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J. Anim. Sci. 2003. 81:2230-2238
© 2003 American Society of Animal Science

Color stability of semitendinosus, semimembranosus, and biceps femoris steaks packaged in a high-oxygen modified atmosphere1

J. M. Behrends2, W. B. Mikel3, C. L. Armstrong and M. C. Newman

Department of Animal Sciences, University of Kentucky, Lexington 40546


    Abstract
 Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 Implications
 Literature Cited
 
The objectives of this study were to evaluate visual and chemical attributes of beefsteaks from various USDA quality grades and muscles packaged in high-oxygen (80% O2/20% CO2) modified-atmosphere packaging (MAP). A total of nine carcasses were selected to represent Select (n = 3), low Choice (n = 3), and high Choice (n = 3) USDA quality grades. The semimembranosus (SM), semitendinosus (ST), and biceps femoris (BF) muscles were removed from each carcass and allotted to two packaging types (MAP or polyvinyl chloride over-wrap) and were displayed for up to 10 d, with evaluation on d 1, 3, 5, 7, and 10. Fifty-four steaks were evaluated on each day by a five-member trained panel for visual color (lean color and discoloration) and were also analyzed with a Minolta Chroma Meter CR-310 for L*and a* values (lightness and redness, respectively). Chemical properties measured included percentage of metmyoglobin formation and fat content. Visual color scores did not differ (P > 0.05) at d 1 and 3 with respect to all quality grades, but decreased after d 3, with a greater reduction (P < 0.05) in high Choice steaks for both lean color and discoloration. The low Choice steaks packaged in MAP displayed higher (P < 0.05) lean color scores and less (P < 0.05) discoloration at d 7 and 10 than did Select and high Choice steaks. Redness (a*) values also decreased (P < 0.05) after d 3, whereas (lightness) L* values declined (P < 0.05) from d 1 to 5. The high Choice steaks had higher (P < 0.05) metmyoglobin content than low Choice and Select steaks, but packaging had no effect (P > 0.05) on metmyoglobin content. Muscle type did affect metmyoglobin content; however, the metmyoglobin content of the SM was greatest (P < 0.05), followed by the BF, with the ST having the lowest (P < 0.05) metmyoglobin formation. Results indicate that low Choice steaks react the best in MAP, and the ST maintained greater storage characteristics regardless of quality grade or packaging.

Key Words: Beef • Meat Quality • Packaging • Steaks


    Introduction
 Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 Implications
 Literature Cited
 
Consumers’ continued demand for new and more convenient products has led to the development of alternative processing and packaging methods. In addition, the competition for the declining retail portion of consumers’ dollars has led to new methods of marketing and merchandising. These methods include new packaging alternatives that can be used to increase the shelf life of fresh meats.

For years, case-ready packaging technologies have been evaluated as methods to improve shelf life and maintain the quality of fresh meat. Case-ready packaging includes two major types of packaging: vacuum-packaging and modified-atmosphere packaging (MAP). These two types of packaging systems differ considerably, and each has proven to have considerable advantages when compared to traditional polyvinyl chloride (PVC) over-wrap (Blinkstad, et al., 1981Go; Asenio et al., 1988Go; Gill and McGinnis, 1995). Therefore, the objective of this study was to evaluate the visual and chemical benefits of high-oxygen (80% O2/20% CO2) MAP on steaks from three muscles of the beef round from three USDA quality grades.


    Materials and Methods
 Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 Implications
 Literature Cited
 
Carcass Selection, Fabrication, and Packaging
Beef carcasses obtained from New Horizons Packing (Cincinnati, OH) were ribbed between the 12th and 13th ribs for yield and quality grade determination (USDA, 1997Go) following a 24-h chill period at 1°C. Carcasses (n = 9) were selected for the study based on USDA quality grades to include three each of Select (Slight10 to Slight50), low Choice (Small30 to Small70), and high Choice (Moderate60 to Moderate100). Rounds from each carcass were fabricated into the semitendinosus (ST), semimembranosus (SM), and biceps femoris (BF). Each muscle was cut in half (ST was cut lengthwise; SM and BF were bisected by the width of the muscle perpendicular to the aitch bone) and muscle halves were allocated randomly to either high-oxygen (80% O2/20% CO2) MAP or PVC over-wrap (OTR = 6,500 cc/M2, 24 h, atm, 25°C) packaging. Muscles were labeled according to corresponding carcass, vacuum-packaged, and held at 4°C for 24 h.

