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자료유형
학술저널
저자정보
Song, Minyu (Animal Products Development and Processing Division, National Institute of Animal Science) Kim, Hyaekang (Department of Agricultural Biotechnology and Research Institute of Agriculture and Life Sciences, Seoul National University) Kwak, Woori (C & K Genomics) Park, Won Seo (Animal Products Development and Processing Division, National Institute of Animal Science) Yoo, Jayeon (Animal Products Development and Processing Division, National Institute of Animal Science) Kang, Han Byul (Animal Products Development and Processing Division, National Institute of Animal Science) Kim, Jin-Hyoung (Animal Products Development and Processing Division, National Institute of Animal Science) Kang, Sun-Moon (Animal Products Development and Processing Division, National Institute of Animal Science) Van Ba, Hoa (Animal Products Development and Processing Division, National Institute of Animal Science) Kim, Bu-Min (Animal Products Development and Processing Division, National Institute of Animal Science) Oh, Mi-Hwa (Animal Products Development and Processing Division, National Institute of Animal Science) Kim, Heebal (Department of Agricultural Bi) Ham, Jun-Sang
저널정보
한국축산식품학회 Food science of animal resources Food science of animal resources 제39권 제4호
발행연도
2019.1
수록면
601 - 609 (9page)

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Bifidobacterium longum KACC 91563 secretes family 5 extracellular solute-binding protein via extracellular vesicle. In our previous work, it was demonstrated that the protein effectively alleviated food allergy symptoms via mast cell specific apoptosis, and it has revealed a therapeutic potential of this protein in allergy treatment. In the present study, we cloned the gene encoding extracellular solute-binding protein of the strain into the histidine-tagged pET-28a(+) vector and transformed the resulting plasmid into the Escherichia coli strain BL21 (DE3). The histidine-tagged extracellular solute-binding protein expressed in the transformed cells was purified using Ni-NTA affinity column. To enhance the efficiency of the protein purification, three parameters were optimized; the host bacterial strain, the culturing and induction temperature, and the purification protocol. After the process, two liters of transformed culture produced 7.15 mg of the recombinant proteins. This is the first study describing the production of extracellular solute-binding protein of probiotic bacteria. Establishment of large-scale production strategy for the protein will further contribute to the development of functional foods and potential alternative treatments for allergies.

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