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JMBS 2019, 10(1): 103-107 |
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Mamandi H, Golestani Eimani B, Pilehchian Langroudi R. Cloning of Tpel Gene of Clostridium perfringens in E. coli. JMBS 2019; 10 (1) :103-107
URL: http://biot.modares.ac.ir/article-22-16561-en.html
URL: http://biot.modares.ac.ir/article-22-16561-en.html
1- Biology Department, Basic Sciences Faculty, Urmia Branch, Islamic Azad University, Urmia, Iran
2- Biology Department, Basic Sciences Faculty, Urmia Branch, Islamic Azad University, Urmia, Iran, Ayatollah Rafsanjani Complex, Urmia Branch, Islamic Azad University, 2 Kilometer of Airport Road, Urmia, Iran ,golestani_bahram@yahoo.com
3- Razi Vaccine & Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Alborz, Karaj, Iran
2- Biology Department, Basic Sciences Faculty, Urmia Branch, Islamic Azad University, Urmia, Iran, Ayatollah Rafsanjani Complex, Urmia Branch, Islamic Azad University, 2 Kilometer of Airport Road, Urmia, Iran ,
3- Razi Vaccine & Serum Research Institute, Agricultural Research, Education and Extension Organization (AREEO), Alborz, Karaj, Iran
Abstract: (7092 Views)
Clostridium perfrinjens is an anaerobics , Gram-positive, rod-shaped and heat resistant bacterium of genus clostridium . C. perfringens is a spore-forming bacterium and widely occurring pathogen. The organism is grouped into 5 types (A, B, C, D, and E) on the basis of the production of 4 major toxins alpha, beta, epsilon, and iota toxins. Tpel Clostridium perfringens (C. perfringens ) toxin have identified with A, B, and C types by cytotoxin activity in recent years. In this study C. perfringens type B had been used. Tpel caused to intestinal disease especially intestinal infections in human and necrotic enteritis in birds. In this study, perfect genomic DNA extracted by phenol-chloroform and Polymerase Chain Reaction (PCR) method used to isolation Tpel gene by a couple exclusive primer of perfect bacterium genomic DNA. PCR product after joining to pTZ57RL/T vector by TA cloning method in E. coli strain TOP10 susceptible became cloned and then colony PCR method used to screening transforming bacterium colonies with recombinant plasmid. Presence of fragment close to 2469bp on 1% agarose gel indicated that Tpel gene in E. coli strain TOP10 have be cloned.
Article Type: Research Paper |
Subject:
Agricultural Biotechnology
Received: 2017/08/15 | Accepted: 2018/02/6 | Published: 2019/03/16
Received: 2017/08/15 | Accepted: 2018/02/6 | Published: 2019/03/16
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