TY - JOUR. T1 - Characterizing the regulation of the Pu promoter in Acinetobacter baylyi ADP1. AU - Huang, Wei E.. AU - Singer, Andrew C.. AU - Spiers, Andrew J.. AU - Preston, Gail M.. AU - Whiteley, Andrew S.. PY - 2008/7. Y1 - 2008/7. N2 - Effective gene trapping and screening requires sensory and regulatory compatibility of both host and exogenous systems. The naturally competent bacterium Acinetobacter baylyi ADP1 is able to efficiently take up and integrate exogenous DNA into the chromosome, making it an attractive host system for a wide range of metagenomic applications. To test the ability of A. baylyi ADP1 to express the XylR regulated Pu promoter from Pseudomonas putida mt-2, we have constructed and examined an A. baylyi ADP1 strain, ADPWH-Pu-lux-xylR. The Pu promoter in ADPWH-Pu-lux-xylR was specifically induced by toluene, m-, p- and o-xylene. The substrate induced Pu promoter was highly dependent on the growth medium: it was repressed in rich media until stationary phase, but was ...

Acinetobacter junii is a species of bacteria. Its type strain is ATCC 17908. It can be pathogenic. This bacterium has been linked to nosocomial infections including catheter-related blood stream infections and cellulitis. Vaneechoutte, M.; De Baere, T.; Nemec, A.; Musilek, M.; Van Der Reijden, T. J. K.; Dijkshoorn, L. (2008). Reclassification of Acinetobacter grimontii Carr et al. 2003 as a later synonym of Acinetobacter junii Bouvet and Grimont 1986. International Journal of Systematic and Evolutionary Microbiology. 58 (4): 937-940. doi:10.1099/ijs.0.65129-0. PMID 18398198. Bouvet, P. J. M.; Grimont, P. A. D. (1986). Taxonomy of the Genus Acinetobacter with the Recognition of Acinetobacter baumannii sp. nov., Acinetobacter haemolyticus sp. nov., Acinetobacter johnsonii sp. nov., and Acinetobacter junii sp. nov. and Emended Descriptions of Acinetobacter calcoaceticus and Acinetobacter lwoffii. International Journal of Systematic Bacteriology. 36 (2): 228-240. doi:10.1099/00207713-36-2-228. ...

TY - JOUR. T1 - Rapid detection of blaOXA in carbapenem-susceptible Acinetobacter radioresistens bacteremia leading to unnecessary antimicrobial administration. AU - Brady, Adam C.. AU - Lewis, James S.. AU - Pfeiffer, Christopher D.. N1 - Publisher Copyright: © 2016 Elsevier Inc. Copyright: Copyright 2018 Elsevier B.V., All rights reserved.. PY - 2016/8/1. Y1 - 2016/8/1. N2 - Rapid molecular techniques to identify resistant pathogens are revolutionizing antibiotic stewardship; however, it is important to recognize the limitations of these techniques. Herein we describe two cases of bacteremia that were both initially identified by genotypic testing as carbapenem-resistant Acinetobacter spp. and subsequently identified phenotypically as carbapenem-susceptible A. radioresistens. The genotypic results prompted unnecessary broad-spectrum antibiotic use and infection control concerns.. AB - Rapid molecular techniques to identify resistant pathogens are revolutionizing antibiotic stewardship; ...

The Acinetobacter radioresistens strain was isolated in our laboratories from an activated sludge pilot plant. It is able to grow in presence of either phenol or benzoate as the sole carbon and energy source, metabolizing them via the ortho pathway. A proteomic approach to the study of the regulation of these catabolic pathways showed that the expression of most of the catabolic enzymes is modulated by the growth substrate (1, 2). Moreover, satellite proteins were identified (porins, chaperonins), specifically induced by aromatics and probably involved in the uptake of these molecules and in the physiological cell response to their presence. In the present research these results have been extended by a more precise kinetic analysis of the bacterial growth on either an aromatic (phenol or benzoate) or a non-aromatic (acetate) carbon source. From these experiments it can be seen that cultures grown in presence of phenol or acetate show similar specific growth rates (=0.769 and 0.766 h-1 ...

