نتایج جستجو برای: bacillus anthracis

تعداد نتایج: 56399  

2014
Maja Nielsen Lars Schreiber Kai Finster Andreas Schramm

Bacillus azotoformans MEV2011, isolated from soil, is a microaerotolerant obligate denitrifier, which can also produce N2 by co-denitrification. Oxygen is consumed but not growth-supportive. The draft genome has a size of 4.7 Mb and contains key genes for both denitrification and dissimilatory nitrate reduction to ammonium.

2013
Solomon P. Matthew Skyelar L. Decker Karthik R. Chamakura Gabriel F. Kuty Everett

Bacillus pumilus is a Gram-positive bacterium widely used in agriculture both as an antifungal and as a growth-promoting symbiont. B. pumilus is rarely infectious but has recently been shown to infect humans. Here, we present the complete genome of B. pumilus phage Glittering, a potential biocontrol agent for B. pumilus.

2016
Daniel R. Reuß Andrea Thürmer Rolf Daniel Wim J. Quax Jörg Stülke

Bacillus subtilis ∆6 is a genome-reduced strain that was cured from six prophages and AT-rich islands. This strain is of great interest for biotechnological applications. Here, we announce the full-genome sequence of this strain. Interestingly, the conjugative element ICEBs1 has most likely undergone self-excision in B. subtilis ∆6.

Journal: :Journal of applied microbiology 2007
J V Rogers Y W Choi W R Richter D C Rudnicki D W Joseph C L K Sabourin M L Taylor J C S Chang

AIMS To evaluate the decontamination of Bacillus anthracis, Bacillus subtilis, and Geobacillus stearothermophilus spores on indoor surface materials using formaldehyde gas. METHODS AND RESULTS B. anthracis, B. subtilis, and G. stearothermophilus spores were dried on seven types of indoor surfaces and exposed to approx. 1100 ppm formaldehyde gas for 10 h. Formaldehyde exposure significantly de...

Journal: :Journal of clinical microbiology 2004
Elizabeth Bode William Hurtle David Norwood

Real-time PCR has become an important method for the rapid identification of Bacillus anthracis since the 2001 anthrax mailings. Most real-time PCR assays for B. anthracis have been developed to detect virulence genes located on the pXO1 and pXO2 plasmids. In contrast, only two published chromosomal targets exist, the rpoB gene and the gyrA gene. In the present study, subtraction-hybridization ...

2014
Inbar Cohen-Gihon Ofir Israeli Adi Beth-Din Haim Levy Ofer Cohen Avigdor Shafferman Anat Zvi Theodor Chitlaru

We report the draft whole-genome sequence of the nonproteolytic Bacillus anthracis V770-NP1-R strain. Compared to those of other B. anthracis strains, the genome exhibits unique mutations in multiple targets potentially affecting proteolytic functions. One of these mutations is a deletion that disrupts the NprR quorum-sensing regulator of the NprA protease.

Journal: :Journal of bacteriology 2004
David D Williams Charles L Turnbough

EA1 is an abundant, highly antigenic, surface layer protein of Bacillus anthracis vegetative cells. Recent studies indicate that EA1 is also a component of B. anthracis spores and a potential marker for spore detection. We show here that EA1 is not a spore component but a persistent contaminant in spore preparations.

2014
Se Kye Kim Won-Hyong Chung Sang Hoon Kim Kyoung Hwa Jung Namshin Kim Young Gyu Chai

Bacillus anthracis is a Gram-positive endospore-forming bacterium that causes the zoonotic disease anthrax. We report a complete genome sequence of B. anthracis strain HYU01, isolated from Changnyung, which belongs to the B branch (B.Br.) 001/002 canonical single nucleotide polymorphism (canSNP) group.

Journal: :The new microbiologica 2006
Giuseppina La Rosa Michele Muscillo Michela Sali Elena De Carolis Cinzia Marianelli Franco Ciuchini Antonio Fasanella Rosanna Adone

This study investigated the genetic bases of attenuation in the Bacillus anthracis vaccine strain "Carbosap" used in Italy against anthrax in cattle and sheep. Twelve genes involved in virulence regulatory pathways underwent sequence analysis in comparison with a B. anthracis virulent strain.

Journal: :Antimicrobial agents and chemotherapy 2008
G C Kedar Vickie Brown-Driver Daniel R Reyes Mark T Hilgers Mark A Stidham Karen Joy Shaw John Finn Robert J Haselbeck

Targeted antisense and gene replacement mutagenesis experiments demonstrate that only the murA1 gene and not the murA2 gene is required for the normal cellular growth of Bacillus anthracis. Antisense-based modulation of murA1 gene expression hypersensitizes cells to the MurA-specific antibiotic fosfomycin despite the normally high resistance of B. anthracis to this drug.

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