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Article

Partial Characterization of Protease Inhibitors of Ulva ohnoi and Their Effect on Digestive Proteases of Marine Fish

by
Antonio Jesús Vizcaíno
*,
Alba Galafat
,
María Isabel Sáez
,
Tomás Francisco Martínez
and
Francisco Javier Alarcón
Departamento de Biología y Geología, Escuela Superior de Ingeniería, Ceimar-Universidad de Almería. La Cañada de San Urbano, 04120 Almería, Spain
*
Author to whom correspondence should be addressed.
Mar. Drugs 2020, 18(6), 319; https://doi.org/10.3390/md18060319
Submission received: 30 April 2020 / Revised: 12 June 2020 / Accepted: 16 June 2020 / Published: 18 June 2020
(This article belongs to the Special Issue Enzyme Inhibitor from Marine Organisms)
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Abstract

:
This piece of research evaluates the presence of protease inhibitors in the macroalga Ulva ohnoi and provides an initial overview of their mode of action. The ability of Ulva protease inhibitors to inhibit digestive proteases of three marine fish species, as well as their capacity to hamper the hydrolysis of a reference protein by those fish proteases, were assessed. In addition, thermal stability and the mode of inhibition on trypsin and chymotrypsin were also studied. Dose-response inhibition curves and in vitro protein hydrolysis assays revealed a noticeable inhibition of fish enzymes when Ulva concentration increased in the assay. The thermal treatment of Ulva reduced markedly the inhibitory effect on fish digestive protease. Finally, Lineweaver–Burk plots indicated that trypsin and chymotrypsin inhibition consisted of a mixed-type inhibition mechanism in which the inhibitory effect depends on Ulva concentration. Overall, the results confirmed the presence of protease inhibitors in Ulva, though heat treatment was enough for inactivating these compounds.

Graphical Abstract

1. Introduction

Anti-nutritional factors (ANFs) can be defined as substances that, by themselves or through their metabolic products, can exert negative effects on food utilization and interfere with the normal growth, reproduction and health of fish [1]. From a nutritional point of view, the presence of these compounds in diets is responsible for the deleterious effects on the absorption of nutrients and micronutrients, which may interfere with the normal functioning of certain organs [2]. This fact is one of the most important issues derived from using novel dietary ingredients in aquaculture, as well as one of the main drawbacks that limits their practical application in formulated feeds [3,4].
In general, ANFs have been mainly related to plant-derived feedstuffs, and they comprise a wide variety of compounds, such as protease inhibitors, phytohemagglutinin, lectins, phytic acid, saponins, phytoestrogens or antivitamins [1,5]. Although less known, recent studies have also documented the presence of these substances in seaweeds, considered currently a potential alternative ingredient for farmed fish [6,7].
Seaweeds have drawn the attention of researchers not only as an important source of dietary protein, but also as functional ingredients in aquafeeds [8]. More specially, some species of the genus Ulva have been successfully evaluated as a dietary ingredient in some farmed fish species, such as gilthead seabream (Sparus aurata) [9,10], Senegalese sole (Solea senegalensis) [8,11] or seabass (Dicentrarchus labrax) [12], with promising results in terms of growth, survival and nutrient utilization. Despite the health benefits reported for seaweeds, some studies have described that the dietary inclusion level of algae above 20% yields detrimental effects on fish growth and other zootechnical parameters. It has been suggested that these effects could be attributed to the existence of ANFs, which might affect the bioavailability and/or digestibility of nutrients [13].
In this regard, Oliveira et al. [14] and Maehre, [6] confirmed the presence of lectins, trypsin and alpha-amylase inhibitors, as well as phytic acid, in some species of marine algae, although polyphenolic compounds are considered the substances most frequently linked to their antinutritional effects [6,14]. It has been described that the presence of lectins in feed alters the intestinal epithelium, resulting in the over-secretion of mucus that may impair the enzymatic and absorptive capacity of fish [15], altogether leading to reduced growth [5]. Phytic acid and polyphenols bind to proteins and polysaccharides producing insoluble high-molecular complexes, a fact that reduces nutrient bioavailability and consequent nutrient deficiency, such as that described for methionine, which is essential for lipid metabolism [15,16]. In addition, other antinutritional compounds of seaweeds, such as phytates, can inhibit the action of gastrointestinal enzymes like tyrosinase, trypsin, pepsin, lipase and amylase [2].
It is also worth mentioning the existence of protease inhibitors, substances that bind to proteolytic enzymes causing not only reduced proteolysis, but also increased pancreatic secretion as an attempt to overcome these antinutritional effects [17]. Despite the evidence suggesting the presence of protease inhibitors in seaweeds and their possible effects on the digestive physiology of aquacultured fish [7,13,17], scarce research is available regarding the characterization of their effects. In this context, this this research aims to assess the presence of protease inhibitors in Ulva ohnoi, evaluating the effects of such inhibitors on fish digestive proteases, characterizing their mode of inhibition, and exploring potential strategies to reduce their detrimental effects on fish digestive enzymes.

