Effects of alginate oligosaccharides treatment on preservation and fresh-keeping mechanism of shrimp during frozen storage

Abstract

In this study, we investigated the influence of alginate oligosaccharides (AOS) coating on the quality of white shrimp (P. vannamei) at 4 ± 1 °C. We measured shrimp quality by surveying changes in certain properties, such as sensory quality, the microbiota, total volatile basic nitrogen (TVB-N), pH, and sensory characteristics. Compared to control group, AOS coating effectively stopped the growth of bacteria and decreased the formation of TVB-N (from 40% down to 30%). The pH of samples treated with AOS was visibly lower than that of the control group. The sensory quality of the AOS coated shrimp resembled microbial and physicochemical properties, and the acceptability was improved. Furthermore, we found the abundance of spoilage microorganisms, such as Shewanella and Pseudoalteromonas, in AOS coated groups is reduced compared to control groups. All these results suggest that our AOS coating treatment may improve storage and preservation of frozen shrimp.

Keywords:
alginate oligosaccharides; shelf life; bacterial diversity; microbial communities; preservation

1 Introduction

Alginate is a polysaccharide consisting of mannuronic and guluronic acids. The polymers of alginate can exist as either homopolymeric sequences of G blocks (GG), M blocks (MM), or as a heteropolymeric sequence containing alternating structures of M and G blocks (MG) (Haug et al., 1974). Alginate is found in brown algae and makes up a large amount of intracellular material while also being present in cell wall. Alginate and its derivatives are generally used in food, agriculture, and pharmaceutical industries due to their gelling ability, stability, and high viscosity (Ci et al., 1999; Johnson et al., 1997).

Alginate lyase is an enzyme that catalyzes the degradation of alginate and exists in a variety of organisms including bacteria, fungi, brown algae, ect. (Rahman et al., 2010; Singh et al., 2011; Wang et al., 2013). Alginate lyase has broad applications, for example in the production of alginate-derived bioactive oligosaccharides (Natsume et al., 1994; Kawada et al., 1997; Iwamoto et al., 2005), treatment of patients infected with mucinous Pseudomonas aeruginosa biofilm (Alkawash et al., 2006) and the isolation of protoplasts from marine algae (Sawabe et al., 1993). Alginate can be depolymerized into alginate oligosaccharide (AOS), which has certain advantages over some chemical and physical methods. These advantages include high yields and the production of specific oligosaccharides (Boucelkha et al., 2016). Recent reports have shown that alginate hydrolysates and their derivatives can promote plant growth and prevent dental cavities. These compounds also show anti-oxidant, anti-tumor, antimicrobial, anti-coagulatory, anti-inflammatory, and immunomodulatory activity (Hu et al., 2004; Miura et al., 2001).

Shrimp have many beneficial organic compounds, such as polyunsaturated fatty acids, amino acids, and peptides. Commercial shrimp can be highly perishable which leads to significant odor and soft texture. This perishability is due to microbial growth and lipid oxidation, which mainly causes the deterioration in the quality of such products (Mastromatteo et al., 2011). Recently, a combined treatment of antibiotics and functional marine oligosaccharides has received increasing attention due to increased demand for health safety (He et al., 2014). As consumer demand for shrimp continues to increase, they are increasingly concerned about the preservation of shrimp. In modern society, the demand for healthy and green food has also increased. Therefore, major focus of the industry has been to develop more biological preservatives to replace chemical preservatives. Thus an increasing amount of research has been directed at the development of natural preservatives to improve shelf life of aquatic products. Two preservatives widely used in food and medicine are chitosan oligosaccharide (COS) and alginate-derived oligosaccharides (ADO) due to their physiological characteristics. ADO is a product of sodium alginate degradation by alginate lyase (Blackwood et al., 1983). However, alginate lyase enzyme activity is reduced at cold temperatures which conflicts with refrigeration storage of aquatic products being one of the main long-term preservation methods. Refrigeration is important since it deters microbial growth while maintaining mouthfeel and nutrient content. However, ADO treatment does not necessarily improve product quality (Gonçalves & Gindri, 2009). Thus, further research is necessary to determine the effect of AOS coating on preservation of shrimp. Alginate hydrolysates and their derivatives possess important properties, which make them a promising candidate for future applications.

