Publication: Investigating the Antioxidant Capacity of Lunasin Expressed in Aspergillus oryzae
dc.contributor.author | KARAMAN E. | |
dc.contributor.author | Albayrak C. | |
dc.contributor.author | UYSAL S. | |
dc.contributor.institutionauthor | KARAMAN, ELİF | |
dc.contributor.institutionauthor | ALBAYRAK, CEM | |
dc.contributor.institutionauthor | UYSAL, SERDAR | |
dc.date.accessioned | 2024-07-03T21:50:35Z | |
dc.date.available | 2024-07-03T21:50:35Z | |
dc.date.issued | 2024-01-01 | |
dc.description.abstract | Objective: Lunasin is a bioactive protein that possesses anti-carcinogenic, anti-inflammatory, and antioxidant properties. Traditional isolation methods are resource-intensive, and chemical synthesis faces cost and environmental issues. This study aims to achieve cost-effective lunasin expression in Aspergillus oryzae with a focus on exploring its antioxidant properties in vitro. Materials and Methods: The expression vector carrying four lunasin sequences fused with amylase and an 8xHis-tag was introduced into pyrG auxotrophic A. oryzae. Subsequently, the recombinant protein was purified using metal affinity chromatography. The study uses sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), western blot analyses, and size-exclusion chromatography to evaluate the composition and purity of the protein, a linoleic acid assay to demonstrate the inhibitory effect on lipid peroxidation, and the 2,2\"-azinobis-[3-ethylbenzothiazoline-6-sulfonic acid] ABTS) assay to evaluate the radical scavenging activity. Results: SDS-PAGE and western blot analyses confirmed sustained lunasin expression in A. oryzae, appearing in both fusion and non-fusion forms. Yields were 5.8 mg/L for non-fusion and 4 mg/L for fusion lunasin expression. Moreover, 0.1 μM non-fusion lunasin surpassed α-tocopherol and butylated hydroxyanisole (BHA; p < 0.05) in reducing lipid peroxidation at 4 and 72 h. Unlike the fusion lunasin, the non-fusion lunasin displayed concentration- and time-independent inhibitory effects on linoleic acid peroxidation as well as significant ABTS scavenging activity (p < 0.05). Conclusion: The study has shown for the first time A. oryzae to efficiently express and secrete both fusion and non-fusion lunasin proteins in a soluble form, with the non-fusion lunasin exhibiting superior antioxidant effectiveness compared to the fusion lunasin. The findings underscore A. oryzae\"s potential as a promising host for producing functional lunasin with antioxidant properties, opening avenues for broader applications in biotechnology and bioactive peptides. | |
dc.identifier.citation | KARAMAN E., Albayrak C., UYSAL S., "Investigating the Antioxidant Capacity of Lunasin Expressed in Aspergillus oryzae", European Journal of Biology, cilt.83, sa.1, ss.67-76, 2024 | |
dc.identifier.doi | 10.26650/eurjbiol.2024.1454771 | |
dc.identifier.endpage | 76 | |
dc.identifier.issn | 2602-2575 | |
dc.identifier.issue | 1 | |
dc.identifier.scopus | 85195805622 | |
dc.identifier.startpage | 67 | |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85195805622&origin=inward | |
dc.identifier.uri | https://hdl.handle.net/20.500.12645/39435 | |
dc.identifier.volume | 83 | |
dc.relation.ispartof | European Journal of Biology | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | Biotechnology | |
dc.subject | Antioxidant | |
dc.subject | Aspergillus oryzae | |
dc.subject | Lunasin | |
dc.title | Investigating the Antioxidant Capacity of Lunasin Expressed in Aspergillus oryzae | |
dc.type | Article | |
dspace.entity.type | Publication | |
local.avesis.id | f286d093-d8ca-4d87-9115-8c6009df20ac | |
local.indexed.at | Scopus | |
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