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Effects of Vietnamese tamarind fish sauce enriched with iron and zinc on green mussel quality
Nguyen Phung Tien12 * , Sunisa Siripongvutikorn1, and Worapong Usawakesmanee1'**
1 Prince of Songkla University, Songkhla, Thailand 2 Vinh Long University of Technology Education, Vinh Long Provine, Viet Nam * e-mail: [email protected] ** e-mail: [email protected] Received September 5, 2018; Accepted in revised form October 10, 2018; Published June 08, 2019
Abstract: Marinating is a traditional technology to improve the shelf - life and quality of products. Enriched Vietnamese tamarind fish sauce was prepared and used to marinate green mussels. Subjects of this research were: green mussels (C1), marinated green mussels (C2), and marinated green mussels packaged in modified atmosphere (M1, M2, and M3). A percentage of O2:CO2:N2 was 5:50:45 for M1, 5:70:25 for M2, and 5:90:5 for M3. Microbiological, chemical, and sensory qualities of the samples were analyzed during storage at 4°C for 30 days. The results indicate that glycogen, iron, and zinc contents as well as pH values decreased in all the cases during storage. In addition, TVB-N and TBARS values as well as mesophilic and lactic acid bacteria increased with time in all the samples. The number of psychrophilic bacteria in marinated samples was small or not detected at all. Escherichia coli, Staphylococcus aureus, Salmonella spp. and Vibrio cholera were below standard values. Based on sensory acceptability, the shelf-life of C1, C2, M1, M2, and M3 samples was 12, 18, 24, 24, and 27 days, respectively.
Keywords: Vietnamese tamarind fish sauce, iron, zinc, marinated green mussel, modified atmosphere packaging (MAP)
Please cite this article in press as: Tien N. P., Siripongvutikorn S., and Usawakesmanee W. Effects of Vietnamese tamarind fish sauce enriched with iron and zinc on green mussel quality. Foods and Raw Materials, 2019, vol. 7, no. 1, pp. 51-59. DOI: http:// doi.org/10.21603/2308-4057-2019-1-51-59.
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Foods and Raw Materials, 2019, vol. 7, no. 1
E-ISSN 2310-9599 ISSN 2308-4057
Research Article Open Access
DOI: http://doi.org/10.21603/2308-4057-2019-1-51-59 Available online at http:jfrm.ru
INTRODUCTION
Green mussel (Perna viridis L.) is a common marine animal in the Asia-Pacific region [1]. This is a large bivalve with smooth, elongated shell typical of several mytilids. Flesh of the green mussel is considered an excellent source of selenium, calcium, iron, magnesium, phosphorous and vitamins (A, Bp B2, B6, B12 and C) [2, 3]. In addition, mussel fat is rich in polyunsaturated fatty acids (PUFA, 37-48% of total fatty acids) mainly ra-3 PUFA [4], which is biologically important and can decrease the risk of cardiovascular disease [5]. However, this filter feeder animal has a high risk of microbiological contamination that lead to a short shelf-life, poor quality, and economic losses. In addition, only well-cooked green mussels are microbiologically safe.
Marinating is a seasoning process mainly using organic acid containing liquids [6]. Liquid marinades ge-
nerally include sugar, spices, oil, and acid such as vinegar, fruit juice or wine. Marinating improves tenderness, juiciness, taste and aroma, as well as improves the shelf-life of red meat, poultry, seafood, and vegetables [7-10].
Vietnamese tamarind fish sauce is popular in its country of origin. The main ingredients are tamarind pulp, fish sauce and sugar, while some fresh garlic and chili are used to enhance taste. The Vietnamese consume this sauce with various foods, such as seafood, fried food, dried food. It is even used as a condiment in various kinds of food products. Ready-to-cook products are expected to gain popularity in South-East Asia as well. Mineral deficiencies, including iron and zinc, remain problematic in developing countries. Thus, the enrichment of food products with minerals can be an effective way to solve this problem. However, according to a market survey, green mussels marinated with enriched tamarind fish sauce are not commercially avai-
Copyright © 2019, Tien et al. This is an open access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material for any purpose, even commercially, provided the original work is properly cited and states its license.
lable, especially when packed in a modified atmosphere. Modified atmosphere packaging (MAP) is a technology that prolongs the shelf-life of food products by retarding microbial growth and biochemical reactions, often with an elevated carbon dioxide level [11]. Moreover, in MAP oxygen may inhibit the growth of anaerobic bacteria and accumulate toxins from Clostridium botulinum, type E [12]. However, botulinum toxins can form at below 2% oxygen [13, 14].
Therefore, the aim of this study was to determine the shelf-life of green mussels marinated with tamarind fish sauce enriched with iron and zinc. The mussels were packed in modified atmosphere and stored at 4°C.
