4.7 Article

Synergistic effects of pH shift and heat treatment on solubility, physicochemical and structural properties, and lysinoalanine formation in silkworm pupa protein isolates

Journal

FOOD RESEARCH INTERNATIONAL
Volume 165, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.foodres.2023.112554

Keywords

Silkworm pupa protein; pH shift; Heat treatment; Solubility; Physicochemical properties; Lysinoalanine formation

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In this study, pH shift and heating treatments were used to improve the solubility of silkworm pupa protein isolates (SPPI) and reduce the content of lysinoalanine (LAL). The results showed that alkaline pH shift + heat treatment had a greater effect on improving solubility compared to acidic pH shift + heat treatment, and it also reduced the LAL content. These findings provide fundamental information for the development and application of SPPI in the food industry.
The application of silkworm pupa protein isolates (SPPI) in food industry was limited because SPPI's solubility is poor and it contains a potential harmful component of lysinoalanine (LAL) which formed during protein extraction. In this study, combined treatments of pH shift and heating were performed to improve the solubility of SPPI and to reduce the content of LAL. The experimental results showed that the promoting effect on SPPI's solubility by alkaline pH shift + heat treatment was greater than that by acidic pH shift + heat. And an 8.62 times increase of solubility was observed after pH 12.5 + 80 degrees C treatment compared to the control SPPI sample which was extracted at pH 9.0 without pH shift treatment. Very strong positive correlation was found between alkali dosage and SPPI solubility (Pearson's correlation coefficient r = 0.938). SPPI with pH 12.5 shift treatment showed the highest thermal stability. Alkaline pH shift combined with heat treatment altered the micromor-phology of SPPI and destroyed the disulfide bonds between macromolecular subunits (72 and 95 kDa), resulting in reduced particle size and increased zeta potential and free sulfhydryl content of the isolates. The fluorescence spectra analysis showed red shifts phenomena with pH increasing and fluorescence intensity increase with temperature increasing, implying the alterations in the tertiary structure of protein. Compared to the control SPPI sample, the amount of LAL reduced by 47.40 %, 50.36 % and 52.39 % using pH 12.5 + 70 degrees C, pH 12.5 + 80 degrees C and pH 12.5 + 90 degrees C treatment, respectively. These findings provide fundamental information for the development and application of SPPI in food industry.

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