On d 6 postmortem, half of each muscle was transported on ice and monitored for temperature control (remaining <4°C) to the Cryovac/Sealed Air Corp. Research and Development Facility (Duncan, SC) for packaging in high-oxygen MAP. Five 2.54-cm-thick steaks were sliced from each muscle and placed in a barrier foam tray (Cryovac/ Sealed Air Corp.), flushed with a 80% O2/20% CO2 mixture, hermetically sealed using an Inpack Nema 4X (Ross, Midland, VA) MAP machine, and randomly assigned to evaluation day. Steaks were then transported in ice chests at <4°C to the University of Kentucky Meat Science Laboratory (Lexington, KY). Five 2.54-cm-thick PVC steaks were sliced from the other half of the corresponding muscles, placed on styrofoam trays, overwrapped using an oxygen-permeable PVC film, and then randomly assigned to evaluation day. All steaks were placed under simulated retail display conditions (on a table 1.25 m directly under the light source; defrost cycles occurred every 4 h for 7 min, maintaining the temperature at ± 1°C) for 1, 3, 5, 7, and 10 d under constant illumination from cool white fluorescent lights (Osram Sylvania Products, Inc., Versailles, KY; model F40/DWWPlus, 3,300 lumens, 750 lx) at 4°C.

Fat Content
Intramuscular fat content for each carcass and muscle was determined from each d-1 steak. Each sample was ground and sent to an independent laboratory; petroleum ether procedures for evaluating fat content followed AOAC (1990)Go guidelines.

Visual Evaluation
Steaks for each of the evaluation days were visually evaluated on the given assigned day (1, 3, 5, 7, and 10 d) by a five-member trained panel before removal from the package. The panel was trained according to AMSA (1995)Go guidelines. Each steak was evaluated for lean color and assigned a score from 8 (bright cherry-red) to 1 (extremely brown or green). Surface discoloration was also evaluated, with scores ranging from 11 (0% surface discoloration) to 1 (90 to 100% surface discoloration; AMSA, 1995Go).

Colorimeter Evaluation
A Minolta Chroma Meter CR-310 (Minolta Co., Ramsey, NJ) with a pulse xenon arc lamp (D65) with a 50-mm aperture size was calibrated each day using a standard white tile and used to examine L* and a* color space value on d 1, 3, 5, 7, and 10 of simulated retail display. Each package was opened and values were recorded (and averaged) from two locations of the cut surfaces of the ST, SM, and BF.

Metmyoglobin Content
Using the procedure of Krzywicki (1982)Go, the relative metmyoglobin content was determined on d 1, 3, 5, 7, and 10 of display. A 4.0-g sample from each steak was blended with 36 mL of a 40 mM PBS (pH 6.8) in a Waring blender (New Hartford, CT). The homogenate was placed into a 50-mL centrifuge tube, placed on ice for 2 h, and then centrifuged at 5°C for 60 minutes at 30,000 x g. The supernatant was filtered using Whatman No. 1 filter paper, and absorbance was recorded at 525, 545, 565, and 572 nm with a spectrophotometer (model 690 STC#690-001; Mountain View, CA) and recorded. Exposure to light was avoided throughout the procedure to reduce further oxidation of the pigment. Metmyoglobin content (mg/g) was calculated from the following formula:


where, R1, R2, and R3 are the absorbance ratios of A572/A525, A565/A525, and A545 /A525, respectively.

Statistical Analysis
Data were analyzed using the GLM procedure of SAS (SAS Inst., Inc., Cary, NC) as a split-plot design with carcass as the whole plot experimental unit and quality grades (high Choice, low Choice, and Select) as treatments. The whole plot error term was quality grades nested within carcasses. The subplot experimental unit was muscle (SM, ST, or BF) with packaging method (MAP or PVC) and display time (1, 3, 5, 7, or 10 d) as treatments (Figure 1Go). The experiment was replicated three times, and all possible pair-wise comparisons were made with a significance level of 5% for the response variables. Main effects were separated using LSD and interactive effect means were separated using the PDIFF option of SAS.



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Figure 1. Design of the experiment.

