Effect of NaCl on the Rheological, Structural, and Gelling Properties of Walnut Protein Isolate-κ-Carrageenan Composite Gels

In this study, we discovered that a certain concentration of Na+ (15 mM) significantly improved the bond strength (12.94 ± 0.93 MPa), thermal stability (72.68 °C), rheological properties, and textural attributes of walnut protein isolate (WNPI)-κ-carrageenan (KC) composite gel. Electrostatic force, hydrophobic interaction, hydrogen bond, and disulfide bond were also significantly strengthened; the α-helix decreased, and the β-sheet increased in the secondary structure, indicating that the protein molecules in the gel system aggregated in an orderly manner, which led to a much denser and more uniform gel network as well as improved water-holding capacity. In this experimental research, we developed a new type of walnut protein gel that could provide technical support for the high-value utilization and quality control of walnut protein.


Introduction
Walnut (Juglans regi L.) is a member of the Juglandaceae family that is particularly popular among consumers for its rich nutritional value [1,2]. China is the world's largest producer and consumer of walnuts, and most walnuts are used for oil extraction due to their extremely high content of polyunsaturated fatty acids [3]. Walnut meal is a byproduct of walnut oil production. Studies have shown that walnut meal contains more than 50% protein, but it is usually discarded, resulting in a waste of walnut protein [4]. In addition, walnut protein can be added to functional food as a natural raw material with good functionals characteristics and biological activity, which plays an important role in promoting human health [5]. Glutelin is the main protein group present in walnut protein (about 70%), and its low water solubility limits the functional performance of walnut protein in food [6]. At present, research on walnut protein is mainly focused on protein components, extraction and preparation methods, physical and chemical properties, and biologically active peptides [7][8][9][10]. There are few reports on gel and adhesion properties of walnut protein. Therefore, improving the gel properties of walnut protein is very important for the development of new gel foods for various applications.
Protein-polysaccharide complexes are commonly used to enhance the physicochemical properties of proteins [11]. Studies have shown that the electrostatic interactions, hydrophobic interactions, hydrogen bonds, and disulfide bonds between proteins and polysaccharides can overcome the repulsion between molecules and improve the final performance of the gel [12,13]. In addition, the filling effect of polysaccharides is conducive 2. Results and Discussion 2.1. Effect of Na + Concentration on the Rheological and Texture Properties of WNPI-KC Composite Gel 2.1. 1

. Rheological Properties
Rheological behavior is often used to evaluate the gelling ability of proteins [22]. As shown in Figure 1A,B, by measuring the changes in G and G of the WNPI-KC composite gel with strain, the linear viscoelastic region was determined to be 1%, and the temperature and frequency of the WNPI-KC composite gel were scanned in this region. During the cooling stage, the G value of all gel samples was significantly lower than G at the same temperature, indicating that an elastic-based gel was formed ( Figure 1C,D). With the increase in Na + concentration from 0 to 15 mM, G and G of the composite gel increased, indicating that during gel formation, stronger molecular interactions occurred between WNPI and KC, which resulted in the enhanced network structure of the composite gel [23]. When Na + concentration reached 20 mM, G and G values of the mixed gel decreased. Similar results were reported by Beck et al. [24]. In addition, G and G increased rapidly, indicating that the composite gel network continuously strengthened. Appropriate salt ion concentration was beneficial to protein aggregation and the formation of an elastic-dominant gel network, but excessive salt ion concentration led to excessive protein aggregation and was not conducive to the formation of gel.
As seen in Figure 1E,F, the modulus G and G values of all gel samples increased with increased angular frequency in the frequency scanning process in a frequency-dependent manner. At the same angular frequency, the G values were significantly lower than the same angular frequency of G , indicating that the gel has strong elastic properties. The G and G of WNPI-KC composite gel increased from 0 to 15 mM with increased Na+ concentration, indicating that there was a stronger molecular interaction between WNPI and KC during gel formation. When Na + concentration reached 20 mM, the G and G of WNPI-KC composite gel decreased. Wang et al. observed similar results, reporting that an appropriate Ca 2+ concentration (0-200 mM) increased the G and G of rice glutelin-sugar beet pectin complex gels, but excessive Ca 2+ (400 mM) decreased these values, which was not conducive to the formation of gel network [25].