STUDY OBJECTS AND METHODS
Materials. Tamarind pulp without seeds, fish sauce, white sugar, finger chili, garlic, and the fresh green mussels (40-50 individuals/kg) were purchased from a supermarket located in Songkhla province. Experiments were carried out at the Food Technology Department, the Agro-Industry Faculty of the Prince of Songkla University, Thailand. Iron sodium ethylenedi-aminotetraacetate (FeNaEDTA3(H2O)) and zinc sulfate (ZnSO4-7(H2O)) were taken from Sigma-Aldrich Company (Steinheim, Germany).
Marinated green mussel preparation. The green mussels were washed during 2 hours with tap water, then blanched in boiling water at 100 °C for 30 s to facilitate meat removal. A ratio of sample to water was 1:2 w/w. Afterwards, the meat of green mussels was separated from the shells. We prepared tamarind fish sauce contained 42% of tamarind slurry, 37% of sugar, and 21% of fish sauce. 236 mg of FeNaEDTA3(H2O) and 88.5 mg of ZnSO47(H2O) were added into 30 g of the sauce, which was 36 mg of Fe and 20 mg of Zn, respectively. The green mussel meat was soaked in the enriched sauce at the ratio of 1:1. The marinated meat was packaged in 15 x 30 cm Havel Vacuum bags, b.v. (Europac Co., Ltd) with O2 transmission rate 46.6 cm3m2 day-1 at 38°C, 1 atm. We tested five samples of green mussels: meat without marinade solution packed under normal air (C1), marinated meat without gases (C2), and meat packed in the modified atmosphere (M1, M2, and M3). A percentage of O2:CO2:N2 was 5:50:45 for M1, 5:70:25 for M2, and 5:90:5 for M3. All samples were stored at 4°C for 30 days. Microbiological, chemical and sensory analyses were performed every 3 days.
pH. The marinated green mussels were blended with sterilized distilled water at the ratio of 1:5 and allowed to stand for 2 min. Then pH was measured by using a pH meter (Mettler 350, Singapore).
Thiobarbituric acid reactive substances (TBARS). The thiobarbituric acid reactive substances (TBARS) were determined by the method described in [15]. 10 g of chopped samples were homogenized with 50 ml of distilled water for 2 min and then transferred to distillation tubes. 47.5 ml of distilled water was additionally infused into the distillation tube to avoid losing the sample. 2.5 ml of 4 N HCl and a few drops of an anti-
foam agent were added. 5 ml from 50 ml of the distillate were mixed with 5 ml of 0.02 M 2-thiobarbituric acid in 90% glacial acetic acid (TBA reagent). The mixture was placed in a vial that was capped and heated in a water bath for 35 min. Afterwards, the vial was cooled down and the sample was measured at 532 nm using a spec-trophotometer (UV/VIS T180, PG Instrument Ltd., UK). The results are expressed in mg malondialdehyde/kg sample.
Glycogen content. Glycogen content was determined based on the method of [16]. 50 mg of chopped marinated green mussels were boiled for 20 min with 400 ^l of 33% KOH, cooled down, and 700 ^l of 96% ethanol was added. The mixture was placed in an ice bath for 2 hours to reach complete precipitation. Thereafter, the mixture was centrifuged at 7,500 g for 20 min using a microlitre centrifuge (Z-233-M2, Hermle-Germany) and the supernatant was collected. The supernatant was mixed with 1 ml of distilled water and sonicated for 5 min using Crest Ultrasonic (575 DAE, Malaysia). Then 100 ^l of the solution and 2 ml of anthrone reagent were kept at 90°C for 20 min in darkness. The reagent consisted of 38 ml of concentrated sulphuric acid with 15 ml of distilled water and 0.075 g of anthrone. The solution was measured at 620 nm using a spectrophotometer. Glycogen concentration was calculated from a standard curve for glycogen from Sigma-Aldrich Company (Steinheim, Germany).
Total volatile base nitrogen (TVB - N). Total volatile base (TVB - N) contents in the green mussels were determined using Conway micro-diffusion method described in [17]. 2 g of a sample were mixed with 8 ml of 4% tricloroacetic acid (TCA), then homogenized with a high-speed homogenizer for 1 min. The supernatant was filtered by Whatman No. 41 filter paper (Whatman International, Ltd., Maidstone, UK). 1 ml of the sample was placed in the outer ring, while 1% boric acid containing the Conway indicator was pipetted into the inner ring. 1 ml of saturated K2CO3 was added to the sample to initiate the reaction after mixing. Thereafter, the mixture was incubated at room temperature for 3 hours. Afterwards, the inner ring solution was titrated using 0.02N HCl until the green color turned to pink similar to a blank sample. TVB-N content was calculated as follows, mg/100 g:
TVB - N (mg/100 g) =
,
Weight of sample
where: N is normality of HCl in titrant; A is titration volume for actual sample; B is titration volume for blank; V is total initial volume of sample with TCA.
