scholarly article | Q13442814 |
P50 | author | Kornelia Smalla | Q33113624 |
Sergey Sokolov | Q49685448 | ||
Marina Titok | Q55816246 | ||
P2093 | author name string | Christopher M Thomas | |
Lewis E H Bingle | |||
Yanina R Sevastsyanovich | |||
Irina A Kosheleva | |||
Anthony S Haines | |||
Renata Krasowiak | |||
Anastassia A Leuchuk | |||
P2860 | cites work | Molecular relationships between Pseudomonas INC P-9 degradative plasmids TOL, NAH, and SAL | Q70172096 |
Plasmids isolated from the sugar beet phyllosphere show little or no homology to molecular probes currently available for plasmid typing | Q72414242 | ||
A pair of PCR primers for Incp-9 plasmids | Q73253358 | ||
PCR-based detection of mobile genetic elements in total community DNA | Q73877527 | ||
Pseudomonas putida--a versatile biocatalyst | Q78864939 | ||
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools | Q24248165 | ||
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs | Q24545170 | ||
A rapid alkaline extraction procedure for screening recombinant plasmid DNA | Q24614998 | ||
The neighbor-joining method: a new method for reconstructing phylogenetic trees | Q25939010 | ||
A comprehensive set of sequence analysis programs for the VAX | Q26778432 | ||
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0 | Q26778434 | ||
Artemis: sequence visualization and annotation | Q27861024 | ||
TreeView: an application to display phylogenetic trees on personal computers | Q27861074 | ||
Organization and evolution of naphthalene catabolic pathways: sequence of the DNA encoding 2-hydroxychromene-2-carboxylate isomerase and trans-o-hydroxybenzylidenepyruvate hydratase-aldolase from the NAH7 plasmid | Q28369173 | ||
Bacterial catabolic transposons | Q33541342 | ||
Transmissible Plasmid Coding Early Enzymes of Naphthalene Oxidation in Pseudomonas putida | Q33784915 | ||
Molecular diversity of plasmids bearing genes that encode toluene and xylene metabolism in Pseudomonas strains isolated from different contaminated sites in Belarus | Q33987152 | ||
Paradigms of plasmid organization | Q33994576 | ||
Comparative biology of IncQ and IncQ-like plasmids | Q34010408 | ||
Mobile elements as a combination of functional modules. | Q34499476 | ||
Genomic and functional analysis of the IncP-9 naphthalene-catabolic plasmid NAH7 and its transposon Tn4655 suggests catabolic gene spread by a tyrosine recombinase | Q34696950 | ||
Biodegradation, biotransformation, and biocatalysis (b3) | Q34905240 | ||
Combination of the tod and the tol pathways in redesigning a metabolic route of Pseudomonas putida for the mineralization of a benzene, toluene, and p-xylene mixture. | Q35184584 | ||
Detection and characterization of broad-host-range plasmids in environmental bacteria by PCR. | Q35192180 | ||
Plasmids isolated from marine sediment microbial communities contain replication and incompatibility regions unrelated to those of known plasmid groups | Q35198340 | ||
Natural horizontal transfer of a naphthalene dioxygenase gene between bacteria native to a coal tar-contaminated field site | Q35201987 | ||
Diversity of Pseudomonas plasmids: to what extent? | Q35654474 | ||
Expression and transfer of engineered catabolic pathways harbored by Pseudomonas spp. introduced into activated sludge microcosms | Q35694307 | ||
The evolution of pTF-FC2 and pTC-F14, two related plasmids of the IncQ-family. | Q36057474 | ||
The evolution of IncP catabolic plasmids. | Q36165508 | ||
Plasmid gene organization: naphthalene/salicylate oxidation | Q36280676 | ||
Mobile catabolic genes in bacteria | Q36289677 | ||
Metabolism of benzoate and the methylbenzoates by Pseudomonas putida (arvilla) mt-2: evidence for the existence of a TOL plasmid | Q36760222 | ||
Identification and classification of bacterial plasmids | Q37064518 | ||
The completely sequenced plasmid pEST4011 contains a novel IncP1 backbone and a catabolic transposon harboring tfd genes for 2,4-dichlorophenoxyacetic acid degradation | Q37583361 | ||
Ecological and molecular maintenance strategies of mobile genetic elements | Q37587418 | ||
Catabolic mobile genetic elements and their potential use in bioaugmentation of polluted soils and waters | Q37587424 | ||
Mosaic plasmids and mosaic replicons: evolutionary lessons from the analysis of genetic diversity in IncFII-related replicons | Q38308567 | ||
Engineering of quasi-natural Pseudomonas putida strains for toluene metabolism through an ortho-cleavage degradation pathway. | Q39560065 | ||
Experimental evolution of catabolic pathways of bacteria | Q39612439 | ||
The relationship of degradative and resistance plasmids of Pseudomonas belonging to the same incompatibility group | Q39673185 | ||
The distribution of β-lactamase genes on plasmids found in Pseudomonas | Q39679825 | ||
Conjugative plasmids isolated from bacteria in marine environments show various degrees of homology to each other and are not closely related to well-characterized plasmids | Q39803598 | ||
