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Recombinant Fusion Protein Containing Plant Nigellothionin Regulates the Growth of Food-Spoiling Fungus (Aspergillus niger).
Barashkova, Anna S; Ryazantsev, Dmitry Yu; Zhuravleva, Anna S; Sharoyko, Vladimir V; Rogozhin, Eugene A.
Affiliation
  • Barashkova AS; Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry Russian Academy of Sciences, Moscow 117937, Russia.
  • Ryazantsev DY; All-Russian Institute for Plant Protection, Pushkin 196608, Russia.
  • Zhuravleva AS; Shemyakin and Ovchinnikov Institute of Bioorganic Chemistry Russian Academy of Sciences, Moscow 117937, Russia.
  • Sharoyko VV; Agrophysical Research Institute, Saint-Petersburg 195220, Russia.
  • Rogozhin EA; Department of General and Bioorganic Chemistry, Pavlov First Saint-Petersburg State Medical University, Saint-Petersburg 197022, Russia.
Foods ; 12(16)2023 Aug 09.
Article in En | MEDLINE | ID: mdl-37628001
ABSTRACT
This study aimed to obtain a recombinant chimeric protein named trx-NsW2 via theheterologous expression of the multifunctional antimicrobial peptide nigellothionin from black cumin (Nigella sativa L.) seeds in the Escherichia coli system. The protein was purified using a combination of Ni-NTA affinity chromatography and reversed-phase HPLC. Based on the HPLC calibration, the total yield of the protein was calculated to be 650 mg/L of bacterial culture. The fungistatic activity of trx-NsW2 against the food-spoiling fungus Aspergillus niger was demonstrated as itinhibited the maturation of conidiawithout affecting conidial germination or fungal growth. In contrast to mature nigellothionin NsW2, the fusion protein showeda low level of cytotoxicity towards both normal and tumor cell lines at concentrationsof up to 100-200 µM. Interestingly, at lower concentrations, it even stimulated cytokinesis. These findings are of critical importance for applying chimeric antimicrobial proteins obtained via microbiological synthesis in applied science.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Foods Year: 2023 Document type: Article Affiliation country: Rusia

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Foods Year: 2023 Document type: Article Affiliation country: Rusia