نتایج جستجو برای: plasmid r773

تعداد نتایج: 35503  

Journal: :avicenna journal of medical biochemistry 0
maryam daneshpour department of molecular medicine and human genetics, school of medicine,hamadan university of medical sciences hamadan, iran nooshin shabab research center for molecular medicine, hamadan university of medical sciences, hamadan, iran massoud saidijam research center for molecular medicine, hamadan university of medical sciences, hamadan, iran; research center for molecular medicine, hamadan university of medical sciences, hamadan, iran , +98 9121324616

objectives the overall goal of this study was to carry out a set of comparative analyses of arsr gene in plasmid r773 and bacterial chromosome from escherichia coli bl-21(de3). methods pdb and ncbi databases and chimera, mega4, clc main workbench software and 3d-jigsaw and embl-ebi servers were applied to perform this study. by using these software and servers, multiple analyses including deter...

Journal: :Biochimica et biophysica acta 1990
B P Rosen C M Hsu C E Karkaria P Kaur J B Owolabi L S Tisa

An anion-translocating ATPase has been identified as the product of the arsenical resistance operon of resistance plasmid R773. When expressed in Escherichia coli this ATP-driven oxyanion pump catalyzes extrusion of the oxyanions arsenite, antimonite and arsenate. Maintenance of a low intracellular concentration of oxyanion produces resistance to the toxic agents. The pump is composed of two po...

Journal: :Biomolecular NMR assignments 2011
Jun Ye Yanan He Jack Skalicky Barry P Rosen Timothy L Stemmler

ArsD is a metallochaperone that delivers As(III) to the ArsA ATPase, the catalytic subunit of the ArsAB pump encoded by the arsRDABC operon of Escherichia coli plasmid R773. Conserved ArsD cysteine residues (Cys(12), Cys(13) and Cys(18)) construct the As(III) binding site of the protein, however a global structural understanding of this arsenic binding remains unclear. We have obtained NMR assi...

Journal: :Analytical biochemistry 2002
Kaisa Hakkila Mikael Maksimow Matti Karp Marko Virta

The selection of a genetic reporter can be difficult because of the wide range of genes available. In order to reduce the selection, we compared the performance of different reporter genes: firefly luciferase (Photinus pyralis lucFF), bacterial luciferase operon (Photorhabdus luminescens luxCDABE), green fluorescent protein (Aequorea victoria gfp), and red fluorescent protein (Discosoma sp. dsr...

Journal: :Applied and environmental microbiology 1998
K Suzuki N Wakao T Kimura K Sakka K Ohmiya

The arsenic resistance (ars) operon from plasmid pKW301 of Acidiphilium multivorum AIU 301 was cloned and sequenced. This DNA sequence contains five genes in the following order: arsR, arsD, arsA, arsB, arsC. The predicted amino acid sequences of all of the gene products are homologous to the amino acid sequences of the ars gene products of Escherichia coli plasmid R773 and IncN plasmid R46. Th...

2014
NEELAM SINGH

Arsenic resistance in bacteria is basically due to a detoxification system encoded by the ars operon. It has been reported in various grams negative as well as gram positive genera. The E. coli chromosomal ars operon and E. coli plasmid R773 borne ars operons were the first ones to be discovered. The ars operon Staphylococcus aureus plasmid pI 258 which shows only 30% structural homology with t...

Journal: :Journal of bacteriology 2003
Renhui Li January D Haile Peter J Kennelly

The deduced protein product of open reading frame slr0946 from Synechocystis sp. strain PCC 6803, SynArsC, contains the conserved sequence features of the enzyme superfamily that includes the low-molecular-weight protein-tyrosine phosphatases and the Staphylococcus aureus pI258 ArsC arsenate reductase. The recombinant protein product of slr0946, rSynArsC, exhibited vigorous arsenate reductase a...

Journal: :Applied and environmental microbiology 2002
Chad W Saltikov Betty H Olson

The occurrence and diversity of the Escherichia coli R773 ars operon were investigated among arsenic-resistant enteric and nonenteric bacteria isolated from raw sewage and arsenic-enriched creek waters. Selected isolates from each creek location were screened for ars genes by colony hybridization and PCR. The occurrence of arsA, arsB, and arsC determined by low-stringency colony hybridization (...

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