Cost-effective batch production process of scFv antibody in Escherichia coli

Cost-effective batch production process of scFv antibody in Escherichia coli


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دانشگاه علوم پزشکی تبریز
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نویسندگان: علی مسگری شادی , ژاله برار , یداله امیدی

کلمات کلیدی: Antibody, arabinose, cost-effective, induction, scFv

نشریه: 14092 , 3 , 26 , 2018

اطلاعات کلی مقاله
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نویسنده ثبت کننده مقاله علی مسگری شادی
مرحله جاری مقاله تایید نهایی
دانشکده/مرکز مربوطه مرکز تحقیقات ریز فناوری دارویی
کد مقاله 62595
عنوان فارسی مقاله Cost-effective batch production process of scFv antibody in Escherichia coli
عنوان لاتین مقاله Cost-effective batch production process of scFv antibody in Escherichia coli
ناشر 4
آیا مقاله از طرح تحقیقاتی و یا منتورشیپ استخراج شده است؟ بلی
عنوان نشریه (خارج از لیست فوق)
نوع مقاله Original Article
نحوه ایندکس شدن مقاله ایندکس شده سطح دو – PubMed
آدرس لینک مقاله/ همایش در شبکه اینترنت

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BACKGROUND: Cost-effective production of antibody (Ab) fragments is of great interests of many pharmaceutical industries, in large part due to their high usages in research, diagnosis and therapy. Thus, the production of Abs necessitates accomplishment of the optimal strategies. OBJECTIVE: In this study, based on the induction start time using arabinose, we implemented a novel strategy for the cost-effective production of single chain variable fragment (scFv) in Escherichia coli (E. coli ). METHODS: Complex and minimum media were used to investigate the batch fermentation in 50 mL batch tubes to find the optimum conditions for the production of a scFv in the Escherichia coli HB2151. RESULTS: Arabinose was used as an appropriate economical alternative of isopropyl β -D-1-thiogalactopyranoside (IPTG) for the production of scFv antibody. The optimum concentration of arabinose as an inducer was 0.1% (w/w), while below this point the scFv production yield (Y P / X ) decreased significantly. The start time of the induction of E. coli HB2151 cells was adjusted during the stationary phase of the growth, and the results showed higher specific scFv production yields up to 0.9 mg scFv/g biomass in the minimum media. The optimum induction duration times for complex and minimum media were about 12 and 24 hours, respectively. CONCLUSIONS: We propose this method to possibly be used for the large-scale production of recombinant proteins/peptides such as scFv and Fab antibodies.

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نویسنده نفر چندم مقاله
علی مسگری شادیاول
ژاله برارسوم
یداله امیدیچهارم

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