No abstract

In the present study, Fourier‐transform infrared spectroscopy (FTIR) is investigated as a method to measure connective tissue components that are important for the quality of Atlantic cod filets (Gadus morhua L.). The Atlantic cod used in this study originated from a feeding trial, which found that fish fed a high starch diet contained relative more collagen type I, while fish fed a low starch (LS) diet contained relative more glycosaminoglycans (GAGs) in the connective tissue. FTIR spectra of pure commercial collagen type I and GAGs were acquired to identify spectral markers and compare them with FTIR spectra and images from connective tissue. Using principal component analysis, high and LS diets were separated due to collagen type I in the spectral region 1800 to 800 cm−1. The spatial distribution of collagen type I and GAGs were further investigated by FTIR imaging in combination with immunohistochemistry. Pixel‐wise correlation images were calculated between preprocessed connective tissue images and preprocessed pure components spectra of collagen type I and GAGs, respectively. For collagen, the FTIR images reveal a collagen distribution that closely resembles the collagen distribution as imaged by immunohistochemistry. For GAGs, the concentration is very low. Still, the FTIR images detect the most GAGs rich regions.

The muscle syndrome woody breast (WB) impairs quality of chicken fillets and is a challenge to the poultry meat industry. There is a need for online detection of affected fillets for automatic quality sorting in process. Near-infrared spectroscopy (NIRS) is a promising method, and in this study we elucidate the spectral properties of WB versus normal fillets. On a training set of 50 chicken fillets (20 normal, 30 WB), we measured NIR, nuclear magnetic resonance (NMR) T2 relaxation distributions, and crude chemical composition. NIRS could estimate protein in the fillets with an accuracy of ±0.64 percentage points. T2 distributions showed that there was a larger share of free water in WB fillets. This difference in water binding generated a shift and narrowing of the water absorption peak in NIR around 980 nm, quantified by a bound water index (BWI). The correlation between BWI and T2 distributions was 0.78, indicating that NIRS contains information about degree of water binding. Discriminant analysis showed that NIRS obtained 100% correct classification of normal versus WB on the training set, and 96% correct classification on a test set of 52 fillets. The main reason for why NIRS can successfully discriminate between WB and normal fillets is the methods sensitivity to both protein content and degree of water binding in the muscle, both established markers for WB. The classification model can be based on NIR spectra only, calibration against protein is not needed. The affected muscle tissue associated with the WB syndrome is unevenly distributed in the fillets, and this heterogeneity was characterized by NIRS and NMR. Clear differences in water binding properties were found between the superficial 1 cm layer and the deeper layer at 1 to 2 cm depth. Significant differences in protein estimates by NIRS at different measurement points along the chicken fillets were obtained for WB fillets. The findings suggest how to obtain optimal sampling with NIRS for best possible discrimination between WB and normal breast fillets.