Iron and zinc content. Samples of 0.5 g in mass were digested in 5 ml of concentrated nitric acid with 2 ml of 30% hydrogen peroxide under pressure in a closed vessel before heating in a microwave oven until the samples were digested. Afterwards, the samples were cooled down and filtered by Whatman filter paper No. 1 with a pore size of 110 nm (Whatman International, Ltd., Maidstone, UK)). Each sample solu-
tion was then transferred into a 25 ml volumetric flask and the volume was made up with distilled water [18]. The extract samples were used to determine iron and zinc by Inductively Couple Plasma Mass Spectrometry (ICP-MS) (Perkin-Elmer SCIEX, Shelton, CT, USA). The RF power was 1,350 W, the plasma gas flow rate was 15 l/min, the carrier gas flow was 0.94 l/min, and make-up gas flow was 0.15 l/min. The sample take rate was 100 ^l/min and the sample depth was 6.0 mm.
Microbiological quality. 25 g of the marinated green mussels were blended with 225 ml of 0.1% sterilized peptone water. From the 10-1 dilution, dilutions to 10-2 and 10-3 were prepared with 0.1°% sterilized peptone water. Mesophilic and psychrophilic bacteria, Esche-richia coli, Salmonella spp, Vibrio cholera, and Staphy-lococcus aureus were determined using the method in [19]. Lactic acid bacteria were determined using de Man Rogosa and Shape agar by pour plate method, with incubation in anaerobic conditions at 35°C for 48 hours before colony count [20].
Sensory evaluation. Marinated samples were baked in a casserole pan (House worth HW-1707S, China) at 180°C for 10 min until the core temperature of the meat sample reached 80 ± 2°C. Then the samples were served to fifty untrained panelists of post-graduate students and technicians from the Department of Food Technology, Prince of Songkla University. The panelists were asked to evaluate the likability scores for appearance, aroma, texture, taste and overall on a nine-point hedonic scale.
Statistical analyses. All experiments were run in triplicates. The data were subjected to Analysis of Variance (ANOVA) and the differences between means were assessed for significance by Duncan's Multiple Range Test [21]. Data analysis was performed with the SPSS package (SPSS 6.0 for Windows, SPSS Inc., Chicago, IL, USA).
RESULTS AND DISCUSSION
We found that the sauce had pH 3.31, total titratable acidity 32.13%, and water activity 0.87. The viscosity of this enriched sauce was 840 cP, with non-Newtonian behavior. The colour coordinates L*, a*, and b* were 26.44, 15.8 and 33.7, respectively.
pH. pH levels of un-treated and treated green mussels are shown in Fig. 1. In general, pH with all treatments decreased with storage time. The initial pH of un-treated green mussels (C1) was 6.77 and decreased to 6.21 at 15 days of storage (p < 0.05). The marinated samples had significantly lower pH than the control group due to acidity of the sauce (pH 3.31) (p < 0.05). The pH of marinated green mussels without gases (C2) was 4.48 on day 1 and declined to 4.07 by day 21 of storage (p < 0.05). The initial pH of marinated green mussel (M1, M2, and M3) was about 4.51-4.64 and dropped to 4.24, 4.2 and 3.95, respectively, at 30 days of storage (p < 0.05). The decrease in pH of meat during chilled storage is normally caused by conversion of glycogen to lactic acid and other volatile acids, as a result of muscle degradation [22]. Cao et al. also reported that the spoilage of mollusk shellfish was partly by fermentation indicated by decreasing pH [23]. Moreover, pH was lower with MAP using gases than with other treatments,
8
6
"3. ^
2
0 J-1-1-1-1-1-,
0 5 10 15 20 25 30 Storage time, days -CI -C2 -Ml -M2 M3
Fig. 1. Dependence of pH values of green mussels on storage time. C1 = control; C2 = marinated with no gases; M1, M2, and M3 = marinated at the O^O^N percentage of 5:50:45; 5:70:25; and 5:90:5, respectively.
due to the dissolution of CO2 that produced carbonic acid [24] and reduced production of alkaline compounds in the marinated samples [24, 25]. Higher concentrations of CO2 (M3 > M2 > M1) gave lower pH levels in our experiments, although without significant differences. The pH value in our experiments was mainly due to the acidic marinade sauce with tamarind pulp.
