Effect of Dietary Processed Sulfur on the Meat Quality in Pork under Aging.

The present study was performed to determine the effect of dietary supplementation with processed sulfur on the quality and stability of vacuum packaged pork during aging time. All groups were designated into two groups; NP, a group fed basal diet and SP, a group fed basal diet and processed sulfur, 3 g/kg feed. Following vacuum packaging, Longissimus dorsi muscles were vacuum-packaged and stored under refrigerated condition (1-2℃) for 21 d. Weight loss of the SP group was lower (p<0.05) than that of the NP group. Interaction effect of shear force and cooking loss was observed (p<0.05). Redness values of the SP group at 14 and 21 d after storage were higher than those of the NP group (p<0.05). Lipid oxidation and volatile basic nitrogen (VBN) levels in the SP group were retarded (p<0.05) compared to that of the NP group during storage. Aspartic and glutamic acid in SP were higher than in NP (p<0.1). There was no significant (p>0.05) difference in TPC between the both groups during storage. Therefore, vacuum packaged pork from pigs fed processed sulfur had better aging yield and storage stability than pork from pigs fed basal diet.

Introduction

In the last decade, meat with vacuum packaging under chilled conditions has been supplied to the fresh market or consumers due to extended shelf-life. Recently, the effect of aging time on pork with vacuum packaging was researched by Tikk . However, vacuum packaging is unattractive to consumers due to perceptible purge loss and color denaturation of meat (Lagerstedt ). In general, the pork has a lower storage ability compared to other meat because of the rapid postmortem glycolysis, the low hygienic status and risks of bacterial growth (Blixt and Borch, 2002).

Elemental sulfur has gained interest in the animal industry because sulfur metabolism can interfere with several enzyme activities and protein metabolism (Metyer ). Sulfur-containing amino acids such as methioinine, cysteine, and taurine play important roles in animals (Shoveller ). According to Brosnan and Brosnan (2006), cysteine is used to form disulfide bonds to link protein structure while methionine is converted into glutathione (an antioxidant enzyme) throughout the transsulfuration pathway. It has been reported that pigs fed high sulfur diet have enhanced antioxidant ability (Song ). Kim demonstrated that the supplementation with 0.3% processed sulfur is acceptable to improve pork quality. However, there is scarce research about how the fresh meat quality of processed sulfur fed pigs changes through wet-aging.

The aim of this study was to evaluate the effect of dietary supplementation with processed sulfur on physicochemical properties (such as proximate compositions, pH, drip loss, cooking loss, color, free amino acids composition and shear force) and storage stability (lipid oxidation, volatile basic nitrogen, and total plate count) of vacuum packaged pork during aging.

Materials and Methods

Animals, sample collection, and treatment

A total of 40 three-way crossbred (Landrace × Yorkshire × Duroc) pigs with an average live weight of 8.51±1.12 kg (n=5 in each pen) were randomly assigned based on weight. Two dietary treatments were prepared for this experiment: Control diet (NP) and diet supplemented with processed sulfur (SP) to obtain 3 g/kg feed during the fattening phase (3 mon). Processed sulfur, which is registered at the Korea Feed Ingredient Association, was obtained from Jungmin Co., Ltd (Korea) and was contained 97.93% of elemental sulfur. The animal experiment was conducted at the abattoir of Pocheon Federation of Livestock Cooperatives. Animals were managed under the animal policy of Konkuk University (Korea). The dose of processed sulfur in the feed was determined according to a previous study (Kim ). No significant difference (p>0.05) in final live weight (about 120 kg) between the two groups was found. After slaughtering procedure, the Longissimus dorsi of pigs were obtained from the carcass. The obtained muscles were cut into pieces (about 500 g each piece) and sealed with vacuum packaging. The samples were stored at a refrigerated room at 1℃. Samples were collected at different time points of the experiment (0, 3, 7, 14, and 21 d during aging). Animal and experimental designs were expressed as Fig. 1.

Fig. 1.

Schematic figure illustrating animal and experimental design.

Proximate compositions

Moisture, crude fat, crude protein, and ash of samples were measured according to the method of AOAC (1995). Data of proximate compositions were expressed as percentages (%).

