, the Box-Behnken design of response surface methodology (RSM) was employed to optimize the response of four independent factors: SPP concentration (X 1 ), initial pH (X 2 ), incubation temperature (X 3 ), and incubation time (X 4 ).The optimization was conducted using the R-software (2021.09.1+372 version), and a total of 27 runs were performed for the optimization.Each factor was tested at three levels: low, medium, and high, represented by the coded values of −1, 0, and +1, respectively.The resultant data were analyzed using R-software to determine the optimal conditions for the chitosanase production.The following secondorder polynomial equation was the effect of four factors: where Y is the predicted response (U/mL); β 0 is the intercept; β

Chitosanase Purification
To purify the chitosanase, the culture supernatant (0.4 L) containing the enzyme was precipitated with (NH 4 ) 2 SO 4 , and the resulting precipitate was re-dissolved in acetate buffer (50 mM, pH 5.5).To remove any residual (NH 4 ) 2 SO 4 , the crude enzyme solution was dialyzed against acetate buffer (50 mM, pH 5.5) for 1 day.Next, the crude enzyme was loaded onto a high S column pre-equilibrated with acetate buffer (50 mM, pH 5.5).The chitosanase bound to the column was eluted using a NaCl gradient (0-0.5 mM).The active fraction containing the enzyme was collected, dialyzed against acetate buffer (50 mM, pH 5.5), and further purified using a CM column (0-0.5 mM).Chitosanase was eluted from the CM column by applying a NaCl gradient.Subsequently, the active fraction was concentrated by the freeze-drying method and loaded onto a Sephacryl S-200 column for final purification.The molecular weight and purity of the purified enzyme were determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) [8].The SDS-PAGE gel was stained by Protein Assay Dye Reagent from BioRad (Hercules, CA, USA).The chitinolytic activity of the purified enzyme was confirmed through native-PAGE containing 0.01% chitosan.In this assay, the chitosanase was loaded onto an acrylamide gel containing 0.01% chitosan and electrophoresed at 140 V and 4 • C. The gel was subsequently incubated overnight at 37 • C in acetate buffer (50 mM, pH 5.5) and finally stained with Congo red (0.1%).The gel was destained with 1 M NaCl; the chitosanase activity band appeared distinct and clear.

Mass Spectrometry and Protein Identification
Briefly, the target band on the SDS-PAGE gel was obtained and subjected to in-gel digestion with trypsin.Following that, the identity of the protein was determined by liquid chromatography-tandem mass spectrometry (LC-MS/MS) analysis performed by Mission Biotech Company (Taipei, Taiwan).The resulting fragment spectra were then searched against the SwissProt database using the MASCOT search engine.

Thin-Layer Chromatography (TLC) Analysis of Hydrolysis Products
The hydrolysis products of chitosan catalyzed by P. elgii TKU051 chitosanase were analyzed according to protocols mentioned in previous works [8].The hydrolysis solutions of 98% DDA chitosan with P. elgii TKU051 chitosanase at 0 h, 1 h, 2 h, 3 h, 4 h, and 5 h were analyzed by the TLC method.The mobile phase was a mixture of propanol/ammonia solution/water (70/10/20, v/v/v).The hydrolysis products were visualized by spraying the TLC plate with 10% H 2 SO 4 in ethanol and heating it at 180 • C.