TBARS. Fig. 2 demonstrates the TBARS levels in green mussels during storage for the various treatments. TBARS is indicator of the malondialdehyde content, which is a secondary lipid oxidation product from polyunsaturated fatty acids [26] causing off-flavors in meat products [27]. The initial TBARS of the control (C1) was 2.62 mg MDA/kg, while the marinated samples (C2, M1, M2, M3) had 0.99, 0.81, 0.92, 0.88 mg MDA/kg, respectively. It should be noted that the marinated green mussels had lower TBARS values than the control samples, apparently due to osmosis during marinating conveying TBARS out from the mussels. Also the bacterial count was higher for C1 than for the other samples, which could also play a role in producing TBARS [28]. The lower TBARS values of the marina-
Storage time, days -CI -C2 -Ml -M2 M3
Fig. 2. Dependence of TBARS values of green mussel on storage time. C1 = control; C2 = marinated with no gases; M1, M2, and M3 = marinated at the O^O^N percentage of 5:50:45; 5:70:25; and 5:90:5, respectively.
Storage time, days
-CI -C2 -Ml -M2 M3
Fig. 3. Dependence of TVB - N values of green mussels on storage time. C1 = control; C2 = marinated with no gases; M1, M2, and M3 = marinated at the O2:CO2:N2 percentage of 5:50:45; 5:70:25; and 5:90:5, respectively.
Storage time, days
-C1 -C2 -M1 -M2 M3
Fig. 4. Dependence of glycogen content of green mussels on storage time. C1 = control; C2 = marinated with no gases; M1, M2, and M3 = marinated at the O2:CO2:N2 percentage of 5:50:45; 5:70:25; and 5:90:5, respectively.
ted green mussels were consistent throughout the storage, and sulfur compounds from garlic in the marinade may have played a role as antioxidants [29]. However, TBARS in all cases increased during storage because of high content of polyunsaturated fatty acids in mussel fat, as mentioned in the introduction. Moreover, MAP packaging reduced TBARS may be due to O2-elimina-tion by enriched CO2 proportion [22]. Masniyom et al. reported that seabass flesh in MAP did not suffer from increased lipid oxidation [30]. The TBARS level of 5-8 mg/kg malonaldehyde is a standard criterion of the poor quality of oily food [31, 32]. TBARS in the control (C1) reached 8.03 mg MDA/kg on day 12 of storage, while C2 had 7.85 mg MDA/kg on day 18. M1, M2, and M3 had TBARS levels below the standard on day 27, namely 7.59, 6.89, and 6.82 mg MDA/kg, respectively. The marinated green mussels packed at the percentage of O2:CO2:N2 equaled 5:90:5 gave the least TBARS level at the end of storage (p > 0.05).
Total volatile base nitrogen (TVB-N). Changes in the TVB-N value of the treated and un-treated green mussels during storage are shown in Fig. 3. The TVB-N increased with storage time. The initial TVB-N of green mussels (C1) was 6.44 mg/100 g and increased gradually to 10.22 mg/100 g during storage. The treated samples C2, M1, M2, and M3 had initial TVB-N values 20.6, 18.97, 19.53 and 18.94 mg/100 g, respectively. By the end of the storage they reached 30.1, 33.33, 33.67, and 29.69 mg/100 g, respectively (p < 0.05). TVB-N is composed of volatile amines, typically dimethylamine, trimethylamine and ammonia [22], that commonly determine the spoilage of seafood [33]. The marinated samples had higher TVB-N values than the control even on day 1, due to volatile amines in the fish sauce [34]. In addition, the marinade contained garlic with sulfur compounds that could also react with boric acid, contributing to TVB-N content [29]. The increasing trend of TVB-N with time in this study agrees with the findings of [35]. Fishery products are acceptable for human consumption when TVB-N does not exceed 30 mg/100 g of sample [34]. Based on this, the shelf-lives of M3, M2,
and M1 samples were 27, 24, and 25 days, respectively. In addition, [36] noticed that for seafood TVB-N indicated the freshness of raw materials and acceptability for human consumption. They pointed out that TVB-N increased with storage time as a result of quality deterioration. However, the initial TVB-N of the marinated products may not indicate the quality, considering that fish sauce and garlic used as ingredients cause erroneous results.