Weight loss and Cooking loss

Each sample with weight of approximately 300 g with vacuum packaging was placed at 1℃. They were weighed on 1, 3, 7, 14, and 21 d. Weight loss was calculated as weight difference expressed in percentage before and after placing in the refrigerated room.

Samples (about 100 g each) collected at 1, 3, 7, 14 and 21 d were vacuum packed and cooked to reach at core temperature 70℃. Cooked samples were cooled down with cold water for 30 min. Cooking loss was calculated as a percentage of weight loss before and after cooking.

pH

Each sample (2 g) was collected and homogenized with 18 mL of distilled water. The pH values of homogenized samples were measured using a pH meter (pH 900, Precisa, Co., UK).

Color measurement

Color of sample after blooming for 1 h was expressed as values of CIE L* (lightness), CIE a* (redness), and CIE b* (yellowness). The lightness, redness, and yellowness values of samples were measured using a handy colorimeter (NR-300, Nippon Denshoku, Japan). The calibration of machine was conducted using a white plate (CIE L*=+94.48, a*=−0.67, b*=+3.31).

Thiobarbituric acid reactive substances (TBARS)

TBARS of sample was measured using the method of Witte . Briefly, 2 g of sample was homogenized with 10 mL of 10% trichloroacetic acid (TCA) solution and 0.04 mL of 0.3% BHT (Butylated hydroxytoluence) solution. The homogenized sample was reacted with 2-thiobarbituric acid solution (TBA) and heated in boiling water for 10 min. After chilling down, the absorbance of sample was measured at 532 nm using a spectrophotometer (Optizen 2120UV, Mecasys, Korea). Data were expressed as malondialdehyde (MDA) mg/kg. Standard curve of MDA formed from 1,1,3,3-tetraethxypropane (TEP) was used for calculation.

Shear force

After cooking loss measurement, samples were cut into parallel strips of 100 mm2 at 30 mm in length. Shear force was recorded as peak force (kg) on a minimum of 10 strips from each sample using TX-XT2 (Stable Micro System Ltd., England) equipped with a triangular blade. The condition of this machine was designed as 50 kg load cell and 200 mm/min cross-head speed.

Volatile Basic Nitrogen (VBN)

VBN measurement was conducted according to the Conway microdiffusion method (Conway, 1950). Briefly, 5 g of sample was homogenized in 45 mL distilled water at 12,000 rpm for 1 min and filtered with Whatman No. 1 filter paper. Filtrated sample (1 mL) was transferred to the outer place of Conway chamber. Then 1 mL of 0.01 N boric acid (H3BO3) solution and 50 μL Conway reagent (0.066% methyl red and 0.066% bromocresol green in ethanol) were added to the inner place of the Conway chamber. The Conway unit was closed immediately after the addition of 1 mL of 50% (w/v) potassium carbonate to the outer place. After incubating at 37℃ for 2 h, titration was progressed with 0.02 N sulfuric acid to the inner place of the chamber. Data were expressed as mg%.

Free amino acid

The extracted sample was prepared according to the slightly modified Analytical Methods of Korean Food Standards Codex (2015a). The meat was sonicated in 75% Ethanol for 1 h and then the sonicated sample was extracted for 24 h at the room temperature. The extraction was filtered through 0.2 um filter (Millipore) to analyze for free amino acids by using an automatic amino acid analyzer (S2100, S4300, S5200, SYKAM, Germany).

Total plate count (TPC)

Two grams of sample and 18 mL of 0.85% NaCl in sterile distilled water were transferred to a sterile stomacher bag and homogenized for 60 s with a bag mixer (Interscience Co., France). A 10−1 dilution was used for subsequent serial dilutions. Aliquot (0.1 mL) of sample with the appropriate dilution was spread onto Petrifirm Aerobic Count Plates (3M, Korea) in triplicates. Plates were incubated at 35℃ for 48 h. Colony forming unit (CFU) was expressed as Log CFU/ g.