The replication and stable-inheritance functions of IncP-9 plasmid pM3. | Q40856696 | ||
Transcriptional control of the Pseudomonas TOL plasmid catabolic operons is achieved through an interplay of host factors and plasmid-encoded regulators | Q41620651 | ||
OXIDATIVE METABOLISM OF PHENANTHRENE AND ANTHRACENE BY SOIL PSEUDOMONADS. THE RING-FISSION MECHANISM. | Q42172460 | ||
Isolation and molecular characterization of a novel broad-host-range plasmid from Bordetella bronchiseptica with sequence similarities to plasmids from gram-positive organisms. | Q42599637 | ||
Complete sequence and genetic organization of pDTG1, the 83 kilobase naphthalene degradation plasmid from Pseudomonas putida strain NCIB 9816-4. | Q42632647 | ||
Sequence and analysis of the 46.6-kb plasmid pA1 from Sphingomonas sp. A1 that corresponds to the typical IncP-1beta plasmid backbone without any accessory gene | Q42679098 | ||
Complete sequence of the IncP-9 TOL plasmid pWW0 from Pseudomonas putida | Q42692935 | ||
Mosaic structure of plasmids from natural populations of Escherichia coli. | Q42966739 | ||
The 64 508 bp IncP-1β antibiotic multiresistance plasmid pB10 isolated from a waste-water treatment plant provides evidence for recombination between members of different branches of the IncP-1β group | Q43368119 | ||
Identification of the key genes of naphthalene catabolism in soil DNA | Q44696470 | ||
The complete sequences of plasmids pB2 and pB3 provide evidence for a recent ancestor of the IncP-1beta group without any accessory genes | Q45140765 | ||
Molecular classification of IncP-9 naphthalene degradation plasmids | Q46940247 | ||
Bacterial aromatic ring-cleavage enzymes are classified into two different gene families. | Q48287182 | ||
PCR primers for detection and characterisation of IncP-9 plasmids. | Q53142772 | ||
Prevalence of Pseudomonas aeruginosa strains possessing R factor in a hospital | Q53795789 | ||
Redesigning metabolic routes: manipulation of TOL plasmid pathway for catabolism of alkylbenzoates. | Q54413058 | ||
[Nah-plasmids of IncP-9 group from natural strains of Pseudomonas]. | Q54572710 | ||
Plasmids from freshwater environments capable of IncQ retrotransfer are diverse and include pQKH54, a new IncP-1 subgroup archetype. | Q54584426 | ||
The multiple antibiotic resistance IncP-1 plasmid pKJK5 isolated from a soil environment is phylogenetically divergent from members of the previously established α, β and δ sub-groups | Q57272595 | ||
Molecular relationships of degradative plasmids determined by in situ hybridisation of their endonuclease-generated fragments | Q67358609 | ||
P433 | issue | Pt 10 | |
P304 | page(s) | 2929-2941 | |
P577 | publication date | 2008-10-01 | |
P1433 | published in | Microbiology | Q11339587 |
P1476 | title | Diversity of IncP-9 plasmids of Pseudomonas | |
P478 | volume | 154 |
Q34490376 | Adaptation for protein synthesis efficiency in a naturally occurring self-regulating operon |
Q35771470 | Assessing environmental drivers of microbial communities in estuarine soils of the Aconcagua River in Central Chile |
Q37538155 | Conjugative plasmids: vessels of the communal gene pool |
Q35108366 | Cultivation-independent screening revealed hot spots of IncP-1, IncP-7 and IncP-9 plasmid occurrence in different environmental habitats |
Q37596957 | Draft Genome Sequence of Pseudomonas moraviensis R28-S. |
Q37332245 | Host range diversification within the IncP-1 plasmid group. |
Q91938921 | Identification of a Novel Plasmid Lineage Associated With the Dissemination of Metallo-β-Lactamase Genes Among Pseudomonads |
Q36175574 | Identification of novel toluene monooxygenase genes in a hydrocarbon-polluted sediment using sequence- and function-based screening of metagenomic libraries |
Q38717933 | Insights into the genomic plasticity of Pseudomonas putida KF715, a strain with unique biphenyl-utilizing activity and genome instability properties |
Q44215989 | Metal oxides, clay minerals and charcoal determine the composition of microbial communities in matured artificial soils and their response to phenanthrene |
Q41962424 | Occurrence of plasmids in the aromatic degrading bacterioplankton of the baltic sea |
Q57072357 | Petroleum contamination and bioaugmentation in bacterial rhizosphere communities from Avicennia schaueriana |
Q34186192 | Plasmids foster diversification and adaptation of bacterial populations in soil |
Q34291217 | Predicting plasmid promiscuity based on genomic signature |
Q33743353 | Shifts in abundance and diversity of mobile genetic elements after the introduction of diverse pesticides into an on-farm biopurification system over the course of a year |
Q35056021 | The rulB gene of plasmid pWW0 is a hotspot for the site-specific insertion of integron-like elements found in the chromosomes of environmental Pseudomonas fluorescens group bacteria |
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