Glycogen content. During storage glycogen content decreased gradually in all samples, but declined rapidly in C2 samples (p < 0.05), as shown in Fig. 4. The initial glycogen content in the control sample (C1) was significantly lower than that in the marinated samples (C2, M1, M2, and M3). Glycogen is a polysaccharide including glucose units in a branched structure. Extraction and hydrolysis were used to obtain simple sugars in the gly-cogen content determination. As mentioned earlier, the marinade solution had 37% of sugar, so it positively contributed to the glycogen content. Jermyn [37] mentioned
Table 1. Iron and zinc content in green mussel samples during storage
Minerals Samples Initially End of storage
Iron content, C1 71.44 ± 0.77a 67.61 ± 0.67b
mg/kg C2 599.62 ± 12.60a 371.47 ± 2.33b
Ml 389.67 ± 1.14a 381.34 ± 1.99b
M2 399.2 ± 1.98a 390.00 ± 1.41b
M3 481.93 ± 1.36a 392.36 ± 0.44b
Zinc content, C1 11.09 ± 0.40a 8.95 ± 0.13b
mg/kg C2 382.19 ± 8.22a 249.00 ± 1.41b
M1 267.20 ± 1.56a 257.74 ± 2.51b
M2 280.35 ± 0.64a 266.17 ± 1.17»
M3 331.00 ± 1.98a 271.11 ± 2.40b
Note: ,-b Means within rows with different superscripts are significantly different (p < 0.05). C1 = control; C2 = marinated with no gases; M1, M2, and M3 = marinated at the O2:CO2:N2 percentage of 5:50:45; 5:70:25; and 5:90:5, respectively
Table 2. Microbiological levels in marinated and non-marinated green mussel kept under different conditions during the storage at 4°C for 30 days.
Bacterial type
Treat-
Storage time, days
ment 1 3 6 9 12 15 18 21 24 27 30
C1 9.3 x 103 7.0 x 104 2.5 x 105 6.3 x 105 8.6 x 105 1.2 x 106
C2 2.8 x 103 3.7 x 103 8.9 x 104 9.8x 104 1.04 x 105 5.3 x 105 7.1 x 105 1.13 x 106
M1 < 100 3.6 x 103 6.5 x 103 7.9 x 103 8.6 x 103 1.30 x 104 1.63 x 104 1.90 x 104 2.45 x 104 9.0 x 104 1.42 x 106
M2 < 100 2.5 x 103 5.2 x 103 5.7 x 103 6.3 x 103 9.2x 102 1.05 x 104 1.47 x 104 2.10 x 104 2.6 x 104 1.12 x 106
M3 < 100 < 100 < 100 3.0 x 103 5.2 x 103 7.4 x 103 9.6 x 103 1.10 x 104 1.80 x 104 2.48 x 104 9.8 x 105
C1 8.5 x 103 1.56 x 104 2.0 x 104 2.13 x 104 2.32 x 104 5.0 x 104
C2 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10
M1 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10
M2 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10
M3 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10 < 10
C1 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
C2 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M1 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M2 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M3 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
C1 ND ND ND ND ND ND ND ND ND ND ND
C2 ND ND ND ND ND ND ND ND ND ND ND
M1 ND ND ND ND ND ND ND ND ND ND ND
M2 ND ND ND ND ND ND ND ND ND ND ND
M3 ND ND ND ND ND ND ND ND ND ND ND
C1 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
C2 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M1 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M2 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M3 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
C1 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
C2 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M1 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M2 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
M3 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0 < 3.0
C1 9.9 x 103 1.5 x 104 1.76 x 104 2.1 x 104 2.6 x 104 3.5 x 104
C2 6.0 x 103 1.02 x 104 1.66 x 104 1.81x 104 2.41 x 104 4.8 x 104 7.2 x 104 1.14 x 105
M1 8.0 x 103 9.5 x 103 1.43 x 104 1.72 x 104 2.10 x 104 2.5 x 104 4.6 x 104 6.2 x 104 8.5 x 104 1.12 x 105 2.12 x 105
M2 6.0 x 103 7.6 x 103 9.4 x 103 1.02 x 104 1.71 x 104 2.38 x 104 2.5 x 104 3.5 x 104 4.1 x 104 5.6 x 104 1.36 x 105
M3 2.5 x 103 3.4 x 103 5.4 x 103 8.3 x 103 1.34 x 104 1.87 x 104 2.25 x 104 3.2 x 104 3.5 x 104 4.2 x 104 6.2 x 104
£ aU
g
yc £ &
M p-
£ Ü
M p-
M p-
3 ~
o [X
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Note: C1 = control, C2 = normal marinated, M1 = marinated i
, M2 =
5%O2:70%CO2:25%N M3
5%O2:90%CO2:5%N2
that in the determination of carbohydrates by anthrone method, other simple sugars in the system interfered. He pointed out that using glycogen content for glycolysis determination, which should decrease with storage time, might not give good results for high sugar products. The glycogen content decreased with storage time due to metabolism by glycolysis pathway in some bacteria [22]. The glycogen content of the control sample (C1) dropped to 61.42 mg/kg by day 12 of storage, while the marinated without MAP sample (C2) had 614.01 mg/kg after 18 days (p < 0.05). In the marinated samples packed with gases (M1, M2, and M3) the glycogen contents were 857.33; 1,005.68; and 1,293.17 mg/kg. The marinade with sugar strongly increased glycogen levels in marinated products. However, in C1the glycogen content decreased from 94.75 to 61.42 mg/kg during 12 days. The rapid decrease in glycogen levels of C2 may due to faster bacterial growth than with the treatments that included MAP, and the garlic from marinade solution seems to accelerate glycogen loss relative to the control (C1) perhaps by
sulfur compounds and prebiotics in garlic that support lactic acid bacterial growth [22].
