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1 ne transfer RNA gene (trnI.2) located in the rRNA operon.
2 nscribed spacer (ITS) regions 1 and 2 of the rRNA operon.
3 odes 4,350 predicted ORFs, 45 tRNAs, and one rRNA operon.
4 nscribed spacer regions (ITS) 1 and 2 of the rRNA operon.
5 ntained a randomly mutagenized plasmid-borne rRNA operon.
6 ely restored to wild-type levels by a cloned rRNA operon.
7  in the 16 S rRNA gene of H. halobium single rRNA operon.
8 7.1 kb BamHI fragment containing part of the rRNA operon.
9 ntary conditions were profiled by sequencing rRNA operons.
10 2,274 predicted proteins, 61 tRNAs, and four rRNA operons.
11 d reestablished the full complement of seven rRNA operons.
12 P1 promoters from the seven Escherichia coli rRNA operons.
13  carry the mutation A2058G in one of two 23S rRNA operons.
14                       There are at least two rRNA operons.
15 mX2, located adjacent to two of the repeated rRNA operons.
16 e leader region of the single ribosomal RNA (rRNA) operon.
17 s 168-type strain contains 10 ribosomal RNA (rRNA) operons.
18 , which possess only one chromosomal copy of rRNA operon, allowed isolation of a number of linezolid-
19 d the single-nucleotide polymorphisms in the rRNA operon and variable numbers of tandem repeats in th
20 hat were similar to the six remaining intact rRNA operons and reestablished the full complement of se
21 e genome contains 4,252 genes, including six rRNA operons and six predicted reductive dehalogenases.
22 ositively correlated with both the number of rRNA operons and the number of tRNA genes.
23 tes for fluorescent proteins adjacent to the rRNA operons and then examining their positions pairwise
24                    There is a single 16S-23S rRNA operon, and there are 30 tRNA coding sequences.
25                                There are two rRNA operons, and 39 tRNA genes are dispersed around the
26 18 base pairs, encoding 2,640 proteins, four rRNA operons, and 56 tRNA genes.
27 hat V. natriegens contains a large number of rRNA operons, and its rRNA promoters are extremely stron
28 us thuringiensis These species have 11 to 14 rRNA operons, and sequence variability occurs among the
29 normal transcription and is also involved in rRNA operon antitermination.
30 a coli strain in which all seven chromosomal rRNA operons are inactivated by deletions spanning the 1
31                                    The seven rRNA operons are nearly identical and separated from eac
32 A synthesis from the P1 promoters of several rRNA operons are reduced 2-fold in a fis null mutant com
33                         In Escherichia coli, rRNA operons are transcribed as 30S precursor molecules
34 argeting primary transcripts from chlamydial rRNA operons as well as dnaA, polA, mutS, minD, ftsK, an
35                             A single E. coli rRNA operon carried by a multicopy plasmid supplies 16S
36 consistent with the hypothesis that multiple rRNA operons constitute a metabolic burden at slow growt
37              Escherichia coli ribosomal RNA (rRNA) operons contain antitermination motifs necessary f
38 database containing annotated information on rRNA operon copy number among prokaryotes.
39      Maximum growth rate in association with rRNA operon copy number expresses a rate-yield trade-off
40                           In prokaryotes the rRNA operon copy number is the important determinant of
41 iting pausing, promoting anti-termination on rRNA operons, coupling transcription with translation on
42 g microorganisms that contain only a foreign rRNA operon derived from either Salmonella typhimurium o
43 hat the cell's innate ability to up-regulate rRNA operons does not compensate for 5S rRNA deficiencie
44  replication of the spacer region from other rRNA operons during the repair of rrnB suggest that the
45                     Sequence analysis of the rRNA operon for all the genomovars indicated that this p
46 s, and demonstrated the use of a T7-promoted rRNA operon for stoichiometrically balanced rRNA synthes
47 ucleotide signature region in the ISR of all rRNA operons for five B. subtilis 168 isolates; sequenci
48 of the trinucleotide signature region in all rRNA operons for these strains.
