ライフサイエンスコーパス: acidophilic

1 this PME is non-processive, halophilic, and acidophilic.

2 )-reducing gene pool in soil is dominated by acidophilic Acidobacteria, including a highly abundant g

3 el payloads after oral administration of the acidophilic algae motors is confirmed using a murine mod

4 , our findings indicate that multifunctional acidophilic algae-based biomotors offer distinct advanta

5 ethanogen (Methanococcus maripaludis S2), an acidophilic and aerobic thermophile (Sulfolobus solfatar

6 gene on oral microbiota and specifically the acidophilic and caries-associated Streptococcus mutans i

7 Though cysteine proteinases are acidophilic and normally confined to the lysosomal netwo

8 2, is one of the first hyperthermophilic and acidophilic archaeal species to be discovered.

9 ent of genomic change that distinguishes the acidophilic archaeon Ferroplasma acidarmanus fer1 from a

10 rixviridae infecting a hyperthermophilic and acidophilic archaeon Saccharolobus islandicus LAL14/1.

11 rter enzyme in expression hosts that are not acidophilic, as well as lactic acid bacteria and other m

12 e identified peptidoglycan from thermophilic acidophilic bacteria (Alicyclobacillus acidocaldarius) a

13 wetland plant species and the association of acidophilic bacteria in the wetland rhizosphere indicate

14 We have examined PurE from the acidophilic bacterium Acetobacter aceti (AaPurE), focusi

15 Here, the CcO of the acidophilic bacterium Acidithiobacillus ferrooxidans is

16 es to investigate an iron oxidizing, extreme acidophilic bacterium, A. ferrooxidans isolate (IO-2C) f

17 ia in comprehensively characterized, natural acidophilic biofilm communities.

18 dom shotgun sequencing of DNA from a natural acidophilic biofilm, we report reconstruction of near-co

19 r of a genomically uncharacterized, natural, acidophilic biofilm.

20 from community genomic data from two natural acidophilic biofilms.

21 perivenular necroinflammatory foci, and many acidophilic bodies scattered throughout the lobule.

22 Acidithiobacillus ferrooxidans is an acidophilic chemolithoautotroph that plays an important

23 Acidophilic chemolithoautotrophic iron(II)-oxidizing bac

24 The abilities of acidophilic chemolithotrophic bacteria and archaea to ac

25 umulation of three lysosomal proteins and an acidophilic dye.

26 ith a second class of endosomes that take up acidophilic dyes (acidic endosomes [AEs]).

27 We identified the acidophilic fungus Acrodontium crateriforme as the domin

28 ro slightly reduced the respiratory burst of acidophilic granulocytes and drastically altered the exp

29 rt that gilthead seabream (Sparus aurata L.) acidophilic granulocytes, which are the functional equiv

30 res which show histopathological findings of acidophilic ground substance in DFNA9 patients.

31 , like those involved in Fe(II) oxidation by acidophilic iron oxidizers or anaerobic photoferrotrophs

32 r Archaea and the frequent occurrence of the acidophilic iron(II)- and sulfur-oxidizing and iron(III)

33 lly) pure cultures of the recently described acidophilic, iron-oxidizing heterotrophic bacterium Acid

34 Here we report a direct interaction of the acidophilic kinase Polo-like kinase 2 (PLK2, also known

35 Oenococcus oeni is an alcohol-tolerant, acidophilic lactic acid bacterium primarily responsible

36 hic marker genes appear more often in highly acidophilic lineages.

37 s of me(v)/me(v) marrow revealed the classic acidophilic macrophage pneumonia of me(v)/me(v) mice, bu

38 Obligate acidophilic members of the thaumarchaeotal genus Candida

39 chrotolerant (Polaromonas), acidotolerant or acidophilic (members of the Acidobacteria), or resistant

40 Here, we demonstrate that acidophilic microalgae biomotors can maintain their swim

41 Metagenomic data from an acidophilic microbial community enabled a genomewide, co

42 referred to as ARMAN (archaeal Richmond Mine acidophilic nanoorganisms), from environmental samples a

43 al evaluation of liver showed more extensive acidophilic necrosis and severe pathological changes in

44 -h recovery groups had higher percentages of acidophilic neurons (65% and 54% respectively) than the

45 Neuronal cell counting revealed 20% acidophilic neurons in dorsal dentate hilus after 40-min

46 a 0-3 scale by estimating the percentage of acidophilic neurons in each of 23 brain regions.

47 the 1-h and 3-h seizure groups (31% vs. 43% acidophilic neurons respectively).

48 CA4), quantitative cell counts of normal and acidophilic neurons were also performed.

49 s (Euryarchaeota) is represented by the most acidophilic organisms known so far that are poorly amena

50 nfects hyperthermophilic (~80 degrees C) and acidophilic (pH ~ 2) archaea.

51 ted on the basic and acidic phosphopeptides: acidophilic phosphorylation sites were predominately enr

52 Alveolar macrophages in acidophilic pneumonia, a major cause of death of aging 1

53 far the most widely studied of all extremely acidophilic prokaryotes.

54 VP30 is a strongly acidophilic protein; RNA binding became stronger as pH w

55 n ancestor via horizontal gene transfer from acidophilic representatives of Euryarchaeota.

56 CK1s are acidophilic serine/threonine kinases with multiple criti

57 esults in dephosphorylation of clustered and acidophilic sites.

58 to autotrophy, to chemoheterotrophy in less acidophilic species.

59 a in all the enrichments and subsequently an acidophilic strain (TR1) was isolated.

60 lopment of AMD-like communities dominated by acidophilic sulfide-oxidizing bacteria on untreated OWR

61 Microbiological suitability of acidophilic sulfur reduction for metal recovery was expl

62 versity biofilms dominated by members of the acidophilic sulfur-oxidizer genus Acidithiobacillus.

63 by inundation, exists corresponding to rapid acidophilic to halophilic plant community change and a c

64 The thermo-acidophilic unicellular red alga Galdieria sulphuraria r