Iron and zinc content. Iron and zinc contents of green mussels with various treatments are presented in Table 1. On day 1, the iron content in C1 was 71.44 mg/kg, while that in the marinated samples C2, M1, M2, and M3 was 599.62; 389.67; 399.2; and 481.93 mg/kg, respectively. The initial zinc contents in C1, C2, M1, M2, and M3 were 11.09; 382.19; 267.2; 280.35; and 331 mg/kg, respectively. The iron and zinc contents may have fluctuated due to uncontrolled factors, such as uneven marinade absorption, the amount of marinade drip from the surface of green mussels during sample preparation for testing, or the small weight (1.0 g) of samples tested. If the samples are not uniform, then consistent results may not be obtained. The iron and zinc content in the marinated samples was higher than that in the control sample due to the absorption of iron and zinc from the marinade. Generally, the iron and zinc contents decreased by the end of the shelf-life to 67.61; 371.47; 381.34; 390.00;
Tien N. P. et al. Foods and Raw Materials, 2019, vol. 7, no. 1, pp. 51-59 Table 3. Sensory acceptability score of green mussel kept under different condition during storage at 4°C for 30 days
Storage time, Treatments Attributes
day Appearance Flavor Colour Texture Taste Overall
1 C1 6.63 ± 0.72a 6.40 ± 0.62b 6.90 ± 0.99a 7.07 ± 0.74ab 6.57 ± 0.68a 6.63 ± 0.73b
C2 6.90 ± 0.76a 7.l0 ± 0.84a 6.90 ± 0.80a 7.30 ± 0.75a 7.03 ± 0.6la 7.l0 ± 0.84a
Ml 6.93 ± 0.98a 6.57 ± 0.63b 6.73 ± 0.69a 6.73 ± 0.52bc 6.77 ± 0.68a 6.60 ± 0.56b
M2 6.83 ± 0.65a 6.80 ± 0.7lab 6.53 ± 0.57a 6.33 ± 0.48c 6.77 ± 0.73a 6.60 ± 0.67b
M3 6.90 ± 0.6la 6.80 ± 0.8lab 6.90 ± 0.96a 6.83 ± 0.70a bc 6.83 ± 0.70a 6.80 ± 0.48ab
3 Cl 6.50 ± 0.73a 6.27 ± 0.98b 6.47 ± 0.78a 6.97 ± 0.85a 6.40 ± 0.93b 6.23 ± 0.94c
C2 6.83 ± 0.9la 6.87 ± 0.94a 6.73 ± 0.83a 6.80 ± 0.7la 6.83 ± 0.83ab 6.80 ± 0.76ab
M1 6.60 ± 0.8la 6.40 ± 0.67b 6.57 ± 0.50a 6.63 ± 0.93ab 6.50 ± 0.86ab 6.53 ± 0.78bc
M2 6.70 ± 0.79a 6.90 ± 0.84a 6.60 ± 0.67a 6.27 ± 0.52b 6.40 ± 0.56b 6.43 ± 0.50bc
M3 6.83 ± 0.79a 6.67 ± 0.76ab 6.83 ± 0.75a 6.77 ± 0.63a 6.93 ± 0.78a 6.97 ± 0.96a
6 Cl 6.23 ± 0.63b 6.l3 ± 0.43c 6.43 ± 0.63ab 6.77 ± 0.82a 6.70 ± 0.53abc 6.l3 ± 0.68c
C2 6.67 ± 0.7la 6.80 ± 0.92a 6.70 ± 0.88a 6.57 ± 0.50abc 6.80 ± 0.76a 6.77 ± 0.90a
Ml 6.60 ± 0.72a 6.30 ± 0.53bc 6.27 ± 0.52b 6.33 ± 0.6lbc 6.43 ± 0.63bc 6.57 ± 0.57ab
M2 6.60 ± 0.56a 6.53 ± 0.63ab 6.40 ± 0.50b 6.20 ± 0.76c 6.40 ± 0.62c 6.27 ± 0.52bc
M3 6.83 ± 0.70a 6.63 ± 0.67ab 6.60 ± 0.67ab 6.70 ± 0.70ab 6.77 ± 0.68ab 6.80 ± 0.7la
9 Cl 6.l7 ± 0.53b 6.03 ± 0.4lc 6.l3 ± 0.68b 6.50 ± 0.5lab 6.03 ± 0.6lb 6.07 ± 0.69b