Textural Properties
Texture performance is an important indicator of gel properties. As shown in Table 1, the hardness, adhesiveness, gumminess, and chewiness of WNPI-KC gel increased slightly with increased NaCl concentration (0-15 mM), but there was no significant difference in springiness, cohesiveness, or resilience (p < 0.05). This is mainly because the appropriate concentration of Na + reduced the repulsion between WNPI and KC and promoted the combination of WNPI and KC [26]. In addition, when the Na + concentration reached 20 mM, the hardness, adhesion, and chewiness of the WNPI-KC gel decreased. This may be due to the excessive aggregation of proteins caused by the addition of 20 mM Na + [27]. This was also consistent with the results of the microstructure. The dense gel network structure improved the texture properties of the gel [28].

Textural Properties
Texture performance is an important indicator of gel properties. As shown in Table 1, the hardness, adhesiveness, gumminess, and chewiness of WNPI-KC gel increased slightly with increased NaCl concentration (0-15 mM), but there was no significant difference in springiness, cohesiveness, or resilience (p < 0.05). This is mainly because the appropriate concentration of Na + reduced the repulsion between WNPI and KC and promoted the combination of WNPI and KC [26]. In addition, when the Na + concentration reached 20 mM, the hardness, adhesion, and chewiness of the WNPI-KC gel decreased. This may be due to the excessive aggregation of proteins caused by the addition of 20 mM Na + [27]. This was also consistent with the results of the microstructure. The dense gel network structure improved the texture properties of the gel [28]. The apparent viscosity of the WNPI-KC composite gel in the presence of NaCl is displayed in Figure 2A. As can be seen from the figure, 15 mM Na + had the highest apparent viscosity. This behavior may be due to the fact that appropriate concentration of Na + strengthened the hydrophobic interaction and the electrostatic interaction between WNPI and KC, and the high-molecular-weight polymers formed by the two may have caused higher apparent viscosity [29].  The apparent viscosity of the WNPI-KC composite gel in the presence of NaCl is displayed in Figure 2A. As can be seen from the figure, 15 mM Na + had the highest apparent viscosity. This behavior may be due to the fact that appropriate concentration of Na + strengthened the hydrophobic interaction and the electrostatic interaction between WNPI and KC, and the high-molecular-weight polymers formed by the two may have caused higher apparent viscosity [29].

Bond Strength
Bond strength is an important indicator for evaluating the adhesiveness of gels [30]. As shown in Figure 2B, the bonding strength of WNPI-KC composite was higher than that of a single protein and polysaccharide. After NaCl treatment, the bonding strength was further improved, with a maximum of 12.94 Mpa at an Na + concentration of 15 mM. This might be due to the fact that Na + promoted the unfolding of the protein molecular structure, increased the molecular force between WNPI and KC, and produced a good binding force, which is consistent with the results of apparent viscosity.

Bond Strength
Bond strength is an important indicator for evaluating the adhesiveness of gels [30]. As shown in Figure 2B, the bonding strength of WNPI-KC composite was higher than that of a single protein and polysaccharide. After NaCl treatment, the bonding strength was further improved, with a maximum of 12.94 Mpa at an Na + concentration of 15 mM. This might be due to the fact that Na + promoted the unfolding of the protein molecular structure, increased the molecular force between WNPI and KC, and produced a good binding force, which is consistent with the results of apparent viscosity. WHC could reflect the ability of protein gel to retain water. As presented in Figure 2C, the WHC of the WNPI-KC gel was the highest at 15 mM Na + , at 90.18%. Na + concentrations among 5-15 mM had no significant effect on the WHC of the composite gel (p > 0.05). It is possible that salt ions induced a dense gel structure. However, 20 mM Na + might cause the gel network to be rough and irregular, resulting in a decrease in WHC. Zhang et al. found that the composite gel of wheat gluten protein and potato isolate protein had a dense network structure under low concentrations of Na + , whereas it was relatively loose under high ionic strength [31]. Studies have shown that a denser three-dimensional network structure better confines water in the gel system, thereby significantly enhancing its WHC [32].