Biohazard level, growth media and temperature, gram stain, industrial applications and more information for Acinetobacter radioresistens.

Researchr is a web site for finding, collecting, sharing, and reviewing scientific publications, for researchers by researchers.. Sign up for an account to create a profile with publication list, tag and review your related work, and share bibliographies with your co-authors. ...

Biosurfactant producers are crucial for incremental oil production in microbial enhanced oil recovery (MEOR) processes. The isolation of biosurfactant-producing bacteria from oil reservoirs is important because they are considered suitable for the extreme conditions of the reservoir. In this work, a novel biosurfactant-producing strain Acinetobacter junii BD was isolated from a reservoir to reduce surface tension and emulsify crude oil. The biosurfactants produced by the strain were purified and then identified via electrospray ionization-Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR-MS). The biosurfactants generated by the strain were concluded to be rhamnolipids, the dominant rhamnolipids were C26H48O9, C28H52O9 and C32H58O13. The optimal carbon source and nitrogen source for biomass and biosurfactant production were NaNO3 and soybean oil. The results showed that the content of acid components increased with the progress of crude oil biodegradation. A glass micromodel test

The highly variable nature of the internal transcribed spacer region (ITS) has been claimed to represent an ideal target for designing species-specific probes/primers capable of differentiating between closely related Acinetobacter species. However, several Acinetobacter species contain multiple ITS copies of variable lengths, and these include Acinetobacter bereziniae, Acinetobacter guillouiae and Acinetobacter baylyi. This study shows these length variations result from inter-genomic insertion/deletion events (indels) involving horizontal transfer of ITS fragments of other Acinetobacter species and possibly unrelated bacteria, as shown previously by us. In some instances, indel incorporation results in the loss of probe target sites in the recipient cell ITS. In other cases, some indel sequences contain target sites for probes designed from a single ITS sequence to target other Acinetobacter species. Hence, these can generate false positives. The largest of the indels that remove probe sites is 683 bp

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TY - JOUR. T1 - An Increase of Abundance and Transcriptional Activity for Acinetobacter junii Post Wastewater Treatment. AU - Jumat, Muhammad. AU - Haroon, Muhammad. AU - Aljassim, Nada I.. AU - Cheng, Hong. AU - Hong, Pei-Ying. N1 - KAUST Repository Item: Exported on 2021-02-19 Acknowledged KAUST grant number(s): BAS/1/1033-01-01 Acknowledgements: The authors would like to thank George Princeton Dunsford for access to the KAUST wastewater treatment plant and Moustapha Harb for providing sampling assistance. The research reported in this publication was supported by the KAUST baseline funding BAS/1/1033-01-01 awarded to Pei-Ying Hong.. PY - 2018/4/6. Y1 - 2018/4/6. N2 - A membrane bioreactor (MBR)-based wastewater treatment plant (WWTP) in Saudi Arabia is assessed over a five-month period in 2015 and once in 2017 for bacterial diversity and transcriptional activity using metagenomics, metatranscriptomics and real time quantitative polymerase chain reaction (RT-qPCR). Acinetobacter spp. are shown ...

Bacteria of the genus Acinetobacter are ubiquitous in nature. These organisms were invariably susceptible to many antibiotics in the 1970s. Since that time, acinetobacters; have emerged as multiresistant opportunistic nosocomial pathogens. The taxonomy of the genus Acinetobacter underwent extensive revision in the mid-1980s, and at least 32 named and unnamed species have now been described. Of these, Acinetobacter baumannii and the closely related unnamed genomic species 3 and 13 sensu Tjernberg and Ursing (13TU) are the most relevant clinically. Multiresistant strains of these species causing bacteraemia, pneumonia, meningitis, urinary tract infections and surgical wound infections have been isolated from hospitalised patients worldwide. This review provides an overview of the antimicrobial susceptibilities of Acinetobacter spp. in Europe, as well as the main mechanisms of antimicrobial resistance, and summarises the remaining treatment options for multiresistant Acinetobacter infections. © ...