2. Results

2.1. Inhibition Assay

The inhibitory effect of Ulva ohnoi on the digestive proteases of gilthead seabream, Senegalese sole and seabass is shown in Figure 1. Dose-response inhibition curves were obtained by measuring the reduction in proteolytic activity on a standardized fish intestinal extract following incubation with different volumes of Ulva extract. The results confirmed the presence of protease inhibitor in crude Ulva (CR-Ulva) able to inhibit up to 70% of Senegalese sole’s proteolytic activity, and by 65% of protease activity in the other two fish species. It was also found that the amount of Ulva able to cause the inhibition of 50% digestive protease activity (IC50) ranged from 0.6 to 0.9 mg Ulva per unit of proteolytic activity (UA). On the other hand, autoclaved Ulva (heat treated; HT-Ulva) reduced significantly its inhibitory capacity (less than 20% inhibition in all cases) compared to CR-Ulva (p < 0.05).
Zymograms of fish digestive proteases after incubation with Ulva extract are shown in Figure 2. The effects of protease inhibitors were compared to a control without Ulva (lane 1). Noticeable reduction in the intensity of the active fractions (with proteolytic activity) was evidenced after incubation with Ulva (lanes 2 to 4). Differences in the inhibitory effect were observed among the three fish species. In the case of gilthead seabream, a progressive decrease in the intensity of all active proteases was observed as the Ulva concentration increased, whereas protease inhibition in the other fish was selective for some specific active fractions.

2.2. In Vitro Casein Hydrolysis

Proteinograms of casein hydrolyzed by fish digestive enzymes are shown in Figure 3. All the main casein fractions (34, 26 and 23 kDa), corresponding to α, β and κ subunits, were hydrolyzed after 30 min.
Figure 4 shows the time-course protein hydrolysis of casein by the fish digestive proteases in the presence of Ulva extracts. Overall, CR-Ulva hampered the capacity of fish proteases to hydrolyze casein. The fate of the casein fractions throughout the in vitro assay was partial and less marked compared to the same assay carried out without Ulva (Figure 3). It was also observed that the inhibitory effect was dose-dependent, given that the higher CR-Ulva concentration in the in vitro assay, the lower the hydrolytic capacity of fish digestive enzymes against casein. The inhibitory effect of Ulva extracts on digestive proteases was reduced remarkably owing to thermal treatment, as revealed by the proteinograms shown in Figure 4 (lanes at the right). Thus, heat-treated seaweed extracts (HT-Ulva) were affected casein hydrolysis to a lesser extent than untreated Ulva (CR-Ulva), in such a way that none of the casein subunits remained after 90 min in any of the assays carried out with HT-Ulva. However, intraspecific and dose-dependent differences were found, and thus increasing concentrations of HT-Ulva also reduced casein hydrolysis, not least for seabream and seabass digestive proteases.
The estimated values of the coefficient of protein degradation (CPD) and total amino acids released after the in vitro hydrolysis of casein are given in Table 1. The CR-Ulva lowered the rate of protein degradation compared to the assay performed without Ulva (p < 0.05). The lowest CPD values were observed for the highest concentrations of CR-Ulva in the reaction mixture (1500 µg per UA). In parallel, the amount of free amino acids released was also affected by the interaction of Ulva extracts with fish proteases, especially for highest concentrations of CR-Ulva. The impact of HT-Ulva on S. aurata and S. senegalensis digestive protease activity was negligible, since neither the CPD nor free amino acids that were released were different from the controls. However, a certain residual inhibitory effect of HT-Ulva was observed on D. labrax enzyme extracts.

2.3. Thermal Stability of Protease Inhibitors

The influence of a thermal treatment on the inhibitory capacity of Ulva on trypsin activity was evaluated. A noticeable reduction in the inhibitory effects of Ulva was observed as the temperature increased (Figure 5). Protease inhibitors of the Ulva extracts were stable at room temperature, but their inhibitory effect significantly reduced (p < 0.05) above 40 °C. The exposure of Ulva extract at 80 °C for 30 min reduced their inhibitory activity up to 50% compared to the untreated controls.
The existence of proteinaceous complexes consisting of Ulva protease inhibitors and trypsin is revealed in Figure 6. The commercial trypsin showed three protein fractions (24, 24.4, and 26 kDa, lane 1), whereas the protein pattern of the Ulva extract contained several protein fractions (lane 2). The incubation of trypsin with crude Ulva before SDS-PAGE (sodium dodecyl sulphate polyacrylamide gel electrophoresis) yielded a characteristic protein profile in which the 24 and 26 kDa fractions of trypsin disappeared. Instead, a new 31 kDa fraction appeared (lanes 3 to 5), which was not present either in trypsin or in Ulva. However, this 31 kDa protein fraction did not appear when trypsin was incubated with heat-treated Ulva (lanes 6 to 8).

