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Detection of Aflatoxin B(1) in Single Peanut Kernels by Combining Hyperspectral and Microscopic Imaging Technologies

To study the dynamic changes of nutrient consumption and aflatoxin B(1) (AFB(1)) accumulation in peanut kernels with fungal colonization, macro hyperspectral imaging technology combined with microscopic imaging was investigated. First, regression models to predict AFB(1) contents from hyperspectral...

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Detalles Bibliográficos
Autores principales: Zhang, Haicheng, Jia, Beibei, Lu, Yao, Yoon, Seung-Chul, Ni, Xinzhi, Zhuang, Hong, Guo, Xiaohuan, Le, Wenxin, Wang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9269126/
https://www.ncbi.nlm.nih.gov/pubmed/35808359
http://dx.doi.org/10.3390/s22134864
Descripción
Sumario:To study the dynamic changes of nutrient consumption and aflatoxin B(1) (AFB(1)) accumulation in peanut kernels with fungal colonization, macro hyperspectral imaging technology combined with microscopic imaging was investigated. First, regression models to predict AFB(1) contents from hyperspectral data ranging from 1000 to 2500 nm were developed and the results were compared before and after data normalization with Box-Cox transformation. The results indicated that the second-order derivative with a support vector regression (SVR) model using competitive adaptive reweighted sampling (CARS) achieved the best performance, with R(C)(2) = 0.95 and R(V)(2) = 0.93. Second, time-lapse microscopic images and spectroscopic data were captured and analyzed with scanning electron microscopy (SEM), transmission electron microscopy (TEM), and synchrotron radiation-Fourier transform infrared (SR-FTIR) microspectroscopy. The time-lapse data revealed the temporal patterns of nutrient loss and aflatoxin accumulation in peanut kernels. The combination of macro and micro imaging technologies proved to be an effective way to detect the interaction mechanism of toxigenic fungus infecting peanuts and to predict the accumulation of AFB(1) quantitatively.