Here we isolated a marine bacterium classified as Flavobacterium sp. strain B2 (described below in detail) from kelp's or abalone's viscera. This bacterium produces alginate lyase enzyme that acts on sodium alginate. The AOS treatment prepared by enzymatic hydrolysis can have a positive effect on the preservation of shrimp, which provides a mechanism for bio-preservation technology.

2 Materials and methods

2.1 Shrimp sample preparation

The white shrimp (P. vannamei) were purchased from Fuqing Yihua Food Co., Ltd. (Fujian, China). Fresh live shrimp were shipped to the lab within 30 minutes and remained alive before experiment. The shrimp were killed with crushed ice and washed with deionized water. Shrimp were soaked based on size for 30 min with sterile distilled water and AOS. Samples treated with different solutions were randomly divided into ziplock bags and placed at 4 ± 1 °C for quality evaluation.

2.2 Preparation of AOS

Bacteria was fermented to get alginate lyase, which was precipitated by ammonium sulfate and dialyzed to get crude protein. Crude protein was filtered by 0.22 μm filter membrane and loaded first onto a DEAE-650C column (1.6×25 CM) from American GE Ltd pre-equilibrated with phosphate buffer (PB) (20 mM, pH 8.0). Unbound protein was removed by rinsing with the PB buffer. Bound protein was eluted with a linear gradient from 0 M to 0.25 M sodium chloride (NaCl) in PB buffer (20 mM, pH 8.0). Finally, the column was eluted with 1M NaCl in PB buffer (20 mM, pH 8.0). Each fraction was tested for enzyme activity. The fraction displaying peak enzyme activity was analyzed by SDS-PAGE (12.5%T, 5%C), and the active fraction loaded onto a Sephacryl S-200 column (1.6×100 CM) pre-equilibrated with PB (20 mM, pH 8.0) before loading. 20 g/L of sodium alginate was degraded by alginate lyase to obtain AOS.

2.3 Physicochemical analysis

Sensory evaluation

The sensory evaluation of shrimp was conducted according to the methods (Erickson et al., 2007; Xu et al., 2014a; Chen et al., 2019) with some changes. The aroma, color and muscle tissue of shrimp samples were evaluated by analysis panel consisting of eight panelists. The sensory quality of the shrimp was comprehensively scored. The score is 10 points. The 9 points or higher are strongly acceptable, the 7-9 points are a slightly acceptable range, and the 6-7 points are acceptable. 5-6 points are unacceptable, and less than 5 points are completely unacceptable.

Texture Profile Analysis (TPA)

TPA determination of shrimp was performed using a texture analyzer (TA-XT plus, UK). The P/5 (d=5 mm) cylindrical probe was used on the second and the third abdominal section of shrimp, with a deformation of 40% and a test speed of 1 mm/s.

Determination of pH

To determine pH of the shrimp after coating, 2 g of minced shrimp was homogenized with 20 mL of distilled water for 30 minutes, and the homogenate was filtered. pH was measured using a digital STARTER 2100 pH meter (OHRUS, Shanghai, China).

Determination of TVB-N

The TVB-N values were calculated by the GB 5009.228-2016 method. 2 g of minced shrimp was homogenized with 4 mL distilled water and 16 mL of 2 g/L trichloroacetic acid (TCA). The mixture was incubated for 30 minutes and then filtered. A 2 mL filter and 5 mL of a 1% (m/v) magnesium oxide (MgO) solution was added to the reactor, respectively. The distillation was collected in a flask containing 10 mL of a 10 g/L aqueous solution of boric acid and then mixed with an indicator containing 30 μL of 1 g/L methyl red and 170 μL of 1 g/L bromocresol green. 0.1 M hydrochloric acid solution was used to titrate the solution. The TVB-N value is shown in milligrams of nitrogen (1 mg/100 g) per 100 g of sample.