2.4. Kinetic Parameter’s

The data obtained for the kinetic studies performed with trypsin and chymotrypsin are shown in Figure 7. The results demonstrated that Ulva protease inhibitors yielded a potential mixed type inhibition, as revealed by the decrease in Vmax as Km increased, compared to the apparent kinetic parameters obtained for both trypsin and chymotrypsin activities in the absence of Ulva (Table 2).

3. Discussion

Seaweeds are considered a promising alternative ingredient for aquafeeds. In addition to having nutrients with potential quantitative interest, the presence of biologically active compounds like polysaccharides, pigments (chlorophylls and carotenoids), sterols, polyphenols, and vitamins also makes seaweeds a valuable functional ingredient for aquafeeds [18,19]. However, it has been reported that macroalgae contain several anti-nutritional factors as well, such as lectins and protease inhibitors that might interfere with digestive processes [8]. In this regard, the present study explores the presence of antinutritional factors in Ulva ohnoi with a potential inhibitory effect on fish digestive proteases and provides an initial overview of their mode of action on those proteolytic enzymes.
Related to Ulva ANFs, the results of the present study confirmed the existence of compounds able to reduce the digestive proteolytic activity of different marine fish species. This fact agrees with previous studies pointing to the existence of protease inhibitors in some macroalgae species, such as Ulva rigida, Ulva ohnoi, Gracilaria cornea and Sargassum sp. [7,8,17]. In our study, inhibition plots and zymograms illustrate the response of fish proteases after incubation with crude Ulva ohnoi. Seabream, Senegalese sole and seabass digestive proteases showed susceptibility to Ulva ANFs, although a high concentration of Ulva was needed to cause high inhibition (>50% of protease inhibition). According to the equations obtained from the inhibition assays, the amount of Ulva required to reach IC50 would represent a dietary inclusion of approximately 40–53% in feeds, which are unusual levels for feed formulation. From a practical point of view, for 40 g fish consuming feeds containing 15% Ulva at an intake rate of 3% of its body weight, a 20% reduction in their digestive protease activity would be expected. In general, fish have physiological mechanisms aimed at compensating the effects of dietary antinutrients [20], although the influence of these compounds is species-specific [21] and may depend on different factors like fish physiology, macroalgae species, duration of feeding period with seaweed-supplemented diets, and the dietary inclusion level [8]. In this regard, there are numerous studies reporting the utilization of dietary seaweeds without compromising growth performance [19,22]. However, others described some negative effects on fish growth, even using seaweed biomass at low dietary inclusion level [8].
The effect of Ulva inhibitors on fish digestive proteases were also evidenced in zymograms. Protease inhibition caused by CR-Ulva on gilthead seabream enzymes could be classified as “unspecific”, owing to the fact that all the protease fractions visualized in the gels were affected similarly. However, the inhibitory effect seemed to be more “specific” in Senegalese sole and seabass, taking into account that the active fractions with molecular masses below 30 kDa were inhibited even with the lowest amount of crude Ulva, whereas heavier proteases were inhibited only using the highest concentration assayed. This reduction in protease activity may negatively affect feed intake and nutrient digestibility in fish [23]. In this context, the in vitro digestive simulations also confirmed that CR-Ulva hampered the hydrolysis of standard (casein) by digestive proteases of three different species of aquaculture fish. Thus, a clear reduction both in CPD values and the amount of amino acids released was evidenced when the concentration of CR-Ulva in the in vitro assay was increased. Considered together, both findings clearly indicate lower protein hydrolysis and also reflect a significant reduction in the hydrolytic action of both the digestive endo- and exo-proteases of fish [24].
The deactivation of ANFs is an important issue in raw materials processing [25]. Basically, ANFs can be divided into two groups: (i) heat-labile ANFs, including protease inhibitors, phytates and lectins; and (ii) heat-stable ANFs, represented by saponins, non-starch polysaccharides and some phenolic compounds [2]. Heat treatment is a simple procedure for inactivating ANFs and improving the nutritional value of raw protein feedstuffs [26]. The results in our study indicate that thermal treatment is effective when it comes to inactivating Ulva ohnoi ANFs that affect fish digestive proteases. The degree of ANFs inactivation depends on factors like temperature, time, particle size, and moisture conditions [2]. In fact, both time and temperature should be controlled carefully in order to minimize losses of nutritional value of a given feed ingredient (for instance, lower availability of amino acids and vitamins, and reduced protein bioaccessibility) as a result of excessive heat denaturation [15,27]. In this regard, the effect of the thermal treatment on the capacity of Ulva to inhibit trypsin activity indicates that such inhibitors are susceptible to relatively slight thermal treatment. A thermal treatment of 80 °C for 15 min reduced the inhibitory capacity by 50%, and above 75% as prolonged times were applied. In agreement, proteinograms (Figure 6, lanes 6 to 8) also confirmed that Ulva protease inhibitors are thermolabile, owing to the lack of detection of the 31 kDa proteinaceous complex following the thermal treatment of Ulva. These results suggest that temperatures reached during the standard industrial processing, for instance, in the extrusion of feeds, would be enough for minimizing the inhibitory capacity of Ulva. Both the preconditioning of the ingredient mixture and the friction forces of the extrusion process itself, which squeezed through a cylinder by a specially designed volute [26] can increase the temperature above 100 °C. Indeed, many researchers have shown that extrusion is an efficient procedure for decreasing the trypsin inhibitory capacity of pulses like soybean without altering the amino acid composition, transforming soybean into a high-quality product [26].
For a better understanding of the potential mode of action of Ulva protease inhibitors, a kinetic study was performed in which commercial trypsin and chymotrypsin were exposed to Ulva extracts. Plant protease inhibitors are characterized by either reversible or irreversible mechanisms [28]. In the present study, kinetics studies revealed a potential reversible inhibition. According to the Lineweaver–Burk plots, both trypsin and chymotrypsin inactivation occurred by a mixed-type inhibition. This type of inhibition is characterized by the ability to bind not only to free enzymes but also to with the enzyme-substrate complexes [29]. In kinetics terms, mixed type inhibition causes changes that result in a progressive decrease in Vmax when Km increases occurs [30]. This type of inhibition cannot be reversed by increasing substrate concentration, given that the inhibitor cannot be displaced by the substrate. Therefore, the extent of the inhibition depends on the concentration of the inhibitor. In addition, differences in Km indicated that Ulva protease inhibitors presented higher affinity for trypsin than for chymotrypsin.
Although plenty of literature regarding the mechanisms of plant protease inhibitors is available, there are no studies assessing the mode of action of seaweed protease inhibitors. Protease inhibitors in soybean and other seeds have been studied extensively. They are grouped into the Bowman–Birk and Kunitz families according to primary structure homology, the position of reactive sites, the number or location of disulfide bonds, and their ability to withstand thermal and acid processing [31]. According to the available literature, Kunitz proteinase inhibitors are usually 18–26 kDa proteins [32]. Overall, they are characterized by several Kunitz domains composed of approximately 60 amino acid residues, stabilized by three conserved disulfide bonds. This family mainly inhibits trypsin and weakly inhibits chymotrypsin [33] and is relatively heat- and acid-sensitive [15]. On the other hand, Bowman–Birk proteinase inhibitors (BBIs) are usually 6–9 kDa proteins with a polypeptide chain bridged by seven conserved disulfide bonds; they have independent sites for trypsin and for chymotrypsin, and they display similar inhibitory capacity for both proteases [31,34]. Disulfide bonds are fundamental for maintaining the structural stability of inhibitors [35]. Unfortunately, this work does not provide information on the structure of purified protease inhibitors of Ulva, their molecular weight, or their amino acid profile; however, the ability to inhibit mainly trypsin and also chymotrypsin, as well as the heat lability observed, suggest a certain similarity with the Kunitz type inhibitors family, although further studies are needed to ascertain this hypothesis.