Thermal Stability
The effect of NaCl treatment on the thermal stability of the gel is presented in Figure 2D. The denaturation temperature of the gel without NaCl treatment was 69.19 • C. With an increase in Na + concentration, the heat denaturation temperature gradually increased and reached a maximum value of 72.68 • C at 15 mM Na + . The rising trend of thermal denaturation temperature was reversed due to the salting-out effect when Na + concentration reached 20 mM. Therefore, it can be inferred that the appropriate concentration of Na + could improve the thermal stability of the composite gel. This might be due to the stronger gel structure and stronger intermolecular interaction of the composite gel induced by Na + , which was consistent with the findings from Zhou et al.

Effect of Na + Concentration on the Moisture Distribution of WNPI-KC Composite Gel
LF-NMR was used to characterize the moisture characteristics of the gel system, and the quality of the gel was reflected by the evaluation of the distribution of water molecules [33]. It can be seen from Figure 3 that the T 2 curve possesses four separate peaks, which represent strongly bound water (T 2b ), weakly bound water (T 2b-1 ), immobilized water (T 21 ), and free water (T 22 ). The concentration of Na + at the T 2b , T 2b-1 , T 21 , and T 22 relaxation times of WNPI-KC composite gel and the corresponding peak areas, P 2b , P 2b-1 , P 21 , and P 22 , are shown in Table 2. Substances with a shorter relaxation time were closer to water molecules than those with a longer relaxation time. The water content of different states in the gel system was determined by comparing the corresponding peak areas. It can be seen from the relaxation times of T 2b and T 2b-1 after adding NaCl that the relaxation time showed a significantly shorter trend (p < 0.05). The T 2b-1 relaxation time of the composite gel with 15 mM Na + was the shortest, and the T 2b relaxation time appeared at the same time, revealing that the combination of WNPI and water molecules was tighter. After adding NaCl, the T 21 relaxation time was shortened, and there was almost no change with different concentrations of NaCl (p > 0.05). The relaxation time of free water appeared at 20 mM Na + , which indicates that excessive Na + concentration loosens the binding of water molecules and proteins. This result is consistent with WHC. It can be seen from the peak area that 15 mM Na + reduced the immobilized water of the composite gel, increased the bound water, and migrated to the strongly bound water. This might be due to the enhanced binding ability of WNPI to water molecules by Na + treatment.   Different letters in the same column indicate significant differences (p < 0.05).

Effect of Na + on the Particle Size and Zeta Potential of WNPI-KC Composite Gel
The particle size distribution reflects the size and uniformity of the particles in the sample solution. D [4,3] represents the volume-weighted average particle diameter, which indicates the degree of protein aggregation. ζ-potential is a vital indicator for evaluating colloidal stability; the lower the absolute value of the potential, the lower the stability of the solution system [34]. The particle size distribution of all samples was roughly bimodal ( Figure 4A), and D [4,3] of the composite gel was minimal at 15 mM NaCl ( Figure 4B). This indicates that the appropriate concentration of Na + ultrasound might cause the protein to unfold and reduce the particle size, thereby forming a much stabler and more uniform system, whereas an excessively high concentration of Na + would cause the formation of protein aggregates, leading to an increase in the particle size. Compared with WNPI and KC alone, the absolute value of the potential of the WNPI-KC composite system increased significantly (p > 0.05) ( Figure 4B). With the increase Na + concentration, it first increased and then decreased, reaching a maximum at 15 mM (46.37 mV). This might be due to the fact that WNPI and KC both carried negative charges, which increased the negative charges in the composite system and electrostatic repulsion between the droplets [35]. NaCl also had a certain amount of negative charge, which resulted in an increase in negative charge on the surface of the droplet. When Na + concentration was 20 mM, the protein reaggregated and shielded some charged groups, which increased the negative charge of WNPI-KC. The results show that the composite system had the smallest particle size and the highest absolute value of potential after treatment with 15 mM Na + , which effectively improved the stability of the composite system.

