牡蛎精氨酸激酶稳定性及同源性分析
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(中国食品发酵工业研究院,北京市蛋白功能肽工程技术研究中心,北京 100015)

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赵晓涵 女 研究生 研究方向为功能食品与食品过敏原 E-mail:zxh08240026@163.com 李国明 男 高级工程师 研究方向为功能食品与生物技术 E-mail:gml_1002@163.com

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中国食品发酵工业研究院强院工程培育专项(院强院20-功能肽-505);国家自然科学基金项目(31671963)


Study on stability and homology analysis of arginine kinase from oyster
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(China National Research Institute of Food & Fermentation Industry,Beijing Engineering Research Center of Protein and Functional Peptides,Beijing 100015, China)

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    摘要:

    目的 鉴定从牡蛎中提取的天然蛋白精氨酸激酶(arginine kinase,AK),并了解其基本性质及同源性。方法 利用硫酸铵盐析、阴离子交换从牡蛎中分离纯化出蛋白,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和圆二色(CD)光谱确定相对分子质量和二级结构,并研究其稳定性;用生物信息学软件对牡蛎AK和其他11种甲壳类、软体类动物过敏原的AK氨基酸序列进行比对,分析它们之间的同源性。结果 分离纯化得到的相对分子量为40 kDa的天然蛋白为牡蛎AK,AK既不耐热也不耐强酸。牡蛎AK与软体类动物过敏原AK氨基酸序列的同源性较高,与甲壳类动物氨基酸序列的同源性在55%~60%之间。结论 从牡蛎中提取得到天然AK,基本了解牡蛎AK的稳定性和同源性,并为牡蛎AK致敏性和致敏机制的全面研究打下基础。

    Abstract:

    Objective To identify the natural protein arginine kinase (AK) extracted from oysters, and to understand its basic properties and homology. Methods AK was isolated and purified from oysters by ammonium sulfate salting out and anion exchange, and the relative molecular mass and secondary structure were determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and circular dichroism (CD) spectroscopy. Its stability was also studied. The amino acid sequences of oyster AK and 11 other crustacean and mollusk allergens were compared by bioinformatics software, and their homology was analyzed. Results The natural protein with a relative molecular weight of 40 kDa was oyster AK. AK was neither heat-resistant nor acid-resistant. Oyster AK has high homology of mollusk allergen AK amino acid sequence, and homology of crustacean amino acid sequence is 55%-60%. Conclusion Natural AK is extracted from oysters, and the stability and homology are basically understood. It will lay the foundation for comprehensive research on sensitization and sensitization mechanism of oysters.

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赵晓涵,刘文颖,方磊,谷瑞增,凌空,李国明,鲁军.牡蛎精氨酸激酶稳定性及同源性分析[J].中国食品卫生杂志,2020,32(4):370-373.

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  • 收稿日期:2020-05-05
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  • 在线发布日期: 2020-08-30
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