4. Materials and Methods

4.1. Ulva Biomass

Ulva ohnoi biomass was ground, sieved (<100 µm), and kept at −20 °C until use. For inhibitory assays, Ulva biomass was separated in two different batches (100 g each), the first batch received no thermal treatment (CR-Ulva), and the second was heat-treated at 120 °C for 20 min (HT-Ulva). Aqueous extracts (0.1 g mL−1) were prepared from CR-Ulva and HT-Ulva, homogenized in distilled water by shaking for 30 min at room temperature, and then for 24 h at 4 °C. The mixture was centrifuged for 20 min at 12,000 g and 4 °C. Supernatants were stored at 4 °C until used in posterior inhibitory assays.

4.2. Fish Enzyme Extracts

Juvenile specimens of gilthead seabream (Sparus aurata), seabass (Dicentrarchus labrax), and Senegalese sole (Solea senegalensis) were used as model aquaculture fish species. Nine fish of each species were anesthetized and sacrificed by severing their spine according to the requirements of the Council Directive 2010/63/UE. The abdomen was opened and the whole viscera were obtained. Intestines of each species were pooled (three pools including three intestines each, one per fish species), and manually homogenized in distilled water at 4 °C to a final concentration of 0.5 g mL−1. Supernatants were obtained after centrifugation (12,000 rpm for 12 min at 4 °C) and stored at −20 °C until further use. The total soluble protein in the enzyme extracts was determined using bovine serum albumin as standard [36]. The total alkaline protease activity in the enzyme extracts was measured spectrophotometrically following the procedures described by Alarcón et al. [37], using 5 g L−1 casein in 50 mM Tris–HCl (pH 9.0) as substrate. One unit of total protease activity of activity (UA) was defined as the amount of enzyme that released 1 µg of tyrosine per min in the reaction mixture, considering an extinction coefficient for tyrosine of 0.008 µg−1 mL−1 cm−1, measured spectrophotometrically at 280 nm.