Determination of K-value

Adenosine triphosphate (ATP) and its degradation products were measured by the improved method of SC/T 3048-2014. 2 g of chopped shrimp were homogenized with 20 mL of 10% (v/v) cold perchloric acid and then centrifuged at 10,000 x g for 10 min. The analyte in the precipitate was extracted with 10 mL of 5% (v/v) cold perchloric acid and centrifuged at 10,000 x g for 10 min. The pH of the two supernatants was adjusted to 6.0 to 6.4 using 10 M sodium hydroxide (NaOH), followed by centrifugation at 10,000 x g for 10 min. The supernatants were filtered with a 0.22 μm membrane filter. The peak at 254 nm was detected by HPLC technique. 0.02 M PB (pH 6.0) was used as the mobile phase. The Formula 1 to determine K-values is as follows:

$$KValue\left(\%\right)=\left[\left(HxR\right)+\left(Hx\right)\right]/\left[\left(ATP\right)+\left(ADP\right)+\left(AMP\right)+\left(IMP\right)+\left(HxR\right)+\left(Hx\right)\right]\times 100$$ (1)

where ATP is adenosine triphosphate concentration in the sample (μmol/g); ADP is adenine diphosphate concentration in the sample (μmol/g); AMP is adenylate concentration in the sample (μmol/g); IMP is inosine concentration in the sample (μmol/g); HxR is the concentration of hypoxanthine nucleoside in the sample (μmol/g); Hx is the concentration of hypoxanthine in the sample (μmol/g).

2.4 Microbial analysis

Microbiological analysis

Microbiological analysis was performed according to the method of GB/T 4789.2-2008. Shrimp was homogenized in a 90 mL 0.9% sterile physiological saline solution by a stomacher stirrer for 2 min. The resulting mixture was serially diluted in a 1:10 ratio in sterile saline. 0.1 mL of the appropriate dilution was plated in triplicate on LB agar plates and incubated at 30 °C for 48 hours. Total bacterial count (TBC) was measured and expressed by log CFU/g.

Microbial diversity analysis

Total genomic DNA extraction kit (Sangon Biotech, Shanghai, China) following manufacturer instructions. High-throughput sequencing of extracted DNA was carried out using Illumina Hiseq2500 system (Illumina, San Diego, CA, USA). The reads from the original DNA fragments were merged by Base Calling analysis and the results were stored in FASTQ file format, which includes reads information and its corresponding sequencing quality information.

CD-HIT was used for clustering raw sequences into operational taxonomic units (OTUs) at a 97% similarity level. The OTU statistics and graphical output were conducted in R program version 1.8.0. The microbial communities were examined by using network analysis and Pearson rank correlations.

2.5 Statistical analysis

Each experiment was repeated three times. Data was processed using Origin 8.5. Data is displayed as mean ± SD. Statistical significance was analyzed by one-way analysis of variance (ANOVA) using SPSS 17.0 (Chicago, IL, USA). p = 0.05 was set to a statistically significant level.

3 Results and discussion

3.1 Physicochemical analysis

Preparation of AOS

Bacteria was grown in a 250 mL flask and alginate lyase was purified via electrophoretic homogeneity by two-step ion exchange chromatography and gel filtration chromatography. Purified fractions show a single band in SDS-PAGE with the correct corresponding molecular weight of approximately 80 kDa (Figure 1, lane 5). AOS was obtained by purified alginate lyase degradation of alginate at 30 °C and pH 8.0.

Figure 1
SDS-PAGE analysis of Strain B2, M: the standard protein molecular weight markers; (1) crude fermentation of Strain B2; (2) PB wash of DEAE-650C column; (3) 0.25 M NaCl in PBS elution of DEAE-650C column; (4) 1 M NaCl in PBS elution of DEAE-650C column; (5) PB by Sephacryl S-200 column.

Sensory evaluation

There was no obvious difference between shrimps treated AOS and the control group on the 2nd day (Table 1). On the 4th day, the sensory score of shrimps treated AOS was 8.38, which was higher than that of the control group. On the 6th day, the treated group score of 7.81 was still within the acceptance, significantly higher than the control group score of 5.81. On the 8th day, the control group score of 3.44 was less than a strongly unacceptable degree, but the treated group score of 6.06 was acceptance. Thus, the results implied that the group treated AOS can extend the shelf life of the shrimps by 2 days.

Table 1
Changes of sensory scores in control group and AOS treated group.