49 nt loci that come into close proximity, with rRNA operons forming a structure reminiscent of the euka
50 ulation of promoters (e.g., the promoters of rRNA operons) from changes in transcription due to chang
51  transcribed spacer 1 (ITS1) and ITS2 of the rRNA operon has played an important role in understandin
52 rther, an active transcription from multiple rRNA operons in chromosome is critical for the compactio
53                                    The seven rRNA operons in Escherichia coli each contain two promot
54 f the expression of additional plasmid-borne rRNA operons in Escherichia coli was exaggerated at slow
55 ers produces a mixture of amplicons from all rRNA operons in the genome, and the sequence data genera
56  of an unreported sequence variation between rRNA operons in this organism.
57  tRNA genes, 3 tRNA modifying systems, and 4 rRNA operons in various combinations.
58 the relative positions of the ribosomal RNA (rRNA) operons in space.
59                   Transcription of an intact rRNA operon is not necessary, although a minimal transcr
60  our data demonstrated that transcription of rRNA operons is a key mechanism affecting genome compact
61  internally transcribed spacer region of the rRNA operon (ITS PCR-RFLP).
62  been studied using only a single locus (the rRNA operon), leaving the origins of many key clades unc
63 sence of the trinucleotide insert in certain rRNA operons may play a role in rRNA maturation and prot
64 osed to selection for rapid growth have more rRNA operons, more tRNA genes and more strongly selected
65 cted O. macclurei blood recovered the entire rRNA operon of this apicomplexan parasite along with the
66         Transcription antitermination in the rRNA operons of Escherichia coli requires a unique nucle
67 biosum was identified in the vicinity of the rRNA operon on a large genomic contig.
68      In the final strain, carrying no intact rRNA operon on the chromosome, rRNA molecules were expre
69 e effect of transcription, specifically from rRNA operons, on the structure of the nucleoid, when the
70                                          Non-rRNA operon pairs did not colocalize, and the magnitude
71             This region contained a complete rRNA operon plus 10 other potential open reading frames
72 y site-directed mutagenesis in the wild-type rRNA operon produced an oxazolidinone resistance phenoty
73    Fecal bacterial community was analyzed by rRNA operon profiling.
74                      Deletion via duplicated rRNA operon promoter (Prrn) sequences was also frequent
75      The test system was the tobacco plastid rRNA operon promoter fused with the E.coli phage T7 gene
76 al transcribed spacer 2 (ITS2) region of the rRNA operon provide accurate identification of clinicall
77 from a multicopy plasmid containing a single rRNA operon (prrn).
78  show that extra, plasmid-borne copies of an rRNA operon recruit RNAP from the nucleoid into the cyto
79  understand the evolutionary implications of rRNA operon redundancy, we have created a phylogenetical
80                        Colocalization of the rRNA operons required the rrn P1 promoter region but not
81                    Expression of the plastid rRNA operon (rrn) during development is highly regulated
82 SR) between the 16S and 23S rRNA genes, five rRNA operons, rrnI-H-G and rrnJ-W, lack a trinucleotide
83              We determined a nearly complete rRNA operon sequence of T. whippelii from specimens from
84 that in B. burgdorferi, an organism with few rRNA operons that grows slowly, the role of (p)ppGpp may
85 m of the replication region and is the first rRNA operon to be sequenced from B. megaterium.
86 utility of two primer pairs, directed to the rRNA operon, to specifically identify the B. cepacia com
87 nce upstream of the -35 element (GTGGGA; the rRNA operon upstream activator [RUA]) that is conserved
88                                 Profiling of rRNA operons using the Oxford MinION yielded 65,706 2-D
89                                           An rRNA operon was located upstream of the replication regi
90                                   The single rRNA operon was targeted with a synthetic 16S rRNA allel
91 ernal transcribed spacer (ITS) region of the rRNA operon was validated for application to equine clin
92 with a plasmid carrying randomly mutagenized rRNA operon, was screened for mutants exhibiting resista
93 g internal transcribed spacer regions of the rRNA operon were simultaneously amplified and interrogat
94 acterial cells containing each cloned mutant rRNA operon were then examined for cell growth, terminat
95     We also were able to replace the E. coli rRNA operon with an E. coli/yeast hybrid one in which th
96                To examine the flexibility of rRNA operons with respect to fundamental organization, t
97 n fragment length polymorphism (RFLP) of the rRNA operons, with three distinct patterns found upon So