Ver más] As a part of a nationwide study in Spain, 15 clinical isolates of Acinetobacter genomic species 3 (AG3) were analyzed. The main objective of the study was to characterize the ampC genes from these isolates and to determine their involvement in B-lactam resistance in AG3. The 15 AG3 isolates showed different profiles of resistance to ampicillin (range of MICs, 12 to ,256 μg/ml). Nucleotide sequencing of the 15 ampC genes yielded 12 new AmpC enzymes (ADC-12 to ADC-23). The 12 AG3 enzymes showed 93.7 to 96.1% amino acid identity with respect to the AmpC enzyme from Acinetobacter baumannii (ADC-1 enzyme). Eight out of fifteen ampC genes were expressed in Escherichia coli cells under the control of a common promoter, and with the exception of one isolate (isolate 65, which showed lower B-lactam MICs), significant differences in overall B-lactam MICs for E. coli cells expressing AG3 ampC genes were not revealed. No significant differences in ampC gene expression in AG3 clinical isolates ...

Optimum conditions for the activity of the new DNA methylase in cell lysate were determined. Methylation of DNAs of bacteriophages λ and T7 and plasmid pBR322 (dcm+) in the 5′-Cm5CWGG-3′ region blocked M.AjnI activity. The specificity of M.AjnI was determined using λ DNA methylated by this enzyme as well as computer modeling and data on the sensitivity of restriction endonucleases Mval, HinfI, and BstMAI to methylation.

COGEM released a comprehensive database of pathogenicity assessment of around 2575 bacterial species in 2011. The database ranks the pathogenicity of species on a scale of 1 to 4. Acinetobacter johnsonii ranks 2 on this scale: Species that can cause diseases in humans or animals, which are unlikely to spread in the human population and for which an adequate prophylaxis or therapy ...

การจำแนกเชื้อ Acinetobacter species สามารถใช้วิธี multiplex PCR เพื่อตรวจหา natural occurring blaOXA gene ที่จำเพาะต่อเชื้อแต่ละ species ได้ ดังนี้ blaOXA23 ในเชื้อ blaOXA134 ในเชื้อ A. lwoffii/A. schindleri, blaOXA211 ในเชื้อ A. johnsonii, blaOXA213 ในเชื้อ A. calcoaceticus, blaOXA214 ในเชื้อ A. haemolyticus, และ blaOXA228 ในเชื้อ A. bereziniae. ...

Three samples of terra rossa were shown to be efficient adsorbents of phosphate [P(V)] from wastewater and removed 29.9-32.6% of P(V). The total iron content in terra rossa was the key factor which determined the P(V) removal from wastewater. The original samples of terra rossa were effective support materials for the immobilization of metabolically active P(V)-accumulating bacteria Acinetobacter junii (0.56-2.47×1010 CFU g-1). The removal of oxalate-extractable iron from original sample of terra rossa increased the number of immobilized bacteria to 1.34×1011 CFU g-1, which is the largest number of immobilized bacteria reported in the literature so far. In reactors containing the A. junii and terra rossa P(V) was removed from wastewater by simultaneous adsorption onto terra rossa and accumulation inside bacterial cells, resulting in 40.5-62.5% of P(V) removal. Terra rossa is a promising substrate for biological P(V) removal from wastewater, acting both as adsorbent of P(V) and carrier of ...

