Okara is a soybean transformation agri-food by-product, the massive production of which currently poses severe disposal issues. However, its composition is rich in seed storage proteins, which, once extracted, can represent an interesting source of bioactive peptides. Antimicrobial and antifungal proteins and peptides have been described in plant seeds; thus, okara is a valuable source of compounds, exploitable for integrated pest management. The aim of this work is to describe a rapid and economic procedure to isolate proteins from okara, and to produce an enzymatic proteolyzed product, active against fungal plant pathogens. The procedure allowed the isolation and recovery of about 30% of okara total proteins. Several proteolytic enzymes were screened to identify the proper procedure to produce antifungal compounds. Antifungal activity of the protein digested for 24 h with pancreatin against Fusarium and R. solani mycelial growth and Pseudomonas spp was assessed. A dose-response inhibitory activity was established against fungi belonging to the Fusarium genus. The exploitation of okara to produce antifungal bioactive peptides has the potential to turn this by-product into a paradigmatic example of circular economy, since a field-derived food waste is transformed into a source of valuable compounds to be used in field crops protection.

Valorization of okara by enzymatic production of anti-fungal compounds for plant protection / S. De Benedetti, V. Girlando, M. Pasquali, A. Scarafoni. - In: MOLECULES. - ISSN 1420-3049. - 26:16(2021 Aug 11), pp. 4858.1-4858.14. [10.3390/molecules26164858]

Valorization of okara by enzymatic production of anti-fungal compounds for plant protection

S. De Benedetti;V. Girlando;M. Pasquali
;
A. Scarafoni
2021

Abstract

Okara is a soybean transformation agri-food by-product, the massive production of which currently poses severe disposal issues. However, its composition is rich in seed storage proteins, which, once extracted, can represent an interesting source of bioactive peptides. Antimicrobial and antifungal proteins and peptides have been described in plant seeds; thus, okara is a valuable source of compounds, exploitable for integrated pest management. The aim of this work is to describe a rapid and economic procedure to isolate proteins from okara, and to produce an enzymatic proteolyzed product, active against fungal plant pathogens. The procedure allowed the isolation and recovery of about 30% of okara total proteins. Several proteolytic enzymes were screened to identify the proper procedure to produce antifungal compounds. Antifungal activity of the protein digested for 24 h with pancreatin against Fusarium and R. solani mycelial growth and Pseudomonas spp was assessed. A dose-response inhibitory activity was established against fungi belonging to the Fusarium genus. The exploitation of okara to produce antifungal bioactive peptides has the potential to turn this by-product into a paradigmatic example of circular economy, since a field-derived food waste is transformed into a source of valuable compounds to be used in field crops protection.
No
English
okara; bioactive peptides; circular economy; biotechnology; proteolysis
Settore BIO/10 - Biochimica
Settore AGR/12 - Patologia Vegetale
Articolo
Esperti anonimi
Ricerca applicata
Pubblicazione scientifica
   Field to Field, Valorisation of biomolecules from soybean drink by-products as defence products and biostimulants for an improved sustainability of crops cultivation
   FONDAZIONE CARIPLO
   2018-0983
11-ago-2021
MDPI
26
16
4858
1
14
14
Pubblicato
Periodico con rilevanza internazionale
crossref
Aderisco
info:eu-repo/semantics/article
Valorization of okara by enzymatic production of anti-fungal compounds for plant protection / S. De Benedetti, V. Girlando, M. Pasquali, A. Scarafoni. - In: MOLECULES. - ISSN 1420-3049. - 26:16(2021 Aug 11), pp. 4858.1-4858.14. [10.3390/molecules26164858]
open
Prodotti della ricerca::01 - Articolo su periodico
4
262
Article (author)
no
S. De Benedetti, V. Girlando, M. Pasquali, A. Scarafoni
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/861553
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