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Identification and Purification of Antioxidant Peptides from Lentils (Lens Culinaris) Hydrolysates

Received: 1 April 2015    Accepted: 11 April 2015    Published: 24 April 2015
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Abstract

Powder derived from Lentils was hydrolyzed sequentially using five different enzymes and their combinations for production of antioxidant peptide. For identifying antioxidant peptides, Lentils hydrolysate was fractionated using Ultra filtration and size exclusion chromatography (Superdex Peptide 10/300 GL) methods. The lentils peptide and its fractions demonstrated antioxidant activities as revealed from studies using a β-carotene-linoleate model system, hydroxyl radical-scavenging, the DPPH radical-scavenging activity assay, and a reducing power evaluation. Molecular characteristics of individual Lentils protein was investigated using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The results demonstrated that Lentils peptide fraction III exhibited the highest antioxidant activity compared to the other Lentils Fraction. The molecular weight and sequence were identified by LC-MS analysis as 587.31 Da and the amino acid sequence was as follows: Ala- Leu- Gly- Pro- Val- Met.

Published in Journal of Plant Sciences (Volume 3, Issue 3)
DOI 10.11648/j.jps.20150303.13
Page(s) 123-132
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Lentils, Lentils Peptide Hydrolysate, Antioxidant Properties, Sdspage

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Cite This Article
  • APA Style

    Muhammad Jamirul Ashad Zehadi, Kingsley Masamba, Yue Li, Maoshen Chen, Xuemei Chen, et al. (2015). Identification and Purification of Antioxidant Peptides from Lentils (Lens Culinaris) Hydrolysates. Journal of Plant Sciences, 3(3), 123-132. https://doi.org/10.11648/j.jps.20150303.13

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    ACS Style

    Muhammad Jamirul Ashad Zehadi; Kingsley Masamba; Yue Li; Maoshen Chen; Xuemei Chen, et al. Identification and Purification of Antioxidant Peptides from Lentils (Lens Culinaris) Hydrolysates. J. Plant Sci. 2015, 3(3), 123-132. doi: 10.11648/j.jps.20150303.13

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    AMA Style

    Muhammad Jamirul Ashad Zehadi, Kingsley Masamba, Yue Li, Maoshen Chen, Xuemei Chen, et al. Identification and Purification of Antioxidant Peptides from Lentils (Lens Culinaris) Hydrolysates. J Plant Sci. 2015;3(3):123-132. doi: 10.11648/j.jps.20150303.13

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  • @article{10.11648/j.jps.20150303.13,
      author = {Muhammad Jamirul Ashad Zehadi and Kingsley Masamba and Yue Li and Maoshen Chen and Xuemei Chen and Hafiz Rizwan Sharif and Fang Zhong},
      title = {Identification and Purification of Antioxidant Peptides from Lentils (Lens Culinaris) Hydrolysates},
      journal = {Journal of Plant Sciences},
      volume = {3},
      number = {3},
      pages = {123-132},
      doi = {10.11648/j.jps.20150303.13},
      url = {https://doi.org/10.11648/j.jps.20150303.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jps.20150303.13},
      abstract = {Powder derived from Lentils was hydrolyzed sequentially using five different enzymes and their combinations for production of antioxidant peptide. For identifying antioxidant peptides, Lentils hydrolysate was fractionated using Ultra filtration and size exclusion chromatography (Superdex Peptide 10/300 GL) methods. The lentils peptide and its fractions demonstrated antioxidant activities as revealed from studies using a β-carotene-linoleate model system, hydroxyl radical-scavenging, the DPPH radical-scavenging activity assay, and a reducing power evaluation. Molecular characteristics of individual Lentils protein was investigated using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The results demonstrated that Lentils peptide fraction III exhibited the highest antioxidant activity compared to the other Lentils Fraction. The molecular weight and sequence were identified by LC-MS analysis as 587.31 Da and the amino acid sequence was as follows: Ala- Leu- Gly- Pro- Val- Met.},
     year = {2015}
    }
    

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  • TY  - JOUR
    T1  - Identification and Purification of Antioxidant Peptides from Lentils (Lens Culinaris) Hydrolysates
    AU  - Muhammad Jamirul Ashad Zehadi
    AU  - Kingsley Masamba
    AU  - Yue Li
    AU  - Maoshen Chen
    AU  - Xuemei Chen
    AU  - Hafiz Rizwan Sharif
    AU  - Fang Zhong
    Y1  - 2015/04/24
    PY  - 2015
    N1  - https://doi.org/10.11648/j.jps.20150303.13
    DO  - 10.11648/j.jps.20150303.13
    T2  - Journal of Plant Sciences
    JF  - Journal of Plant Sciences
    JO  - Journal of Plant Sciences
    SP  - 123
    EP  - 132
    PB  - Science Publishing Group
    SN  - 2331-0731
    UR  - https://doi.org/10.11648/j.jps.20150303.13
    AB  - Powder derived from Lentils was hydrolyzed sequentially using five different enzymes and their combinations for production of antioxidant peptide. For identifying antioxidant peptides, Lentils hydrolysate was fractionated using Ultra filtration and size exclusion chromatography (Superdex Peptide 10/300 GL) methods. The lentils peptide and its fractions demonstrated antioxidant activities as revealed from studies using a β-carotene-linoleate model system, hydroxyl radical-scavenging, the DPPH radical-scavenging activity assay, and a reducing power evaluation. Molecular characteristics of individual Lentils protein was investigated using sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). The results demonstrated that Lentils peptide fraction III exhibited the highest antioxidant activity compared to the other Lentils Fraction. The molecular weight and sequence were identified by LC-MS analysis as 587.31 Da and the amino acid sequence was as follows: Ala- Leu- Gly- Pro- Val- Met.
    VL  - 3
    IS  - 3
    ER  - 

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Author Information
  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

  • State Key Laboratory of Food Science and Technology, School of Food Science and Technology, Jiangnan University, Wuxi, Jiangsu, Peoples Republic China

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