Quantification of Major Royal Jelly Protein 1 in Fresh Royal Jelly by Ultraperformance Liquid Chromatography-Tandem Mass Spectrometry

被引:20
作者
Lin, Na [1 ]
Chen, Si [3 ,4 ]
Zhang, Hong [1 ]
Li, Junmin [1 ]
Fu, Linglin [2 ]
机构
[1] Zhejiang Gongshang Univ, Sch Food Sci & Biol Engn, Hangzhou 310018, Zhejiang, Peoples R China
[2] Zhejiang Gongshang Univ, Food Safety Key Lab Zhejiang Prov, Sch Food Sci & Biotechnol, Hangzhou 310018, Zhejiang, Peoples R China
[3] Marine Fisheries Res Inst Zhejiang Prov, Key Lab Mariculture & Enhancement, Zhoushan 316000, Peoples R China
[4] Zhejiang Ocean Univ, Marine & Fisheries Res Inst, Zhoushan 316000, Zhejiang, Peoples R China
基金
美国国家科学基金会;
关键词
MRJP1; royal jelly; quantitative method; signature peptide; stable isotope-labeled internal standard peptide; UPLC-MS/MS; DIFFERENT STORAGE-CONDITIONS; TNF-ALPHA RELEASE; APIS-MELLIFERA; APALBUMIN; PEPTIDES; HONEYBEE; FAMILY; QUANTITATION; PRODUCTS; ELISA;
D O I
10.1021/acs.jafc.7b05698
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Major royal jelly protein 1 (MRJP1) is the most abundant protein in royal jelly (RJ), and the level of MRJP1 has been suggested as a promising parameter for standardization and evaluation of RJ authenticity in quality. Here, a quantitative method was developed for the quantification of MRJP1 in RJ based on a signature peptide and a stable isotope-labeled internal standard peptide FFDYDFGSDER*(R*, C-13(6), N-15(4)) by ultraperformance liquid chromatography-tandem mass spectrometry. Recoveries of the established method ranged from 85.33 to 95.80%, and both the intra- and interday precision were RSD < 4.97%. Quantification results showed that content of MRJP1 in fresh RJ was 41.96-55.01 mg/g. Abnormal levels of MRJP1 were found in three commercial RJs and implied that these samples were of low quality and might be adulterated. Results of the present work suggested that the developed method could be successfully applied to quantify MRJP1 in RJ and also could evaluate the quality of RJ.
引用
收藏
页码:1270 / 1278
页数:9
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