Effect of Na + on the Particle Size and Zeta Potential of WNPI-KC Composite Gel
The particle size distribution reflects the size and uniformity of the particles in the sample solution. D [4,3] represents the volume-weighted average particle diameter, which indicates the degree of protein aggregation. ζ-potential is a vital indicator for evaluating colloidal stability; the lower the absolute value of the potential, the lower the stability of the solution system [34]. The particle size distribution of all samples was roughly bimodal ( Figure 4A), and D [4,3] of the composite gel was minimal at 15 mM NaCl ( Figure 4B). This indicates that the appropriate concentration of Na + ultrasound might cause the protein to unfold and reduce the particle size, thereby forming a much stabler and more uniform system, whereas an excessively high concentration of Na + would cause the formation of protein aggregates, leading to an increase in the particle size. Compared with WNPI and KC alone, the absolute value of the potential of the WNPI-KC composite system increased significantly (p > 0.05) ( Figure 4B). With the increase Na + concentration, it first increased and then decreased, reaching a maximum at 15 mM (46.37 mV). This might be due to the fact that WNPI and KC both carried negative charges, which increased the negative charges in the composite system and electrostatic repulsion between the droplets [35]. NaCl also had a certain amount of negative charge, which resulted in an increase in negative charge on the surface of the droplet. When Na + concentration was 20 mM, the protein reaggregated and shielded some charged groups, which increased the negative charge of WNPI-KC. The results show that the composite system had the smallest particle size and the highest absolute value of potential after treatment with 15 mM Na + , which effectively improved the stability of the composite system.

FTIR
FTIR can be used to study the interaction between the various components in composite gel [36]. As shown in Figure 5A, the composite gel had several characteristic absorption peaks located at 3365 cm −1 , 1660 cm −1 , 1543 cm −1 , and 1240 cm −1 . No new peaks were observed in any of the samples, confirming that no new functional groups were generated by Na + treatment. When the Na + concentration was 0-15 mM, the broadband intensity from 3100 to 3500 cm −1 increased, indicating that the hydrogen bond strength was enhanced, but the high concentration of Na+ partially broke the hydrogen bond, resulting in a decrease in the broadband strength [37]. Similarly, peak intensities of amide I, amide II, and amide III bands were enhanced at low Na + concentrations (0-15 mM), which might be another important reason why Na + promoted the formation of a dense and stable network structure in WNPI-KC composite gel. The peak intensity decreased at a higher Na + concentration (20 mM), which might be due to the weakened interaction between WNPI and KC, as well as the decreased thermal stability caused by changes in the protein during heating.
The secondary structure of WNPI was fitted according to the amide I region in FTIR [38] ( Figure 5B). The α-helix content reduced from 15.64 (0 mM) to 12.39% (15 mM), whereas the β-sheet content increased from 35.23 to 39.02%. Studies have shown that an increase in β-sheet content is conducive to the formation of a dense and uniform gel network [39]. Zhao et al. also reported that the transformation of the α-helix to β-sheet of sweet potato protein was conducive to the formation of gel after adding salt ions [40]. In addition, with an increase in Na + concentration (20 mM), the random coil content increased, indicating that the structure of the protein gradually became irregular.  FTIR can be used to study the interaction between the various components in composite gel [36]. As shown in Figure 5A, the composite gel had several characteristic absorption peaks located at 3365 cm −1 , 1660 cm −1 , 1543 cm −1 , and 1240 cm −1 . No new peaks were observed in any of the samples, confirming that no new functional groups were generated by Na + treatment. When the Na + concentration was 0-15 mM, the broadband intensity from 3100 to 3500 cm −1 increased, indicating that the hydrogen bond strength was enhanced, but the high concentration of Na+ partially broke the hydrogen bond, resulting in a decrease in the broadband strength [37]. Similarly, peak intensities of amide I, amide II, and amide III bands were enhanced at low Na + concentrations (0-15 mM), which might be another important reason why Na + promoted the formation of a dense and stable network structure in WNPI-KC composite gel. The peak intensity decreased at a higher Na + concentration (20 mM), which might be due to the weakened interaction between WNPI and KC, as well as the decreased thermal stability caused by changes in the protein during heating.

