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Home > Archive>Volume 22, Issue 1, 2021 >149-156. DOI:10.13430/j.cnki.jpgr.20200618001 Online First
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Detection Method of Allergen Gly m Bd 30K and Identification of Elite Accessions with Low Allergenicity in Soybean (Glycine max (L.) Merr.)
DOI:
10.13430/j.cnki.jpgr.20200618001
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  • ZHOU Ming-ming 1

    ZHOU Ming-ming

    Yangtze University, College of Agriculture, Hubei Jingzhou
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  • ZHANG Ming-jun 1

    ZHANG Ming-jun

    Yangtze University, College of Agriculture, Hubei Jingzhou
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  • WANG Jun 1

    WANG Jun

    Yangtze University, College of Agriculture, Hubei Jingzhou
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  • QIU Li-juan 2

    QIU Li-juan

    National Key Facility for Crop Gene Resources and Genetic Improvement / Key Laboratory of Soybean Biology in Beijing( MOA) / Institute of Crop Sciences, Chinese Academy of Agricultural Sciences
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Affiliation:

1Yangtze University, College of Agriculture, Hubei Jingzhou 434025; 2National Key Facility for Crop Gene Resources and Genetic Improvement / Key Laboratory of Soybean Biology in Beijing( MOA) / Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081

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    Abstract:

    Gly m Bd 30K protein is recognized as a major immunodominant allergen in soybean, and this protein can lead to anaphylaxis such as diarrhea and intestinal inflammation in humans and livestock. The exploration of germplasms with lower Gly m Bd 30K content is important in breeding for elite functional soybean varieties. In this study, we generated the polyclonal antibody targeting to the 190-379aa peptides of the Gly m Bd 30K protein, followed by quantifying the Gly m Bd 30K protein using Western blot in 30 soybean accessions that were derived from Shanxi province. The genomic sequence of the Gly m Bd 30K gene and its transcriptional level was further conducted. As a result, two germplasms( 134, ZDD02046, Daqingdou, ZDD02174) with lower Gly m Bd 30K protein content have been identified, the identification efficiency is 6.9%. Both accessions displayed 8 and 42 TA repeats respectively in the promoter of the Gly m Bd 30K gene if compared with that of Willams82. The transcription level in 134( ZDD02046) was found to be significantly lower than that of Daqingdou( ZDD02174) . It is speculated that TA polymorphism in the promoter may associate with the Gly m Bd 30K expression. Collectively, this study established a strategy on the quantification of Gly m Bd 30K protein content and identified two accessions with lower Gly m Bd 30K protein, which will provide technical and material supports in breeding for new soybean varieties with high-quality proteins.

    Key words:soybean; allergen; Gly m Bd 30K; germplasm screening; western blot
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History
  • Received:June 18,2020
  • Revised:August 29,2020
  • Adopted:August 31,2020
  • Online: January 07,2021
  • Published:
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