Statistical analysis

This experiment was designed as a factorial model 2 supplementation (NP and SP) × 5 storage periods (0, 3, 7, 14 and 21 d) in triplicates using two-way analysis of variance (ANOVA). Differences among storage periods were evaluated by Duncan’s multiple range test using the General Linear Model (GLM) procedure of SPSS version 18.0 (SPSS, 2003).

Results and Discussion

Changes in proximate compositions of vacuum packaged loins from pigs fed with processed sulfur during aging are shown in Table 1. Moisture content of SP showed a higher tendency than that of NP (p<0.1). Moisture content of samples on days 3 was the lowest and showed an decline tendency during storage compared to sample on day 0 (p<0.001), whereas protein content slightly increased during storage (p<0.05), respectively. Ash contents in both NP and SP groups were increased at 3 d compared to other days. In addition, the ash content of the SP group was higher than that of the NP group (p<0.01). Increasing moisture and ash contents in pork from pigs fed processed sulfur supplementation, while processed sulfur supplementation decreased in lipid content in muscle (Kim ). Crude fat content of the SP showed a lower tendency than that of NP (p<0.1), whereas crude fat was not affected by aging time (p>0.05).

Table 1.

Changes in proximate compositions of vacuum packaged meat from pigs fed processed sulfur during aging (%)

(%)	Supplementation			Aging time (d)					p-value
	NP1)	SP	SEM	0	3	7	14	21	SEM	Supplementation	Time	Interaction
Moisture	69.80	70.68	0.13	71.49a	68.78d	70.89ab	70.46bc	69.59cd	0.21	0.075	<0.001	0.118
Crude protein	25.69	25.23	0.26	24.11b	25.89ab	25.83ab	26.21b	25.26ab	0.43	0.240	0.014	0.287
Crude fat	2.82	2.69	0.33	2.89	2.77	3.48	2.03	2.59	0.53	0.054	0.155	0.726
Crude Ash	1.32	1.40	0.02	1.35b	1.45a	1.33b	1.36b	1.31b	0.03	0.005	0.023	0.975

1)NP, normal diet fed pigs; SP, sample from 0.3% processed sulfur fed pigs. 2)Different superscript letters in the same row indicate significant differences during aging time, p<0.05.

pH, drip loss, cooking loss, and shear force

Changes in pH, drip loss, cooking loss, and shear force of NP and SP groups during the aging storage are shown in Table 2. The pH values of both NP and SP groups increased (p<0.05) during the storage. High pH meat can improve the water-holding capacity and decrease cooking loss during ageing (Silva ). Increased pH of meat during storage is associated with the formation of ammonia due to degradation of protein and amino acid (Nychas ). However, no significant difference between the treatments was proved (p>0.05).

Table 2.

Changes in pH, weight loss, cooking loss, and shear force of meat from pigs fed processed sulfur during aging

(%)	Supplementation			Aging time (d)					p-value
	NP1)	SP	SEM	0	3	7	14	21	SEM	Supplementation	Time	Interaction
pH	5.64	5.65	0.01	5.55b	5.63a	5.70a	5.70a	5.65a	0.02	0.826	<0.001	0.157
Weight loss (%)	14.14	12.78	0.71	10.59a	16.22b	12.78ab	15.46b	12.25ab	1.13	0.035	0.007	0.981
Cooking loss (%)	21.82	20.62	0.54	22.51ab	24.08a	18.71b	19.55b	21.27ab	0.85	0.134	0.001	0.031
Shear force (Kg)	3.78	3.95	0.10	3.77a	4.29a	3.98a	4.17a	3.13b	0.16	0.261	<0.001	0.008

1)NP, normal diet fed pigs; SP, sample from 0.3% processed sulfur fed pigs. 2)Different superscript letters in the same row indicate significant differences during aging time, p<0.05.

