ライフサイエンスコーパス: pseudomonad

1 sification of fluorescent and nonfluorescent pseudomonads.

2 loring the assimilation of alpha-KG in other pseudomonads.

3 o both virulence and survival in fluorescent pseudomonads.

4 t difficult to generalize a role for FlhF in pseudomonads.

5 e for the characteristic fluorescence of the pseudomonads.

6 D designated QuiC1, which is present in some pseudomonads.

7 n-gene cistron in P. aeruginosa and in other Pseudomonads.

8 ctional osmoregulatory transporters in other pseudomonads.

9 hesis in P. aeruginosa likely apply to other pseudomonads.

10 regulatory system to evolutionary fitness of pseudomonads.

11 -3-methylglutaryl-coenzyme A pathway seen in pseudomonads.

12 ncoded conversion of benzoate to catechol in pseudomonads.

13 to be conserved in adjacent loci in certain pseudomonads.

14 m other root-colonizing and plant pathogenic pseudomonads.

15 aromatic hydroxylation complexes of the soil pseudomonads.

16 similarity exists between the two sequenced Pseudomonads, 976 protein-encoding genes are unique to P

17 udomonas alcaligenes, we isolated, from both pseudomonads, a third DKP, which was chemically characte

18 Possible roles of CinA and CinQ to help pseudomonads adapt and survive under prolonged copper st

19 ee different loci in the genomes of the four pseudomonads analyzed.

20 tion systems are also found in nonpathogenic pseudomonads and in species of symbiotic nitrogen-fixing

21 SDH) and is involved in valine catabolism in pseudomonads and mammals, was cloned and sequenced from

22 PA2449 is conserved among pseudomonads and might be universally involved in the as

23 ed a periplasmic transaminase in fluorescent pseudomonads and other proteobacteria that we termed Pta

24 In pseudomonads and related organisms, sugar uptake is not

25 to identify Psi subunits from several other Pseudomonads and to predict probable translational start

26 Pseudomonads are cosmopolitan microorganisms able to pro

27 resistance genes found in enterobacteria and pseudomonads are part of small mobile elements known as

28 The pseudomonads are unusual in that they often contain mult

29 has two flagellar stators, conserved in all pseudomonads as well as some other gram-negative bacteri

30 trpBA operon of three species of fluorescent Pseudomonads, bends the DNA when it forms either of two

31 scription of the trpBA operon of fluorescent pseudomonads, bends the DNA when it forms either of two

32 synthesis is conserved among the fluorescent pseudomonads, but the promoters recognized by PvdS ortho

33 er, Helicobacter and Wolinella; PseudoDB for pseudomonads; ClostriDB for clostridia; RhizoDB for Rhiz

34 patients are commonly infected by pathogenic Pseudomonads due to their immunocompromised state.

35 orin production could have arisen within the pseudomonads during the assembly of these biosynthetic g

36 han twofold higher than those of both of the pseudomonad enzymes.

37 uery genomes of DC3000 and other fluorescent pseudomonads for similar motifs.

38 With access to a fifth complete pseudomonad genome sequence, we were able to identify 3,

39 crylate dehalogenase (CaaD), isolated from a pseudomonad growing in these soils, hydrolytic dechlorin

40 igh sequence identity with SPases from other pseudomonads (>/= 78%).

41 The genome sequences of several pseudomonads have revealed a gene cluster containing gen

42 in, participates in catabolite repression in pseudomonads, helping to coordinate metabolism.

43 s IncPalpha plasmids and may have evolved in pseudomonad hosts.

44 y to important pathogenic and non-pathogenic pseudomonads in host habitats.

45 that support disparate levels of fluorescent Pseudomonads in natural soils; 16S ribosomal RNA sequenc

46 a substance which is excreted by fluorescent pseudomonads in order to scavenge iron from their enviro

47 indigenous antibiotic-producing fluorescent pseudomonads in the widespread decline of take-all in re

48 -guluronic acid, is produced by a variety of pseudomonads, including Pseudomonas syringae.

49 henazine-nonproducing strains of fluorescent pseudomonads indicated that each of the biosynthetic ope

50 thiocarboxylate) (PDTC), produced by certain pseudomonads, is a sulfur-containing siderophore that bi

51 Promysalin is a species-specific Pseudomonad metabolite with unique bioactivity.

52 ants suggested that catabolite repression in pseudomonads might, in part, involve control of BkdR lev

53 ptible strains of Gram-negative enteric rods/pseudomonads (nine individuals).

54 diverse bacteria including sediment-dwelling pseudomonads, nitrogen-fixing bradyrhizobia and cyanobac

55 putida strain mt-2 and by other fluorescent pseudomonads occurs in response to water limitations and

56 strains, it is apparently absent from other pseudomonad plant pathogens and prokaryotic genomes that

57 In this report a gene cluster encoding a pseudomonad polyketide has been completely sequenced and

58 at in response to water-limiting conditions, pseudomonads produce alginate, which influences biofilm

59 Certain members of the fluorescent pseudomonads produce and secrete phenazines.

60 Many pseudomonads produce redox active compounds called phena

61 The root-colonizing pseudomonad Pseudomonas putida (Pp) appears to produce t

62 In comparison to other pseudomonads, Pseudomonas aeruginosa grows poorly in L-l

63 high degree of similarity with two sequenced pseudomonads, Pseudomonas putida and Pseudomonas aerugin

64 e elements (ILEs) found in six environmental pseudomonads (strains FH1-FH6).

65 scens WCS365, but are absent from pathogenic pseudomonads such as P. aeruginosa and P. syringae.

66 lap genes are conserved among environmental pseudomonads such as P. putida KT2440, P. fluorescens Pf

67 al for siderophore biogenesis in fluorescent pseudomonads, such as pathogenic Pseudomonas aeruginosa

68 family of tyrosinases present in fluorescent pseudomonads that are required for siderophore maturatio

69 89%) are bacterial genes, including several Pseudomonads that have been shown to use P3N as growth s

70 of a choline pool in P. aeruginosa and other pseudomonads that, with the glycine betaine pool, regula

71 In pseudomonads, the occurrence of ptaA correlates with the

72 It is largely unknown, however, how pseudomonads themselves respond to - and survive in the

73 the normal hosts of these viruses seem to be pseudomonads, those viruses that attach directly to the

74 tural products produced by 42 bacilli and 18 pseudomonads through the generation of amino acid sequen

75 ty siderophores produced by a broad range of pseudomonads to enhance growth under iron deficiency.

76 on phenazine made by all phenazine-producing pseudomonads, to help P. aeruginosa alleviate Fe(III) li

77 lfur/cysteine for PDTC biosynthesis and that pseudomonads utilize sulfite reduction enzymology distin

78 Gram-negative enteric rods/pseudomonads were subjected to ciprofloxacin disk-diffus

79 on of DgcP (diguanylate cyclase conserved in Pseudomonads), whose activity in the olive tree pathogen

80 Arginine metabolism in pseudomonads with multiple catabolic pathways for its ut

81 genomic analysis revealed differences among pseudomonads with respect to alanine racemase genes that

82 acid phosphoribosyltransferase and, in some Pseudomonads, with nicotinamidase.