Treatment	Storage time (days)
	0	2	4	6	8
Control	10 ± 0.00	8.56 ± 0.42ab	7.56 ± 0.42c	5.81 ± 0.26d	3.44 ± 0.42e
AOS		8.88 ± 0.23a	8.38 ± 0.35b	7.81 ± 0.26c	6.06 ± 0.32d

Values were expressed using means ±standard deviation. Different letters in each data indicate a statistically significant different (p < 0.05).

Texture Profile Analysis (TPA)

From the perspective of consumer acceptability, texture is a very important sensory indicator. Shrimp was coated by AOS or stored in distilled H20 to evaluate their quality after storage at 4 ± 1 °C for 8 days. As shown in Figure 2, the hardness and chewiness of the AOS and water decreased over the 8 days period. However, the AOS treatment group had a higher hardness and chewiness compared to the control group. This result is similar to the results of other studies (Hsu et al., 2016; Feng et al., 2016; Huang et al., 2015). Overall, the chewiness of shrimp treated with AOS tended to be better than the control group. This is indicative that AOS coating was effective in improving the rheological properties of the treated shrimp. However, the hardness was not significantly higher in the AOS treatment compared to the control group and may be due to the low initial quality of shrimp used in our study.

Figure 2
Texture changes of shrimp during cold storage, AOS: treated with alginate oligosaccharides; Control: treated with distilled water; each bar represents mean ± SD. *p < 0.05, based on the Student’s t-test, and significant differences can be seen for both treatments. (a) for hardness; (b) for chewiness.

pH value

The pH of the AOS treated shrimp was significantly lower compared to the distilled water control group during refrigerated storage (p < 0.05) (Figure 3). The AOS coated shrimp reached an acceptable level of pH 7.74 on the 6th day. However, the pH of the control group approached 7.91 on the 6th day. This pH is designated as reaching the end of the stored shrimps shelf life and is consistent with the previous results (Galvão et al., 2017). There was a great relationship between the enzymes present in the shrimp tissues and the changes of microbial metabolites, which effected the pH of the sample. The increase in pH is attributed bacterial growth and protein decomposition by enzymes to produce basic compounds (Wu et al., 2014). The pH of the stored shrimp is also influenced by other factors, such as the type of fish and the growth environment. Therefore, pH of the sample can be used as a supplementary indicator to represent the quality of the stored shrimp.

Figure 3
pH changes of shrimp during cold storage, AOS: treated with alginate oligosaccharides; Control: treated with distilled water; Each bar represents mean ± SD. *p < 0.05, based on the Student’s t-test, and significant differences can be seen for both treatments.

TVB-N

Total volatile basic-nitrogen (TVB-N) is another major indicator of shelf life for seafood. In general, shrimp's TVB-N content increased over the time of refrigerated storage regardless of treatment. However, we found that the TVB-N content of shrimp treated with AOS was lower than that of the control group (p < 0.05). As was shown in Figure 4, the final TVB-N content was about 23.3 mg/100 g for AOS coated shrimp, which is lower than reported by Bonilla et al. (2018). TVB-N content in the control group was approximately 30.3 mg/100 g at day 8 of storage. A limit TVB-N of 30 mg/100 g for shrimp products is usually regarded as spoiled. The above results are consistent with previous studies in which the TVB-N value of shrimp treated with a chitosan-carvacrol coating had been found to be significantly decreased (Wang et al., 2018). The results indicate, based off of TVB-N content of stored shrimp, that AOS coating can be used to extend the shelf life of shrimp by 2 days during storage.

Figure 4
TVB-N content of shrimp during cold storage, AOS: treated with alginate oligosaccharides; Control: treated with distilled water; Each bar represents mean ± SD. *p < 0.05, based on the Student’s t-test, and significant differences can be between both treatments.

K-value

Figure 5 shows the change in K-value of the two different treatments of shrimp during refrigeration. The K-value increased over time in both the AOS coated shrimp and the control group. The K-value of the AOS coated shrimp was lower (p < 0.05) than the control group over the measured time period. As the storage time increases, many biochemical reactions occur in the stored shrimp that may affect freshness, including adenosine triphosphate (ATP) degradation to hypoxanthine. The increase in K-value was associated with the accumulation of hypoxanthine and inosine, which can be attributed to enzyme action. AOS coating may reduce the rate of ATP degradation by inhibiting endogenous autolytic enzyme activity, which can increase the quality of shrimp during storage.

