نتایج جستجو برای: kanr

تعداد نتایج: 38  

2003
JEAN T. GREENBERG

The tripeptide glutathione (L-y-glutamyl-L-cysteinylglycine) (GSH) is the predominant low-molecular-weight thiol in many organisms and has been proposed to protect cells from oxidative damage such as that formed by H202 and ionizing radiations (19). Escherichia coli deficient in GSH because of mutations in the gshA gene was found previously (3) to exhibit normal resistance to X irradiation in t...

Journal: :Applied sciences 2021

In recent years, many researchers have devoted time to designing algorithms used introduce external information from knowledge graphs, solve the problems of data sparseness and cold start, thus improve performance recommendation systems. Inspired by these studies, we proposed KANR, a graph-enhanced attention aggregation network for making recommendations. This is an end-to-end deep learning mod...

Journal: :Genetics 1987
O Huisman W Raymond K U Froehlich P Errada N Kleckner D Botstein M A Hoyt

We describe here a new variant of transposon Tn10 especially adapted for transposon analysis of cloned yeast genes; it can equally well be used for analysis of prokaryotic genes. We have applied this element to analysis of the LEU2, RAD50, and CDC48 genes of Saccharomyces cerevisiae. This transposon, nicknamed mini-Tn10-LUK, contains a lacZ gene without efficient transcription or translation st...

Journal: :Nucleic acids research 1990
D. Bell-Pedersen S. Quirk J. Clyman M. Belfort

Although mobility of the phylogenetically widespread group I introns appears to be mechanistically similar, the phage T4 intron-encoded endonucleases that promote mobility of the td and sunY introns are different from their eukaryotic counterparts. Most notably, they cleave at a distance from the intron insertion sites. The td enzyme was shown to cleave 23-26 nt 5' and the sunY endonuclease 13-...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه تربیت مدرس - دانشکده علوم زیستی 1393

هدف از این مطالعه، داخل کردن کاست بیانی آنتی سنس درون کروموزوم باکتریایی جهت کاهش بیان طولانی مدت ژن هدف، و استفاده از کاست بیانی آنتی سنس (ابزار اصلی ناک داون ژنی) برای انجام حذف ژنی (ناک اوت) در سیستم باکتریایی، بود. لذا این روش برای حذف همزمان ژن کدکننده آنزیم پروزامین سنتتاز (per) و کاهش بیانی ژن virb1 در باکتری بروسلا ملی تنسیس سویه rev1 برای دستیابی به سویه جهش یافته ضعیف شده ای از آن بکا...

Journal: :Nucleic acids research 1998
D York K Welch I Y Goryshin W S Reznikoff

We have exploited the intramolecular transposition preference of the Tn 5 in vitro transposition system to test its effectiveness as a tool for generation of nested families of deletions and inversions. A synthetic transposon was constructed containing an ori, an ampicillin resistance (Ampr) gene, a multi-cloning site (MCS) and two hyperactive end sequences. The donor DNA that adjoins the trans...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1990
N Sternberg

The development of a bacteriophage P1 cloning system capable of accepting DNA fragments as large as 100 kilobase pairs (kbp) is described. The vectors used in this system contain a P1 packaging site (pac) to package vector and cloned DNA into phage particles, two P1 loxP recombination sites to cyclize the packaged DNA once it has been injected into a strain of Escherichia coli containing the P1...

Journal: :Journal of bacteriology 1989
R J Martinez

Resistance to the bactericidal action of normal human serum is one of the characteristics of virulent Yersinia enterocolitica. This property is attributable to the virulence plasmid harbored by pathogenic strains of the species. Serum resistance in Y. enterocolitica is thermoregulated, and its expression correlates well with the presence of virulence plasmid-encoded outer membrane proteins. To ...

Journal: :Microbiology 1996
A J Bradbury M J Gruer K E Rudd J R Guest

The second aconitase (AcnB) of Escherichia coli was partially purified from an acnA::kanR mutant lacking AcnA, and the corresponding polypeptide identified by activity staining and weak cross-reactivity with AcnA antiserum. The acnB gene was located at 2 center dot 85 min (131 center dot 6 kb) in a region of the chromosome previously assigned to two unidentified ORFs. Aconitase specific activit...

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