C2 6.57 ± 0.68a 6.70 ± 0.79a 7.00 ± 0.79a 6.20 ± 0.6lbc 6.57 ± 0.90a 6.63 ± 0.76a
Ml 6.47 ± 0.5lab 6.27 ± 0.69bc 6.l3 ± 0.63b 6.23 ± 0.73bc 6.30 ± 0.65ab 6.37 ± 0.56bc
M2 6.53 ± 0.63a 6.43 ± 0.50ab 6.30 ± 0.47b 6.l3 ± 0.57c 6.30 ± 0.60ab 6.l7 ± 0.59b
M3 6.47 ± 0.73ab 6.53 ± 0.73ab 6.50 ± 0.78b 6.60 ± 0.67a 6.63 ± 0.6la 6.70 ± 0.60a
12 Cl 6.l0 ± 0.55ab 5.73 ± 0.58b 6.03 ± 0.4lc 6.l7 ± 0.53b 5.87 ± 0.57c 6.00 ± 0.45b
C2 6.03 ± 0.76b 6.27 ± 0.45a 6.57 ± 0.68a 6.l3 ± 0.63b 6.20 ± 0.48bc 6.l3 ± 0.43b
Ml 6.37 ± 0.49ab 6.l7 ± 0.38a 6.07 ± 0.52c 6.l7 ± 0.59b 6.l7 ± 0.53b 6.27 ± 0.58b
M2 6.47 ± 0.57a 6.40 ± 0.72a 6.23 ± 0.50c 6.07 ± 0.58b 6.23 ± 0.63ab 6.l0 ± 0.66b
M3 6.30 ± 0.53ab 6.37 ± 0.56a 6.43 ± 0.82ab 6.50 ± 0.63a 6.50 ± 0.63a 6.57 ± 0.63a
15 C2 5.90 ± 0.66a 6.l7 ± 0.9la 6.40 ± 0.77a 6.l0 ± 0.76a 6.l3 ± 0.76a 6.l0 ± 0.6lb
Ml 6.23 ± 0.57a 6.07 ± 0.78a 6.00 ± 0.9lb 6.l0 ± 0.40a 6.07 ± 0.37a 6.l3 ± 0.63ab
M2 6.20 ± 0.6la 6.27 ± 0.45a 6.l7 ± 0.38ab 6.03 ± 0.49a 6.20 ± 0.66a 6.03 ± 0.67a
M3 6.27 ± 0.52a 6.23 ± 0.68a 6.33 ± 0.6la 6.43 ± 0.68a 6.27 ± 0.45a 6.37 ± 0.76a
18 C2 5.83 ± 0.79a 5.93 ± 0.78a 6.27 ± 0.78a 6.03 ± 0.67a 5.97 ± 0.76a 5.90 ± 0.66b
Ml 6.l3 ± 0.57a 6.03 ± 0.56a 5.87 ± 0.455b 6.07±0.45a 6.00 ± 0.79a 6.07 ± 0.64ab
M2 6.l7 ± 0.75a 6.l3 ± 0.63a 6.l0 ± 0.66ab 6.00 ± 0.69a 6.l3 ± 0.43a 6.00 ± 0.74ab
M3 6.l7 ± 0.38a 6.l7 ± 0.53a 6.27 ± 0.58a 6.30 ± 0.47a 6.l8 ± 0.46a 6.30 ± 0.47a
21 Ml 6.07 ± 0.52a 5.90 ± 0.6la 5.70 ± 0.75b 6.00 ± 0.53a 5.93 ± 0.52a 6.03 ± 0.72a
M2 6.l0 ± 0.76a 6.07 ± l.lla 6.07 ± 0.64a 5.90 ± 0.55b 6.07 ± 0.58a 5.97 ± 0.6la
M3 6.l0 ± 0.55a 6.l3 ± 0.63a 6.l7 ± 0.59a 6.23 ± 0.43a 6.l0 ± 0.3la 6.23 ± 0.50a
24 Ml 6.03 ± 0.72a 5.90 ± 0.80a 5.70 ± 0.84a 5.97 ± 0.67a 5.80 ± 0.7la 5.97 ± 0.76a
M2 6.00 ± 0.53a 6.03 ± 0.76a 5.93 ± 0.64a 5.90 ± 0.6la 6.00 ± 0.37a 5.87 ± 0.63a
M3 6.03 ± 0.72a 6.03 ± 0.56a 6.l0 ± l.09a 6.l3 ± 0.5la 6.00 ± 0.45a 6.l3 ± 0.82a
27 M3 5.93 ± 0.37 5.97 ± 0.72 5.93 ± 0.58 5.90 ± 0.55 6.00 ± 0.26 6.07 ± 0.37
Note: Mean ± SD from 50 panalists; ■ fMeans within a column with different superscripts are significantly different (p < 0.05). C1 = control C2 = marinated with no gases; M1, M2, and M3 = marinated at the O2:CO2:N2 percentage of 5:50:45; 5:70:25; and 5:90:5, respectively
and 392.36 mg/kg for C1, C2, M1, M2, and M3, respectively. The zinc contents similarly were 8.95; 249.00; 257.74; 266.17; and 271.11 mg/kg for the same samples. The decrease in iron and zinc contents during storage may be due to the degradation of proteins by browning reaction, which may easily interact with iron and zinc.
