scholarly article | Q13442814 |
P50 | author | Kornelia Smalla | Q33113624 |
Eva M Top | Q91595750 | ||
Holger Heuer | Q40482933 | ||
Hirokazu Yano | Q42760500 | ||
P2093 | author name string | Celeste J Brown | |
Linda M Rogers | |||
Molly G Knox | |||
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Plasmid donor affects host range of promiscuous IncP-1beta plasmid pB10 in an activated-sludge microbial community | Q33995911 | ||
Complete nucleotide sequence of TOL plasmid pDK1 provides evidence for evolutionary history of IncP-7 catabolic plasmids | Q34119158 | ||
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Divergence of mobile genetic elements involved in the distribution of xenobiotic-catabolic capacity. | Q35613132 | ||
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Piggery manure used for soil fertilization is a reservoir for transferable antibiotic resistance plasmids | Q46537060 | ||
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Genomic organization and genomic structural rearrangements of Sphingobium japonicum UT26, an archetypal γ-hexachlorocyclohexane-degrading bacterium. | Q52731547 | ||
Gentamicin resistance genes in environmental bacteria: prevalence and transfer. | Q53953915 | ||
Transcription of repA, the gene of the initiation protein of the Pseudomonas plasmid pPS10, is autoregulated by interactions of the RepA protein at a symmetrical operator. | Q54012553 | ||
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Plasmids from freshwater environments capable of IncQ retrotransfer are diverse and include pQKH54, a new IncP-1 subgroup archetype. | Q54584426 | ||
Variation in permissiveness for broad-host-range plasmids among genetically indistinguishable isolates of Dickeya sp. from a small field plot | Q57238322 | ||
Frequent conjugative transfer accelerates adaptation of a broad-host-range plasmid to an unfavorable Pseudomonas putida host | Q57238328 | ||
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 | ||
Homology in the transfer origins of broad host range IncP plasmids: definition of two subgroups of P plasmids | Q70924676 | ||
Host range of conjugation and replication functions of the Escherichia coli sex plasmid Flac. Comparison with the broad host-range plasmid RK2 | Q71645704 | ||
Roles of long and short replication initiation proteins in the fate of IncP-1 plasmids. | Q35806093 | ||
KorA protein of promiscuous plasmid RK2 controls a transcriptional switch between divergent operons for plasmid replication and conjugative transfer | Q35862902 | ||
Autorepressor properties of the pi-initiation protein encoded by plasmid R6K. | Q36132816 | ||
P1 plasmid replication: measurement of initiator protein concentration in vivo | Q36240951 | ||
Regions of broad-host-range plasmid RK2 involved in replication and stable maintenance in nine species of gram-negative bacteria | Q36278381 | ||
Inferring the evolutionary history of IncP-1 plasmids despite incongruence among backbone gene trees | Q36474943 | ||
Recombination between plasmids of incompatibility groups P-1 and P-2 | Q36578723 | ||
Genomics of IncP-1 antibiotic resistance plasmids isolated from wastewater treatment plants provides evidence for a widely accessible drug resistance gene pool | Q36841958 | ||
Using Mahalanobis distance to compare genomic signatures between bacterial plasmids and chromosomes. | Q37014746 | ||
Progress towards understanding the fate of plasmids in bacterial communities | Q37174799 | ||
Diverse broad-host-range plasmids from freshwater carry few accessory genes | Q37335561 | ||
The diversity of conjugative relaxases and its application in plasmid classification | Q37461189 | ||
Plasmid transfer from Escherichia coli to Bacteroides fragilis: differential expression of antibiotic resistance phenotypes | Q37577714 | ||
P1 plasmid replication: multiple functions of RepA protein at the origin | Q37685319 | ||
Call of the wild: antibiotic resistance genes in natural environments | Q37700168 | ||
The behavior and significance of degradative plasmids belonging to Inc groups in Pseudomonas within natural environments and microcosms. | Q37876072 | ||