Fluorescence Spectroscopy
Fluorescence spectroscopy has been widely used to determine tertiary structural changes in proteins [41]. As described in Figure 5C, the fluorescence intensity of the KC solution was close to 0, and the other samples all had maximum fluorescence emissions  The secondary structure of WNPI was fitted according to the amide I region in FTIR [38] ( Figure 5B). The α-helix content reduced from 15.64 (0 mM) to 12.39% (15 mM), whereas the β-sheet content increased from 35.23 to 39.02%. Studies have shown that an increase in β-sheet content is conducive to the formation of a dense and uniform gel network [39]. Zhao et al. also reported that the transformation of the α-helix to β-sheet of sweet potato protein was conducive to the formation of gel after adding salt ions [40]. In addition, with an increase in Na + concentration (20 mM), the random coil content increased, indicating that the structure of the protein gradually became irregular.

Fluorescence Spectroscopy
Fluorescence spectroscopy has been widely used to determine tertiary structural changes in proteins [41]. As described in Figure 5C, the fluorescence intensity of the KC solution was close to 0, and the other samples all had maximum fluorescence emissions at 335 nm. Compared with WNPI alone, the fluorescence intensity of WNPI-KC composite solution was significantly reduced. As the concentration of Na + increased, the fluorescence intensity first increased and then decreased reaching the lowest value at 15 mM (475). This might be due to the fact that Na+ accelerated the WNPI molecule-deployable structure and the chromophore was exposed to the solvent, which changed the polarity of the environment and reduced the fluorescence intensity [42]. Pallarès et al. revealed that the decrease in fluorescence intensity might be due to the tight tertiary conformation in WNPI shielding tryptophan residues [43]. The increased fluorescence intensity at high concentrations of Na + (20 mM) might be due to the weakening of the interaction between WNPI and KC.

Sulfhydryl Content
Sulfhydryl content can reveal changes in protein conformation and the degree of protein denaturation, which play an important role in the functional properties of the protein. With an increase in Na + concentration, the content of -SH in the composite solution increased gradually, and the highest sulfhydryl content was 141.54 µmol/g at 15 mM ( Figure 5D). Na + -induced protein unfolding was beneficial to the exposure of internal -SH groups, resulting in an increase in -SH content. Liu et al. reported that the disulfide bonds induced by sulfhydryl groups facilitated the formation of a gel network during thermal gelation [44]. In addition, the increase in free sulfhydryl groups enhanced the hydrophobic interaction between WNPI molecules and induced the composite system to form a stable gel. However, 20 mM Na + caused protein molecules to aggregate, and sulfhydryl groups were buried, resulting in a decrease in their content.

Surface Hydrophobicity
Surface hydrophobicity can reflect changes in protein structural properties [45]. The surface hydrophobicity showed an increasing trend when the Na + concentration increased from 0 mM to 15 mM and decreased at 20 mM Na + ( Figure 5E). The maximum surface hydrophobicity of the composite solution was 209.00 at 15 mM Na + . This may be because Na+ promotes the unfolding of the WNPI structure, exposing the hydrophobic group originally embedded in WNPI on the surface. However, excessive Na + (20 mM) caused salting out, and the hydrophobic groups and -SH groups would be hidden, which might affect the gel performance of the protein [46].

