Fluorescence studies by quenching and protein unfolding on the interaction of bioactive compounds in water extracts of kiwi fruit cultivars with human serum albumin - Publikacja - MOST Wiedzy

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Fluorescence studies by quenching and protein unfolding on the interaction of bioactive compounds in water extracts of kiwi fruit cultivars with human serum albumin

Abstrakt

The main aim of this investigation was to characterize new kiwi fruit cultivars after cold storage treatment and to determine the similarities and differences between them, using spectroscopic methods. The chemometric comparison of kiwi fruit cultivars based on physicochemical indices during cold storage was carried out. All kiwi fruit cultivars showed a high level of correlation between the contents of phenolic compounds (polyphenols, tannins and flavonoids) and their antioxidant capacities. The interactions of soluble polyphenols of different kiwi fruit cultivars with human serum albumin (HSA) were investigated by fluorescence. The obtained statistical and fluorescence results allow to classify the investigated kiwi fruit cultivars according to their properties. The antioxidant properties of different cultivars monitored by β-carotene assay showed that the highest percentage of antioxidant activity (%AA) at the end of the cold storage was detected for ‘SKK-12’ (27.61±2.44) %AA with the lowest shelf life (8 weeks) and the lowest was found for ‘Hayward’ variety (8.33±0.74) %AA with the highest shelf life (24 weeks). The averaged amount of polyphenols in ‘Bidan’ and ‘SKK-12’ 13.97±1.95 mg GAE/g was much higher than in other cultivars 3.93±3.26 mg GAE/g, without respect on time of cold storage. The HSA-binding capacities of these cultivars were the highest and correlated with their antioxidant capacities. To our knowledge this is the first report showing differences and similarities in new kiwi fruit cultivars, using spectroscopic techniques. The fact that fluorescence spectral methods are applied as a powerful tool to show the photophysical properties of intrinsic fluorophores in protein molecules in the presence of fruit extracts is important in this study. In conclusion, the obtained knowledge would contribute to the pharmaceutical development and clinical application of kiwi fruit extracts.

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Autorzy (10)

  • Zdjęcie użytkownika  Yong-Seo Park

    Yong-Seo Park

    • Mokpo National University Department of Horticultural Science
  • Zdjęcie użytkownika  Martin Polovka

    Martin Polovka

    • Food Research Institute National Agricultural and Food centre
  • Zdjęcie użytkownika  Alma Leticia Martinez-Ayala

    Alma Leticia Martinez-Ayala

    • Insituto Politecnico Nacional Centro de Desarrollo de Productos Bioticos
  • Zdjęcie użytkownika  Gustavo González-Aguilar

    Gustavo González-Aguilar

    • Research Center fod Food and Development CIAD
  • Zdjęcie użytkownika  Kyung-Sik Ham

    Kyung-Sik Ham

    • Mokpo National University Departemnt of Food Engineering
  • Zdjęcie użytkownika  Seong-Gook Kang

    Seong-Gook Kang

    • Mokpo National University Departemnt of Food Engineering
  • Zdjęcie użytkownika  Yang-Kyun Park

    Yang-Kyun Park

    • Mokpo National University Departemnt of Food Engineering
  • Zdjęcie użytkownika  Buk-Gu Heo

    Buk-Gu Heo

    • Naju Foundation of natural Dyeing Culture Naju
  • Zdjęcie użytkownika  Shela Gorinstein

    Shela Gorinstein

    • Hebraw University Institute for Drug research

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Informacje szczegółowe

Kategoria:
Publikacja w czasopiśmie
Typ:
artykuł w czasopiśmie wyróżnionym w JCR
Opublikowano w:
JOURNAL OF LUMINESCENCE nr 160, strony 71 - 77,
ISSN: 0022-2313
Język:
angielski
Rok wydania:
2015
Opis bibliograficzny:
Park Y., Polovka M., Martinez-Ayala A., González-Aguilar G., Ham K., Kang S., Park Y., Heo B., Namieśnik J., Gorinstein S.: Fluorescence studies by quenching and protein unfolding on the interaction of bioactive compounds in water extracts of kiwi fruit cultivars with human serum albumin// JOURNAL OF LUMINESCENCE. -Vol. 160, (2015), s.71-77
DOI:
Cyfrowy identyfikator dokumentu elektronicznego (otwiera się w nowej karcie) 10.1016/j.jlumin.2014.11.044
Weryfikacja:
Politechnika Gdańska

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