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1 ential trait for rhizosphere colonization by pseudomonads.
2 e (Pss) and other plant- and soil-associated pseudomonads.
3 regulatory system to evolutionary fitness of pseudomonads.
4 sification of fluorescent and nonfluorescent pseudomonads.
5 loring the assimilation of alpha-KG in other pseudomonads.
6 o both virulence and survival in fluorescent pseudomonads.
7 t difficult to generalize a role for FlhF in pseudomonads.
8 e for the characteristic fluorescence of the pseudomonads.
9 n-gene cistron in P. aeruginosa and in other Pseudomonads.
10 ctional osmoregulatory transporters in other pseudomonads.
11 hesis in P. aeruginosa likely apply to other pseudomonads.
12 -3-methylglutaryl-coenzyme A pathway seen in pseudomonads.
13 ncoded conversion of benzoate to catechol in pseudomonads.
14  to be conserved in adjacent loci in certain pseudomonads.
15 m other root-colonizing and plant pathogenic pseudomonads.
16 aromatic hydroxylation complexes of the soil pseudomonads.
17 D designated QuiC1, which is present in some pseudomonads.
18 e for completing the biosynthetic pathway in pseudomonads.
19  similarity exists between the two sequenced Pseudomonads, 976 protein-encoding genes are unique to P
20 udomonas alcaligenes, we isolated, from both pseudomonads, a third DKP, which was chemically characte
21  Under iron-limiting conditions, fluorescent pseudomonads acquire iron from the environment by secret
22      Possible roles of CinA and CinQ to help pseudomonads adapt and survive under prolonged copper st
23                                 Our isolated Pseudomonads also grow on biguanide, suggesting the exis
24 ee different loci in the genomes of the four pseudomonads analyzed.
25 tion systems are also found in nonpathogenic pseudomonads and in species of symbiotic nitrogen-fixing
26 SDH) and is involved in valine catabolism in pseudomonads and mammals, was cloned and sequenced from
27                    PA2449 is conserved among pseudomonads and might be universally involved in the as
28 ed a periplasmic transaminase in fluorescent pseudomonads and other proteobacteria that we termed Pta
29                                           In pseudomonads and related organisms, sugar uptake is not
30 ndances of known beneficial bacteria such as Pseudomonads and Rhizobium.
31 zines to increase the growth of iron-limited pseudomonads and that these effects depend on whether ps
32  to identify Psi subunits from several other Pseudomonads and to predict probable translational start
33  The KinB-AlgB-BphP module is present in all pseudomonads, and we demonstrate that AlgB is the partne
34                                              Pseudomonads are cosmopolitan microorganisms able to pro
35 ads and that these effects depend on whether pseudomonads are grown on glucose, succinate, or pyruvat
36                                Although most pseudomonads are mesophilic in nature, isolates such as
37                                Although most pseudomonads are mesophilic in nature, isolates such as
38 resistance genes found in enterobacteria and pseudomonads are part of small mobile elements known as
39                                              Pseudomonads are ubiquitous bacteria with importance in
40                                          The pseudomonads are unusual in that they often contain mult
41     Using phenazine antibiotic production by pseudomonads as a case study, we show that phenazines ar
42  has two flagellar stators, conserved in all pseudomonads as well as some other gram-negative bacteri
43 trpBA operon of three species of fluorescent Pseudomonads, bends the DNA when it forms either of two
44 scription of the trpBA operon of fluorescent pseudomonads, bends the DNA when it forms either of two
45 synthesis is conserved among the fluorescent pseudomonads, but the promoters recognized by PvdS ortho
46                         We recently isolated Pseudomonads capable of growing on metformin as the sole
47 er, Helicobacter and Wolinella; PseudoDB for pseudomonads; ClostriDB for clostridia; RhizoDB for Rhiz
48 patients are commonly infected by pathogenic Pseudomonads due to their immunocompromised state.
49 orin production could have arisen within the pseudomonads during the assembly of these biosynthetic g
50 t in the sulfur starvation-induced response, Pseudomonads employ two-component flavin-dependent monoo
51                         Total viable counts, pseudomonads, enterobacteria, and specific fish spoilers
52 han twofold higher than those of both of the pseudomonad enzymes.
53 uery genomes of DC3000 and other fluorescent pseudomonads for similar motifs.
54              With access to a fifth complete pseudomonad genome sequence, we were able to identify 3,
55 crylate dehalogenase (CaaD), isolated from a pseudomonad growing in these soils, hydrolytic dechlorin
56 igh sequence identity with SPases from other pseudomonads (>/= 78%).
57 hages of both diverse enteric bacteria and a pseudomonad have these properties.
58              The genome sequences of several pseudomonads have revealed a gene cluster containing gen
59 in, participates in catabolite repression in pseudomonads, helping to coordinate metabolism.