4.3. Testing the Presence of Protease Inhibitors in Ulva

The inhibitory effects of CR-Ulva and HT-Ulva on the intestinal proteases of gilthead seabream, Senegalese sole and seabass were determined using a modification of the method described by Alarcón et al. [38]. This method is based on the measurement of the residual proteolytic activity after the preincubation of fish extracts with different volumes of CR-Ulva and HT-Ulva extracts providing a ratio mg Ulva per fish protease activity ranged from 0.0 mg Ulva UA−1 to 1.5 mg Ulva UA−1. Enzyme inhibition was expressed as a percentage of protease inhibition after comparing with a control assay carried out without any Ulva extract. In addition, the amount of Ulva requested for 50% protease inhibition (IC50) was estimated.
In order to visualize the effect of Ulva on active fish intestinal proteases, substrate-SDS-PAGE electrophoresis gels were performed. Intestinal extracts were preincubated for 60 min with different volumes of CR-Ulva or HT-Ulva extracts. Then, the samples were mixed (1:1) with SDS sample buffer (0.125 M Tris HCl, pH 6.8; 4% (w/v) SDS; 20% (v/v) glycerol; 0.04% (w/v) bromophenol blue) and SDS-PAGE was performed according to Laemmli, [39] using 11% polyacrylamide gels (100 V per gel, 45 min at 4 °C). Zymograms revealing protease active bands were made according to Alarcón et al. [37]. After electrophoresis, gels were washed with distilled water and incubated in 0.75% (w/v) casein solution prepared in 50 mM Tris–HCl buffer, pH 9.0, for 30 min at 4 °C. The gels were then incubated in the same solution for 90 min at 37 °C without agitation. Finally, the gels were washed and fixed in 12% TCA for 10 min to stop the reaction prior to staining with Coomassie Brilliant Blue R-250 in a solution of methanol–acetic acid–water for 12 h. Distaining was done using a methanol–acetic acid–water solution. Clear gel zones revealed the presence of active proteases with caseinolytic activity.

4.4. Effect of Ulva on Fish Digestive Proteases

The capacity of Ulva to inhibit the hydrolysis of casein by fish intestinal proteases was also assessed using an in vitro assay in the presence of different concentrations of crude (CR) and heat-treated (HT) algae biomass providing 0.5, 1.0 and 1.5 mg Ulva UA−1.
The in vitro casein hydrolysis was simulated in 10 mL-jacketed reaction vessels connected to a circulating water bath at 37 °C, under continuous agitation by a magnetic stirrer. The temperature was selected in order to increase the activity of the enzymes for reducing the time requested for each analysis [40]. An amount of casein, providing 80 mg of crude protein per vessel, was suspended in 50 mM Tris HCl buffer pH 9.0. After 15 min stirring, the hydrolysis was started by the addition of the enzymatic extract providing 200 UA of total alkaline proteolytic activity [24]. The alkaline hydrolysis was maintained for 90 min, and samples of the reaction mixture (0, 15, 30, 60 and 90 min) were withdrawn. The products of the hydrolysis were separated by sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE), and total amino acids released were also measured at each sampling time, in order to estimate the sequential degradation of casein [41]. All determinations were performed in triplicate. Blank assays with casein but without Ulva biomass were carried out for each fish species.
In order to visualize the casein hydrolysis of SDS-PAGE-separated casein fractions, electrophoresis gels were performed. The procedure was carried out as previously described. The rate of hydrolysis was expressed by a numerical value obtained considering both the percentage of reduction in optical density for each protein after the enzymatic hydrolysis and the relative proportion that such protein represented in the total proteins [38]. The value obtained was called the coefficient of protein degradation (CPD), and it was estimated using the following mathematical expression:
C D P = ∑ i = 1 n [ O D i ( t = 0 ) − O D i ( t = 90 min ) O D i ( t = 0 )   x   100 ]   x   O D i ( t = 0 ) ∑ i = 1 n O D i ( t = 0 )
where i are the proteins identified, ODi is the optical density of the proteins, and t is the time of reaction.
In addition, the total released amino acids in each sampling time were also quantified at 340 nm in a spectrophotometer (Shimadzu UV-1800, Shimadzu, Kyoto, Japan), using L-leucine as standard [41]. The results were expressed as accumulated values of amino acid released during the enzymatic hydrolysis (g 100 g protein−1).

