Jatropha curcas L. Seed Cake Residue as an Alternative Source for Obtaining Curcin: A Type 1 Ribosome-Inactivating Protein

被引:5
作者
da Silva Barroso, Wallady [1 ]
Leite, Talita Abrante [1 ]
de Abreu Feitosa, Vanessa [1 ]
da Penha, Samara Sena [1 ]
Freire, Elionai Gomes [1 ]
de Castro e Silva, Vinicius Rodrigues [1 ]
de Souza, Bartolomeu Warlene Silva [2 ]
da Silva, Andre Luis Coelho [1 ]
机构
[1] Univ Fed Ceara, Dept Bioquim & Biol Mol, Lab Biotecnol Mol LabBMol, BR-60455970 Fortaleza, Ceara, Brazil
[2] Univ Fed Ceara, Dept Engn Pesca, BR-60356000 Fortaleza, Ceara, Brazil
关键词
Curcin; Type; 1; RIP; RRNA-N-glycosidase; Jatropha curcas seed cake; RICIN-A-CHAIN; SENSITIVE METHOD; PHORBOL-ESTER; TOXIC LECTIN; CHROMATOGRAPHY; PURIFICATION; PLANTS; OIL;
D O I
10.1007/s12649-021-01412-2
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Jatropha curcas seed cake is a byproduct of oil extraction from biodiesel industry. Although it has high protein content, its valorization is hampered by its toxicity. Curcin is a type 1 ribosome-inactivating protein (type 1 RIP) that contributes to the Jatropha seed cake toxicity. The present study aimed to evaluate the feasibility of using Jatropha seed cake as an alternative source to obtain bioactive curcin. Extracts from the seed cake stored for 15, 30, 45, 60, 75, and 90 days were used to produce protein fractions (JcPFC15, JcPFC30, JcPFC45, JcPFC60, JcPFC75, and JcPFC90), which were further used in purifying curcin via size exclusion chromatography. All JcPFCs comprised curcin. The purified JcPFC curcins apparently had a molecular mass of 28 kDa, which was similar to the seed curcin. Western blot using antibody anti-curcin revealed a single band, corresponding to curcin. No significant differences were observed in the curcin concentrations in all JcPFCs throughout storage. Furthermore, JcPFCs' curcins presented conformational similarities to those of seed curcin, on evaluation by circular dichroism and intrinsic fluorescence spectroscopy. The RIP characteristic activity was assayed by rRNA-N-glycosidase activity test and in vitro protein synthesis inhibition assay, which revealed that the enzymatic activity was maintained in all JcPFCs' curcins. Moreover, the toxicity test did not indicate significant differences between JcPFCs' curcins and seed curcin. Accordingly, based on the results obtained, it is possible to affirm that J. curcas seed cake is a viable source of active curcin even after 90 days of storage. [GRAPHICS] .
引用
收藏
页码:5587 / 5597
页数:11
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