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碱性蛋白酶 2.4 L 和氯化钙用于水相提取花生油的组合。

Combination of Alcalase 2.4 L and CaCl for aqueous extraction of peanut oil.

机构信息

College of Food Science and Technology, Henan University of Technology, Zhengzhou, 450001, China.

College of Food Science, Northeast Agricultural University, Harbin, 150030, China.

出版信息

J Food Sci. 2020 Jun;85(6):1772-1780. doi: 10.1111/1750-3841.15158. Epub 2020 Jun 2.

DOI:10.1111/1750-3841.15158
PMID:32484970
Abstract

The combined application of CaCl and Alcalase 2.4 L to the aqueous extraction process of peanuts was evaluated as a method to destabilize the oil body (OB) emulsion and improve the oil yield. After adding 5 mM CaCl , the oil yield was reached to 92.0% which was similar with that obtained using Alcalase 2.4 L alone, and the required enzyme loading was decreased by approximately 60 times. In addition, the demulsification mechanism during aqueous extraction process was also investigated. Particle size and zeta-potential measurements indicated that the stability of the peanut OB emulsion dramatically decreased when CaCl was added. Under these conditions, the demulsification of Alcalase 2.4 L performed was more efficiently. SDS-PAGE results showed that adding CaCl changed the subunit structure of the peanut OB interface proteins and promoted the cross-linking among the arachin Ara h3 isoforms, resulting in unstable emulsions.

摘要

氯化钙和 Alcalase 2.4 L 的联合应用评估为一种破坏花生油体(OB)乳液并提高出油率的方法。添加 5 mM 氯化钙后,出油率达到 92.0%,与单独使用 Alcalase 2.4 L 获得的出油率相似,所需酶用量减少了约 60 倍。此外,还研究了水提取过程中的脱乳化机制。粒径和 Zeta 电位测量表明,添加氯化钙后花生 OB 乳液的稳定性显著降低。在这些条件下,Alcalase 2.4 L 的脱乳化效果更为高效。SDS-PAGE 结果表明,添加氯化钙改变了花生 OB 界面蛋白的亚基结构,并促进了 arachin Ara h3 同工型之间的交联,导致乳液不稳定。

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