Microstructure
The influence of Na + concentration on the three-dimensional network structure of WNPI-KC composite gel was directly observed by laser scanning confocal microscopy. WNPI was marked as red by rhodamine B, and KC was marked as dark black ( Figure 6A-G). At low concentrations of Na + (0-15 mM), the protein molecules gradually unfolded, and the microstructure of the WNPI-KC gel gradually became homogeneous, indicating that the interaction between WNPI and KC was enhanced. However, 20 mM Na + aggregated protein molecules, suggesting that the microstructure was destroyed by excessive Na + . Zhang et al. reported that an appropriate concentration of Na + promoted the cross linking and polymerization of wheat gluten protein and potato isolate protein molecules, forming a uniform and dense gel network; however, with a continuous increase in Na + , the network structure of the gel was destroyed.
the cross linking and polymerization of wheat gluten protein and potato isolate protein molecules, forming a uniform and dense gel network; however, with a continuous increase in Na + , the network structure of the gel was destroyed.
The morphology of the WNPI-KC gel was further observed by scanning electron microscopy. The single protein had a sheet-like structure, and the polysaccharide had a rodlike structure (Figure 6a-g). The complex gel network without salt ions was relatively rough and had large gaps. With Na + concentration increased from 5 mM to 15 mM, the gel became dense with smaller pores, but at higher Na + concentrations, the gel matrix presented a concave-convex surface with many holes, which is consistent with the observation results of CLSM. Yang et al. also found that an appropriate concentration of Na + caused the protein form a uniform and dense network structure during heating. Excessive salt ions disrupted the balance and formed protein aggregation, resulting in a rough and uneven morphology, which might lead to reduced WHC and textural properties [47].  The morphology of the WNPI-KC gel was further observed by scanning electron microscopy. The single protein had a sheet-like structure, and the polysaccharide had a rodlike structure (Figure 6a-g). The complex gel network without salt ions was relatively rough and had large gaps. With Na + concentration increased from 5 mM to 15 mM, the gel became dense with smaller pores, but at higher Na + concentrations, the gel matrix presented a concave-convex surface with many holes, which is consistent with the observation results of CLSM. Yang et al. also found that an appropriate concentration of Na + caused the protein form a uniform and dense network structure during heating. Excessive salt ions disrupted the balance and formed protein aggregation, resulting in a rough and uneven morphology, which might lead to reduced WHC and textural properties [47].

Effect of Na + on the Intermolecular Force of WNPI-KC Composite Gel
The intermolecular forces were determined by measuring the solubility of WNPI-KC gel in different solutions [48]. It can be seen from Figure 7 that the main interaction force in the composite gel was hydrophobic interaction, which is consistent with the research results of Xia et al. [49]. The low concentration of Na + (5-15 mM) enhanced the electrostatic interaction, but as the Na + concentration further increased, the electrostatic interaction weakened. This may be due to the fact that a moderate concentration of NaCl can reduce the electrostatic repulsion between proteins and polysaccharides, thereby narrowing the distance between the two and promoting the formation of aggregates. In addition, the salt bridge formed by Na + and protein molecules also reduced the electrostatic repulsion. However, excessive Na + caused the protein particles aggregate and precipitate quickly, thereby reducing the electrostatic repulsion. Compared with composite gels that did not contain Na + , 15 mM Na + enhanced hydrophobic interactions. This indicates that Na + exposed the hydrophobic groups inside the protein molecules. However, WNPI might form irregular aggregates at 20 mM NaCl, reducing hydrophobic interactions. When the concentration of NaCl is 15mM, the hydrogen bonding effect is the strongest, which may be due to the fact that Na+ promoted the interaction between WNPI and water molecules [50]. The strength of disulfide bonds showed the same trend as that of hydrogen bonds. It is well known that sulfhydryl groups can induce the generation of disulfide bonds and promote the cross linking of proteins and polysaccharides during heating. The concentration of Na + at 15 mM induced the production of more -SH, so the content of disulfide bonds increased. distance between the two and promoting the formation of aggregates. In addition, the salt bridge formed by Na + and protein molecules also reduced the electrostatic repulsion. However, excessive Na + caused the protein particles aggregate and precipitate quickly, thereby reducing the electrostatic repulsion. Compared with composite gels that did not contain Na + , 15 mM Na + enhanced hydrophobic interactions. This indicates that Na + exposed the hydrophobic groups inside the protein molecules. However, WNPI might form irregular aggregates at 20 mM NaCl, reducing hydrophobic interactions. When the concentration of NaCl is 15mM, the hydrogen bonding effect is the strongest, which may be due to the fact that Na+ promoted the interaction between WNPI and water molecules [50]. The strength of disulfide bonds showed the same trend as that of hydrogen bonds. It is well known that sulfhydryl groups can induce the generation of disulfide bonds and promote the cross linking of proteins and polysaccharides during heating. The concentration of Na + at 15 mM induced the production of more -SH, so the content of disulfide bonds increased.