The SOS response to DNA damage that induces up to 10% of the prokaryotic genome requires RecA action to relieve LexA transcriptional repression. In Acinetobacter species, which lack LexA, the error-prone polymerase accessory UmuDAb is instead required for ddrR induction after DNA damage, suggesting it might be a LexA analog. RNA-Seq experiments defined the DNA damage transcriptome (mitomycin C-induced) of wild type, recA and umuDAb mutant strains of both A. baylyi ADP1 and A. baumannii ATCC 17978. Of the typical SOS response genes, few were differentially regulated in these species; many were repressed or absent. A striking 38.4% of all ADP1 genes, and 11.4% of all 17978 genes, were repressed under these conditions. In A. baylyi ADP1, 66 genes (2.0% of the genome), including a CRISPR/Cas system, were DNA damageinduced, and belonged to four regulons defined by differential use of recA and umuDAb. In A. baumannii ATCC 17978, however, induction of 99% of the 152 mitomycin C-induced genes depended on recA,

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Strategy for In Situ Detection of Natural Transformation-Based Horizontal Gene Transfer Events - they used a pUC derived plasmid called pCLT that they got from Palmen and Hellingwerf ...

After 30 d incubation, the NA experiment showed removal effi ciency of 6.8% only (5,017 to 4,848 mg kg−1) as shown in Table 3. NA appears ineffective in removal of the bio-recalcitrant fraction C18-C22, containing the non-volatile hydrocarbons with indigenous bacteria (102 CFU g−1). Soil washing by spraying sterile water without disturbing the soil in the Ctrl experiment showed that 11.2% of the hydrocarbons were removed from the soil (Fig. 2(b)). Wu et al. [28] have shown a similar pattern of removal rate (16%) of TPH when sterile water was added to soil. Water tends to flush out hydrocarbons and other contaminants from soil [36]. In the BIO microcosms, there was no marked difference in degradation until 15 d of incubation (Table 3). A notable increase in degradation rate was observed after 15 d, and resulted in 56.4% of C18-C22 hydrocarbons being removed by the end of the experiment, which The initial concentration of hydrocarbons was 5,202 mg kg−1. Values represent average of triplicate ...

Acinetobacter sp. ATCC ® 49467D™ Designation: Genomic DNA from Acinetobacter sp. strain AmMS 248 TypeStrain=False Application:

1EO2: Structure of Acinetobacter strain ADP1 protocatechuate 3, 4-dioxygenase at 2.2 A resolution: implications for the mechanism of an intradiol dioxygenase.

1EOC: Structure of Acinetobacter strain ADP1 protocatechuate 3, 4-dioxygenase at 2.2 A resolution: implications for the mechanism of an intradiol dioxygenase.

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Based on imipenem resistance in an Acinetobacter genospecies 3 clinical isolate, we were able to identify, for the first time in this genomic species, a plasmid-encoded blaOXA-58 gene that was 100% homologous to the same ...

The World Health Organization has just released its list of the 12 bacteria that pose the greatest risk to humanitys existence, stating that new antibiotics are urgently needed to counter them. WHO held a press conference recently to unveil the list of the most dangerous superbugs, which are resistant to most antibiotics making them difficult or nearly impossible to treat.. The bacteria Acinetobacter baumannii topped the list. This disease can result in pneumonia, blood infections, and more. It affects people with compromised immune systems, and it attacks organ systems with a high fluid content, like the respiratory or urinary tract. ...

Microbial taxonomy remains a conservative discipline, relying on phenotypic information derived from growth in pure culture and techniques that are time-consuming and difficult to standardize, particularly when compared to the ease of modern high-throughput genome sequencing. Here, drawing on th ...

Acinetobacter sp. ATCC ® 49137™ Designation: AmMS 203 TypeStrain=False Application: Quality control strain Quality control strain for MicroScan [Reg TM] products

Domain architectures containing the following SCOP superfamilies _gap_,52518,52518,52922,_gap_ in Acinetobacter sp. ADP1. Domain architectures illustrate each occurrence of _gap_,52518,52518,52922,_gap_.