4.5. Partial Characterization of Ulva Protease Inhibitors

4.5.1. Effect of Temperature on Protease Inhibitors

The effect of temperature on Ulva protease inhibitors was assessed by heating the aqueous Ulva extract (0.1 g mL−1) at different temperatures (25, 40, 60, 80, 90, 100 °C) during 60 min and then immediately cooled in a water bath. Samples of Ulva from each temperature treatment were withdrawn at 5, 15, 30 and 60 min, and then preincubated with a solution of bovine trypsin (1 µg mL−1. T8003 from Sigma Aldrich, SL. Saint Louis, MO, USA) during 60 min at room temperature at a ratio of 500 µg of Ulva per µg trypsin. After that, trypsin activity was assayed according to Erlanger et al. [42] using BAPNA (Nα-Benzoyl-DL-arginine 4-nitroanilide hydrochloride) as substrate. Enzyme inhibition was expressed as the percentage of trypsin inhibition after comparing with a control assay carried out without Ulva. SBTI was used as positive control of the inhibition assay.
In addition, the formation of proteinaceous enzyme-inhibitor complexes was determined by using substrate-SDS-PAGE electrophoresis gels. Samples were prepared by preincubating crude or heat-treated (100 °C, 5 min) Ulva extracts with a trypsin solution (1 µg mL−1) at a ratio of 500 µg of Ulva per µg trypsin for 0, 30 and 60 min at room temperature. Samples were mixed (1:1) with SDS sample buffer (0.125 M Tris HCl, pH 6.8; 4% (w/v) SDS; 10% (v/v) β-mercaptoethanol; 20% (v/v) glycerol; 0.04% (w/v) bromophenol blue and SDS-PAGE was performed according to Laemmli [39] using 12% polyacrylamide gels (100 V per gel, 45 min, 4 °C). After electrophoresis, gels were washed with distilled water prior to staining with Coomassie Brilliant Blue R-250 in a methanol-acetic acid solution overnight. Finally, distaining was done with a methanol-acetic acid-water solution. In addition, 5 μL of a wide-range molecular weight marker (S-84445 SigmaMarker™, St. Louis, MO, USA) were included in each gel. The molecular marker consisted of 12 proteins ranging from 6.5 kDa (aprotinin, bovine lung) to 200 kDa (myosin, porcine heart).

4.5.2. Trypsin and Chymotrypsin Inhibition Kinetics

Inhibition kinetics were conducted according to Bijina et al. [30], with minor modifications, using trypsin and chymotrypsin from bovine pancreas (T8003 and C4129 from Sigma Aldrich, SL) and different concentrations of the synthetic substrate. An aliquot of 10 µL of each protease (1 mg mL−1) was pre-incubated with different concentrations of Ulva (from 0 to 500 µg Ulva per µg trypsin) for 60 min. Later on, trypsin and chymotrypsin activities of the pre-incubated mixtures were assayed using various concentrations of BAPNA (Nα-Benzoyl-DL-arginine 4-nitroanilide hydrochloride) (from 0.10 to 0.75 mM) according to Erlanger et al. [42], or SAPNA (N-succinyl-(Ala)2-Pro-Phe-P-nitroanilide) (from 0.05 to 0.5 mM) according to DelMar et al. [43], respectively, in 50mM Tris-HCl, 10mM CaCl2 buffer, pH 8.5.
The activity of the enzymatic reaction (v) based on the rate of change in absorbance (405 nm) of the reaction mixture was determined for each substrate concentration [S] assayed. Lineweaver–Burk curves, 1/v versus 1/[S], were plotted and the Michaelis constant (Km) and the maximum rate of reaction (Vmax) were calculated for classifying the pattern of inhibition generated by the Ulva extract (competitive, uncompetitive or non-competitive).

4.6. Statistical Analysis

The results were expressed as mean ± standard deviation. In order to test data normality and variance homogeneity, the Kolmogorov–Smirnov test and Levene’s F-test were used, respectively. Data with parametric distribution were analyzed using one-way analysis of variance (ANOVA), and the significant differences between treatments (p < 0.05) were determined using Tukey’s multiple comparison test. Data with nonparametric distribution were analyzed by using Kruskal–Wallis test, and significant differences were determined using box-and-whisker plot graphs. All statistical analyses were performed using the Statgraphics Plus 4.0 (Rockville, MD, USA) software.

5. Conclusions

This work showed the presence of protease inhibitors in Ulva able to inhibit digestive proteases of commercial fish species. The inhibitory capacity was dose-dependent. From a physiological point of view, high dietary inclusion of crude Ulva would be requested to achieve higher inhibition values. The thermal treatment during feed processing is high enough to inactivate the inhibitors from U. ohnoi; hence, it can be used efficiently as potential sustainable ingredient for aquafeeds.

Author Contributions

A.J.V., M.I.S. and A.G. performed experiments and analyzed data. A.J.V. wrote the manuscript. F.J.A. and T.F.M. conceptualized, designed the research, revised and corrected the paper. All authors agreed with the final submitted version. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the projects SABANA (grant # 727874) from the European Union’s Horizon 2020 Research and Innovation program, DORALGAE (RTI2018-096625-B-C31) from the Ministry of Sciences, Innovation and Universities (Spain) and the European Regional Development Fund (ERFD), and the knowledge transfer action grant GREEN4FEED # 5917 from the Ministry of Economy, Knowledge, Business and University of the Regional Government of Andalusia (Spain) and ERFD.

Acknowledgments

Authors thank IFAPA El Toruño center (Cádiz, Spain) for providing Senegalese sole specimens and Ulva ohnoi biomass. Gilthead seabream and seabass juveniles were kindly provided by Predomar (Almería, Spain).

Conflicts of Interest

The authors declare no conflict of interest.

