ライフサイエンスコーパス: extremophile

1 Microbiology special issue 'Ecophysiology of Extremophiles'.

2 we now see as yet another niche harbouring 'extremophiles'.

3 mostly microbes - are often referred to as 'extremophiles'.

4 eny, physiology and genomic features of this extremophile.

5 by a decrease in lipid desaturation in this extremophile.

6 ic and metabolic adaptive plasticity in this extremophile.

7 that nematodes are widely pre-adapted to be extremophiles.

8 lt in variation within the proteome of these extremophiles.

9 es and evolutionary adaptation strategies of extremophiles.

10 l metabolic transcription factor in archaeal extremophiles.

11 ue in learning about viruses infecting these extremophiles.

12 ties for the biotechnological exploration of extremophiles.

13 s other animal and plant pathogens and (poly)extremophiles.

14 viding a novel perspective on the ecology of extremophiles.

15 ent excludes most organisms except microbial extremophiles, a few invertebrates (mostly insects), hig

16 y informed analysis of the metabolome of the extremophile Amycolatopsis sp. DEM30355 has allowed for

17 -NT) is homologous to proteins found only in extremophiles and is the only such protein that is fused

18 All treatments were dominated by typical extremophiles and lithotrophs, typically Truepera, Thiob

19 lar biology, underscoring the versatility of extremophiles and providing a deeper mechanistic underst

20 erstand and control pathogens and to exploit extremophiles and their enzymes in bioremediation and in

21 of two organisms, Pyrococcus horikoshii (an extremophile) and Haemophilus influenzae (a parasite wit

22 including two model bacteria, a pathogen, an extremophile, and an animal were robustly active in pure

23 we examine critically what it means to be an extremophile, and the implications of this for evolution

24 Extremophile archaeal organisms overcome problems of mem

25 As more new extremophiles are brought into laboratory culture, they

26 Extremophiles are remarkable examples of life's resilien

27 -inspired approaches, such as those based on extremophiles, are also discussed.

28 ngly more closely related to the saprophytic extremophile Bacillus haladurans and Bacillus subtilis t

29 quired through horizontal gene transfer from extremophile bacteria which live in symbiosis within the

30 The extremophile bacterium D. radiodurans boasts a distincti

31 In the extremophile bacterium Deinococcus radiodurans, the oute

32 Natranaerobius thermophilus is an unusual extremophile because it is halophilic, alkaliphilic and

33 These extremophile behaviors challenge understanding of normal

34 hat are found predominantly in pathogens and extremophiles, called R2-like ligand-binding oxidases (R

35 on of biomolecules from two pure cultures of extremophiles (Chroococcidiopsis cubana cyanobacteria an

36 crobiome, we performed a meta-omic survey of extremophile communities inhabiting halite (salt) nodule

37 references (amino acid usage profiles) in an extremophile compared to its non-extremophile relative r

38 al genomes comes from the highly specialized extremophiles, Cyanidiophyceae.

39 na Bardawil, shares this attribute but is an extremophile found in hypersaline environments.

40 ditions, but remain unknown, particularly in extremophiles growing under multiple extremes.

41 Under conditions of limited iron, the extremophile Halobacterium salinarum, a salt-loving arch

42 e compare beta-glucosidase A (BglA) from the extremophile Halothermothrix orenii H168 expressed in Es

43 sits that homologous proteins from different extremophiles have comparable flexibilities at the optim

44 Extremophiles have much to reveal about the biology of r

45 (formerly known as Thlaspi caerulescens), an extremophile heavy metal hyperaccumulator model plant in

46 The discovery of extremophiles helped enable the development of groundbre

47 we report the results of the ISS experiment EXTREMOPHILES, including the analysis of microbial commu

48 velopmental and reproductive success in this extremophile insect.

49 H-) of membranes that were made of synthetic extremophile-inspired phospholipids with systematically

50 derstanding the water relations of microbial extremophiles is imperative to our ability to increase a

51 Research involving exopolysaccharides from extremophiles is only recently gaining attention.

52 distinctive genetic elements underlying the extremophile lifestyle of this species.

53 s, suggest a possible basis for T. parvula's extremophile lifestyle.