 

    Results and Discussion
 Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 Implications
 Literature Cited
 
Fat content
Select carcasses had a lower (P < 0.05) intramuscular fat content (2.02%) than low Choice and high Choice carcasses (3.76 and 5.69%, respectively). Although there were no differences (P > 0.05) between muscles, steaks from the BF tended to have numerically higher intramuscular fat contents (4.71%) than both ST (3.56%) and SM (3.20%) muscles (data not shown).

Color
Visual Lean Color.
Results indicated that low Choice steaks received higher (P < 0.05) lean color values (6.4) than either high Choice or Select steaks (5.8 and 5.9, respectively). Many consumers evaluate steak quality by using color to make their purchasing decision. Beefsteak quality has been equated to a bright red color. Consumers look unfavorably toward discoloration and any variation from this bright red standard. Kennick et al. (1971)Go reported color desirability was higher for steaks in the Choice grades then those in the Select and Prime grades.

Evaluation of quality grades in different packaging types displayed differences at d 5, 7, and 10 for lean color (packaging method x quality grade; P < 0.05), with low Choice steaks in MAP and PVC receiving the highest (P < 0.05) in lean color values and high Choice steaks in PVC receiving the lowest (P < 0.05) on d 5, 7, and 10 (Figure 2Go, Panel A). Moreover, lean color scores were higher (P < 0.05) for steaks packaged in MAP than PVC (6.3 vs. 5.9). The interactive effect (P < 0.05) of packaging method and muscle suggested inherent differences in muscles affected their reaction to packaging. Both ST and BF steaks were rated higher (P < 0.05) for lean color in MAP than PVC, whereas packaging method did not (P > 0.05) affect color scores of steaks from the SM (Figure 2Go, Panel B). Even though lean color values decreased (P < 0.05) with increasing display time (data not shown), ST steaks in MAP were rated higher (P < 0.05) for lean color on d 5, 7, and 10, whereas BF steaks in PVC, and SM steaks in PVC and MAP, received the lower (P < 0.05) lean color scores after 5, 7, and 10 d of simulated retail display (Figure 2Go, Panel B). The lean color values decreased (P < 0.05) as display time increased. Much of the variation in lean color could be attributed to overall oxidation levels of the cuts from increased metmyoglobin formation and possible lipid oxidation.



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Figure 2. Packaging method x quality grade interaction (P > 0.05; SEM = 0.12) and packaging method x steak interaction (P < 0.05; SEM = 0.14) over display time for lean color values. Lean color scale = 1 to 8 (1 = extremely dark red or brown; 8 = extremely bright red) was visually appraised on steaks of muscles (BF = biceps femoris; ST = semitendinosus; SM = semimembranosus) from carcasses with different quality grades (SL = Select; LC = low Choice; HC = high Choice) displayed in either a modified-atmosphere package (MAP) or overwrapped with a polyvinyl chloride film (PVC).

 
Discoloration.
Discoloration is a major deterrent to consumers. Evaluation of surface discoloration scores indicated less discoloration for low Choice steaks packaged in MAP and PVC than high Choice and Select steaks on d 5, 7, and 10 (packaging method x quality grade; P < 0.05). Moreover, low Choice steaks packaged in MAP had less (P < 0.05) discoloration at d 7 and 10 than all other quality grades packaged in either MAP or PVC (Figure 3Go, Panel A). The BF and ST muscles packaged in MAP had less (P < 0.05) discoloration than corresponding muscles packaged in PVC, whereas discoloration scores were similar (P > 0.05) in the SM regardless of packaging method (Figure 3Go, Panel B). Furthermore, there was less (P < 0.05) discoloration at d 7 and 10 for ST steaks compared with steaks from either the BF or SM; however, on d 1, 3, and 5, there were no (P > 0.05) differences between muscles (Figure 3Go, Panel A). There was a noticeable increase (P < 0.05) in discoloration after 5 d; however, Sorheim et al. (1999)Go reported color scores were stable throughout 11 d of storage. Panel evaluation scores were different between packaging with less (P < 0.05) discoloration for MAP than PVC steaks (8.3 vs. 7.8).



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Figure 3. Packaging method x quality grade (P > 0.05; SEM = 0.19) interaction and packaging method x steak interaction (P < 0.05; SEM = 0.22) over display time for discoloration values. Discoloration scale = 1 to 11 (1 = 90 to 100% discoloration; 11 = 0% discoloration) was visually appraised on steaks of muscles (BF = biceps femoris; ST = semitendinosus; SM = semimembranosus) from carcasses with different quality grades (SL = Select; LC = low Choice; HC = high Choice) displayed in either a modified atmosphere package (MAP) or overwrapped with a polyvinyl chloride film (PVC).