Screening of Carbon/Nitrogen Source and Culture Factors for the Chitosanase Productivity of Paenibacillus elgii TKU051
Several low-cost and abundantly available chitin-rich fishery wastes (squid pens, crab shells, shrimp heads, and shrimp shells) were screened for their suitability for chitosanase production (Figure 1a).Among the materials, SPP was the best C/N source for chitosanase production (yielding 0.779 U/mL on the third day), followed by CC (0.718 U/mL on the Polymers 2023, 15, 3724 5 of 19 fifth day).CSP, SSP, and SHP did not appear to be appropriate C/N sources for producing chitosanase, as the enzyme productivity of P. elgii TKU051 on the mediums containing these C/N sources was insignificant.Likewise, SPP has been a suitable substrate for chitosanase production by Paenibacillus sp.TKU042 [33], Paenibacillus macerans TKU029 [36], and Paenibacillus sp.TKU047 [8].However, Paenibacillus mucilaginosus TKU032 exhibited the highest chitosanase productivity when SHP was the C/N source [9].CC is typically considered the optimal substrate for the synthesis of chitinolytic enzymes by various microbial strains [17,[37][38][39][40][41]; however, CC is a chitin form produced through chemical treatment, potentially resulting in high production costs and environmental pollution [38].These drawbacks limit the utilization of CC for large-scale production of chitinolytic enzymes.In this study, P. elgii TKU051 demonstrated greater efficiency in chitosanase production when utilizing SPP instead of CC.Thus, SPP emerges as a viable and effective alternative to CC for chitosanase production by P. elgii TKU051.Furthermore, when using different amounts of SPP as substrates for chitosanase production, 5% of SPP gave the best yield of chitosanase (1.757 U/mL on day 7) (Figure 1b).
of Paenibacillus elgii TKU051 Several low-cost and abundantly available chitin-rich fishery wastes (squid pens, crab shells, shrimp heads, and shrimp shells) were screened for their suitability for chitosanase production (Figure 1a).Among the materials, SPP was the best C/N source for chitosanase production (yielding 0.779 U/mL on the third day), followed by CC (0.718 U/mL on the fifth day).CSP, SSP, and SHP did not appear to be appropriate C/N sources for producing chitosanase, as the enzyme productivity of P. elgii TKU051 on the mediums containing these C/N sources was insignificant.Likewise, SPP has been a suitable substrate for chitosanase production by Paenibacillus sp.TKU042 [33], Paenibacillus macerans TKU029 [36], and Paenibacillus sp.TKU047 [8].However, Paenibacillus mucilaginosus TKU032 exhibited the highest chitosanase productivity when SHP was the C/N source [9].CC is typically considered the optimal substrate for the synthesis of chitinolytic enzymes by various microbial strains [17,[37][38][39][40][41]; however, CC is a chitin form produced through chemical treatment, potentially resulting in high production costs and environmental pollution [38].These drawbacks limit the utilization of CC for large-scale production of chitinolytic enzymes.In this study, P. elgii TKU051 demonstrated greater efficiency in chitosanase production when utilizing SPP instead of CC.Thus, SPP emerges as a viable and effective alternative to CC for chitosanase production by P. elgii TKU051.Furthermore, when using different amounts of SPP as substrates for chitosanase production, 5% of SPP gave the best yield of chitosanase (1.757 U/mL on day 7) (Figure 1b).Next, the effect of pH, temperature, and incubation time on the chitosanase production of P. elgii TKU051 was explored.As seen in Figure 1c, the chitosanase activity of the culture supernatants was observed at a broad pH range of 6.6 to 9.6, with maximum productivity at pH 8.6 (1.789 U/mL on day 6).Chitosanase production was significantly dependent on cultivation temperature (Figure 1d) and reached a maximum of 1.916 U/mL at 37 • C after six days of culturing.Based on these results, pH 8.6, 37 • C, and six days of culturing were selected as the optimal conditions for producing chitosanase in subsequent experiments.
At present, squid pens are considered an unappealing by-product of the squid processing sector [42].Nevertheless, several distinctive features of squid pens suggest their potential suitability as a viable chitin source [43].For sustainable methodologies, the use of squid pens as a viable C/N source in microbial fermentation processes is a promising avenue for producing high-value-added bioactive materials [44][45][46][47].In this study, squid pens were potentially promising in the production of chitosanase by P. elgii TKU051.Further, the culture conditions were optimized to enhance the production of chitosanase.