Weight loss of SP showed an increasing tendency at 3 d after aging and a decreasing tendency from 3 d to 21 d (p<0.1). Weight loss of SP was significantly lower than that of the NP (p<0.05). Lee proved that the drip loss of sulfur compounds fed pigs decreased. Cooking loss of NP and SP groups showed no significant difference. The cooking loss of SP on day 3 was significantly increased compared to other days (p<0.05). Similar result was shown by Straadt et al. (2007), who reported that cooking loss increased during the initial four days of aging because of the degradation of fibers such as collagen. The cooking loss of SP reversely decreased from 3 d to 14 d and then the cooking loss increased from 14 d to 21 d (p<0.05). This result was might be related to increasing cooking time of aged meat due to decreasing heat conduction of aged meat. George-Evins proved the relation between increasing cooking loss and cooking time of aged beef. Moreover, there was a significant interaction between diet and aging (p<0.05). This result was caused that NP had a decline tendency of cooking loss, whereas cooking loss of SP increased on day 3 and decreased on day 21. High collagen solubility of pork from processed sulfur fed pigs was reported by Kim . Kristensen and Purslow (2000) have also reported that degradation of cytoskeleton proteins such as desmin, vinculin, and talin during aging can enhance the water-holding capacity of meat due to inflow of extracellular water.

Processed sulfur supplementation did not influence shear force value (p>0.05), while aging time affected the shear force of pork (p<0.001). Aging time and treatment interaction of shear force was observed (p<0.05). Shear force of the NP group was not significantly decreased during aging time, while the shear force of the SP group on day 21 was lower than that at 0 d (p<0.05). Reduction in shear force of pork during aging has been reported by Juarez . Significant difference in time and treatment interaction of shear force was found (p<0.01). Shear force of meat is associated with several factors such as intramuscular fat content and crosslink protein such as collagen (Wang ). As mentioned above, the increase proteolysis index and collagen solubility of meat from the processed sulfur fed pig were reported by Kim .

Color

Changes in color (lightness, redness, and yellowness) of vacuum packaged meat from pigs fed processed sulfur during aging are shown in Fig. 2. The lightness (CIE L*) value of samples gradually increased during storage (p<0.01). The supplementation and aging time interaction effect on lightness was detected (p<0.05). The lightness value of the SP group had a tendency to be higher than that of the NP group on days 21 after aging (p<0.1). Oliete have observed that the lightness value of meat is increased during aging. The lightness of aged meat is coincided with disk Z degradation during aging, resulting in expression of lighter meat (Swatland, 1982).

Fig. 2.

Changes in colors (lightness, redness and yellowness) of meat from pigs fed processed sulfur during aging.

Redness (CIE a*) of SP was higher than that of NP because of processed sulfur supplementation effect (p<0.01). Redness of samples on days 21 significantly lower than that of samples aged 0, 7 and 14 d (p<0.05), whereas the interaction effect was also proved (p<0.01). Redness values of the NP group at 3 d and 7 d after aging were higher (p<0.05) compared to those at 0 d. However, the redness values of the NP group at 14 d and 21 d were lower (p<0.05) compared to those at 0 d. Similarly, the redness values of the SP group at 7 d and 14 d were higher (p<0.05) compared to those at 0 d. They were decreased (p<0.05) on day 21. Seydim have reported that myoglobin oxidation can decrease the redness of meat when the pH of meat is high. Previous study has shown that pigment oxidation of processed sulfur fed pigs is retarded compared to that of pigs fed basal diet (Kim ). In this study, the redness values of the SP group at 14 d and 21 d were higher (p<0.05) compared to those of the NP group. Consumer acceptance of meat has a positive correlation with redness value of meat (Renerre, 2000). Therefore, the high redness of the processed supplementation might increase acceptability of consumer.

Yellowness (CIE b*) values of both NP and SP groups remained stable (p>0.05) during the aging. In addition, there was no significant (p>0.05) difference in yellowness between the NP and SP groups during aging.

TBARS

TBA values of both NP and SP groups of vacuum packaged meat during aging are shown in Fig. 3. Processed sulfur supplementation inhibited the increasing TBA value (p<0.001). The TBA values of both groups were gradually increased (p<0.05) during storage and the interaction effect on TBA was observed (p<0.05). The SP group had lower TBA values at 14 d and 21 d than the NP group (p<0.05). Inhibition of lipid oxidation in meat from processed sulfur fed pigs has been proved by Kim . Song et al. (2013) have found that sulfur-containing antioxidants in meat such as methionine, taurine, and glutathione enzyme are increased if pigs are fed high sulfurcontaining diet. In the transsulfuration pathway, methionine is transformed into cysteine and then the cysteine is converted into glutathione (McBean, 2012).