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Acinetobacter calcoaceticus is a bacterial species of the genus Acinetobacter. It is a nonmotile, gram negative coccobacillus. It grows under aerobic conditions, is catalase positive and oxidase negative. It is part of the normal human intestinal flora. Together with A. baumannii, it is referred to as the A. calcoaceticus-A. baumannii complex, which is relatively simple to identify based on the beforementioned phenotypic characteristics. To identify other Acinetobacter species genotyping is required. A. calcoaceticus is a soil bacterium. It has been shown to be prevalent in the tiger mosquito Aedes albopictus microflora. Phloroglucinol carboxylic acid is a degradation product excreted by A. calcoaceticus grown on (+)-catechin as the sole source of carbon. A. calcoaceticus can be pathogenic and cause an opportunistic infection in patients with multiple underlying diseases. A. calcoaceticus can be used as an alternative to A. baumannii in the laboratory setting. The interchangeability of the two ...

Wax ester synthases (WSs) can synthesize wax esters from alcohols and fatty acyl coenzyme A thioesters. The knowledge of the preferred substrates for each WS allows the use of yeast cells for the production of wax esters that are high-value materials and can be used in a variety of industrial applications. The products of WSs include fatty acid ethyl esters, which can be directly used as biodiesel. Here, heterologous WSs derived from five different organisms were successfully expressed and evaluated for their substrate preference in Saccharomyces cerevisiae. We investigated the potential of the different WSs for biodiesel (that is, fatty acid ethyl esters) production in S. cerevisiae. All investigated WSs, from Acinetobacter baylyi ADP1, Marinobacter hydrocarbonoclasticus DSM 8798, Rhodococcus opacus PD630, Mus musculus C57BL/6 and Psychrobacter arcticus 273-4, have different substrate specificities, but they can all lead to the formation of biodiesel. The best biodiesel producing strain was found to be

Bacteria of the genus Acinetobacter, with their numerous species common in various habitats, play a significant role as pathogens. Their ability to adapt to different living conditions is largely due to the presence of numerous plasmids containing the necessary adaptive genes. At the same time the diversity of Acinetobacter plasmids and their evolutionary dynamics have not been sufficiently studied. Here, we characterized 44 plasmids isolated from five permafrost Acinetobacter lwoffii strains, examined their relationship with plasmids of modern Acinetobacter strains and identified groups of related plasmids. For this purpose, we have developed a combined approach for classifying all known Acinetobacter plasmids. The classification took into account the size of plasmids, the presence and structure of the rep and mob genes, as well as the structure of their backbone and accessory regions. Based on the analysis, 19 major groups (lineages) of plasmids were identified, of which more than half were small

Acinetobacter calcoaceticus MopR protein: Member of the NtrC family of transcriptional activators with significant homology to XylR and DmpR from Pseudomonas; regulates phenol degradation in Acinetobacter calcoaceticus; has ATP-binding activity; binds phenol; GenBank CAA93242

Acinetobacter Infections - Pipeline Review, H1 2017 Summary Latest Pharmaceutical and Healthcare disease pipeline guide Acinetobacter Infections - Pipeline

Teck Wee Boo, Molecular characterisation of carbapenem resistance of Acinetobacter species in an Irish tertiary care hospital, [thesis], Trinity College (Dublin, Ireland). School of Medicine. Discipline of Clinical Microbiology, 2010, pp 377 ...

Genus and Species: Acinetobacter calcoaceticus (strepomycin sensitive) Domain: Prokaryote Optimal Growth Medium: Brain Heart Infusion Agar Optimal Growth Temperature: 30° C Package: MicroKwik Culture® Vial Biosafety Level: 2 Gram Stain: Gram-Negative Shape: Bacillus (rod-shaped)

Domain architecture and assignment details (superfamily, family, region, evalue) for HMPREF0012_00695T0 from Acinetobacter calcoaceticus ruh2202. Plus protein sequence and external database links.