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Marinedrugs 18 00319 g001 550
Figure 1. Dose-response inhibition plot of S. aurata (A), S. senegalensis (B) and D. labrax (C) intestinal proteases activity following the incubation with increasing concentrations of crude (CR-Ulva) and heat-treated Ulva extracts (HT-Ulva). Each point represents the mean of triplicates ± SD. IC50: mg of Ulva needed to cause 50% protease inhibition.
Figure 1. Dose-response inhibition plot of S. aurata (A), S. senegalensis (B) and D. labrax (C) intestinal proteases activity following the incubation with increasing concentrations of crude (CR-Ulva) and heat-treated Ulva extracts (HT-Ulva). Each point represents the mean of triplicates ± SD. IC50: mg of Ulva needed to cause 50% protease inhibition.
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Figure 2. Substrate-SDS-PAGE (sodium dodecyl sulphate polyacrylamide gel electrophoresis) obtained after incubation of S. aurata, S. senegalensis and D. labrax intestinal extracts with different concentrations of Ulva extract. Lane 1: control without inhibitor (distilled water was used instead of Ulva extract); lane 2: 500 µg Ulva per unit of proteolytic activity (UA); lane 3: 1000 µg Ulva per UA; lane 4: 1500 µg Ulva per UA. The molecular mass markers (kDa) were phosphorylase b (94), bovine serum albumin (66), ovalbumin (45), carbonic anhydrase (30), and soybean trypsin inhibitor (20).
Figure 2. Substrate-SDS-PAGE (sodium dodecyl sulphate polyacrylamide gel electrophoresis) obtained after incubation of S. aurata, S. senegalensis and D. labrax intestinal extracts with different concentrations of Ulva extract. Lane 1: control without inhibitor (distilled water was used instead of Ulva extract); lane 2: 500 µg Ulva per unit of proteolytic activity (UA); lane 3: 1000 µg Ulva per UA; lane 4: 1500 µg Ulva per UA. The molecular mass markers (kDa) were phosphorylase b (94), bovine serum albumin (66), ovalbumin (45), carbonic anhydrase (30), and soybean trypsin inhibitor (20).
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Figure 3. The time-course of in vitro proteolysis of casein by S. aurata, S. senegalensis and D. labrax digestive proteases in the absence of any inhibitory extract. Images show SDS-PAGE hydrolysis patterns obtained at different sampling times (0, 30, and 90 min). Numbers on the left of the electrophoresis gel stand for the molecular mass of proteins fractions (kDa).
Figure 3. The time-course of in vitro proteolysis of casein by S. aurata, S. senegalensis and D. labrax digestive proteases in the absence of any inhibitory extract. Images show SDS-PAGE hydrolysis patterns obtained at different sampling times (0, 30, and 90 min). Numbers on the left of the electrophoresis gel stand for the molecular mass of proteins fractions (kDa).
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Figure 4. The time-course of in vitro proteolysis of casein by S. aurata (A), S. senegalensis (B) and D. labrax (C) digestive proteases in the presence of increasing concentrations of crude (CR-Ulva) and heat-treated (HT-Ulva) Ulva. The images show SDS-PAGE hydrolysis patterns obtained at different sampling times (0, 30, and 90 min). The numbers on the left of the electrophoresis gels stand for the molecular mass of the protein fractions (kDa).
Figure 4. The time-course of in vitro proteolysis of casein by S. aurata (A), S. senegalensis (B) and D. labrax (C) digestive proteases in the presence of increasing concentrations of crude (CR-Ulva) and heat-treated (HT-Ulva) Ulva. The images show SDS-PAGE hydrolysis patterns obtained at different sampling times (0, 30, and 90 min). The numbers on the left of the electrophoresis gels stand for the molecular mass of the protein fractions (kDa).
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Figure 5. The effects of thermal treatments on the inhibitory effect of Ulva on trypsin activity. * Denote significant differences among treatments (p < 0.05).
Figure 5. The effects of thermal treatments on the inhibitory effect of Ulva on trypsin activity. * Denote significant differences among treatments (p < 0.05).
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Figure 6. SDS-PAGE carried out to detect trypsin-Ulva inhibitor complexes. Lane 1 = trypsin (1 mg mL−1). Lane 2 = Ulva (0.1 g mL−1). Lanes 3 to 5 = trypsin preincubated with CR-Ulva during 0, 30 and 60 min. Lanes 6 to 8 = trypsin pre-incubated with heat-treated Ulva during 0, 30 and 60 min.
