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بیان بالای fragmentC توکسین کزاز در اشرشیا کلی

آقایی پور, خسرو ، تیمورپور, رقیه (1397) بیان بالای fragmentC توکسین کزاز در اشرشیا کلی. Archives of Razi Institute ــ 73 (1). ص.ص.27-38. شاپا 0365-3439

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آدرس اینترنتی رسمی : http://archrazi.areeo.ac.ir/article_114057.html


عنوان انگليسی

High-level expression of tetanus toxin fragment C in Escherichia coli

خلاصه انگلیسی

Fragment C is the C-terminal domain of the heavy chain of tetanus toxin that can promote the immune response against the lethal dose of this toxin. Therefore, this portion can be considered as a candidate vaccine against tetanus infection, which occurs by Clostridium tetani. The present study aimed to compare the expression of tetanus toxin fragment C in Escherichia coli BL21 (DE3) pLysS cells having a high tolerance to toxins between two different expression vectors, namely pET22b and pET28a, using the sodium dodecyl sulfate polyacrylamide gel electrophoresis and western blot analyses. After DNA extraction from Harvard CN49205 strain of C. tetani, the gene of interest was amplified using polymerase chain reaction, and then sequenced and cloned into the expression vectors of pET22b and pET28a, transformed into competent BL21 (DE3) pLysS cells, and finally expressed using an optimized protocol. The cells were induced with isopropyl β-D-1-thiogalactopyranoside (IPTG) at four different incubation temperatures (i.e., 37, 33, 30, and 25 °C) and three different incubation times (i.e., 1, 2, and 3 h). Although the SDS-PAGE and western blot analyses confirmed the expression of the recombinant fragment C (r-fragment C) ligated into both of the expression vectors, pET28a showed a higher rfragment C expression level than the other vector (38.66 mg/L versus 32.33 mg/L, P<0.05). An optimal expression condition was acquired 3 h after 1 mM IPTG induction at 25 °C. The results demonstrated that E. coli BL21 (DE3) pLysS as an expression host in combination with pET-28a as an expression vector was a more compatible expression system to express the fragment C of tetanus toxin, compared to E. coli BL21 (DE3) pLysS/pET-22b expression system. Overall, these results may represent an opportunity to improve the expression system for the production of tetanus toxin vaccine using recombinant protein strategy.

نوع سند :مقاله
زبان سند : انگلیسی
نویسنده مسئول :خسرو آقایی پور
نویسنده :رقیه تیمورپور
ضریب تاثیر و نمایه مجلات:Indexed in: PubMed/Medline, Scopus, Zoological Record
کلیدواژه ها (انگلیسی):Clostridium tetani, Fragment C, pET22b expression vector, pET28a expression vector, E. coli BL21 (DE3) pLysS
موضوعات :QW میکروب شناسی و ایمنی شناسی
بخش های دانشگاهی :دانشكده پزشكي > گروه علوم پایه > بخش میکروبیولوژی
کد شناسایی :9947
ارائه شده توسط : دکتر رقیه تیمورپور
ارائه شده در تاریخ :21 مهر 1398 08:33
آخرین تغییر :21 مهر 1398 08:33

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