El-Din et al. [38] mentioned that when iron and zinc minerals were added into dairy products, such as milk, the iron was bound with amino acids into casein micelles. Zinc associated with colloidal calcium phosphate in the casein micelles. Therefore, the contents of available iron and zinc may be reduced. In addition, it
was noted that the drip increased with storage time due to high salt content (~ 5.5% NaCl) and acidity of the marinade, leaching iron and zinc out from the mussels. Baygar et al. [39] observed that water content decreased during marinating.
Microbiological quality. Mesophilic and lactic acid bacteria were found in all treated samples throughout the experiment. However, psychrophilic bacteria were found only in the control sample (C1), while Escherichia coli, Staphylococcus aureus, Salmonella spp., and Vibrio cholera were very low or not detected, as shown in Table 2. Psychrophilic bacteria in the marinated sam-
ples (C2, M1, M2, and M3) were present in the amount of no more than 10 CFU/g. This indicates that the hurdle effect of the sauce (aw 0.87, pH 3.31, TA 32.13%, and salt 5.26%) strongly controlled psychrophilic bacterial growth. During storage, mesophilic and lactic acid bacteria increased with time (p < 0.05). Not surprisingly that the bacterial count in the control sample (C1) was the highest, followed by the marinated samples (C2), (M1), (M2) and (M3) in this order. ICMSF [40] recommended 106CFU/g as the standard limit of total viable count in freshwater fish and seafood. By this threshold the shelf-life of the control was 12 days, while the marinated green mussel (C2) had 18 days. With higher CO2 contents lower bacterial counts were found. This suggests that MAP can prolong the shelf-life when CO2 inhibits microbial growth. Farber [25] also stated that CO2 becomed more antibacterial as its concentration increased. CO2 can decarboxylate enzymes and inhibit the metabolic activity of microflora, thereby extending the lag phase and reducing logarithimic phase growth of spoilage bacteria [25, 41, 12]. Goulas et al. [42] reported that when mussels (Mytilus gallo-provincialis) were kept in 80%CO2:20%N2 atmosphere, the total viable count of bacteria was retarded compared to other tested conditions. Masniyom et al. [43] also reported that MAP with 80-100% of CO2 effectively extended the shelf-life of green mussels (Perna viridis). Our current study indicates that 90% CO2 atmosphere is the most effective to prolong the shelf-life of marinated green mussels. Therefore, combined acidity, salt and atmospheric CO2 were effective in retarding microbial growth.
Sensory evaluation. Generally, sensory evaluation is applied in the estimation of seafood quality and correlates well with the microbiological and chemical analyses [44]. The sensorial scores from fifty non-trained panelists for green mussels with the
various treatments during storage are summarized in Table 3. The scores from panelists became worse with storage time (p < 0.05). The threshold score for rejection was chosen to be 6, and only aroma showed significant differences between un-treated and treated green mussels during storage (Table 3). While all the sensory attributes with any treatment degraded towards the end of shelf-life, the scores remained on an acceptable level. Unexpectedly, the marinated mussels did not score better than the control group. This may be due to too soft texture, and unusual aroma and taste from the sauce that was highly acidic and contained iron and zinc. This altered the good natural aroma and texture of the mussels. This type of sauces is served as dips in Vietnam, not as marinades.
CONCLUSION
TVB-N, TBARS, TVC, and lactic acid bacteria increased in all samples during storage, while pH, glyco-gen, iron, and zinc contents decreased. The shelf-life of marinated green mussel was extended from 12 to 18, 24, or 27 days based on microbiological quality, TBARS and TVB-N value, by use of CO2 rich MAP packaging. For marinated green mussels, high concentration of CO2 (90%) appears to be both feasible and beneficial to shelf-life.
CONFLICT OF INTEREST
The authors declare no conflict of interest.
ACKNOWLEDGMENTS
This work was supported by the Higher Education Research Promotion and the Thailand's Education Hub for Southern Region of ASEAN Countries Project Office of the Higher Education Commission.
We would like to thank the team of the Research and Development Office (RDO) of the Prince of Songkla University, Thailand for the assistance with English.
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ORCID IDs
Nguyen Phung Tien https://orcid.org/0000-0001-8688-7930
