نتایج جستجو برای: pET26b

تعداد نتایج: 42  

2014
Mohammad Rabiee-Faradonbeh Davood Darban-Sarokhalil Mohammad Mehdi Feizabadi Amirhooshang Alvandi Hasan Momtaz Neda Soleimani Abolfazl Gholipour

BACKGROUND Tuberculosis has been announced as a global emergency by World Health Organization and the second infectious agent of mortality worldwide. The general policy in the development of new vaccines is to develop some vaccines with higher efficiency not only for infants but also for adults compared with the Bacillus Calmette-Guerin vaccine. Recently, cytochrome P450 cyp141 has been introdu...

Journal: :Jundishapur journal of microbiology 2015
Ali Mohammad Latifi Khosro Khajeh Gholamreza Farnoosh Kazem Hassanpour Samaneh Khodi

BACKGROUND Organophosphorus hydrolase (OPH) is a type of organophosphate-degrading enzyme which is widely used in the bioremediation process. OBJECTIVES In this study, the periplasmic and cytoplasmic productions and the activity of recombinant OPH in Escherichia coli were investigated and compared using two pET systems (pET21a and pET26b). MATERIALS AND METHODS The sequence encoding the opd...

Journal: :Protein expression and purification 2004
Oki K Dzivenu Hyun Ho Park Hao Wu

We have designed and constructed a novel pair of bacterial co-expression vectors to facilitate the production of substantial amounts of recombinant multiprotein complexes for biochemical, biophysical, and structural studies. pOKD4 (kanamycin-resistant) and pOKD5 (ampicillin-resistant) are derivatives of pACYC177 cloning and pET26b expression vectors. As a result, pOKD4 and pOKD5 are T7-based ex...

2017
Sobhan Faezi Ahmad Reza Bahrmand Mehdi Mahdavi Seyed Davar Siadat Iraj Nikokar Soroush Sardari

Type IV pili (T4P) are major virulence factors of Pseudomonas aeruginosa (P. aeruginosa) that are associated with primary adhesion, biofilm formation and twitching motility. This study focuses on the introduction of a novel biologically active subunit vaccine derived from the disulfide loop (DSL) of P. aeruginosa pilin. We investigated the expression of the novel PilA in-frame with pET26b vecto...

Journal: :iranian red crescent medical journal 0
mohammad rabiee-faradonbeh department of microbiology and immunology, faculty of medicine, cellular and molecular research center, shahrekord university of medical sciences, shahrekord, ir iran; department of microbiology, shahrekord branch, islamic azad university, shahrekord,ir iran davood darban sarokhalil department of microbiology and immunology, faculty of medicine, alborz university of medical sciences, karaj, ir iran mohammad mehdi feizabadi department of microbiology, faculty of medicine, tehran university of medical sciences, tehran, ir iran amirhooshang alvandi department of microbiology, faculty of medicine, tehran university of medical sciences, tehran, ir iran hasan momtaz department of microbiology, shahrekord branch, islamic azad university, shahrekord,ir iran neda soleimani department of pathology, al-zahra hospital, isfahan university of medical sciences, isfahan, ir iran

conclusions the results of this study demonstrated that the p450 cyp141 gene was successfully cloned into a pet26b plasmid vector as an expression vector. in this paper, for the first time in iran, this gene was cloned for more purposes, including the expression and purification of the recombinant cytochrome p450 cyp141 protein. results the cloning of p450 cyp141 gene was confirmed by the enzym...

Journal: :jundishapur journal of microbiology 0
ali mohammad latifi applied biotechnology research centre, baqiyatallah university of medical sciences, tehran, ir iran khosro khajeh department of biochemistry, faculty of science, tarbiat modares university, tehran, ir iran gholamreza farnoosh applied biotechnology research centre, baqiyatallah university of medical sciences, tehran, ir iran; applied biotechnology research centre, baqiyatallah university of medical sciences, tehran, ir iran. tel/fax: +98-9155437109 kazem hassanpour medical school, sabzevar university of medical sciences, sabzevar, ir iran samaneh khodi applied biotechnology research centre, baqiyatallah university of medical sciences, tehran, ir iran

conclusions the activities studied by the production of pnp were determined by following the increase at 410 nm. the maximum pnp was produced at 30°c with an optical density of 10.62 in the presence of cytoplasmic expression of oph (pet21a-opd). consequently, our results suggest cytoplasmic expression system as an appropriate candidate with a high amount of oph in spite of inclusion body format...

پایان نامه :وزارت علوم، تحقیقات و فناوری - پژوهشگاه ملی مهندسی ژنتیک وزیست فناوری 1393

آنزیم های محدودکننده توالی خاصی از dna را شناسایی می کنند و اسکلت قند-فسفات dna را در آن یا نزدیکی آن برش می زنند. این آنزیم ها اکثرا منشا باکتریایی دارند و در سامانه ی اصلاح و برش باکتری ایفای نقش می کنند. آنزیم های محدودکننده در همسانه سازی ژن-ها و مهندسی ژنتیک نقش اصلی را ایفا می کنند و بسیاری تکنیک-های مولکولی دیگر نیز بر پایه ی توانایی آن ها در برش دادن توالی های اختصاصی از dna تعریف شده ا...

ژورنال: Vaccine Research 2017

Introduction: Hepatitis E virus (HEV) is a fecal-oral transmitting virus which causes a chronic liver disease. ORF2 is an immunogen capsid protein of HEV that has been proposed to be used for Hepatitis E vaccine design. It is a 660-amino acid protein which includes an immunogenic region (residues 112-607). This protein has been expressed in complete and truncated forms, using different expressi...

2008
S. Matroudi M.R. Zamani M. Motallebi

In this study Trichoderma atroviride was selected as over producer of chitinase enzyme among 30 different isolates of Trichoderma sp. on the basis of chitinase specific activity. From this isolate the genomic and cDNA clones encoding chit33 have been isolated and sequenced. Comparison of genomic and cDNA sequences for defining gene structure indicates that this gene contains three short introns...

Journal: :Acta Crystallographica Section F: Structural Biology and Crystallization Communications 2006
Tomoko Adachi Atsushi Izumi Dean Rea Sam-Yong Park Jeremy R. H. Tame David I. Roper

The gene encoding 2-oxo-hept-3-ene-1,7-dioic acid (OHED) hydratase (HpcG) was cloned into the high-expression plasmid pET26b and overexpressed in Escherichia coli BL21(DE3). The enzyme was purified in three steps to greater than 95% purity prior to crystallization. Crystals were obtained by the hanging-drop vapour-diffusion method at 277 K in a number of screening conditions. Crystals measuring...

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