Production Optimization of Paenibacillus elgii TKU051 Chitosanase
Important parameters, including the amount of SPP (X 1 ), initial pH of the medium (X 2 ), incubation temperature (X 3 ), and incubation time (X 4 ), were optimized by using the RSM based on the Box-Behnken design to achieve the highest production of chitosanase.The experimental design was based on 27 experiments, including three central points (Table 1).The chitosanase activity of the cultural mediums ranged from 0.230 U/mL to 1.966 U/mL under different culture conditions.The effect of four factors was the following second-order polynomial equation: The results of regression analysis and analysis of variance are presented in Tables 2 and 3.The F-statistic of the model was evaluated to be 19.87,implying the significance of the model.The lack-of-fit F-value of 2.007 implies the non-significance of the lack of fit relative to the pure error, further confirming that the model was significant.The value of the determination coefficient was 0.9586, indicating that only 4.14% of total variations could not be explained by the model.The adjusted determination coefficient (adjusted R 2 ) of all models was also high (0.9104) and confirmed the significance of the model.The chitosanase productivity was strongly affected by the linear terms of X 3 and X 4 , the 2-factor interactions terms of X 1 X 2 , X 1 X 4 , and X 2 X 3, and the quadratic term (Table 2).The relationship between the dependent and independent variables and the determination of their optimal levels were explored by generating 2-dimensional (2D) contour plots and 3D response surface plots by plotting one of the responses against any two independent variables while holding the third variable as a constant at its midpoint (0) level (Figure 2).The 3D response surface plots were expected to exhibit a convex shape, with the plot peak indicating the optimal combination of the two factors being tested.Meanwhile, the 2D contour plots displayed an oval shape, indicating a significant interaction between the two variables that were plotted [48].Thus, the chitosanase activity of the culture medium was susceptible to changes in the tested factors.Specifically, as depicted in Figure 2, the chitosanase activity of the culture medium increased initially and then decreased with the increase in the SPP amount, initial pH of the medium, incubation temperature, and fermentation time.
The maximum predicted chitosanase activity of 1.974 U/mL could be attained by setting the initial pH, incubation temperature, incubation time, and amount of SPP at 8.93, 38 • C, 5.73 days, and 5.278%, respectively.The fermentation was executed in triplicate using the recommended fermentation conditions to validate the optimization findings.P. elgii TKU051 demonstrated chitosanase productivity of 2.023 ± 0.072 U/mL under the optimal conditions (Table 4), consistent with the predicted maximum activity and greater than its chitosanase productivity under unoptimized conditions (0.777 ± 0.076 U/mL) and optimization by employing the OFAT method (1.899 ± 0.031 U/mL).Therefore, the production process of chitosanase from P. elgii TKU051 using SPP as the sole C/N source could be successfully optimized.The relationship between the dependent and independent variables and the determination of their optimal levels were explored by generating 2-dimensional (2D) contour plots and 3D response surface plots by plotting one of the responses against any two independent variables while holding the third variable as a constant at its midpoint (0) level (Figure 2).The 3D response surface plots were expected to exhibit a convex shape, with the plot peak indicating the optimal combination of the two factors being tested.Meanwhile, the 2D contour plots displayed an oval shape, indicating a significant interaction between the two variables that were plotted [48].Thus, the chitosanase activity of the culture medium was susceptible to changes in the tested factors.Specifically, as depicted in Figure 2, the chitosanase activity of the culture medium increased initially and then decreased with the increase in the SPP amount, initial pH of the medium, incubation temperature, and fermentation time.The maximum predicted chitosanase activity of 1.974 U/mL could be attained by setting the initial pH, incubation temperature, incubation time, and amount of SPP at 8.93, 38 °C, 5.73 days, and 5.278%, respectively.The fermentation was executed in triplicate using the recommended fermentation conditions to validate the optimization findings.P. elgii TKU051 demonstrated chitosanase productivity of 2.023 ± 0.072 U/mL under the optimal conditions (Table 4), consistent with the predicted maximum activity and greater than its chitosanase productivity under unoptimized conditions (0.777 ± 0.076 U/mL) and optimization by employing the OFAT method (1.899 ± 0.031 U/mL).Therefore, the production process of chitosanase from P. elgii TKU051 using SPP as the sole C/N source could be successfully optimized.

Enzyme Purification and Identification
The chitosanase was purified before its characteristics could be investigated further.The crude chitosanase was obtained from the culture supernatant of P. elgii TKU051 using the (NH4)2SO4 precipitation method.It was then purified using Macro-Prep High S, CM, and Sephacryl S-200 columns (Figure 3).A unique peak of chitosanase fraction was ob-

Enzyme Purification and Identification
The chitosanase was purified before its characteristics could be investigated further.The crude chitosanase was obtained from the culture supernatant of P. elgii TKU051 using the (NH 4 ) 2 SO 4 precipitation method.It was then purified using Macro-Prep High S, CM, and Sephacryl S-200 columns (Figure 3).A unique peak of chitosanase fraction was observed during the purification process.As shown in Table 5, the purified chitosanase demonstrated a 141.081-fold increase in specific activity, and 4% of the total activity could be recovered from the culture supernatant using the purification process.