54 Extremophile lineages inspire questions about how organi

55 e synthesis of the structurally novel fungal extremophile metabolite berkelic acid, an effort leading

56 es of abiotic organic chemical synthesis and extremophile microorganisms, and unparalleled faunal bio

57 Extremophiles, microorganisms thriving in extreme enviro

58 by making pore-only proteins from two other extremophile Na(V)s: one from the hydrocarbon degrader A

59 Salt cress is an extremophile native to harsh environments and can reprod

60 nsmembrane electrical potential in the 'poly extremophile'Natranaerobius thermophilus are the context

61 and hypersaline Mono Lake (CA, US) [7-9] for extremophile nematodes.

62 The genomic resources established for this extremophile offer new perspectives for understanding th

63 The desert moss Syntrichia caninervis, an extremophile, offers novel insights into surviving desic

64 mophile viruses; the survival of terrestrial extremophiles on the surface of Mars; biological soils c

65 These resilient organisms, known as extremophiles or polyextremophiles, owe their survival d

66 Extremophile organisms are known that can metabolize at

67 g natural selection in extreme environments, extremophile organisms may commonly exhibit multivariate

68 When we think of extremophiles, organisms adapted to extreme environments

69 cellular viability - especially for certain extremophiles - over geological timescales.

70 The molecular basis of this extremophile phenotype, involving strain isolates with a

71 lution, and particularly in the evolution of extremophile physiology, is unclear.

72 ra of forward and reverse genetic studies of extremophile plant biology.

73 hypertolerance and hyperaccumulation in the extremophile plant species Arabidopsis halleri.

74 Extremophile plants thrive in places where most plant sp

75 nhabiting active volcanic soil is a discrete extremophile population that has evolved by tolerating a

76 e or spread on surfaces but are endowed with extremophile properties, for example, resistance to osmo

77 AP2 from Cyanidioschyzon merolae (Cyani), an extremophile red algae that grows at acidic pH at 45 deg

78 iles) in an extremophile compared to its non-extremophile relative recurs in the organisms of similar

79 olecular structure-function relationships in extremophiles requires methodologies adapted to extremes

80 volcanic hot springs in which these archaeal extremophiles reside.

81 ontrast, neither the catalytic properties of extremophile RNases III nor the structures and reactivit

82 that the mesophile Escherichia coli and the extremophile Shewanella piezotolerans both expanded thei

83 Comparisons to two non-extremophile sister species [12] reveal that arsenic res

84 Antifreeze proteins are produced by extremophile species to control ice formation and growth

85 wild sunflower relatives, including numerous extremophile species.

86 Here we present the draft genome for this extremophile species.

87 The study of natural extremophiles such as Deinococcus radiodurans has reveal

88 microorganisms ranging from common yeasts to extremophiles such as hyperthermophilic archaea can also

89 The use of enzymes from extremophiles, such as thermophiles or alkaliphiles, off

90 The molluscan archive is dominated by extremophile taxa, including those containing endosymbio

91 advanced hypothesis that this species is an extremophile that has traded viral resistance for precoc

92 ria and Archaea include mainly anaerobes and extremophiles that are involved in the sulfur, nitrogen,

93 chitectures of four phylogenetically diverse extremophiles that span the range of operon stabilities

94 ogists characterized the Archaea as obligate extremophiles that thrive in environments too harsh for

95 e we present the first genome assembly of an extremophile, the first dipteran in the family Chironomi

96 Compared to ribosomes from extremophiles, the M. acetivorans ribosome has a simplif

97 iscovered in a distinct bacterial lineage of extremophiles, the Thermus-Deinococcus group.

98 The extremophile Thermotoga maritima possesses a remarkable

99 CsoR-like protein, TTHA1953, from the model extremophile Thermus thermophilus HB8 using the iterativ

100 In extremophiles, these small heme proteins must have featu

101 Rusticyanin from the extremophile Thiobacillus ferrooxidans is a blue copper

102 nnihilation of not just human life, but also extremophiles, through the boiling of all water in Earth

103 resence of SlpA enhances the capacity of the extremophile to adjust to high pH.

104 ters, and thermal acidic springs; biology of extremophile viruses; the survival of terrestrial extrem

105 the standard melting transition relevant to extremophiles, we estimate the effects of superhelical s

106 rate simultaneously to an archaeon and to an extremophile whose cytoplasmic pH and normal growth temp

107 unclear to what degree mutant phenotypes of extremophiles will resemble those of their counterparts

108 Many Archaea are extremophiles, with species that are capable of growth a