60 s IncPalpha plasmids and may have evolved in pseudomonad hosts.
61 y to important pathogenic and non-pathogenic pseudomonads in host habitats.
62 that support disparate levels of fluorescent Pseudomonads in natural soils; 16S ribosomal RNA sequenc
63 a substance which is excreted by fluorescent pseudomonads in order to scavenge iron from their enviro
64 enomic analysis was carried out on epiphytic pseudomonads in the UK orchards.
65  indigenous antibiotic-producing fluorescent pseudomonads in the widespread decline of take-all in re
66 -guluronic acid, is produced by a variety of pseudomonads, including Pseudomonas syringae.
67 henazine-nonproducing strains of fluorescent pseudomonads indicated that each of the biosynthetic ope
68 thiocarboxylate) (PDTC), produced by certain pseudomonads, is a sulfur-containing siderophore that bi
69             Promysalin is a species-specific Pseudomonad metabolite with unique bioactivity.
70 ants suggested that catabolite repression in pseudomonads might, in part, involve control of BkdR lev
71 ptible strains of Gram-negative enteric rods/pseudomonads (nine individuals).
72 diverse bacteria including sediment-dwelling pseudomonads, nitrogen-fixing bradyrhizobia and cyanobac
73  putida strain mt-2 and by other fluorescent pseudomonads occurs in response to water limitations and
74 he results of our studies will help generate Pseudomonad omega-TAs and omega-TAs from other organisms
75 hway has recently been fully elucidated, the pseudomonad pathway is still mostly elusive.
76  strains, it is apparently absent from other pseudomonad plant pathogens and prokaryotic genomes that
77     In this report a gene cluster encoding a pseudomonad polyketide has been completely sequenced and
78 at in response to water-limiting conditions, pseudomonads produce alginate, which influences biofilm
79           Certain members of the fluorescent pseudomonads produce and secrete phenazines.
80                                         Many pseudomonads produce redox active compounds called phena
81                          The root-colonizing pseudomonad Pseudomonas putida (Pp) appears to produce t
82                       In comparison to other pseudomonads, Pseudomonas aeruginosa grows poorly in L-l
83 high degree of similarity with two sequenced pseudomonads, Pseudomonas putida and Pseudomonas aerugin
84 e elements (ILEs) found in six environmental pseudomonads (strains FH1-FH6).
85 scens WCS365, but are absent from pathogenic pseudomonads such as P. aeruginosa and P. syringae.
86  lap genes are conserved among environmental pseudomonads such as P. putida KT2440, P. fluorescens Pf
87                                  Fluorescent pseudomonads such as Pseudomonas aeruginosa or Pseudomon
88 al for siderophore biogenesis in fluorescent pseudomonads, such as pathogenic Pseudomonas aeruginosa
89  substitutions across a phylogeny of related Pseudomonads suggests these mutations may be common in n
90 family of tyrosinases present in fluorescent pseudomonads that are required for siderophore maturatio
91  89%) are bacterial genes, including several Pseudomonads that have been shown to use P3N as growth s
92 of a choline pool in P. aeruginosa and other pseudomonads that, with the glycine betaine pool, regula
93 ssion of PhaG, an enzyme first identified in Pseudomonads, that transfers 3-hydroxy acyl-chains betwe
94                                           In pseudomonads, the occurrence of ptaA correlates with the
95          It is largely unknown, however, how pseudomonads themselves respond to - and survive in the
96 the normal hosts of these viruses seem to be pseudomonads, those viruses that attach directly to the
97 tural products produced by 42 bacilli and 18 pseudomonads through the generation of amino acid sequen
98 minase and biguanide hydrolase enzymes allow Pseudomonads to convert either metformin or biguanide to
99 ty siderophores produced by a broad range of pseudomonads to enhance growth under iron deficiency.
100 , and phenazines, RAMs made by soil-dwelling pseudomonads, to ask whether plant and microbial RAMs mi
101 on phenazine made by all phenazine-producing pseudomonads, to help P. aeruginosa alleviate Fe(III) li
102 r subsequent regulatory activity, and (b) in pseudomonads, transcripts under CCR control are represse
103 lfur/cysteine for PDTC biosynthesis and that pseudomonads utilize sulfite reduction enzymology distin
104                   Gram-negative enteric rods/pseudomonads were subjected to ciprofloxacin disk-diffus
105 on of DgcP (diguanylate cyclase conserved in Pseudomonads), whose activity in the olive tree pathogen
106                       Arginine metabolism in pseudomonads with multiple catabolic pathways for its ut
107  genomic analysis revealed differences among pseudomonads with respect to alanine racemase genes that
108  acid phosphoribosyltransferase and, in some Pseudomonads, with nicotinamidase.

 
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