Identification of bacterial plasmids based on mobility and plasmid population biology. | Q37895333 | ||
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The role of the natural environment in the emergence of antibiotic resistance in gram-negative bacteria | Q38076545 | ||
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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 | ||
Mangrove microniches determine the structural and functional diversity of enriched petroleum hydrocarbon-degrading consortia | Q39841497 | ||
IncP-1ε Plasmids are Important Vectors of Antibiotic Resistance Genes in Agricultural Systems: Diversification Driven by Class 1 Integron Gene Cassettes | Q40482877 | ||
Crosstalk between plasmid vegetative replication and conjugative transfer: repression of the trfA operon by trbA of broad host range plasmid RK2. | Q40533403 | ||
Diversity of IncP-9 plasmids of Pseudomonas | Q41071792 | ||
Host range and transfer efficiency of incompatibility group HI plasmids | Q41503073 | ||
Functional Characterization of Replication and Stability Factors of an Incompatibility Group P-1 Plasmid from Xylella fastidiosa | Q41706669 | ||
Interactions of DnaA proteins from distantly related bacteria with the replication origin of the broad host range plasmid RK2. | Q41728432 | ||
Phylogeny of replication initiator protein TrfA reveals a highly divergent clade of incompatibility group P1 plasmids | Q41874268 | ||
The IncP-1 plasmid backbone adapts to different host bacterial species and evolves through homologous recombination | Q42092273 | ||
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Plasmid pBP136 from Bordetella pertussis represents an ancestral form of IncP-1beta plasmids without accessory mobile elements. | Q42605811 | ||
The genome sequence of the incompatibility group Iγ plasmid R621a: evolution of IncI plasmids | Q42609350 | ||
Dissection of the switch between genes for replication and transfer of promiscuous plasmid RK2: basis of the dominance of trfAp over trbAp and specificity for KorA in controlling the switch | Q42651003 | ||
The Population Biology of Bacterial Plasmids: A PRIORI Conditions for the Existence of Conjugationally Transmitted Factors. | Q42974347 | ||
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 | ||
All IncP-1 plasmid subgroups, including the novel epsilon subgroup, are prevalent in the influent of a Danish wastewater treatment plant | Q43369333 | ||
Modulation of pPS10 host range by DnaA. | Q44169692 | ||
Expansion of the IncX plasmid family for improved identification and typing of novel plasmids in drug-resistant Enterobacteriaceae | Q46440410 | ||
P433 | issue | Pt 11 | |
P304 | page(s) | 2303-2315 | |
P577 | publication date | 2013-09-03 | |
P1433 | published in | Microbiology | Q11339587 |
P1476 | title | Host range diversification within the IncP-1 plasmid group | |
P478 | volume | 159 |
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Q37335561 | Diverse broad-host-range plasmids from freshwater carry few accessory genes |
Q36735017 | Diversification of broad host range plasmids correlates with the presence of antibiotic resistance genes |
Q33884746 | Emerging patterns of plasmid-host coevolution that stabilize antibiotic resistance |
Q64076745 | Fate of Antibiotic Resistant Pseudomonas putida and Broad Host Range Plasmid in Natural Soil Microcosms |
Q40515882 | Lateral gene transfer, bacterial genome evolution, and the Anthropocene |
Q41948466 | Novel assay to measure the plasmid mobilizing potential of mixed microbial communities |
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Q38833121 | Scoping the effectiveness and evolutionary obstacles in using plasmid-dependent phages to fight antibiotic resistance |
Q37126788 | Source-sink plasmid transfer dynamics maintain gene mobility in soil bacterial communities. |
Q99619624 | Universal whole-sequence-based plasmid typing and its utility to prediction of host range and epidemiological surveillance |
Q41876631 | Widespread dissemination of class 1 integron components in soils and related ecosystems as revealed by cultivation-independent analysis |
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