Journal
FOOD CHEMISTRY
Volume 240, Issue -, Pages 32-42Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.foodchem.2017.07.048
Keywords
Near-infrared spectroscopy; Wheat protein; Cereals; Rapid measurement; Chemical imaging; Single kernel assessment; Hyperspectral imaging
Funding
- Biotechnology and Biological Sciences Research Council [BB/I532902/1]
- Biotechnology and Biological Sciences Research Council [BB/N021126/1, BB/N020979/2] Funding Source: researchfish
- BBSRC [BB/N021126/1, BB/N020979/2, BB/N020979/1] Funding Source: UKRI
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Hyperspectral imaging (HSI) combines Near-infrared (NIR) spectroscopy and digital imaging to give information about the chemical properties of objects and their spatial distribution. Protein content is one of the most important quality factors in wheat. It is known to vary widely depending on the cultivar, agronomic and climatic conditions. However, little information is known about single kernel protein variation within batches. The aim of the present work was to measure the distribution of protein content in whole wheat kernels on a single kernel basis, and to apply HSI to predict this distribution. Wheat samples from 2013 and 2014 harvests were sourced from UK millers and wheat breeders, and individual kernels were analysed by HSI and by the Dumas combustion method for total protein content. HSI was applied in the spectral region 980-2500 nm in reflectance mode using the push-broom approach. Single kernel spectra were used to develop partial least squares (PLS) regression models for protein prediction of intact single grains. The protein content ranged from 6.2 to 19.8% (as-is basis), with significantly higher values for hard wheats. The performance of the calibration model was evaluated using the coefficient of determination (R-2) and the root mean square error (RMSE) from 3250 samples used for calibration and 868 used for external validation. The calibration performance for single kernel protein content was R-2 of 0.82 and 0.79, and RMSE of 0.86 and 0.94% for the calibration and validation dataset, enabling quantification of the protein distribution between kernels and even visualisation within the same kernel. The performance of the single kernel measurement was poorer than that typically obtained for bulk samples, but is acceptable for some specific applications. The use of separate calibrations built by separating hard and soft wheat, or on kernels placed on similar orientation did not greatly improve the prediction ability. We simulated the use of the lower cost InGaAs detector (1000-1700 nm), and reported that the use of proposed HgCdTe detectors over a restricted spectral range gave a lower prediction error (RMSEC = 0.86% vs 1.06%, for HgCdTe and InGaAs, respectively), and increased R-2 value (R-c(2) = 0.82 vs 0.73). (C) 2017 The Authors. Published by Elsevier Ltd.
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