Fig. 3.

Changes in TBA value of meat from pigs fed processed sulfur during aging.

Changes in VBN of vacuum packaged meat are shown in Fig. 4. Although VBN was not significantly affected by processed sulfur supplementation, NP showed a slightly incline tendency compared to SP (p<0.1). VBN contents of samples were significantly increased during aging (p<0.05). VBN contents of the NP group at 0 d and 14 d were higher (p<0.05) than those of the SP group. However, there was no significant difference in VBN between NP and SP on day 21 after aging (p>0.05). VBN is considered as an important factor that determines the degree of microbial contamination and protein degradation in meat (Hur ). According to Korea Food and Drug Administration (2002), the VBN of fresh raw and packaged meat is allowed below 20mg%. The VBN contents of both NP and SP groups did not exceed the standard value until 21 d.

Fig. 4.

Changes in volatile basic nitrogen (VBN) of meat from pigs fed processed sulfur during aging.

Free amino acids

The changes in free amino acid contents in the NP and SP are expressed in Table 3. Free amino acids are an important indicator to determine aromatic flavor of meat with Maillard reaction and Strecker degradation (Barbieri ; Ventanas ). According to Nishmura and Kato (1988), the enhancement of meat taste during storage was proved due to the increasing free amino acids and each free amino acid has a characteristic taste such as sweetness (Gly and Ala), bitterness (Phe, Tyr, Trp, Leu, Val) and umami (Glu). In this study, the composition of all free amino acid was not different between both groups during storage (p>0.05). Most free amino acids in both groups significantly increased during storage (p<0.05), whereas the glutamine content was not changed during storage (p>0.05). The formation of glutamine is generated from the enzymatic reaction with glutamic acid and ammonia (Dura ). Keynan demonstrated that the reaction related to glutamine and glutamic acid was inhibited under anaerobic condition. Therefore, the result could be affected by vacuum packaging of meat. Although the taurine accounts for about 20% of free amino acid in meat, the taurine is not part of the muscle protein component (Aristoy and Toldra, 1998; Beriain ). Taurine of samples at 3 d was decreased compared to the samples at 0 d (p<0.05). The interaction with treatment and time on taurine content was found (p<0.05). Taurine contained in drip loss of meat (Lambert ). Therefore, this result may be related to water-holding capacity of meat. Cysteine was not detected in both groups, whereas the Met of SP was not significantly different compared to the NP (p>0.05). Aspartic and glutamic acid of SP showed incline tendencies than those of NP (p<0.1) and these free amino acids contents of both groups increased in day 21 without significant difference. Umami taste is enhanced when the Asp and Gln are combined with Inosine 5’-monophosphate (Rotzoll ). Proline of SP was also a higher tendency than that of NP (p<0.01). Rezaei suggested that the proline acts as the component of collagen protein in pigs. This result could be associated with collagen synthesis of processed sulfur fed pigs (Kim ).

Table 3.