Figure 5
K-value changes of shrimp during cold storage, AOS: treated with alginate oligosaccharides; Control: treated with distilled water; Each bar represents mean ± SD. *p < 0.05, based on the Student’s t-test, and significant differences can be seen between both treatments.

3.2 Microbial analysis

Total Bacteria Count (TBC)

During cold storage, the shelf life of seafood can be negatively affected due to bacterial growth. Shrimp lose market value due to the total bacteria count (TBC) exceeding spoilage level. The initial TBC of both the AOS coated and control groups was about 2.52 log CFU/g, indicating a high quality of the shrimp. This measurement is consistent with the results of the previous studies by Li et al. (2017) and Arancibia et al. (2015). The TBC of both groups gradually increased during storage, however the increase of TBC was slower in the AOS treatment compared to the control treatment (Figure 6). This may be due to AOS treatments potentially having antibacterial activity against Pseudomonas as reported in other studies using low molecular weight alginate oligomers (Pritchard et al., 2017b).

Figure 6
TBC number of shrimps during cold storage, AOS: treated with alginate oligosaccharides; Control: treated with distilled water; Each bar represents mean ± SD. *p < 0.05, based on the Student’s t-test, and significant differences can be seen for both treatments.

Composition analysis of the intestinal microbial community

Figure 7 shows differences in the intestinal microbial communities from both AOS treated shrimp and control groups. Our results show an obvious differences in the shrimp intestinal bacterial community between AOS treated group and the control group. Most bacteria found in the shrimp intestinal contents belonged to the phylum Escherrichia-Shigella, but it should be noted that bacteria from the phylum Shewanella and Pseudoalteromonas are major spoilage bacteria found on shrimp. The amount of bacteria from the Shewanella and Pseudoalteromonas phylum in AOS treated group was lower compared to the control group. Furthermore, cluster analysis indicates that AOS treatment changes the bacterial community structure, with bacteria from the Candidatus-Bacilloplasma phylum decreasing in AOS treated group. The data also revealed that bacteria from the Vibrio phylum was reduced after AOS treatment, which is widely found in shellfish.

Figure 7
The main phylums of bacteria found in shrimp intestinal bacterial communities among different samples, AOS: treated with alginate oligosaccharides; Control: treated with distilled water.

The analysis also revealed changes in bacterial composition between AOS and control groups after 8 days of storage. The predominant bacteria found in seafood was bacteria from the Shewanella and Pseudoalteromonas phylums (Mejlholm & Dalgaard, 2015; Serio et al., 2014; Ikutegbe & Sikoki, 2014; Capita et al., 2018; Fu et al., 2018). AOS has been shown to have antibacterial activity (Pritchard et al., 2017a; Tøndervik et al., 2014; Xu et al., 2014b; Li et al., 2018). Moreover, the abundance of bacterial composition in samples varied greatly between the AOS treated shrimp and shrimp stored in distilled water. This emphasizes that AOS coating has considerable effects on the composition of the microbial community.

4 Conclusions

The results of this paper show that AOS coating can better increase the quality of white shrimp compared to untreated white shrimp. This is supported by AOS treatment not only maintaining better sensory scores and characteristics of texture but by also showing a higher capacity to inhibit microbial counts, a lower TVB-N formation, and a lowered K-value and pH during storage. Therefore, AOS and similar kinds of biological preservative may have a vital effect on the preservation of future seafood.

Acknowledgements

The authors appreciate the financial support by the Program of Finance Department of Fujian Province in China (Grant No. (2014)1262), the Program of Finance Department of Fujian Province in China (Grant No. (2015)1297), the Program of Science and Technology of Fuzhou University in China (Grant No. 2014-XQ-20), the Program of Science and Technology of Fuzhou city in China (Grant No. 2017-G-66), “Thirteenth Five-Year Plan” Marine Economy Innovation and Development Demonstration Project (Grant No. FZHJ19).

• Practical Application: The preservation effect of AOS coating on shrimp.

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Publication Dates

• Publication in this collection
  29 May 2020
• Date of issue
  Dec 2020

History

• Received
  10 Oct 2019
• Accepted
  03 Dec 2019