Biochemical Characteristic of Paenibacillus elgii TKU051 Chitosanase
Figure 5a presents the effect of pH on the activity of P. elgii TKU051 chitosanase.The enzyme exhibited its highest activity at pH 5.5 and was stable within the pH range of 5 to 9, retaining over 90% of its residual activity.These findings indicate that the chitosanase from P. elgii TKU051 is an acidic enzyme.Similar characteristics have been reported for chitosanases from other P. barengoltzii (pH 5.5) [30], P. mucilaginosus TKU032 (pH 6) [9], and Paenibacillus sp.1794 (pH 4.8) [50].In contrast, some chitosanases show optimal activity under the neutral condition (pH 7), such as those from P. macerans TKU029 [36], Paenibacillus sp.TKU047 [8], and P. dendritiformis [49].Chitosanases demonstrating optimal catalytic activity in acidic environments are advantageous for producing COS because the solubility of chitosan is enhanced at a pH less than 6.0 [59].Also, with its stability over a broad pH range and optimal acidic pH, P. elgii TKU051 chitosanase shows potential for applications in chitosan saccharification processes.
and Paenibacillus sp.1794 (pH 4.8) [50].In contrast, some chitosanases show optimal activity under the neutral condition (pH 7), such as those from P. macerans TKU029 [36], Paenibacillus sp.TKU047 [8], and P. dendritiformis [49].Chitosanases demonstrating optimal catalytic activity in acidic environments are advantageous for producing COS because the solubility of chitosan is enhanced at a pH less than 6.0 [59].Also, with its stability over a broad pH range and optimal acidic pH, P. elgii TKU051 chitosanase shows potential for applications in chitosan saccharification processes.The optimum temperature for the P. elgii TKU051 chitosanase was 60°C (Figure 5b), similar to that of several other reported chitosanases, such as P. macerans TKU029 [36] and Paenibacillus sp.TKU047 [8], but higher than that of P. dendritiformis (45 °C ) [49].P. elgii TKU051 chitosanase exhibited the highest relative activity towards 98% DDA chitosan solution (100.00%), followed by 75% DDA chitosan solution (80%), colloidal chitin (17%), chitosan powder (1%), and chitin powder (1%), and exhibited no activity towards other polysaccharide substrates (Figure 5d).Hence, the activity of P. elgii TKU051 chitosanase is specific to the GlcN-GlcN linkages.Likewise, a similar phenomenon was observed earlier in chitosanase from Paenibacillus sp.TKU047 [8], P. dendritiformis [49].Most GH 46 chitosanases displayed strict substrate specificity towards chitosan with high DDA [49,53].This result also indicates that the physical form of the substrate significantly affects the activity of chitosanase, with better hydrolytic activity of the enzyme in chitosan solution compared to chitosan powder.Finally, the K m and V max of P. elgii TKU051 chitosanase were determined at chitosan concentrations ranging from 0.195 mg/mL to 25 mg/mL in sodium acetate buffer (pH 5.5) at 60 • C. The Lineweaver-Burk plot was used to calculate the K m and V max, which were at 32.83 mg/mL and 9.200 µM/min, respectively, and the K cat was 1645 s −1 .Likewise, the K cat value of Bacillus sp.KCTC 0377BP chitosanase was estimated to be 1600 s −1 [61].

Hydrolysis Products
The reaction products of P. elgii TKU051 chitosanase were examined using a 98% DDA chitosan solution.In the initial stage of the reaction (from 0 h to 1 h), P. elgii TKU051 chitosanase rapidly hydrolyzed chitosan, resulting in the formation of (GlcN) 2 , (GlcN) 3 , and (GlcN) 4 (Figure 6), indicating that P. elgii TKU051 chitosanase functions as an endochitosanase.From 1 h onward, the levels of (GlcN) 4 gradually decreased over time, suggesting the hydrolysis of (GlcN) 4 to generate (GlcN) 2 .Notably, no GlcN product was detected, indicating that P. elgii TKU051 chitosanase does not possess exo-β-D-glucosaminidase activity and cannot further degrade (GlcN) 2 and (GlcN) 3 into smaller forms.Briefly, P. elgii TKU051 chitosanase was determined to be an endo-chitosanase, generating (GlcN) 2 and (GlcN) 3 as primary products.Studies have confirmed that certain chitosanases derived from the Paenibacillus genus act as endo-chitosanases.This finding is highly consistent with the report by Zhang et al. (2021) [15], who showed that the GH46 family chitosanase CsnY produced (GlcN) 2 and (GlcN) 3 as reaction products (Table 7).Most chitosanases from GH 46 display endo-type properties with no activity toward (GlcN) 2 and (GlcN) 3 .In addition, the majority of GH46 chitosanases seem to favor the generation of COS with lower DP, specifically 2 and 3 [13].In this study, P. elgii TKU051 chitosanase could effectively hydrolyze chitosan to produce COS with a DP of 2-3, and no DP 1 products were observed.Thus, these results underscore the practical application of P. elgii TKU051 chitosanase for the production of COS.[15], who showed that the GH46 family chitosanase CsnY produced (GlcN)2 and (GlcN)3 as reaction products (Table 7).Most chitosanases from GH 46 display endo-type properties with no activity toward (GlcN)2 and (GlcN)3.In addition, the majority of GH46 chitosanases seem to favor the generation of COS with lower DP, specifically 2 and 3 [13].In this study, P. elgii TKU051 chitosanase could effectively hydrolyze chitosan to produce COS with a DP of 2-3, and no DP 1 products were observed.Thus, these results underscore the practical application of P. elgii TKU051 chitosanase for the production of COS.

