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Characterization and evaluation of antibacterial and antiproliferative activities of crude protein extracts isolated from the seed of Ricinus communis in Bangladesh.
Al-Mamun, M Abdulla; Akter, Zerin; Uddin, Md Josim; Ferdaus, K M K B; Hoque, K M F; Ferdousi, Z; Reza, M Abu.
Afiliación
  • Al-Mamun MA; Department of Genetic Engineering and Biotechnology, Protein Science Lab, University of Rajshahi, Rajshahi, 6205, Bangladesh.
  • Akter Z; Department of Genetic Engineering and Biotechnology, Protein Science Lab, University of Rajshahi, Rajshahi, 6205, Bangladesh.
  • Uddin MJ; Department of Pharmacy, Faculty of Science and Engineering, International Islamic University Chittagong, Chittagong, 4203, Bangladesh.
  • Ferdaus KM; Department of Genetic Engineering and Biotechnology, Protein Science Lab, University of Rajshahi, Rajshahi, 6205, Bangladesh.
  • Hoque KM; Department of Genetic Engineering and Biotechnology, Protein Science Lab, University of Rajshahi, Rajshahi, 6205, Bangladesh.
  • Ferdousi Z; Department of Genetic Engineering and Biotechnology, Protein Science Lab, University of Rajshahi, Rajshahi, 6205, Bangladesh.
  • Reza MA; Department of Genetic Engineering and Biotechnology, Protein Science Lab, University of Rajshahi, Rajshahi, 6205, Bangladesh. reza.gen@ru.ac.bd.
BMC Complement Altern Med ; 16: 211, 2016 Jul 12.
Article en En | MEDLINE | ID: mdl-27405609
BACKGROUND: Ricinus communis (Euphorbiaceae) has previously been reported to possess analgesic, antihistamine, antioxidant and anti-inflammatory activities. This study was designed for isolation, characterization and evaluation of antibacterial and anti-proliferative activities of R. communis seed protein. METHODS: The concentration and molecular weight of R. communis seed protein were estimated by SDS-PAGE and spectrophotometric analysis, respectively. Lectin activity was evaluated by hemagglutination assay on mice blood. In vitro susceptibility of four human pathogenic bacteria including Escherichia coli, Pseudomonas aeruginosa, Enterobacter aerogenes and Staphylococcus aureus was detected using disk diffusion assay, and minimum inhibitory concentration (MIC) value was determined using micro-dilution method. A total of twenty four Swiss albino mice containing Ehrlich's ascites carcinoma (EAC) cells were treated with the crude protein of R. communis at 50 and 100 µg/ml/d/mouse for 6 days. Growth inhibitory activity of R. communis seed protein on EAC cells was determined by haemocytometer counting using trypan blue dye and DAPI (4΄,6-diamidino-2-phenylindole) staining was used to assess apoptotic cells. RESULTS: The protein concentration of six R. communis (castor) varieties ranged between 21-35 mg/ml and molecular weight between 14-200 kDa. Castor protein agglutinated mice blood at 3.125 µg/wall. The seed protein shows considerable antimicrobial activity against E. coli, P. aeruginosa and S. aureus, exhibiting MIC values of 250, 125 and 62.5 µg/ml, respectively. Administration of seed protein led to 54 % growth inhibition of EAC cells at 100 µg/ml. DAPI staining indicates marked features of apoptosis including condensation of cytoplasm, nuclear fragmentation and aggregation of apoptotic bodies etc. CONCLUSION: Our study suggests that the lectin rich R. communis seed protein has strong antibacterial and anticancer activities.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Semillas / Extractos Vegetales / Ricinus communis / Proliferación Celular / Antibacterianos / Antineoplásicos Límite: Animals País/Región como asunto: Asia Idioma: En Revista: BMC Complement Altern Med Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2016 Tipo del documento: Article País de afiliación: Bangladesh

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Semillas / Extractos Vegetales / Ricinus communis / Proliferación Celular / Antibacterianos / Antineoplásicos Límite: Animals País/Región como asunto: Asia Idioma: En Revista: BMC Complement Altern Med Asunto de la revista: TERAPIAS COMPLEMENTARES Año: 2016 Tipo del documento: Article País de afiliación: Bangladesh
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