Effect of Na + on the Schematic Mechanism of WNPI-KC Composite Gel
Based on the above research results, the gelling mechanisms of different concentrations of NaCl on WNPI-KC composite are shown in Figure 8. In the absence of NaCl, WNPI-KC composite gel did not show good gel strength, so the bond strength was low. At 15 mM NaCl, WNPI-KC composite gel had the best gel properties. This is because the combination of electrostatic shielding and ion bridging cause the protein molecule to unfold, and more sulfhydryl groups and hydrophobic groups in the protein molecule were exposed and enhanced the interaction between WNPI and KC, which promoted the ordered aggregation of the composite system, forming an ordered network structure with the best gel performance. However, salting out occurred at 20 mM NaCl, which led to excessive aggregation of the composite system, resulting in a rough and irregular structure in the gel system, so it had poor gel strength. In conclusion, 15 mM NaCl improved the gel properties of the WNPI-KC composite system.

Effect of Na + on the Schematic Mechanism of WNPI-KC Composite Gel
Based on the above research results, the gelling mechanisms of different concentrations of NaCl on WNPI-KC composite are shown in Figure 8. In the absence of NaCl, WNPI-KC composite gel did not show good gel strength, so the bond strength was low. At 15 mM NaCl, WNPI-KC composite gel had the best gel properties. This is because the combination of electrostatic shielding and ion bridging cause the protein molecule to unfold, and more sulfhydryl groups and hydrophobic groups in the protein molecule were exposed and enhanced the interaction between WNPI and KC, which promoted the ordered aggregation of the composite system, forming an ordered network structure with the best gel performance. However, salting out occurred at 20 mM NaCl, which led to excessive aggregation of the composite system, resulting in a rough and irregular structure in the gel system, so it had poor gel strength. In conclusion, 15 mM NaCl improved the gel properties of the WNPI-KC composite system.

Conclusions
In this study, we explored the influence of NaCl concentration on the rheological, structural, and gelling properties of WNPI-KC composite gel. The results showed that an appropriate concentration of Na + (15 mM) significantly increased the free sulfhydryl content and surface hydrophobicity of WNPI-KC and promoted the transformation of its

Conclusions
In this study, we explored the influence of NaCl concentration on the rheological, structural, and gelling properties of WNPI-KC composite gel. The results showed that an appropriate concentration of Na + (15 mM) significantly increased the free sulfhydryl content and surface hydrophobicity of WNPI-KC and promoted the transformation of its structure from α-helix to β-sheet, which was beneficial to promote the orderly aggregation of the composite system and formation of an orderly network structure. A concentration of 15 mM Na + also enhanced the interaction force between WNPI and KC; thus, the cohesiveness, rheological properties, texture properties, and WHC of the composite gel were significantly improved. However, excessive Na + (20 mM) led to excessive aggregation of the composite system, resulting in irregular gel structure and damage to the gel and bond strength. With this experiment, we constructed a new type of salt-ion-regulated walnut protein gel system, which could represent a new method for improving the gel properties of WNPI. It could also provide technical support for its application in the food industry and other related industries. Further research is needed concerning the mechanism of action and practical application scenarios.

Materials
Walnuts were obtained from a local market in Wuhan (Hubei, China). κ-carrageenan was obtained from Henan Chinuo Food Ingredients Co., Ltd. (Henan, China). Other chemicals were obtained from Sinopharm Chemical Reagent Co., Ltd. (Shanghai, China).

Preparation of WNPI and WNPI-KC Composite Gels
WNPI was prepared according to the method described in a previous study [51]. A given amount of WNPI, KC, and NaCl was mixed in deionized water and stirred magnetically at 25 • C for 2 h. The final concentration of WNPI and KC in the composite solutions was 5% (w/v) and 0.5% (w/v), respectively. The Na + concentrations were 0, 5, 10, 15, and 20 mmol/L. Then, the composite solution was heated in a 90 • C water bath for 30 min, immediately cooled, and then kept at 4 • C for 12 h to prepare WNPI-KC composite gel.

Determination of Bond Strength
Three samples of the same size were glued together with a gel sample using corrugated cardboard as a material. The bonding strength was measured with an electromechanically universal testing machine with a tensile speed of 10 mm/min. The average value of each sample was taken, and the corresponding test was carried out six times [54].

Water-Holding Capacity (WHC)
An amount of 5 g gel sample was placed in a centrifuge tube and centrifuged at 8000 r/min for 10 min. WHC is expressed as the ratio of the gel weight after centrifugation to the gel weight before centrifugation [55].