Figure 6. SDS-PAGE carried out to detect trypsin-Ulva inhibitor complexes. Lane 1 = trypsin (1 mg mL−1). Lane 2 = Ulva (0.1 g mL−1). Lanes 3 to 5 = trypsin preincubated with CR-Ulva during 0, 30 and 60 min. Lanes 6 to 8 = trypsin pre-incubated with heat-treated Ulva during 0, 30 and 60 min.
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Figure 7. Lineweaver–Burk plots showing the inhibition of trypsin (A) and chymotrypsin (B) by Ulva protease inhibitors (a: 0; b: 200; c: 300; d: 400 and e: 500 µg Ulva per µg enzyme).
Figure 7. Lineweaver–Burk plots showing the inhibition of trypsin (A) and chymotrypsin (B) by Ulva protease inhibitors (a: 0; b: 200; c: 300; d: 400 and e: 500 µg Ulva per µg enzyme).
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Table
Table 1. The values of the estimated coefficient of protein degradation (CPD) and total amino acids released measured after 90 min of in vitro hydrolysis of casein by fish digestive proteases in the presence of different concentrations (0, 500, 1000 and 1500 µg Ulva per UA) of crude (CR-Ulva) and heat-treated (HT-Ulva) Ulva ohnoi.
Table 1. The values of the estimated coefficient of protein degradation (CPD) and total amino acids released measured after 90 min of in vitro hydrolysis of casein by fish digestive proteases in the presence of different concentrations (0, 500, 1000 and 1500 µg Ulva per UA) of crude (CR-Ulva) and heat-treated (HT-Ulva) Ulva ohnoi.
Fish vs. Ulva ConcentrationCPD
(%)		Total Amino Acids Released
(g 100 g protein−1)
Sparus aurata
Control 91.6 ± 2.3 d22.1 ± 2.3 d
CR-Ulva 50077.9 ± 2.0 c15.4 ± 0.1 c
CR-Ulva 100062.6 ± 4.1 b11.1 ± 0.7 b
CR-Ulva 150045.9 ± 2.0 a7.4 ± 2.4 a
HT-Ulva 50091.4 ± 2.1 d20.7 ± 1.0 d
HT-Ulva 100090.6 ± 1.0 d20.8 ± 1.6 d
HT-Ulva 150089.2 ± 1.7 d20.7 ± 2.7 d
p<0.001<0.001
Solea senegalensis
Control 91.9 ± 2.2 d22.1 ± 1.5 c
CR-Ulva 50084.3 ± 0.4 c19.6 ± 0.8 c
CR-Ulva 100066.1 ± 1.5 b12.8 ± 0.3 b
CR-Ulva 150041.8 ± 4.4 a8.5 ± 1.0 a
HT-Ulva 50089.9 ± 1.2 d21.9 ± 1.8 c
HT-Ulva 100089.1 ± 2.1 d21.5 ± 2.0 c
HT-Ulva 150088.2 ± 1.3 d20.8 ± 0.8 c
p<0.001<0.001
Dicentrarchus labrax
Control 96.2 ± 1.2 c22.3 ± 2.5 d
CR-Ulva 50091.2 ± 0.8 b16.3 ± 1.0 c
CR-Ulva 100069.9 ± 1.4 a11.8 ± 0.3 b
CR-Ulva 150066.6 ± 2.5 a8.2 ± 0.3 a
HT-Ulva 50095.1 ± 1.8 b,c22.0 ± 2.3 d
HT-Ulva 100094.1 ± 3.2 b,c21.3 ± 0.6 d
HT-Ulva 150093.4 ± 1.4 b20.1 ± 0.6 d
p<0.001<0.001
The values are mean ± SD of triplicate determinations. Within each fish species, the values in the same column with different lowercase letters indicate significant differences (p < 0.05) owing to Ulva extract. a,b,c,d the superscripts indicate the treatments with significant differences.
Table
Table 2. Kinetic analysis of trypsin and chymotrypsin enzymes in the presence of Ulva.
Table 2. Kinetic analysis of trypsin and chymotrypsin enzymes in the presence of Ulva.
Ulva ConcentrationTrypsin Chymotrypsin
Km
(mM)		Vmax
(µMmol pNA min−1)		Km
(mM)		Vmax
(µMmol pNA min−1)
Without Ulva0.657.030.155.92
200 µg Ulva per µg enzyme0.735.540.205.57
300 µg Ulva per µg enzyme0.874.710.213.15
400 µg Ulva per µg enzyme1.584.430.232.38
500 µg Ulva per µg enzyme2.534.120.251.65
Km: Michaelis constant; Vmax: maximum rate of reaction; pNA: para-nitroaniline.

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Vizcaíno, A.J.; Galafat, A.; Sáez, M.I.; Martínez, T.F.; Alarcón, F.J. Partial Characterization of Protease Inhibitors of Ulva ohnoi and Their Effect on Digestive Proteases of Marine Fish. Mar. Drugs 2020, 18, 319. https://doi.org/10.3390/md18060319

AMA Style

Vizcaíno AJ, Galafat A, Sáez MI, Martínez TF, Alarcón FJ. Partial Characterization of Protease Inhibitors of Ulva ohnoi and Their Effect on Digestive Proteases of Marine Fish. Marine Drugs. 2020; 18(6):319. https://doi.org/10.3390/md18060319

Chicago/Turabian Style

Vizcaíno, Antonio Jesús, Alba Galafat, María Isabel Sáez, Tomás Francisco Martínez, and Francisco Javier Alarcón. 2020. "Partial Characterization of Protease Inhibitors of Ulva ohnoi and Their Effect on Digestive Proteases of Marine Fish" Marine Drugs 18, no. 6: 319. https://doi.org/10.3390/md18060319

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