این سایت در حال حاضر پشتیبانی نمی شود و امکان دارد داده های نشریات بروز نباشند
Iranian Journal of Basic Medical Sciences، جلد ۲۰، شماره ۴، صفحات ۳۸۰-۳۸۵

عنوان فارسی
چکیده فارسی مقاله
کلیدواژه‌های فارسی مقاله

عنوان انگلیسی Recombinant production and affinity purification of the FraC pore forming toxin using hexa-His tag and pET expression cassette
چکیده انگلیسی مقاله Objective(s): A newly-introduced protein toxin from a sea anemone, namely fragaceatoxin C is a protein with molecular weight of 20 kDa and pore-forming capability against cell membranes has recently grasped great attentions for its function. In this study, its coding sequence cloned as a fusion protein with His-tag for simple production and rapid purification. Materials and Methods: After PCR amplification using NcoI and HindIII-harboring primers, the gene fragment was cloned into pET-28a(+). Escherichia coli BL21 was used for expression of constructed vector and toxin expression was verified by SDS-PAGE. For one-step purification Ni-NTA sepharose  affinity chromatography was employed. For examination of purified toxin function, RBC hemolytic test was conducted. Results: The results showed that the FraC-coding gene was successfully cloned between NcoI and HindIII restriction sites and purified with affinity chromatography. Densitometric analysis represented the purity of approximately 97%. Hemolytic test indicated the purified FraC had remarkable lytic activity on RBC and almost lysed 50% of cells at the concentration value of 6.25 nM. Conclusion: The results indicated that not only purified toxin preserved its activity during expression and purification processes but also exerted its function at lower concentrations so that even the 0.09 nM displayed hemolytic effect.
کلیدواژه‌های انگلیسی مقاله

نویسندگان مقاله مهدی ایمانی | mehdi imani
department of basic sciences, faculty of veterinary medicine, urmia university, urmia, iran|department of cellular and molecular biotechnology, institute of biotechnology, urmia university, urmia, iran

سازمان اصلی تایید شده: دانشگاه ارومیه (Urmia university)

حسین زارعی جلیانی | hossein zarei jaliani
department of genetics, school of medicine, shahid sadoughi university of medical sciences, yazd, iran


محمد حسن خیراندیش | mohammad hassan kheirandish
department of genetics, school of medicine, shahid sadoughi university of medical sciences, yazd, iran


مهناز آزادپور | mahnaz azadpour
department of genetics, school of medicine, shahid sadoughi university of medical sciences, yazd, iran



نشانی اینترنتی http://ijbms.mums.ac.ir/article_8577.html
فایل مقاله دریافت فایل مقاله
کد مقاله (doi)
زبان مقاله منتشر شده en
موضوعات مقاله منتشر شده
نوع مقاله منتشر شده Original Article
برگشت به: صفحه اول پایگاه   |   نسخه مرتبط   |   نشریه مرتبط   |   فهرست نشریات