scholarly article | Q13442814 |
review article | Q7318358 |
P2093 | author name string | Manuel Espinosa | |
Elisabeth Grohmann | |||
Günther Muth | |||
P2860 | cites work | Characterization of the effectors required for stable inheritance of Streptococcus pyogenes pSM19035-derived plasmids in Bacillus subtilis | Q72665939 |
Enterococcal pheromone-like activity derived from a lipoprotein signal peptide encoded by a Staphylococcus aureus plasmid | Q73791905 | ||
Regulation of intron function: efficient splicing in vivo of a bacterial group II intron requires a functional promoter within the intron | Q74130101 | ||
Conjugal transfer of chromosomal DNA in Mycobacterium smegmatis | Q74667585 | ||
Evolution of conjugative plasmids from gram-positive bacteria | Q77317214 | ||
Whole sequence of spoIIIE-like, sporulation-inhibitory, and transfer gene (spi) in a conjugative plasmid, pSA1.1, of Streptomyces azureus and detection of spi-like gene in the actinomycete chromosome | Q77361464 | ||
Mobilisation of the streptococcal plasmid pMV158: interactions of MobM protein with its cognate oriT DNA region | Q77964941 | ||
Expression of the mobM gene of the streptococcal plasmid pMV158 in Lactococcus lactis subsp. lactis | Q78065469 | ||
Linkage and the mechanism of recombination in Streptomyces coelicolor | Q78769990 | ||
The minimal replicon of the Streptomyces ghanaensis plasmid pSG5 identified by subcloning and Tn5 mutagenesis | Q80766803 | ||
The terminal proteins of linear Streptomyces chromosomes and plasmids: a novel class of replication priming proteins | Q95806309 | ||
In vivo induction of virulence and antibiotic resistance transfer in Enterococcus faecalis mediated by the sex pheromone-sensing system of pCF10. | Q24537165 | ||
Components of the RP4 conjugative transfer apparatus form an envelope structure bridging inner and outer membranes of donor cells: implications for related macromolecule transport systems | Q24548983 | ||
Conserved sequence motifs in the initiator proteins for rolling circle DNA replication encoded by diverse replicons from eubacteria, eucaryotes and archaebacteria | Q24604023 | ||
Splicing of a group II intron involved in the conjugative transfer of pRS01 in lactococci | Q24683313 | ||
Crystal structure of the hexameric traffic ATPase of the Helicobacter pylori type IV secretion system | Q27629331 | ||
The bacterial conjugation protein TrwB resembles ring helicases and F1-ATPase | Q27629965 | ||
Structure of the cell-puncturing device of bacteriophage T4 | Q27637576 | ||
Type IV secretion: intercellular transfer of macromolecules by systems ancestrally related to conjugation machines | Q28213223 | ||
AAA proteins: in search of a common molecular basis. International Meeting on Cellular Functions of AAA Proteins | Q28364398 | ||
FtsK Is a DNA motor protein that activates chromosome dimer resolution by switching the catalytic state of the XerC and XerD recombinases | Q28427479 | ||
DNA processing reactions in bacterial conjugation | Q30417103 | ||
Terminal proteins essential for the replication of linear plasmids and chromosomes in Streptomyces | Q30993228 | ||
Biochemistry of type IV secretion | Q33536554 | ||
Conformational alterations in the ermC transcript in vivo during induction | Q33591974 | ||
Conjugative transfer in the dissemination of beta-lactam and aminoglycoside resistance | Q33607977 | ||
Enterococcus faecalis pheromone binding protein, PrgZ, recruits a chromosomal oligopeptide permease system to import sex pheromone cCF10 for induction of conjugation | Q33614856 | ||
Sequence and organization of pXO1, the large Bacillus anthracis plasmid harboring the anthrax toxin genes | Q33638407 | ||
Helicobacter pylori virulence and genetic geography | Q33639332 | ||
The TolQRA proteins are required for membrane insertion of the major capsid protein of the filamentous phage f1 during infection | Q33727468 | ||
Complete nucleotide sequence of pSK41: evolution of staphylococcal conjugative multiresistance plasmids. | Q33736381 | ||
Minimal and contributing sequence determinants of the cis-acting locus of transfer (clt) of streptomycete plasmid pIJ101 occur within an intrinsically curved plasmid region | Q33792706 | ||
Bacterial type IV secretion: conjugation systems adapted to deliver effector molecules to host cells | Q33987714 | ||
The T-pilus of Agrobacterium tumefaciens | Q33987720 | ||
Mutational analysis of the tra locus of the broad-host-range Streptomyces plasmid pIJ101. | Q33994483 | ||
Expression characteristics of the transfer-related kilB gene product of Streptomyces plasmid pIJ101: implications for the plasmid spread function | Q33995601 | ||
Mobilization function of the pBHR1 plasmid, a derivative of the broad-host-range plasmid pBBR1 | Q33995841 | ||
Transformation of plasmid DNA into Streptomyces at high frequency | Q34267610 | ||
Sequence and functional analysis of the Streptomyces phaeochromogenes plasmid pJV1 reveals a modular organization of Streptomyces plasmids that replicate by rolling circle | Q34297229 | ||
Identification of the cAD1 sex pheromone precursor in Enterococcus faecalis | Q34308128 | ||
TraG-like proteins of DNA transfer systems and of the Helicobacter pylori type IV secretion system: inner membrane gate for exported substrates? | Q34311340 | ||
Cell-cell communication in gram-positive bacteria | Q34443665 | ||
Conjugal type IV macromolecular transfer systems of Gram-negative bacteria: organismal distribution, structural constraints and evolutionary conclusions | Q34460955 | ||
Vancomycin-resistant Staphylococcus aureus: a new model of antibiotic resistance | Q34547868 | ||
Peptidoglycan as a barrier to transenvelope transport | Q39842837 | ||
Inducible resistance to macrolides, lincosamides and streptogramin type B antibiotics: the resistance phenotype, its biological diversity, and structural elements that regulate expression--a review | Q39849531 | ||
A plasmid from the methylotrophic actinomycete Amycolatopsis methanolica capable of site-specific integration. | Q39899109 | ||
Regulation of the transfer genes of Streptomyces plasmid pSN22: in vivo and in vitro study of the interaction of TraR with promoter regions | Q39899254 | ||
Genetic complementation analysis of the Agrobacterium tumefaciens virB operon: virB2 through virB11 are essential virulence genes | Q39932342 | ||
A combined genetic and physical map of the Streptomyces coelicolor A3(2) chromosome | Q39936258 | ||
The mating pair formation system of plasmid RP4 defined by RSF1010 mobilization and donor-specific phage propagation | Q39937288 | ||
Role of the imp operon of the Streptomyces coelicolor genetic element SLP1: two imp-encoded proteins interact to autoregulate imp expression and control plasmid maintenance | Q39937486 | ||
The active form of the KorB protein encoded by the Streptomyces plasmid pIJ101 is a processed product that binds differentially to the two promoters it regulates | Q39937585 | ||
The oriT region of the Agrobacterium tumefaciens Ti plasmid pTiC58 shares DNA sequence identity with the transfer origins of RSF1010 and RK2/RP4 and with T-region borders | Q39940776 | ||
Identification of a new insertion element, similar to gram-negative IS26, on the lactose plasmid of Streptococcus lactis ML3. | Q39963100 | ||
Genetic and physical characterization of recombinant plasmids associated with cell aggregation and high-frequency conjugal transfer in Streptococcus lactis ML3 | Q39968671 | ||
Transfer of resistance plasmids from Staphylococcus epidermidis to Staphylococcus aureus: evidence for conjugative exchange of resistance | Q39988363 | ||
Characterization of a plasmid from Streptomyces coelicolor A3(2) | Q40034434 | ||
In vitrocleavage of double- and single-stranded DNA by plasmid RSF1010-encoded mobilization proteins | Q40411335 | ||
Unconstrained bacterial promiscuity: the Tn916–Tn1545 family of conjugative transposons | Q40466981 | ||
Common sequence motifs in DNA relaxases and nick regions from a variety of DNA transfer systems | Q40504722 | ||
Nucleotide sequence of the mini-plasmid pSLG33 from Streptomyces lavendulae-grasserius RIA746. | Q40519896 | ||
Expression and characterisation of thekorBgene product from theStreptomyces lividansplasmid plJ101 inEscherichia coliand determination of its binding site on thekorBandkilBpromoters | Q40533139 | ||
Similarity of minus origins of replication and flanking open reading frames of plasmids pUB110, pTB913 and pMV158. | Q40537469 | ||
Processes at the nick region link conjugation, T-DNA transfer and rolling circle replication | Q40637095 | ||
Inactivation of antibiotics and the dissemination of resistance genes | Q40737331 | ||
Common mechanisms in bacterial conjugation and Ti-mediated T-DNA transfer to plant cells | Q40751626 | ||
Bacterial sex pheromone-induced plasmid transfer | Q40891376 | ||
Conjugative transposition | Q40945171 | ||
Role of cell-specific SpoIIIE assembly in polarity of DNA transfer | Q41045727 | ||
Enzymology of DNA transfer by conjugative mechanisms | Q41080217 | ||
Unidirectional theta replication of the structurally stable Enterococcus faecalis plasmid pAM beta 1. | Q41081761 | ||
Sequence similarities between the RP4 Tra2 and the Ti VirB region strongly support the conjugation model for T-DNA transfer | Q41096466 | ||
Nicking by transesterification: the reaction catalysed by a relaxase | Q41627061 | ||
Identity and interspecific transfer of gentamicin-resistance plasmids in Staphylococcus aureus and Staphylococcus epidermidis | Q41644576 | ||
Genetic Evidence for Plasmid-Linked Lactose Metabolism in Streptococcus lactis subsp. diacetylactis. | Q41840473 | ||
Dimerization of the Agrobacterium tumefaciens VirB4 ATPase and the effect of ATP-binding cassette mutations on the assembly and function of the T-DNA transporter | Q41923043 | ||
The E-box motif in the proximal ABCA1 promoter mediates transcriptional repression of the ABCA1 gene | Q42517848 | ||
Complete nucleotide sequence of the Streptomyces nigrifaciens plasmid, pSN22: genetic organization and correlation with genetic properties | Q42595887 | ||
Sequence analysis of plasmid pKJ50 from Bifidobacterium longum | Q42599934 | ||
Molecular characterisation of a 5.75-kb cryptic plasmid from Bifidobacterium breve NCFB 2258 and determination of mode of replication | Q42602248 | ||
Intergeneric transfer of the Enterococcus faecalis plasmid pIP501 to Escherichia coli and Streptomyces lividans and sequence analysis of its tra region. | Q42602274 | ||
Molecular, genetic, and functional analysis of the basic replicon of pVA380-1, a plasmid of oral streptococcal origin | Q42604204 | ||
Sequence, assembly and analysis of pX01 and pX02. | Q42609306 | ||
Enterococcal sex pheromone precursors are part of signal sequences for surface lipoproteins | Q42617101 | ||
Characterization of transposon Tn1549, conferring VanB-type resistance in Enterococcus spp. | Q42627595 | ||
Identification of the minimal replicon of plasmid pMEA300 of the methylotrophic actinomycete Amycolatopsis methanolica. | Q42627853 | ||
The mobilization and origin of transfer regions of a Thiobacillus ferrooxidans plasmid: relatedness to plasmids RSF1010 and pSC101. | Q42635449 | ||
Characterization of six linked open reading frames necessary for pIP501-mediated conjugation | Q42639407 | ||
Completion of the nucleotide sequence of the Enterococcus faecalis conjugative virulence plasmid pAD1 and identification of a second transfer origin | Q42660964 | ||
Sequence of the 50-kb conjugative multiresistance plasmid pRE25 from Enterococcus faecalis RE25. | Q42665054 | ||
Streptomyces ghanaensis Plasmid pSG5: Nucleotide Sequence Analysis of the Self-Transmissible Minimal Replicon and Characterization of the Replication Mode | Q42678651 | ||
Sequence and analysis of the 60 kb conjugative, bacteriocin-producing plasmid pMRC01 from Lactococcus lactis DPC3147. | Q42683961 | ||
The conjugative plasmid pSG5 from Streptomyces ghanaensis DSM 2932 differs in its transfer functions from other Streptomyces rolling-circle-type plasmids | Q42685715 | ||
Vancomycin resistance plasmid in Enterococcus faecalis that encodes sensitivity to a sex pheromone also produced by Staphylococcus aureus | Q42730579 | ||
The large Bacillus plasmid pTB19 contains two integrated rolling-circle plasmids carrying mobilization functions | Q43017347 | ||
A large transmissible plasmid is required for crystal toxin production in Bacillus thuringiensis variety israelensis | Q43032767 | ||
Type IVB secretion by intracellular pathogens | Q34557143 | ||
Functional analysis of TraA, the sex pheromone receptor encoded by pPD1, in a promoter region essential for the mating response in Enterococcus faecalis | Q34840253 | ||
Sequence-related protein export NTPases encoded by the conjugative transfer region of RP4 and by the cag pathogenicity island of Helicobacter pylori share similar hexameric ring structures | Q35104840 | ||
The genetic basis of the aggregation system in Bacillus thuringiensis subsp. israelensis is located on the large conjugative plasmid pXO16. | Q35586229 | ||
A new Escherichia coli cell division gene, ftsK | Q35597632 | ||
A functional origin of transfer (oriT) on the conjugative transposon Tn916 | Q35598843 | ||
Identification and characterization of the origin of conjugative transfer (oriT) and a gene (nes) encoding a single-stranded endonuclease on the staphylococcal plasmid pGO1. | Q35611166 | ||
Intergeneric and interspecies gene exchange in gram-positive cocci | Q35653480 | ||
Conjugational transfer of gentamicin resistance plasmids intra- and interspecifically in Staphylococcus aureus and Staphylococcus epidermidis | Q35739840 | ||
Self-transmissible plasmids in staphylococci that encode resistance to aminoglycosides | Q35748665 | ||
A lipoprotein signal peptide encoded by the staphylococcal conjugative plasmid pSK41 exhibits an activity resembling that of Enterococcus faecalis pheromone cAD1 | Q35975413 | ||
Genetic analysis of regions of the Lactococcus lactis subsp. lactis plasmid pRS01 involved in conjugative transfer. | Q36061930 | ||
DNA sequence and units of transcription of the conjugative transfer gene complex (trs) of Staphylococcus aureus plasmid pGO1. | Q36103138 | ||
Transcriptional regulation by TrsN of conjugative transfer genes on staphylococcal plasmid pGO1 | Q36108293 | ||
Transfer functions of the conjugative integrating element pSAM2 from Streptomyces ambofaciens: characterization of a kil-kor system associated with transfer | Q36121521 | ||
Mobilization of small plasmids in Bacillus thuringiensis subsp. israelensis is accompanied by specific aggregation | Q36123050 | ||
Five genes involved in self-transmission of pSN22, a Streptomyces plasmid | Q36148723 | ||
Mobilization of the relaxable Staphylococcus aureus plasmid pC221 by the conjugative plasmid pGO1 involves three pC221 loci | Q36175513 | ||
Region of the streptococcal plasmid pMV158 required for conjugative mobilization | Q36181454 | ||
Identification and analysis of transcriptional regulatory signals for the kil and kor loci of Streptomyces plasmid pIJ101 | Q36183353 | ||
Genetic organization of the bacterial conjugative transposon Tn916 | Q36185860 | ||
Conjugative transfer of cadmium resistance plasmids in Rhodococcus fascians strains | Q36203363 | ||
Plasmid transfer in Streptomyces lividans: identification of a kil-kor system associated with the transfer region of pIJ101 | Q36264944 | ||
Structural analysis of plasmid and chromosomal loci involved in site-specific excision and integration of the SLP1 element of Streptomyces coelicolor | Q36296965 | ||
Streptococcus faecalis sex pheromone (cAM373) also produced by Staphylococcus aureus and identification of a conjugative transposon (Tn918). | Q36305871 | ||
Evidence for a chromosome-borne resistance transposon (Tn916) in Streptococcus faecalis that is capable of "conjugal" transfer in the absence of a conjugative plasmid | Q36323591 | ||
Conjugative transposons: an unusual and diverse set of integrated gene transfer elements. | Q36670389 | ||
A fourth class of theta-replicating plasmids: the pAM beta 1 family from gram-positive bacteria. | Q36720247 | ||
An in vivo membrane fusion assay implicates SpoIIIE in the final stages of engulfment during Bacillus subtilis sporulation. | Q36748616 | ||
Conjugative transfer genes in staphylococcal isolates from the United States | Q36757408 | ||
Agrobacterium tumefaciens T-complex transport apparatus: a paradigm for a new family of multifunctional transporters in eubacteria | Q36860645 | ||
Regulation of the pAD1 sex pheromone response of Enterococcus faecalis by direct interaction between the cAD1 peptide mating signal and the negatively regulating, DNA-binding TraA protein | Q37420850 | ||
A family of lysozyme-like virulence factors in bacterial pathogens of plants and animals | Q37502145 | ||
TolA: a membrane protein involved in colicin uptake contains an extended helical region | Q37544989 | ||
Active site of the replication protein of the rolling circle plasmid pC194. | Q37636400 | ||
Movable genetic elements and antibiotic resistance in enterococci | Q37874969 | ||
MobA, the DNA strand transferase of plasmid R1162: the minimal domain required for DNA processing at the origin of transfer | Q38292165 | ||
The Lactococcus lactis sex-factor aggregation gene cluA. | Q38308705 | ||
Concerted action of three distinct domains in the DNA cleaving-joining reaction catalyzed by relaxase (TraI) of conjugative plasmid RP4. | Q38311809 | ||
Identification of a new genetic determinant for cell aggregation associated with lactose plasmid transfer in Lactococcus lactis | Q38337381 | ||
The origin of transfer (oriT) of the enterococcal, pheromone-responding, cytolysin plasmid pAD1 is located within the repA determinant | Q38349995 | ||
Mechanisms of initiation and termination reactions in conjugative DNA processing. Independence of tight substrate binding and catalytic activity of relaxase (TraI) of IncPalpha plasmid RP4. | Q38357475 | ||
KorSA from the Streptomyces integrative element pSAM2 is a central transcriptional repressor: target genes and binding sites | Q39499223 | ||
Functional and mutational analysis of p19, a DNA transfer protein with muramidase activity | Q39503619 | ||
Analysis of functional domains of the Enterococcus faecalis pheromone-induced surface protein aggregation substance | Q39505011 | ||
Extrachromosomal systems and gene transmission in anaerobic bacteria | Q39510836 | ||
The N- and C-terminal portions of the Agrobacterium VirB1 protein independently enhance tumorigenesis | Q39538857 | ||
Conjugative junctions in RP4-mediated mating of Escherichia coli. | Q39539170 | ||
Enzymology of type IV macromolecule secretion systems: the conjugative transfer regions of plasmids RP4 and R388 and the cag pathogenicity island of Helicobacter pylori encode structurally and functionally related nucleoside triphosphate hydrolases | Q39539230 | ||
Tn916 family conjugative transposons and dissemination of antimicrobial resistance determinants | Q39558171 | ||
An origin of transfer (oriT) on the conjugative element pRS01 from Lactococcus lactis subsp. lactis ML3. | Q39560424 | ||
The transfer origin for Bacteroides mobilizable transposon Tn4555 is related to a plasmid family from gram-positive bacteria | Q39564325 | ||
Efficient transfer of the pheromone-independent Enterococcus faecium plasmid pMG1 (Gmr) (65.1 kilobases) to Enterococcus strains during broth mating. | Q39567752 | ||
IncP plasmids are unusually effective in mediating conjugation of Escherichia coli and Saccharomyces cerevisiae: involvement of the tra2 mating system | Q39568984 | ||
Identification of the mob genes of plasmid pSC101 and characterization of a hybrid pSC101-R1162 system for conjugal mobilization | Q39587721 | ||
The tra region of the conjugative plasmid pIP501 is organized in an operon with the first gene encoding the relaxase | Q39678428 | ||
TrwD, the hexameric traffic ATPase encoded by plasmid R388, induces membrane destabilization and hemifusion of lipid vesicles | Q39678500 | ||
Genes required for plasmid R64 thin-pilus biogenesis: identification and localization of products of the pilK, pilM, pilO, pilP, pilR, and pilT genes | Q39694629 | ||
The complete genome sequence of the Streptomyces temperate phage straight phiC31: evolutionary relationships to other viruses | Q39728020 | ||
Pheromone-inducible conjugation in Enterococcus faecalis: interbacterial and host-parasite chemical communication | Q39835619 | ||
Bacterial conjugation mediated by plasmid RP4: RSF1010 mobilization, donor-specific phage propagation, and pilus production require the same Tra2 core components of a proposed DNA transport complex | Q39838022 | ||
Identification and functional analysis of the transfer region of plasmid pMEA300 of the methylotrophic actinomycete Amycolatopsis methanolica. | Q39839103 | ||
Identification and properties of a novel clt locus in the Streptomyces phaeochromogenes plasmid pJV1. | Q39842077 | ||
Conjugal transfer of plasmid pMV158: uncoupling of the pMV158 origin of transfer from the mobilization gene mobM, and modulation of pMV158 transfer in Escherichia coli mediated by IncP plasmids | Q43169455 | ||
Control of genes for conjugative transfer of plasmids and other mobile elements | Q43453420 | ||
Transfer of the plJ101 plasmid in Streptomyces lividans requires a cis-acting function dispensable for chromosomal gene transfer | Q43675430 | ||
Conjugative plasmid protein TrwB, an integral membrane type IV secretion system coupling protein. Detailed structural features and mapping of the active site cleft | Q43826798 | ||
Transfer origins in the conjugative Enterococcus faecalis plasmids pAD1 and pAM373: identification of the pAD1 nic site, a specific relaxase and a possible TraG-like protein | Q44067992 | ||
Enterococcal plasmid transfer: sex pheromones, transfer origins, relaxases, and the Staphylococcus aureus issue | Q44235273 | ||
Construction of the mobilizable plasmid pMV158GFP, a derivative of pMV158 that carries the gene encoding the green fluorescent protein | Q44442833 | ||
Co-transfer of vancomycin and other resistance genes from Enterococcus faecalis NCTC 12201 to Staphylococcus aureus | Q44453944 | ||
Mutations that affect regulation of the korB gene of Streptomyces lividans plasmid plJ101 alter plasmid transmission | Q46222639 | ||
Identification of DNA involved in Rhodococcus chromosomal conjugation and self-incompatibility | Q46547373 | ||
The homologous terminal sequence of the Streptomyces lividans chromosome and SLP2 plasmid | Q47865026 | ||
The mobilization protein, MobM, of the streptococcal plasmid pMV158 specifically cleaves supercoiled DNA at the plasmid oriT. | Q48052704 | ||
Characterization of pra, a gene for replication control in pSAM2, the integrating element of Streptomyces ambofaciens | Q48071588 | ||
A conjugation-like mechanism for prespore chromosome partitioning during sporulation in Bacillus subtilis | Q48073032 | ||
Nucleotide sequence of the 18-kb conjugative transposon Tn916 from Enterococcus faecalis | Q48078321 | ||
Analysis of a transfer region from the staphylococcal conjugative plasmid pSK41. | Q48087284 | ||
Analysis of the transfer region of the Streptomyces plasmid SCP2. | Q48100209 | ||
Comparative analysis of five related Staphylococcal plasmids | Q48324751 | ||
The integrative element pSAM2 from Streptomyces: kinetics and mode of conjugal transfer | Q48336440 | ||
Two atypical mobilization proteins are involved in plasmid CloDF13 relaxation | Q48375967 | ||
[DNA nucleotide sequence of the actinomycete plasmid pSB24.2] | Q53853588 | ||
Bacterial secrets of secretion: EuroConference on the biology of type IV secretion processes. | Q53975481 | ||
A variety of gram-positive bacteria carry mobile mef genes. | Q54081322 | ||
Conjugative transposition of Tn916: preferred targets and evidence for conjugative transfer of a single strand and for a double-stranded circular intermediate. | Q54213224 | ||
Site-specific integration of the Streptomyces plasmid pSAM2 in Mycobacterium smegmatis | Q54288189 | ||
Purification and characterization of Tet(M), a protein that renders ribosomes resistant to tetracycline. | Q54301855 | ||
A conjugative plasmid encoding production of a diffusible pigment and resistance to aminoglycosides and macrolides in Staphylococcus aureus. | Q54442739 | ||
The Streptomyces plasmid SCP2*: its functional analysis and development into useful cloning vectors. | Q54461947 | ||
pIJ101, a multi-copy broad host-range Streptomyces plasmid: Functional analysis and development of DNA cloning vectors | Q54526169 | ||
Plasmid transfer and expression of the transfer (tra) gene product of plasmid pIJ101 are temporally regulated during the Streptomyces lividans life cycle. | Q54592503 | ||
The copR gene product of plasmid pIP501 acts as a transcriptional repressor at the essential repR promoter. | Q54625357 | ||
Tn1545: a conjugative shuttle transposon. | Q54767799 | ||
Giant linear plasmids in Streptomyces which code for antibiotic biosynthesis genes | Q59052978 | ||
Genetic Recombination in Streptomyces | Q59098350 | ||
Computer-assisted dissection of rolling circle DNA replication | Q64389862 | ||
Molecular rearrangement of lactose plasmid DNA associated with high-frequency transfer and cell aggregation in Lactococcus lactis 712 | Q67595467 | ||
A 38 base-pair segment of DNA is required in cis for conjugative mobilization of broad host-range plasmid R1162 | Q68220841 | ||
Mobilization of the non-conjugative plasmid RSF1010: a genetic analysis of its origin of transfer | Q70176541 | ||
Physical analysis of the conjugative shuttle transposon Tn1545 | Q70176985 | ||
Structure of cCF10, a peptide sex pheromone which induces conjugative transfer of the Streptococcus faecalis tetracycline resistance plasmid, pCF10 | Q70405422 | ||
Plasmids in different strains of Streptomyces ambofaciens: free and integrated form of plasmid pSAM2 | Q70970114 | ||
Plasmids, recombination and chromosome mapping in Streptomyces lividans 66 | Q71073525 | ||
The TraB protein, which mediates the intermycelial transfer of the Streptomyces plasmid pSN22, has functional NTP-binding motifs and is localized to the cytoplasmic membrane | Q71577095 | ||
Mobilization of "nonmobilizable" plasmids by the aggregation-mediated conjugation system of Bacillus thuringiensis | Q71859585 | ||
Excision of chromosomal DNA sequences from Streptomyces coelicolor forms a novel family of plasmids detectable in Streptomyces lividans | Q72030653 | ||
Staphylococcal plasmid cointegrates are formed by host- and phage-mediated general rec systems that act on short regions of homology | Q72398778 | ||
Plasmid formation in Streptomyces: Excision and integration of the SLP1 replicon at a specific chromosomal site | Q72403230 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | gram-positive bacteria | Q857288 |
P304 | page(s) | 277-301, table of contents | |
P577 | publication date | 2003-06-01 | |
P1433 | published in | Microbiology and Molecular Biology Reviews | Q6839270 |
P1476 | title | Conjugative plasmid transfer in gram-positive bacteria | |
P478 | volume | 67 |
Q97074069 | (Fluoro)quinolones and quinolone resistance genes in the aquatic environment: A river catchment perspective |
Q48106193 | 1H, 15N and 13C chemical shift assignment of the Gram-positive conjugative transfer protein TraHpIP501. |
Q41244785 | A Multiprotein DNA Translocation Complex Directs Intramycelial Plasmid Spreading during Streptomyces Conjugation |
Q35671863 | A classification scheme for mobilization regions of bacterial plasmids. |
Q35127298 | A functional peptidoglycan hydrolase characterized from T4SS in 89K pathogenicity island of epidemic Streptococcus suis serotype 2 |
Q33493807 | A genome-scale proteomic screen identifies a role for DnaK in chaperoning of polar autotransporters in Shigella. |
Q36165506 | A natural barrier to lateral gene transfer from prokaryotes to eukaryotes revealed from genomes: the 70 % rule |
Q35111243 | A new and improved host-independent plasmid system for RK2-based conjugal transfer |
Q38751357 | A review of food-grade vectors in lactic acid bacteria: from the laboratory to their application |
Q41986487 | A septal chromosome segregator protein evolved into a conjugative DNA-translocator protein |
Q42121219 | A transferable 20-kilobase multiple drug resistance-conferring R plasmid (pKL0018) from a fish pathogen (Lactococcus garvieae) is highly homologous to a conjugative multiple drug resistance-conferring enterococcal plasmid. |
Q42108962 | A type IV-secretion-like system is required for conjugative DNA transport of broad-host-range plasmid pIP501 in gram-positive bacteria |
Q37181824 | Actinomycete integrative and conjugative elements |
Q33971396 | Adaptative potential of the Lactococcus lactis IL594 strain encoded in its 7 plasmids |
Q40827176 | Alignment-free detection of horizontal gene transfer between closely related bacterial genomes |
Q40883375 | An accessory protein is required for relaxosome formation by small staphylococcal plasmids |
Q37194619 | An updated view of plasmid conjugation and mobilization in Staphylococcus |
Q37739111 | Analysis of the Listeria monocytogenes Population Structure among Isolates from 1931 to 2015 in Australia. |
Q33517437 | Analysis of the mobilization functions of the vancomycin resistance transposon Tn1549, a member of a new family of conjugative elements |
Q48007955 | Antibiotic resistance among cultured bacterial isolates from bioethanol fermentation facilities across the United States |
Q36942502 | Antibiotics and resistance genes: influencing the microbial ecosystem in the gut. |
Q51323778 | Antimicrobial resistance (AMR) and plant-derived antimicrobials (PDAms) as an alternative drug line to control infections. |
Q35880192 | Antimicrobial resistance gene delivery in animal feeds |
Q49998550 | Assessment of conjugal transfer of antibiotic resistance genes in Salmonella Typhimurium exposed to bile salts. |
Q42073502 | Autoregulation of the synthesis of the MobM relaxase encoded by the promiscuous plasmid pMV158. |
Q64075322 | Biofilm Forming Antibiotic Resistant Gram-Positive Pathogens Isolated From Surfaces on the International Space Station |
Q34449723 | Biogenesis, architecture, and function of bacterial type IV secretion systems |
Q30927042 | Biological diversity of prokaryotic type IV secretion systems. |
Q49959019 | Botulinum neurotoxin-encoding plasmids can be conjugatively transferred to diverse clostridial strains. |
Q34991084 | Branching sites and morphological abnormalities behave as ectopic poles in shape-defective Escherichia coli |
Q38221309 | Bringing them together: plasmid pMV158 rolling circle replication and conjugation under an evolutionary perspective. |
Q41958555 | CRISPR-Cas systems preferentially target the leading regions of MOBF conjugative plasmids. |
Q54338939 | Characterization of a mobile and multiple resistance plasmid isolated from swine manure and its detection in soil after manure application. |
Q34328681 | Characterization of plasmids in a human clinical strain of Lactococcus garvieae. |
Q36710478 | Characterization of replication and conjugation of Streptomyces circular plasmids pFP1 and pFP11 and their ability to propagate in linear mode with artificially attached telomeres |
Q34470496 | Characterization of replication and conjugation of plasmid pWTY27 from a widely distributed Streptomyces species |
Q35187695 | Characterization of the integration and modular excision of the integrative conjugative element PAISt in Streptomyces turgidiscabies Car8 |
Q33962931 | Characterization of the replication, transfer, and plasmid/lytic phage cycle of the Streptomyces plasmid-phage pZL12 |
Q36039019 | Cloning vectors based on cryptic plasmids isolated from lactic acid bacteria: their characteristics and potential applications in biotechnology |
Q48232599 | Clostridium sordellii Pathogenicity Locus Plasmid pCS1-1 Encodes a Novel Clostridial Conjugation Locus |
Q36914997 | Combating bacteria and drug resistance by inhibiting mechanisms of persistence and adaptation. |
Q37525764 | Comparative Genomics of the Listeria monocytogenes ST204 Subgroup |
Q33764142 | Comparative genome analysis of pathogenic and non-pathogenic Clavibacter strains reveals adaptations to their lifestyle |
Q52884884 | Comparison of antibiotic resistance, biofilm formation and conjugative transfer of Staphylococcus and Enterococcus isolates from International Space Station and Antarctic Research Station Concordia. |
Q36297131 | Competition between conjugation and M13 phage infection in Escherichia coli in the absence of selection pressure: a kinetic study |
Q92257111 | Complete genome sequencing of Lactobacillus plantarum CAUH2 reveals a novel plasmid pCAUH203 associated with oxidative stress tolerance |
Q42646691 | Complete nucleotide sequence of pGS18, a 62.8-kb plasmid from Geobacillus stearothermophilus strain 18. |
Q42762762 | Conjugal plasmid transfer in Streptomyces resembles bacterial chromosome segregation by FtsK/SpoIIIE |
Q36435336 | Conjugal transfer of a virulence plasmid in the opportunistic intracellular actinomycete Rhodococcus equi |
Q42288594 | Conjugal transfer of the Salmonella enterica virulence plasmid in the mouse intestine |
Q26864206 | Conjugative DNA transfer in Streptomyces by TraB: is one protein enough? |
Q82856872 | Conjugative Gene Transfer in the Gastrointestinal Environment |
Q24816881 | Conjugative plasmid pAW63 brings new insights into the genesis of the Bacillus anthracis virulence plasmid pXO2 and of the Bacillus thuringiensis plasmid pBT9727 |
Q42117053 | Conjugative transfer of the integrative and conjugative element ICEBs1 from Bacillus subtilis likely initiates at the donor cell pole. |
Q38152896 | Conjugative type IV secretion systems in Gram-positive bacteria |
Q51916481 | Continuous model for the rock-scissors-paper game between bacteriocin producing bacteria. |
Q30577128 | Crystallization and first data collection of the putative transfer protein TraN from the Gram-positive conjugative plasmid pIP501 |
Q34577917 | Crystallization and preliminary structure determination of the transfer protein TraM from the Gram-positive conjugative plasmid pIP501 |
Q35091869 | Cultivation-independent examination of horizontal transfer and host range of an IncP-1 plasmid among gram-positive and gram-negative bacteria indigenous to the barley rhizosphere |
Q90027369 | Current and Promising Approaches to Identify Horizontal Gene Transfer Events in Metagenomes |
Q38187016 | DNA transfer in the gastric pathogen Helicobacter pylori |
Q55407952 | Description and Comparative Genomics of Macrococcus caseolyticus subsp. hominis subsp. nov., Macrococcus goetzii sp. nov., Macrococcus epidermidis sp. nov., and Macrococcus bohemicus sp. nov., Novel Macrococci From Human Clinical Material With Virul |
Q33268287 | Detection of conjugation related type four secretion machinery in Aeromonas culicicola |
Q38642195 | Development of SimCells as a novel chassis for functional biosensors. |
Q34747974 | Discovery of a conjugative megaplasmid in Bifidobacterium breve. |
Q34151028 | Dissemination of an Enterococcus Inc18-Like vanA plasmid associated with vancomycin-resistant Staphylococcus aureus |
Q34453835 | Distributive Conjugal Transfer: New Insights into Horizontal Gene Transfer and Genetic Exchange in Mycobacteria |
Q38226322 | Diverse regulatory circuits for transfer of conjugative elements |
Q36616678 | Dynamics of the IncW genetic backbone imply general trends in conjugative plasmid evolution. |
Q28742032 | Efficient gene transfer in bacterial cell chains |
Q38657199 | Emerging resistance to aminoglycosides in lactic acid bacteria of food origin-an impending menace |
Q38608495 | Enterococcus faecalis PcfC, a spatially localized substrate receptor for type IV secretion of the pCF10 transfer intermediate |
Q33457228 | Evaluation of plasmid content and tetracycline resistance conjugative transfer in Enterococcus italicus strains of dairy origin |
Q89802688 | Evaluation of two transformation protocols and screening of positive plasmid introduction into Bacillus cereus EB2, a gram-positive bacterium using qualitative analyses |
Q30336393 | Evolution of Staphylococcus aureus by large chromosomal replacements. |
Q41992246 | Evolution of conjugation and type IV secretion systems |
Q36120212 | Expansion of a plasmid classification system for Gram-positive bacteria and determination of the diversity of plasmids in Staphylococcus aureus strains of human, animal, and food origins |
Q50498568 | Expression analysis of the spi gene in the pock-forming plasmid pSA1.1 from Streptomyces azureus and localization of its product during differentiation. |
Q92372589 | Extrachromosomal oncogene amplification in tumour pathogenesis and evolution |
Q37187865 | Fight evolution with evolution: plasmid-dependent phages with a wide host range prevent the spread of antibiotic resistance |
Q91738379 | First Report of the Local Spread of Vancomycin-Resistant Enterococci Ascribed to the Interspecies Transmission of a vanA Gene Cluster-Carrying Linear Plasmid |
Q48144926 | Fluorescence microscopy of Streptomyces conjugation suggests DNA-transfer at the lateral walls and reveals the spreading of the plasmid in the recipient mycelium |
Q33697032 | Fully efficient chromosome dimer resolution in Escherichia coli cells lacking the integral membrane domain of FtsK. |
Q36077754 | Functional Comparison of Bacteria from the Human Gut and Closely Related Non-Gut Bacteria Reveals the Importance of Conjugation and a Paucity of Motility and Chemotaxis Functions in the Gut Environment |
Q34697932 | Functional identification of conjugation and replication regions of the tetracycline resistance plasmid pCW3 from Clostridium perfringens |
Q38315967 | Functional properties and structural requirements of the plasmid pMV158-encoded MobM relaxase domain |
Q41962018 | Gene targeting in gram-negative bacteria by use of a mobile group II intron ("Targetron") expressed from a broad-host-range vector |
Q43242610 | Genetic analysis of the Enterococcus vancomycin resistance conjugative plasmid pHTbeta: identification of the region involved in cell aggregation and traB, a key regulator gene for plasmid transfer and cell aggregation |
Q39615016 | Genetic analysis of transfer-related regions of the vancomycin resistance Enterococcus conjugative plasmid pHTbeta: identification of oriT and a putative relaxase gene |
Q36747848 | Genetic and functional characterization of the type IV secretion system in Wolbachia |
Q41459172 | Genetic cargo and bacterial species set the rate of vesicle-mediated horizontal gene transfer |
Q37461159 | Genome dynamics in major bacterial pathogens. |
Q90705141 | Genomic Insights Into Five Strains of Lactobacillus plantarum With Biotechnological Potential Isolated From chicha, a Traditional Maize-Based Fermented Beverage From Northwestern Argentina |
Q60910564 | Genomic characterisation of the new Dickeya fangzhongdai species regrouping plant pathogens and environmental isolates |
Q42134029 | Genomic comparison of archaeal conjugative plasmids from Sulfolobus |
Q40597464 | Green fluorescent protein-labeled monitoring tool to quantify conjugative plasmid transfer between Gram-positive and Gram-negative bacteria. |
Q94468608 | High variability of plasmid uptake rates in Escherichia coli isolated from sewage and river sediments |
Q42053435 | High-frequency conjugation system facilitates biofilm formation and pAMbeta1 transmission by Lactococcus lactis |
Q30356535 | High-level mupirocin resistance within methicillin-resistant Staphylococcus aureus pandemic lineages |
Q34308000 | Homologous Recombination-Experimental Systems, Analysis, and Significance |
Q34203823 | Horizontal gene transfer and the genomics of enterococcal antibiotic resistance |
Q42872099 | ICESluvan, a 94-kilobase mosaic integrative conjugative element conferring interspecies transfer of VanB-type glycopeptide resistance, a novel bacitracin resistance locus, and a toxin-antitoxin stabilization system. |
Q42024565 | Identification of the origin of transfer (oriT) and DNA relaxase required for conjugation of the integrative and conjugative element ICEBs1 of Bacillus subtilis |
Q41340424 | Identification of the origin of transfer (oriT) and a new gene required for mobilization of the SXT/R391 family of integrating conjugative elements |
Q27312351 | Induction of Plasmid Conjugation in Bacillus subtilis Is Bistable and Driven by a Direct Interaction of a Rap/Phr Quorum-sensing System with a Master Repressor. |
Q33489278 | Integrative and sequence characteristics of a novel genetic element, ICE6013, in Staphylococcus aureus |
Q38273295 | Integrons in the intestinal microbiota as reservoirs for transmission of antibiotic resistance genes |
Q42602274 | Intergeneric transfer of the Enterococcus faecalis plasmid pIP501 to Escherichia coli and Streptomyces lividans and sequence analysis of its tra region. |
Q42218598 | Investigating the basis of substrate recognition in the pC221 relaxosome |
Q39964412 | Involvement of a plasmid-encoded type IV secretion system in the plant tissue watersoaking phenotype of Burkholderia cenocepacia |
Q91849348 | Is there a Function for a Sex Pheromone Precursor? |
Q53182182 | Isolation and identification of new inner membrane-associated proteins that localize to cell poles in Escherichia coli. |
Q39769615 | Key components of the eight classes of type IV secretion systems involved in bacterial conjugation or protein secretion |
Q33860454 | Lateral gene transfer of streptococcal ICE element RD2 (region of difference 2) encoding secreted proteins |
Q33558004 | Linear plasmid SLP2 is maintained by partitioning, intrahyphal spread, and conjugal transfer in Streptomyces |
Q38958615 | Localization pattern of conjugation machinery in a Gram-positive bacterium. |
Q28270244 | Mechanisms of, and barriers to, horizontal gene transfer between bacteria |
Q90697869 | Mobile Genetic Elements Associated with Antimicrobial Resistance |
Q37784107 | Mobility of plasmids. |
Q35034341 | Mobility of the native Bacillus subtilis conjugative plasmid pLS20 is regulated by intercellular signaling |
Q34980063 | Mobilizable Rolling-Circle Replicating Plasmids from Gram-Positive Bacteria: A Low-Cost Conjugative Transfer |
Q44967946 | Mobilization functions of the bacteriocinogenic plasmid pRJ6 of Staphylococcus aureus |
Q33394554 | Molecular bacterial diversity and distribution in waste from a steel plant |
Q27676045 | Molecular basis of antibiotic multiresistance transfer in Staphylococcus aureus |
Q22255652 | Multidrug resistance in bacteria |
Q35892099 | Nucleotide sequence and evolution of the five-plasmid complement of the phytopathogen Pseudomonas syringae pv. maculicola ES4326. |
Q47143810 | Opinion of the Scientific Panel on additives and products or substances used in animal feed (FEEDAP) on the updating of the criteria used in the assessment of bacteria for resistance to antibiotics of human or veterinary importance |
Q46368442 | Pathogenic Vibrio species isolated from estuarine environments (Ceará, Brazil) - antimicrobial resistance and virulence potential profiles. |
Q34809289 | Phytoplasmas: bacteria that manipulate plants and insects. |
Q36220009 | Plasmid Complement of Lactococcus lactis NCDO712 Reveals a Novel Pilus Gene Cluster |
Q24815279 | Plasmid-mediated dimethoate degradation by Bacillus licheniformis isolated from a fresh water fish Labeo rohita |
Q34480448 | Plasmids from Food Lactic Acid Bacteria: Diversity, Similarity, and New Developments |
Q28488958 | Polar positioning of a conjugation protein from the integrative and conjugative element ICEBs1 of Bacillus subtilis |
Q38694088 | Processing of Nonconjugative Resistance Plasmids by Conjugation Nicking Enzyme of Staphylococci. |
Q34291074 | Pyrosequencing-based comparative genome analysis of Vibrio vulnificus environmental isolates |
Q48157155 | Rapid conjugative mobilization of a 100 kb segment of Bacillus subtilis chromosomal DNA is mediated by a helper plasmid with no ability for self-transfer. |
Q40883380 | Reconstitution of a staphylococcal plasmid-protein relaxation complex in vitro |
Q27317426 | Recruitment, assembly, and molecular architecture of the SpoIIIE DNA pump revealed by superresolution microscopy |
Q28081298 | Resistance and tolerance to foreign elements by prokaryotic immune systems - curating the genome |
Q45865549 | Revealing the latent mobilization capability of the staphylococcal bacteriocinogenic plasmid pRJ9. |
Q47137352 | Revisiting Antibiotic Resistance Spreading in Wastewater Treatment Plants - Bacteriophages as a Much Neglected Potential Transmission Vehicle |
Q58758056 | Role of plasmid plasticity and mobile genetic elements in the entomopathogen Bacillus thuringiensis serovar israelensis |
Q34495229 | SecReT4: a web-based bacterial type IV secretion system resource |
Q37416226 | Secretion by numbers: Protein traffic in prokaryotes |
Q35075608 | Sequence analysis of the lactococcal plasmid pNP40: a mobile replicon for coping with environmental hazards |
Q34564313 | Sequence analysis of three plasmids harboured in Rhodococcus erythropolis strain PR4. |
Q28473626 | Sequencing and genetic variation of multidrug resistance plasmids in Klebsiella pneumoniae |
Q89636198 | Single-Cell Analysis Reveals that the Enterococcal Sex Pheromone Response Results in Expression of Full-Length Conjugation Operon Transcripts in All Induced Cells |
Q33297912 | SmeA, a small membrane protein with multiple functions in Streptomyces sporulation including targeting of a SpoIIIE/FtsK-like protein to cell division septa |
Q38663510 | Stochasticity in the enterococcal sex pheromone response revealed by quantitative analysis of transcription in single cells |