HTF MI published a new industry research that focuses on Acinetobacter Infections Treatment market and delivers in-depth market analysis and future prospec

Complementing our current clinical pipeline, we have three additional drug candidates in preclinical development. AR-501 has broad bactericidal activity against Gram-negative and Gram-positive bacteria, including antibiotic-resistant strains. AR-201 is a human IgG1 mAb directed against the F-protein of respiratory syncytial virus (RSV). AR-401 is a mAb discovery program to treat infections caused by the Gram-negative bacterium Acinetobacter baumannii.. ...

I am interested in DNA repair mechanisms and recombination. These processes are essential for the protection of organisms from DNA-damaging agents such as ultraviolet light and chemical mutagens. These mechanisms also contribute to the evolution of new traits. Projects in my lab involve using genetic and molecular techniques to study DNA repair and recombination in the bacteria Escherichia coli and Acinetobacter baylyi. In E. coli, DNA damage causes the induction of over 20 genes and this is termed the SOS response. Although the SOS system has served as a model for understanding DNA repair and recombination in other systems such as yeast, plants and humans, there is still much that we dont understand about the SOS response in E. coli. For example, we have not yet identified the precise inducing signal of the SOS response or the biological functions of many of the SOS gene products. It is not yet clear whether A. baylyi exhibits an E. coli-like SOS response. Characterization of DNA repair and ...

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By Stewart MacInnis. Spectrum Volume 18 Issue 21 - February 22, 1996 John L. Johnson, whose pioneering research on differential Bacteroides species won him international recognition as a microbiologist, died last Friday (Feb. 16) at his Blacksburg home after a long illness. He was 59.. He was an outstanding scientist, he was an excellent teacher, and he really cared about his work, said W.E.C. Moore, a friend and former colleague of Johnsons. The world lost a top scientist in microbiology.. Moore, then head of the anaerobe laboratory, brought Johnson to Virginia Tech from his post-doctoral studies at the University of Washington-Seattle in 1968. John did his best work here, Moore said.. That work earned Johnson the 1980 Bergeys Manual Trust Award, one of the most prestigious international awards given in his field. The Pasteur Institute of Paris named a bacterial species for Johnson, Acinetobacter johnsonii. That, Moore said, is a sign of exceptional respect and an indication of the ...

Resistência aos antibióticos β-lactâmicos em isolados clínicos de Acinetobacter spp : caracterização molecular de novas carbapenemases, IMP-5 e OXA-33, e estudo da relação clonal entre os isolados resistentes ao ...

SUMMARY Steel and Cowan (1964) designated Schaub's Biol. 1 as the type strain for Bacterium anitratum Schaub and Hauber 1948. However, this strain was not included among those originally studied by Schaub and Hauber (1948) and cannot be recognized (Rule 9d, Note b, Intl. Code of Nomenclature of Bacteria). One of the original strains used by Schaub and Hauber (Schaub 81, American Type Culture Collection (ATCC) 19606, RH 2208) is here designated as the type for B. anitratum Schaub and Hauber 1948. The morphology, physiology, and per cent guanine plus cytosine of strain 81 are described and more than sixty characters of the strain recorded. The characteristics of strain 81 were found to be in good agreement with those given in the original description by Schaub and Hauber (1948).

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Accepted name: 2-hydroxycyclohexanone 2-monooxygenase. Reaction: 2-hydroxycyclohexan-1-one + NADPH + H+ + O2 = 6-hydroxyhexan-6-olide + NADP+ + H2O. Systematic name: 2-hydroxycyclohexan-1-one,NADPH:oxygen 2-oxidoreductase (1,2-lactonizing). Comment: the product decomposes spontaneously to 6-oxohexanoic acid (adipic semialdehyde).. Links to other databases: BRENDA, EXPASY, KEGG, Metacyc, CAS registry number: 62628-31-3. References. 1. Davey, J.F. and Trudgill, P.W. The metabolism of trans-cyclohexan-1,2-diol by an Acinetobacter species. Eur. J. Biochem. 74 (1977) 115-127. [PMID: 856571]. ...

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