Chemical compositions and physical properties of mixed-sex Thai indigenous (Gallus domesticus) and broiler (commercial breed, CP707) chicken biceps femoris and pectoralis muscles were determined. Indigenous chicken muscles contained higher protein contents but lower fat and ash contents compared to broiler muscles (P < 0.001). The amino acid profile of the indigenous chicken muscles was similar to that of the broiler muscles except they were slightly richer in glutamic acid (P < 0.05). The indigenous chicken muscles contained more saturated and less polyunsaturated fatty acids than the broiler muscles. There were no differences in the monounsaturated fatty acid contents between the breeds. The total collagen contents of indigenous pectoralis and biceps femoris muscles were 5.09 and 12.85 mg/g, respectively, which were higher than those found in broiler pectoralis (3.86 mg/g) and biceps femoris muscles (8.70 mg/g) (P < 0.001). Soluble collagen contents were lower for indigenous pectoralis and biceps femoris muscles, 22.16 vs. 31.38% and 26.06 vs. 33.87%, respectively. The CIE system values of lightness (L*), redness (a*), and yellowness (b*) of indigenous chicken muscles were higher than those of broiler muscles. The shear values of indigenous chicken muscles either raw or cooked were higher than those of broiler muscles (P < 0.05). After cooking, the shear values decreased for broiler biceps femoris and pectoralis muscles (P < 0.05), whereas no change was observed for indigenous chicken biceps femoris muscle (P > 0.05). Shear values increased for indigenous chicken pectoralis muscle (P < 0.05).

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The microstructure and thermal characteristics of Thai indigenous (Gallus domesticus) and broiler chicken (commercial line CP707) biceps femoris and pectoralis muscles were determined. Perimysium thicknesses were 14.2 microm for biceps femoris muscle and 7.10 microm for pectoralis muscle of indigenous chicken muscles, thicker than those of broiler muscles, which were 9.93 microm for biceps femoris muscle and 3.87 microm for pectoralis muscle (P < 0.05). Five endothermic peaks with peak transition temperatures (Tp) of 54.9, 61.7, 65.4, 70.6, and 76.1 degrees C were obtained for broiler pectoralis muscle, whereas only 3 endothermic peaks (Tp of 56.6, 62.6, and 74.9 degrees C) were obtained for broiler biceps femoris muscle. Thai indigenous biceps femoris and pectoralis muscles had endothermic peaks with Tp ranges of 53.5 to 54.8, 60.7 to 61.9, and 75.9 to 76.9 degrees C. The fiber diameters of Thai indigenous chicken muscles were greater (P < 0.05) than those of the broiler, 31.7 vs. 20.4 microm for biceps femoris muscle and 28.9 vs. 26.6 microm for pectoralis muscle, respectively. After cooking at 80 degrees C for 10 min, the fiber diameter of indigenous chicken muscles significantly decreased while those of the broiler significantly increased. The mean of sarcomere lengths of the raw muscles ranged from 1.56 to 1.64 microm and decreased to 0.92 to 1.32 microm (P < 0.001) for broiler muscles and 1.22 to 1.35 microm (P < 0.001) for indigenous chicken muscles after cooking. The perimysium and endomysium of broiler muscles melted after cooking at 80 degrees C, however, only slight disintegration was observed in these tissues in the indigenous chicken muscles.

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