ライフサイエンスコーパス: extremophile

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

2 by a decrease in lipid desaturation in this extremophile.

3 ic and metabolic adaptive plasticity in this extremophile.

4 es and evolutionary adaptation strategies of extremophiles.

5 l metabolic transcription factor in archaeal extremophiles.

6 ue in learning about viruses infecting these extremophiles.

7 ties for the biotechnological exploration of extremophiles.

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

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

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

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

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

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

14 Extremophile archaeal organisms overcome problems of mem

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

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

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

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

19 These extremophile behaviors challenge understanding of normal

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

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

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

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

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

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

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

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

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

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

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

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

32 Extremophiles, microorganisms thriving in extreme enviro

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

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

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

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

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

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

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

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

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

42 Extremophile plants thrive in places where most plant sp

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

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

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

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

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

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

49 wild sunflower relatives, including numerous extremophile species.

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

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

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

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

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

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

56 The extremophile Thermotoga maritima possesses a remarkable

57 Rusticyanin from the extremophile Thiobacillus ferrooxidans is a blue copper

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

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

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

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

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

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