نتایج جستجو برای: heterologous expression

تعداد نتایج: 880880  

2014
Masaki J. Fujita Ryuichi Sakai

The siderophore avaroferrin (1), an inhibitor of Vibrio swarming that was recently identified in Shewanella algae B516, was produced by heterologous expression of the biosynthetic gene cluster cloned from a deep-sea sediment metagenomic DNA, together with two analogues, bisucaberin (2) and putrebactin (3). Avaroferrin (1) is a macrocyclic heterodimer of N-hydroxy-N-succinyl cadaverine (4) and N...

2002
VAL J. WATTS

The nine membrane-bound isoforms of the enzyme adenylate cyclase (EC 4.6.1.1) are highly regulated by neurotransmitters and drugs acting through G protein-coupled receptors to modulate intracellular cAMP levels. In general, acute activation of G s-coupled receptors stimulates cAMP accumulation, whereas acute activation of G i/o-coupled receptors typically inhibits cAMP accumulation. It is also ...

Journal: :Applied sciences 2021

Optimal gene expression is central for the development of both bacterial systems heterologous protein production, and microbial cell factories industrial metabolite production. Our goal to fulfill industry-level overproduction demands optimally, as measured by following key performance metrics: titer, productivity rate, yield (TRY). Here we use a multiscale model incorporating dynamics (i) popu...

H Rajabi Memari M Dadar, M.R Seifi Abad Shapouri R Peyghan

Infectious Pancreatic Necrosis Virus (IPNV) is a member of the family Birnaviridae that has been linked to high mortalities in salmonids. Bacterial based systems as live vectors for the delivery of heterologous antigens offer a number of advantages as vaccination strategies. VP2 is a structural viral protein of IPNV with immunogenicity effects. In this study IPNV was isolated from diseased fry ...

Journal: :applied food biotechnology 0
zahra goudarzi seyed abbas shojaosadati department of chemical engineering, tarbiat modares university, tehran reza hassan sajedi amir maghsoudi

background and objectives: auto-induction is usually employed to achieve high cell density and overproduction of proteins with a simple and low-cost operation. the efficiency of heterologous protein expression in escherichia coli is determined by different parameters. interactions between these parameters usually complicate the identification of those that contribute more to the improvement of ...

Journal: :Current opinion in biotechnology 1999
E Ailor M J Betenbaugh

The baculovirus-insect cell system is a valuable tool for the expression of heterologous proteins. Due to limitations in the intracellular processing environment, however, heterologous secreted and membrane proteins are often insoluble, poorly processed, or contain 'non-human' modifications. Recent attempts to modify the insect cell secretory pathway by overexpressing processing factors have de...

2010
Saul N Rocha José Abrahão-Neto María E Cerdán María I González-Siso Andreas K Gombert

BACKGROUND In spite of its advantageous physiological properties for bioprocess applications, the use of the yeast Kluyveromyces marxianus as a host for heterologous protein production has been very limited, in constrast to its close relative Kluyveromyces lactis. In the present work, the model protein glucose oxidase (GOX) from Aspergillus niger was cloned into K. marxianus CBS 6556 and into K...

Journal: :cell journal 0

introduction: at present, most recombinant proteins are produced in prokaryotes especially e coli. yeasts and cho also are used as eukaryotic hosts. leishmania tarentolae, a parasite of lizards, a member of trypanosomatidae family is one of the new systems for expression of heterologous proteins. in this system, some of the parasitic protozoa features are used in expression of mammalian protein...

Journal: :jundishapur journal of natural pharmaceutical products 0
fatemeh moazen department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran peyman eshaghi djabali department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran naemeh parsapour department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran fatemeh mohamadzadeh department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran abbas jafarian dehkordi department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran hamid mir mohammad sadeghi department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran; department of pharmaceutical biotechnology, isfahan pharmaceutical science research center, school of pharmacy and pharmaceutical sciences, isfahan university of medical science, isfahan, ir iran. tel: +98-3117922616, fax: +98-3116680011

conclusions full factorial design experimental approach helped to identify the critical culture condition parameters in heterologous expression of v2r. it would allow studying the parameters affecting the function of this protein in future experiments. results the maximum amount of protein production was obtained by the addition of 0.75 mm iptg at 37°c after three hours. the most important fact...

Journal: :research in molecular medicine 0
maryam zangi iranian research organization for science and technology (irost) sh. ehsani rad st., enqelab st., parsa sq., ahmadabad mostoufi rd., azadegan highway, p. o. box 3353-5111, tehran 3353136846, i. r. iran tel: (+9821)56276031-2 (+9821)56276026 p. o. box 3353 hamideh ofoghi iranian research organization for science and technology (irost) sh. ehsani rad st., enqelab st., parsa sq., ahmadabad mostoufi rd., azadegan highway, p. o. box 3353-5111, tehran 3353136846, i. r. iran tel: (+9821)56276031-2 (+9821)56276026 p. o. box 3353 zahra amini-bayat iranian research organization for science and technology (irost) sh. ehsani rad st., enqelab st., parsa sq., ahmadabad mostoufi rd., azadegan highway, p. o. box 3353-5111, tehran 3353136846, i. r. iran tel: (+9821)56276031-2 (+9821)56276026 p. o. box 3353 parastoo ehsani molecular biology dept. pasteur institute of iran, tehran, iran.

background: the potential of plants as a safe and eukaryotic systems, are considered for producing recombinant therapeutic human protein today; but the expression level of heterologous proteins is limited by the post-transcriptional gene silencing (ptgs) response in this new technology. the use of viral suppressors of gene silencing can prevent ptgs and improve transient expression level of for...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید