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1 rised a two-gene operon located on the 49-kb linear plasmid.
2 ith B. burgdorferi N40 DNA on a single 48-kb linear plasmid.
3  bha128, a 453-nucleotide gene of the 175-kb linear plasmid.
4  the 9.0-kb circular plasmid and the 27.5-kb linear plasmid.
5  B. hermsii had a 180-kb circular instead of linear plasmid.
6 of Escherichia coli known to lysogenize as a linear plasmid.
7 rmed 'pJAZZ' vector) that is maintained as a linear plasmid.
8 t Borrelia burgdorferi is located in a 54-kb linear plasmid.
9 BHA007 protein, which is encoded by a 174-kb linear plasmid.
10    This new element was demonstrated to be a linear plasmid.
11 d either a 90-kb (pCSL1) or a 140-kb (pCSL2) linear plasmid.
12 cent DNA rearrangement among a number of the linear plasmids.
13 ceeds much faster with supercoiled than with linear plasmids.
14  subfamilies were sequenced and localized to linear plasmids.
15 ns, including a 950-kb linear chromosome and linear plasmids.
16 mosome and a number of variable circular and linear plasmids.
17  and multiple antibiotics, and possess large linear plasmids.
18 ch regions can be efficiently manipulated in linear plasmids.
19 n of circular subgenomes with CMS-S-specific linear plasmids.
20 rgdorferi has over 20 different circular and linear plasmids.
21  linear plasmid (lp25), and either the 28-kb linear plasmid 1 or 4 (lp28-1 and lp28-4, respectively)
22                              Strains missing linear plasmid 25 (lp25(-)) are able to infect mice if t
23 dification (R-M) systems, BBE02 contained on linear plasmid 25 (lp25) and BBQ67 contained on lp56, ha
24  tick vector and mammalian host both require linear plasmid 25 (lp25).
25                                              Linear plasmid 25, which is often lost in laboratory str
26 rated a deletion mutant designated ES10 in a linear plasmid 25-negative isolate of B. burgdorferi str
27 nactivation and genetic complementation of a linear plasmid-25-encoded gene (bbe16) to assess its rol
28     B. burgdorferi spirochetes that lack the linear plasmid 28-1 (lp28-1) succumb to the host's immun
29 of putative tick-specific determinants (e.g. linear plasmid 28-4 genes).
30                               B. burgdorferi linear plasmid 36 (lp36) is critical for mammalian infec
31                               B. burgdorferi linear plasmid 38 (lp38) contains several genes that are
32 onger infectious and lacked genes encoded on linear plasmids 38 and 28-1, among other differences.
33 revealed significant upregulation of several linear plasmid 54 (lp54)-encoded open reading frames (OR
34 mid-encoded genes of B. burgdorferi, several linear plasmid 54 (lp54)-encoded open reading frames (OR
35 the core Borrelia genome (linear chromosome, linear plasmid 54 and circular plasmid 26) that encode f
36 ates numerous genes encoding lipoproteins on linear plasmid 54 in response to environmental cues.
37 rupt CBP1 in H. capsulatum using a telomeric linear plasmid and a two-step genetic selection.
38  a mutant of 297 (M297) that lacks the 49-kb linear plasmid and expression of outer surface proteins
39 evealed that the gene was located on a 53-kb linear plasmid and that there was only one locus for the
40    Bidirectional replication of Streptomyces linear plasmids and chromosomes from a central origin pr
41                                              Linear plasmids and chromosomes of the bacterial genus S
42     By modification of palindrome-generating linear plasmids and development of a novel procedure tha
43  locations within telomeres of streptomycete linear plasmids and investigated mechanisms that enable
44                                 Streptomyces linear plasmids and linear chromosomes can replicate als
45 zed and contains a linear chromosome, twelve linear plasmids and nine circular extra-chromosomal elem
46 d with cells that lost the 24.7- and 27.5-kb linear plasmids and the 9.0-kb circular plasmid.
47  exchange of genetic information between the linear plasmids and the right end of the linear chromoso
48 ent Borrelia hermsii, located it in a 180-kb linear plasmid, and demonstrated its expression.
49 n B31 MI consists of a linear chromosome, 12 linear plasmids, and 9 circular plasmids.
50      Fourteen isolates harbored all B31-like linear plasmids, and seven isolates simultaneously lacke
51         Here we report that long-palindromic linear plasmids are formed in Streptomyces following dou
52 a burgdorferi contains abundant circular and linear plasmids, but the mechanism of replication of the
53  conversion of a unique expression site on a linear plasmid by an archived variable antigen gene.
54  able to repair transformed dephosphorylated linear plasmids by non-homologous end joining with consi
55 ilar but not identical to those reported for linear plasmids carried by these organisms.
56 richia coli accumulate high-molecular-weight linear plasmid concatemers when transformed with plasmid
57 . rochei chromosome and to 100-kb and 206-kb linear plasmids contained in S. rochei, were isolated an
58 e recombinant loci generated by insertion of linear plasmids containing either base-pair substitution
59 s serve as templates for synthesis of duplex linear plasmids containing long palindromes.
60 e rlrA/rorA locus of pSLA2 were seen also on linear plasmids derived from the unrelated SLP2 replicon
61 r Genomic Research) maps to one of the 28-kb linear plasmids (designated lp28-4) that is not present
62 he maternal (stromal) parent possessed three linear plasmids, designated Callan-a (7.5 kb), Aubonne-a
63              The loss of the 27.5- and 40-kb linear plasmids did not decrease the infectivity of thes
64 in vitro patterns of KMnO(4) modification in linear plasmid differed from that in supercoiled plasmid
65 ed isolated supercoiled, relaxed-circular or linear plasmid DNA and isolated mtDNA.
66 a, or ku80delta hdf1delta strains: repair of linear plasmid DNA and repair of an HO endonuclease-indu
67                            The assay employs linear plasmid DNA containing DNA DSBs produced by the r
68 tive within the procapsid and recircularizes linear plasmid DNA containing two terminal loxP recognit
69  The ability of each homologue to cross-link linear plasmid DNA has been determined, with a rank orde
70 products suggests that high-molecular-weight linear plasmid DNA is a substrate for RecBCD-mediated re
71 dimer forms stable complexes at both ends of linear plasmid DNA that protect the DSBs from digestion
72 clease-null AdnAB is a helicase that unwinds linear plasmid DNA without degrading the displaced singl
73 propyl)carbodiimide (EDC) in the presence of linear plasmid DNA.
74 d media was also transformed by pure CCC and linear plasmid DNA.
75 ization of cohesive and blunt-end terminated linear plasmid DNAs following transformation.
76 lution and the mobilities of circular versus linear plasmid DNAs were also affected by the chemical f
77 ent and genomic diversity among isolates are linear plasmid driven.
78 inding protein (SSB) in reactions containing linear plasmid dsDNA allowed us to study the AdnAB helic
79              A DNA library of pRJ28, a large linear plasmid encoding mercury resistance, was construc
80 s) of polintons, virophages, and cytoplasmic linear plasmids encompass an N-terminal domain homologou
81 ccomplish replication of telomere-containing linear plasmids, expression of rlrA, which encodes two L
82  frequent occurrence of ectopic integration, linear plasmid formation, and spontaneous resistance to
83 t least two successive rounds of addition of linear plasmid genetic material to the chromosomal right
84           Whole-genome sequencing revealed a linear plasmid in high-inflammatory isolates within simi
85 e near the right telomere are often found on linear plasmids in B. burgdorferi (sensu stricto) isolat
86  and circular forms in B. turicatae but only linear plasmids in B. parkeri, which should be of intere
87 spirochetes and is carried on variably sized linear plasmids in both Borrelia parkeri and B. turicata
88 y presents evidence of a common ancestor for linear plasmids in Micrococcus and suggests that horizon
89 some approximately 1 Mb in size and multiple linear plasmids in the 16- to 200-kb size range.
90 ently renamed mlp, was found on circular and linear plasmids in the genome sequence of B. burgdorferi
91 d-derived DNA probes used were also found on linear plasmids in the related Eurasian Lyme agents Borr
92 vspB of B. turicatae were near the centre of linear plasmids instead of near the telomeres.
93 lar to protelomerase and parA genes found in linear plasmid-like phages with telomeric ends.
94 protein paralogs from distinct circular- and linear-plasmid loci.
95                 Some plasmids, including the linear plasmid lp17, are never or rarely reported to be
96  a noncoding region of the 200-kb B. hermsii linear plasmid lp200.
97 s that possess the gene carry it on a 200-kb linear plasmid (lp200), whereas isolates that lack the g
98 mosomal telomere with a large portion of the linear plasmid lp21, which is present in the strain B31
99                                    The 25-kb linear plasmid lp25 and one of the 28-kb linear plasmids
100 e of replacing the requirement for the 25 kb linear plasmid lp25 during mammalian infection.
101 n-modification gene product expressed by the linear plasmid lp25.
102                     Two vectors derived from linear plasmids lp25 and lp28-1 were constructed and sho
103 tal data suggest that two of these elements, linear plasmids lp25 and lp28-1, play essential roles fo
104                          The presence of the linear plasmids lp25 and lp56 of Borrelia burgdorferi B3
105 y the 9-kb circular plasmid (cp9), the 25-kb linear plasmid (lp25), and either the 28-kb linear plasm
106       vlsE, a gene localized near one end of linear plasmid lp28-1 and encoding a surface-exposed lip
107                                  The loss of linear plasmid lp28-1, which contains the vls antigenic
108 -kb linear plasmid lp25 and one of the 28-kb linear plasmids (lp28-1) are required for experimental i
109 aracterize the role of one of the four 28-kb linear plasmids, lp28-3, we generated strains specifical
110         To investigate the role of the 36 kb linear plasmid, lp36 (also designated the B. burgdorferi
111                                The conserved linear plasmid lp54 encodes several proteins important f
112                                              Linear plasmid lp54 is one of the most highly conserved
113                           The absence of the linear plasmid lp56, which carries another putative rest
114 tion, but the genetic elements necessary for linear plasmid maintenance have not been experimentally
115 er chromosomes by transient integration, but linear plasmids may lead the donor chromosome end-first
116   Our observations suggest that Streptomyces linear plasmids may occupy an evolutionarily intermediat
117 d encodes, in its chromosome and each of the linear plasmids, members of the lambda exonuclease famil
118   These vectors identify internal regions of linear plasmids necessary for autonomous replication in
119 hbA is a single genetic locus that maps to a linear plasmid of approximately 220 kb.
120                                      A 28 kb linear plasmid of B. burgdorferi B31 (lp28-1) was found
121 y, we demonstrate that a factor encoded on a linear plasmid of B. burgdorferi, lp17, can negatively r
122 lp6.6 gene, which was localized to the 49-kb linear plasmid of B. burgdorferi, subsequently was clone
123                                            A linear plasmid of Borrelia burgdorferi had 16,927 bp, a
124                                pSCL, a 12 kb linear plasmid of Streptomyces clavuligerus, contains, n
125 ied protein attached to the end of the pSLA2 linear plasmid of Streptomyces rochei, determined the N-
126  covalently bound to protein, pSLA2, a 17 kb linear plasmid of Streptomyces rochei, initiates replica
127                             Atypically large linear plasmids of 92 to 105 kb have been identified in
128  and little characterized to date, are large linear plasmids of approximately 160 kb, or approximatel
129 enes were most similar to those of the 54-kb linear plasmids of LD species.
130                        Multiple circular and linear plasmids of Lyme disease and relapsing fever Borr
131 ethods, we determined the sequences of large linear plasmids of two New World species: Borrelia herms
132 sequence of the 51,601-bp Klebsiella oxytoca linear plasmid pKO2, and we demonstrate experimentally t
133 Additionally, the successful transfer of the linear plasmid pLMA1 by a DNase-insensitive, conjugation
134                      pVAPN is similar to the linear plasmid pNSL1 from Rhodococcus sp. NS1 and harbor
135 lasmids with sequence similarities to the 12 linear plasmids present in the B. burgdorferi type strai
136                                          The linear plasmid profile of CA434 was similar to that of C
137 ng an evolutionary heritage from an N15-like linear plasmid prophage ancestor.
138                                          The linear plasmid prophage form of PhiHAP-1 begins with the
139 only phages N15 and PY54 are known to have a linear plasmid prophage with closed hairpin telomeres.
140                                    The 17-kb linear plasmid pSLA2 has been a useful model in studies
141                             The Streptomyces linear plasmid pSLA2 initiates DNA replication bidirecti
142 all B. burgdorferi clinical isolates contain linear plasmids related to each other, but the structure
143 n analyzed biochemically, and their roles in linear plasmid repair in vivo have been verified genetic
144                NHEJ can religate transformed linear plasmids, repair ionizing radiation (IR)-induced
145 alyses provide insight into the mechanism of linear plasmid replication and the mechanisms by which p
146 parently not required for either circular or linear plasmid replication.
147 gene cluster, which is located on the 356-kb linear plasmid SCP1 of Streptomyces coelicolor A3(2).
148 ermination of the 365,023 bp sequence of the linear plasmid SCP1.
149                              The majority of linear plasmids showed variation both in terms of presen
150 ion of infectivity with strains possessing a linear plasmid (size range, 24 to 36 kb) that hybridized
151 ded Orfs encoded by several ORFs of the lp36 linear plasmid, such as BBK07 and BBK19, and proteins of
152                                              Linear plasmid templates for RNA polymerases (Pols) I an
153 a suggest that Polintons have evolved from a linear plasmid that acquired a retroviral integrase at l
154      Here we identify 11 genes localizing to linear plasmids that are up-regulated at pH 7.0 relative
155                  Notably, they harbour large linear plasmids that contribute to their catabolic diver
156 ing; and (iii) formation of long palindromic linear plasmids that duplicate the intact telomere by a
157 relia carry a linear chromosome and numerous linear plasmids that have covalently closed hairpin telo
158 vspA and vspB were each located on different linear plasmids that were the same in both serotypes.
159                        Although derived from linear plasmids, the vectors are maintained in circular
160              Rather, the loss of the 27.5-kb linear plasmid was associated with a more disseminated i
161     A 3.0-kb HindIII fragment of the 24.7-kb linear plasmid was used as a probe to determine the pres
162     The central approximately 25 kb of all 4 linear plasmids was syntenic for orthologous genes for p
163                                              Linear plasmids were transformed into Escherichia coli s
164                      This was located on one linear plasmid, which was defined by the upstream sequen
165                                              Linear plasmids with noncompatible ends introduced to We
166 dorferi (sensu stricto), for the presence of linear plasmids with sequence similarities to the 12 lin
167 p subfamily of alleles, which are carried on linear plasmids within each cell and maintained in sever

 
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