Q36224504 | Structural and dynamic properties of bacterial type IV secretion systems (review). |
Q27670563 | Structure of the VirB4 ATPase, alone and bound to the core complex of a type IV secretion system |
Q27695577 | Structure of the double-stranded DNA-binding type IV secretion protein TraN from Enterococcus |
Q38019704 | Synthetic biology of secondary metabolite biosynthesis in actinomycetes: Engineering precursor supply as a way to optimize antibiotic production |
Q36314921 | TcpA, an FtsK/SpoIIIE homolog, is essential for transfer of the conjugative plasmid pCW3 in Clostridium perfringens |
Q47145574 | Technical guidance ‐ Update of the criteria used in the assessment of bacterial resistance to antibiotics of human or veterinary importance |
Q27675280 | The 2.5 A Structure of the Enterococcus Conjugation Protein TraM resembles VirB8 Type IV Secretion Proteins |
Q38287387 | The ABC-type multidrug resistance transporter LmrCD is responsible for an extrusion-based mechanism of bile acid resistance in Lactococcus lactis. |
Q42190290 | The Bacillus subtilis conjugative transposon ICEBs1 mobilizes plasmids lacking dedicated mobilization functions |
Q38214898 | The Lactococcus lactis plasmidome: much learnt, yet still lots to discover |
Q35017792 | The MobM relaxase domain of plasmid pMV158: thermal stability and activity upon Mn2+ and specific DNA binding. |
Q64076174 | The Pan-Plasmidome |
Q37120439 | The RepA_N replicons of Gram-positive bacteria: a family of broadly distributed but narrow host range plasmids |
Q28255343 | The TetR family of transcriptional repressors. |
Q42671073 | The VanE operon in Enterococcus faecalis N00-410 is found on a putative integrative and conjugative element, Tn6202. |
Q42363792 | The Very Long Chain Fatty Acid (C26:25OH) Linked to the Lipid A Is Important for the Fitness of the Photosynthetic Bradyrhizobium Strain ORS278 and the Establishment of a Successful Symbiosis with Aeschynomene Legumes |
Q38475885 | The carboxyl-terminal domain of TraR, a Streptomyces HutC family repressor, functions in oligomerization |
Q36000509 | The complete genome sequence of the acarbose producer Actinoplanes sp. SE50/110. |
Q37275377 | The expanding bacterial type IV secretion lexicon |
Q36328634 | The ins and outs of DNA transfer in bacteria. |
Q35579496 | The outs and ins of bacterial type IV secretion substrates |
Q41907983 | The presence of conjugative plasmid pLS20 affects global transcription of Its Bacillus subtilis host and confers beneficial stress resistance to cells. |
Q37191498 | The putative coupling protein TcpA interacts with other pCW3-encoded proteins to form an essential part of the conjugation complex |
Q34005318 | The repertoire of ICE in prokaryotes underscores the unity, diversity, and ubiquity of conjugation |
Q45902600 | The resolution and regeneration of a cointegrate plasmid reveals a model for plasmid evolution mediated by conjugation and oriT site-specific recombination. |
Q24669928 | The selective value of bacterial shape |
Q42139372 | The stability region of the Streptomyces lividans plasmid pIJ101 encodes a DNA-binding protein recognizing a highly conserved short palindromic sequence motif. |
Q37406990 | The structural biology of type IV secretion systems |
Q27689998 | The type IV secretion protein TraK from the Enterococcus conjugative plasmid pIP501 exhibits a novel fold |
Q34307587 | The versatile bacterial type IV secretion systems |
Q37573978 | Thirty-eight C-terminal amino acids of the coupling protein TraD of the F-like conjugative resistance plasmid R1 are required and sufficient to confer binding to the substrate selector protein TraM. |
Q38334075 | TraA and its N-terminal relaxase domain of the Gram-positive plasmid pIP501 show specific oriT binding and behave as dimers in solution |
Q42201100 | TraG encoded by the pIP501 type IV secretion system is a two-domain peptidoglycan-degrading enzyme essential for conjugative transfer. |
Q61051851 | TraN: A novel repressor of an Enterococcus conjugative type IV secretion system |
Q36593851 | Transcriptional and translational control of the mlr operon, which confers resistance to seven classes of protein synthesis inhibitors |
Q64091795 | Transfer of a mobile Staphylococcus saprophyticus plasmid isolated from fermented seafood that confers tetracycline resistance |
Q36956388 | Transfer of the methicillin resistance genomic island among staphylococci by conjugation |
Q36816234 | Transport capabilities of eleven gram-positive bacteria: comparative genomic analyses |
Q46314591 | Transposon Tn5281 is the main distributor of the aminoglycoside modifying enzyme gene among isolates of Enterococcus faecalis in Tehran hospitals |
Q42121598 | Two different tetracycline resistance mechanisms, plasmid-carried tet(L) and chromosomally located transposon-associated tet(M), coexist in Lactobacillus sakei Rits 9. |
Q51401840 | Two distinct conjugal transfer systems on Streptomyces plasmid pZL1. |
Q35100533 | Two novel membrane proteins, TcpD and TcpE, are essential for conjugative transfer of pCW3 in Clostridium perfringens |
Q37673221 | Two-step and one-step secretion mechanisms in Gram-negative bacteria: contrasting the type IV secretion system and the chaperone-usher pathway of pilus biogenesis |
Q38077206 | Type IV secretion machinery: molecular architecture and function |
Q37774038 | Type IV secretion systems: versatility and diversity in function |
Q34368266 | Type IV secretion: the Agrobacterium VirB/D4 and related conjugation systems |
Q34056764 | Unique helicase determinants in the essential conjugative TraI factor from Salmonella enterica serovar Typhimurium plasmid pCU1. |
Q30480319 | VirB1* promotes T-pilus formation in the vir-Type IV secretion system of Agrobacterium tumefaciens |
Q27320858 | VirB8-like protein TraH is crucial for DNA transfer in Enterococcus faecalis |
Q81729768 | [Molecular analysis of some genes from plasmid p19 of the soil strain Bacillus subtilis 19 involved in conjugation] |
Q34979537 | pGIAK1, a heavy metal resistant plasmid from an obligate alkaliphilic and halotolerant bacterium isolated from the Antarctic Concordia station confined environment |
Q42529745 | pSK41-like plasmid is necessary for Inc18-like vanA plasmid transfer from Enterococcus faecalis to Staphylococcus aureus in vitro |
Q35334147 | pTC Plasmids from Sulfolobus Species in the Geothermal Area of Tengchong, China: Genomic Conservation and Naturally-Occurring Variations as a Result of Transposition by Mobile Genetic Elements |
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