 
Objective Colorimeter Measurements
Lightness (L*) Values.
There was a packaging x muscle interaction (P < 0.05) of for L* values (Figure 4Go, Panel B). Steaks from the ST in MAP displayed the highest (P < 0.05) L* values after 3, 5, 7, and 10 d of simulated retail display. Additionally, ST steaks were lighter (P < 0.05) than either BF or SM steaks (41.7, 38.9, and 40.7, respectively; data not shown). High Choice steaks were darker (lower L* value) than low Choice and Select steaks (39.2, 41.1, and 41.1, respectively; data not shown). In addition, L* values were higher (P < 0.05) for MAP (41.4) steaks than PVC (39.5) steaks. The low Choice and Select steaks packaged in MAP had higher L* values than low Choice and Select steaks packaged in PVC and high Choice steaks in either packaging type (quality grade x packaging interaction; P < 0.05; Figure 4Go, Panel A).



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Figure 4. Packaging method x quality grade interaction (P > 0.05; SEM = 0.32) and packaging method x steak interaction (P < 0.05; SEM = 0.30) over display time for L* values (lightness) on steaks of muscles (BF = biceps femoris; ST = semitendinosus; SM = semimembranosus) from carcasses with different quality grades (SL = Select; LC = low Choice; HC = high Choice) displayed in either a modified atmosphere package (MAP) or overwrapped with a polyvinyl chloride film (PVC).

 
Redness (a*) Values.
Redness, as indicated by a* values, is a good indicator of color acceptability. There was an effect of quality grade on redness values with low Choice having greater (P < 0.05) a* values than high Choice and Select steaks (13. 9, 12.1, and 12.6, respectively; data not shown). Select and high Choice steaks packaged in PVC tended to be less red (P < 0.05) than low Choice steaks on d 3, 5, and 7 or retail display (quality grade x packaging interaction; P < 0.05; Figure 5Go, Panel A). Steaks package in MAP had higher (P < 0.05) a* values than steaks packaged in PVC, with the greatest difference between packaging methods occurring after 5 d of display (data not shown), and the magnitude of the difference between packaging methods was most noticeable in steaks from the BF and ST muscles (Figure 5Go, Panel B). Moreover, ST steaks in MAP tended to have greater (P < 0.05) a* values after 3, 5, 7, and 10 d of simulated retail display than BF steaks in MAP. Sorheim et al. (1999)Go reported a* values after 3 d of display for steaks packaged in high oxygen were also redder; however, these beef loin steaks discolored gradually between d 3 and 10 of display.



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Figure 5. Packaging method x quality grade interaction (P > 0.05; SEM = 0.31) and packaging method x steak interaction (P < 0.05; SEM = 0.32) over display time for a* values (redness) on steaks of muscles (BF = biceps femoris; ST = semitendinosus; SM = semimembranosus) from carcasses with different quality grades (SL = Select; LC = low Choice; HC = high Choice) displayed in either a modified atmosphere package (MAP) or overwrapped with a polyvinyl chloride film (PVC).

 
Metmyoglobin Content
Metmyoglobin conversion in beef products is very important because consumers’ purchasing decisions of red meats are based, to a high degree, on product color. High Choice steaks had higher (P < 0.05) metmyoglobin concentrations than low Choice and Select steaks. Initial (d 1) values indicated that no metmyoglobin formation had yet occurred. Correal et al. (1986)Go also found differences in metmyoglobin content among strip steaks from the three grades (Prime, Choice, and Good) and attributed the differences to inherent characteristics of the muscles. Low Choice steaks in MAP presented the lowest metmyoglobin formation after 10 d of display (quality grade x packaging interaction; P < 0.05; Figure 6Go, Panel A).



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Figure 6. Packaging method x quality grade interaction (P > 0.05; SEM = 0.02) and packaging method x steak interaction (P < 0.05; SEM = 0.02) over display time for metmyoglobin content (mg/g) on steaks of muscles (BF = biceps femoris; ST = semitendinosus; SM = semimembranosus) from carcasses with different quality grades (SL = Select; LC = low Choice; HC = high Choice) displayed in either a modified atmosphere package (MAP) or overwrapped with a polyvinyl chloride film (PVC).