Changes in free amino acids of meat from pigs fed processed sulfur during aging

Amino acid (mg/100g)	Supplementation			Aging time (d)					p-value
	NP	SP	SEM	0	3	7	14	21	SEM	Supplementation	Time	Interaction
Asp	6.7103	9.1806	0.58	2.24c	2.51c	3.96c	11.18b	19.84a	2.16	0.088	0.001	0.447
Glu	161.9537	161.7992	17.64	117.55c	111.96c	144.96c	194.96b	239.95a	11.74	0.989	<0.001	0.611
Asn	27.1634	26.9343	4.53	15.44c	14.28c	22.36c	34.69b	48.47a	2.39	0.920	<0.001	0.459
Ser	73.7565	74.824	9.52	49.75cd	45.95d	67.09c	92.24b	116.43a	5.93	0.849	<0.001	0.449
Gln	105.9815	110.6208	1.71	99.03ns	93.64	106.59	126.58	115.67	9.53	0.093	0.162	0.338
His	30.171	28.6223	4.33	18.31c	17.66c	24.43c	36.73b	49.86a	2.42	0.482	<0.001	0.355
Gly	58.9448	62.4699	6.88	45.84cd	38.96d	56.12bc	70.81b	91.81a	4.92	0.437	<0.001	0.383
Thr	63.5952	63.309	8.98	40.22cd	37.44d	54.98c	79.97b	104.65a	4.95	0.952	<0.001	0.485
Arg	60.3796	69.7159	7.64	45.44c	43.10	61.05bc	83.15ab	92.49a	7.18	0.177	0.002	0.600
Ala	511.968	501.2456	21.59	451.86c	431.07c	528.82b	532.11b	589.18a	17.20	0.433	<0.001	0.037
Tau	72.8372	71.9731	2.63	77.49a	63.38b	78.44a	70.10ab	72.63ab	3.29	0.735	0.035	0.040
Tyr	47.4961	51.7935	5.49	34.23c	33.35c	47.73b	61.40a	71.51a	4.12	0.279	<0.001	0.560
Val	57.7023	60.0223	9.00	35.23c	34.79c	49.02c	73.34b	101.93a	4.83	0.591	<0.001	0.296
Met	42.5924	42.6349	5.10	28.14d	27.99d	38.59c	52.33b	66.03a	2.39	0.098	<0.001	0.348
Trp	21.1916	21.8912	1.23	18.29c	17.92c	21.12b	23.11b	27.26a	0.78	0.308	<0.001	0.263
Phe	49.0572	50.0997	6.14	33.63d	32.04cd	44.09c	59.56b	78.57a	3.31	0.737	<0.001	0.413
Ile	44.0688	45.9961	6.39	28.02c	27.36c	38.67c	55.94b	75.17a	3.38	0.545	<0.001	0.443
Leu	85.9777	89.8923	11.10	59.00cd	56.21d	78.15c	106.31b	140.01a	6.20	0.502	<0.001	0.444
Lys	92.7646	99.9375	13.51	63.04b	56.15b	86.61b	128.93a	147.03a	11.05	0.523	0.001	0.736
Pro	45.854	48.9553	1.20	32.38b	31.10b	41.40b	56.43a	75.72b	4.71	0.082	<0.001	0.250
TFAA2)	1661.636	1690.448	149.27	1295.12d	1216.85cd	1594.17c	1949.86b	2324.20a	98.6	0.763	<0.001	0.525

1)NP, normal diet fed pigs; SP, sample from 0.3% processed sulfur fed pigs. 2)TFAA, total free amino acid 3) Different superscript letters in the same row indicate significant differences during aging time, p<0.05.

Total Plate Count (TPC)

Change in total plate count of meat during storage is shown in Fig. 5. We speculated that the processed sulfur supplementation inhibited the growth total plate count since antibacterial effect of sulfur-containing compounds was proved by Kim . However, TPC was not affected by the processed sulfur supplementation effect (p>0.05). TPC of both NP and SP groups were significantly increased during storage (p<0.001). However, the TPC of both groups on day 21 did not exceed 6 Log CFU/g sample. Similar increased tendency of total plate count of vacuum packaged pork was observed by Blixt and Boch (2003) who reported that growth bacteria was more affected by slaughter hygience than species. Meat spoilage sign with off-odor production has been proved when TPC in raw meat is over 8.0 Log CFU/g (Egan and Grau, 1981). Therefore, the aspects of microbial safety, the post mortem conditions (hygiene and storage condition) might be more critical than pre-mortem condition (supplementation effect, species, etc.).

Fig. 5.

Changes in total plate count (TPC, Log CFU/g) of meat from pigs fed processed sulfur during aging.

Conclusion

In conclusion, the aging yield and storage stability of pork from pigs fed processed sulfur were improved at 1-2℃ during ageing compared to those of pork from pigs fed basal diet. Low weight loss of pork from pigs fed processed sulfur was found during aging time in this study. The redness of pork from pigs fed processed sulfur was also higher than those of pigs fed basal diet. In addition, the lipid oxidation of pork from pigs fed processed sulfur was lower than that of pork from pigs fed basal diet. Therefore, pork from pigs fed processed sulfur resulted in improved meat quality and storage stability during aging.