Thermal Stability
A Micro-DSCIII differential scanning calorimeter (DSC) (TA Instruments, New Castle, DE, USA) was used to determine the thermal stability of the composite gel [56]. A given amount of lyophilized gel powder was added to the crucible, and then the heating rate and scanning temperature were set to 10 • C/min and 25-125 • C, respectively.

Low-Field Nuclear Magnetic Resonance (LF-NMR)
The moisture distribution of the composite gel was determined using an LF-NMR analyzer (MesoMR, Niumag Electronic Technology Co., Ltd., Shanghai, China) as described by Zhang et al., with minor modifications [57]. The number of scans, echo time, and waiting time were set to 4, 0.5, and 5000 ms, respectively. A total of 4000 echoes were collected for analysis. DLX software was used to analyze the results through the corresponding relative signal amplitude.

Particle Size and Potential
The D [3,4]

Fourier Transform Infrared (FTIR) Spectroscopy
The freeze-dried gel sample was scanned 64 times in the range of 4000 cm −1 to 400 cm −1 with a resolution of 4 cm −1 using an FTIR spectrometer [59]. The changes in secondary structure of amide I bonds in the 1600-1700 cm −1 range were analyzed by Omnic and PeakFit software. The content of each secondary structure was calculated by absorption peak area.

Fluorescence Spectroscopy
The fluorescence spectra of composite solutions (1 mg/mL) were measured by a fluorescence spectrofluorometer. The parameters were set as follows: excitation wavelength, 280 nm; scanning range, 300-400 nm; scanning speed, 1200 nm/min; slit width, 5 nm.

SH Content
A volume of 4 mL of WNPI-KC composite solution (1 mg/mL) was mixed with 40 µL DTNB solution, and the reaction was incubated at 25 • C for 30 min in the dark [60]. The calculation method was as follows: Sul f hydryl (µmol/100 mg) = A 412 × D × 10 5 13,600 × C pr (1) where A 412 represents the absorbance at 412 nm; D represents the dilution factor; and C p r represents the sample concentration (mg/mL).

Surface Hydrophobicity
The surface hydrophobicity of the samples was measured according to the method of Wang et al., with slight modifications [61]. The samples treated with different concentrations of NaCl were diluted into solutions with a concentration of 0.1-0.5 mg/mL, and 20 µL of 8 mmol/L ANS was added to 4 mL of different concentrations of solution. The reaction was performed in the dark for 20 min at 25 • C, and then the fluorescence intensity was measured with a fluorescence spectrophotometer. The measurement parameters were set as: excitation wavelength, 390 nm; emission wavelength, 470 nm; slit, 5 nm; scanning speed, 240 nm/min. Finally, the fluorescence intensity was plotted versus protein concentration, and its initial slope was used as an index of protein surface hydrophobicity.

Microstructure
The CLSM of the composite gels was observed using a laser confocal microscope(Tecnai G2 Spirit BIOTWIN, FEI, Rochester, NY, USA). Before observation, the composite solution (20 µL/mL) was stained with 0.02% rhodamine B reagent. The surface morphology of the WNPI-KC gel was observed at 1000 times magnification using SEM as described by Feng et al. [62].

Molecular Interaction Forces
The intermolecular forces during WNPI-XG gel formation were measured according to the method described by Sun et al. [63]. An amount of 0.5 g of gel samples was mixed with ultrapure water (pH 8.0), 0.086 M Tris-0.09 M glycine-4 mM-Na2EDTA (pH 8.0), 0.5% SDS, 8 M urea, and 2% β-mercaptoethanol. After 20 min of reaction, samples were centrifuged (5000× g, 15 min) and the supernatant (8000× g, 10 min) was obtained, and the solubility of the protein in the supernatant was calculated according to the Biuret method.

Statistical Analysis
Analysis of variance (ANOVA) and Tukey's test were performed on the data using SPSS 25.0, and Origin 2017 was used for graph drawing. Differences were considered statistically significant when p < 0.05. Each experiment was performed in triplicate, and the results are expressed as the mean ± standard deviation.