 
Gill (1996)Go reported color stability is largely a matter of slowing or preventing the formation of brown metmyoglobin at the muscle surface. Metmyoglobin content was not different (P > 0.05) between PVC (0.27 mg/g) and MAP (0.29 mg/g). In contrast, Ordonez and Ledward (1977)Go reported an increase in oxygen concentration caused a significant decrease in the rate of metmyoglobin content, indicating that less than 30% of the total surface pigment concentration was metmyoglobin even after 15 d of storage in 80% O2/20% CO2.

In the present study, despite the increase in oxygen concentration in the packaging system, the concentrations of metmyoglobin continued to increase over display time, indicating stability of oxymyoglobin can be affected by the differences in the muscle’s chemical makeup. Semitendinosus steaks had less (P < 0.05) metmyoglobin formation than steaks for BF and SM muscles, regardless of packaging method (0.22, 0.28, and 0.35 mg/g, respectively). Metmyoglobin content for muscle x packaging increased over time for all muscles (Figure 6Go), which is consistent with Ordonez and Ledward (1977)Go, who reported a 55% increase in metmyoglobin over display time.


    Implications
 Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 Implications
 Literature Cited
 
Muscles react differently to packaging systems, and certain muscles may, in fact, have lower color stability in high-oxygen modified atmosphere packaging. Therefore, individual muscles must be evaluated for the most appropriate packaging method, and alternatives for cuts from these muscles are needed to continue the advances in centralized packaging.


    Footnotes
 
1 The authors would like to thank the Kentucky Beef Council and Cryovac/Sealed Air Corporation for their support of this research. Back

2 Present address: Department of Animal Science, Texas A & M University, College Station 77843. Back

3 Correspondence: 205 W. P. Garrigus Bldg. (phone: 859-257-7550; fax: 859-257-5318; E-mail: wmikel{at}ca.uky.edu).

Received for publication May 14, 2002. Accepted for publication May 29, 2003.


    Literature Cited
 Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 Implications
 Literature Cited
 


AMSA. 1995. Research Guidelines for Cookery, Sensory Evaluation and Instrumental Tenderness Measurements of Fresh Meat. Am. Meat Sci. Assoc., Chicago, IL.

AOAC. 1990. Official Methods of Analysis. 15th ed. Assoc. Offic. Anal. Chem., Washington, DC.

Asenio, M. A., J. A. Ordonez, and B. Sanz. 1988. Effects of carbon dioxide and oxygen enriched atmosphere on the shelf-life of refrigerated pork packed in plastic bags. J. Food Prot. 51:356–360.

Blinkstad, E., S.-O. Enfors, and G. Molin. 1981. Effect of hyperbaric carbon dioxide pressure on the microbial flora of pork stored at 4 or 14°C. J. Appl. Bacteriol. 50:493–498.

Christopher, F. M., C. Vanderzant, Z. L. Carpenter, and G. C. Smith. 1979. Microbiology of pork packaged in various gas atmospheres. J. Food Prot. 42:323–327.

Correal, K. K., J. W. Savell, D. B. Griffin, G. R. Acuff, and C. Vanderzant. 1986. Microbiological and sensory characteristics of beef loin steaks: Role of intramuscular fat. Meat Sci. 18:161–172.

Gill, C. O. 1996. Extending the storge life of raw chilled meats. Meat Sci. 43:S99–S109.

Kennick, W. H., R. S. Turner, D. K. Buck, L. S. McGill, and N. A. Hartmann, Jr. 1971. Effect of marbling and other variables on case life of New York steaks. J. Food Sci. 36:767–769.

Krzywicki, K. 1982. The determination of haem pigments in meat. Meat Sci. 7:29–36.

Ordonez, J. A., and D. A. Ledward. 1977. Lipid and myoglobin oxidation in pork stored in oxygen and carbon dioxide-enriched atmospheres. Meat Sci. 1:41–48.

Sorheim, O., H. Nissen, and T. Nesbakken. 1999. The storage life of beef and pork packaged in an atmosphere with low carbon monoxide and high carbon dioxide. Meat Sci. 52:157–164.

USDA. 1997. Official United States Standards for Grades of Carcass Beef. Agric. Marketing Serv., USDA, Washington, DC.

Witte, V. C., G. F. Krause, and M. E. Bailey. 1970. A new extraction method for determining 2-thiobarbituric acid values of pork and beef during storage. J. Food Sci. 35:582–588.


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