Conclusions
Numerous studies have been done on the production of chitosanase by microbes; nonetheless, there is a dearth of information regarding the statistical optimization of chitosanase production by P. elgii utilizing squid pens as a C/N source.Thus, the results of this study may be a novel contribution to this field.In this work, the production optimization of P. elgii TKU051 chitosanase using squid pens as the substrate resulted in a 2.6-fold increase (2.023 U/mL) in chitosanase production compared to that in unoptimized conditions.A chitosanase with a molecular weight of 25 kDa was isolated, purified, and biochemically characterized from P. elgii TKU051 culture medium.P. elgii TKU051 chitosanase was classified under the GH46 family and exhibited optimal activity at 60 • C and pH 5.5.Furthermore, the chitosanase produced by P. elgii TKU051 was found to be an endo-type enzyme capable of catalyzing chitosan hydrolysis into low-DP COS.The remarkable characteristics exhibited by the chitosanase of P. elgii TKU051 serve as a basis for its use in synthesizing COS.

Figure 1 .
Figure 1.Screening of culture factors for the chitosanase production of Paenibacillus elgii TKU051.(a), Kind of C/N source; (b), amount of SPP; (c), initial pH of the medium; (d), incubation temperature.CC, colloidal chitin; C/N, carbon/ nitrogen; SPP, squid pen powder; SHP, shrimp head powder; SSP, shrimp shell powder.The error bars represent the standard deviation (SD) of the means of three replicates.

Figure 2 .
Figure 2. Response surface plots and 2-dimensional contour plots showing the effect of the amount of squid pens powder (SPP), initial pH of medium, temperature, and incubation time on chitosanase productivity of Paenibacillus elgii TKU051.(a), response surface plot and (b), 2-dimensional contour plot showing the effect of amount of SPP and initial pH; (c), response surface plot and (d), 2dimensional contour plot showing the effect of amount of SPP and temperature; (e), response surface plot and (f), 2-dimensional contour plot showing the effect of amount of SPP and incubation time; (g), response surface plot and (h), 2-dimensional contour plot showing the effect of initial pH and temperature; (i), response surface plot and (j), 2-dimensional contour plot showing the effect of initial pH and incubation time; (k), response surface plot and (l), 2-dimensional contour plot showing the effect of temperature and incubation time.

Figure 6 .
Figure 6.The thin layer chromatography profile of the hydrolysis products of chitosan with 98% degree of deacetylation chitosan solution using Paenibacillus elgii TKU051 chitosanase.

Figure 6 .
Figure 6.The thin layer chromatography profile of the hydrolysis products of chitosan with 98% degree of deacetylation chitosan solution using Paenibacillus elgii TKU051 chitosanase.

Table 2 .
Results of regression analysis of Box-Behnken design.

Table 3 .
Analysis of variance for the fitted quadratic polynomial model.

Table 4 .
Production comparison of Paenibacillus elgii TKU051 chitosanase on different culture conditions.

Table 4 .
Production comparison of Paenibacillus elgii TKU051 chitosanase on different culture conditions.
OFAT, one factor at a time; RSM, response surface methodology.

Table 5 .
A summary of the purification of Paenibacillus elgii TKU051 chitosanase.

Table 6 .
Identification of Paenibacillus elgii TKU051 chitosanase by liquid chromatography with tandem mass spectrometry analysis.

Table 6 .
Identification of Paenibacillus elgii TKU051 chitosanase by liquid chromatography with tandem mass spectrometry analysis.

Table 7 .
Conversion of chitosan to chitooligosaccharides by some endo-chitosanases.

Table 7 .
Conversion of chitosan to chitooligosaccharides by some endo-chitosanases.