ライフサイエンスコーパス: archaebacterium

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1 ram-negative bacterium and P. furiosus is an archaebacterium.

2 idium-like eubacterium and a Sulfolobus-like archaebacterium.

3 s in various prokaryotes, eukaryotes, and an archaebacterium.

4 the E. coli bacterium and the M. jannaschii archaebacterium.

5 The archaebacterium, a thermoacidophil resembling extant The

6 rical origin of Eukaryotes as a fusion of an archaebacterium and a eubacterium that could not have be

7 ymbiogenesis by syntrophic merger between an archaebacterium and a eubacterium.

8 proteolysis by 20 S proteasomes from another archaebacterium and mammals.

9 re indirectly connected through a "eukaryote-archaebacterium-eubacterium-eukaryote" similarity path.

10 t K+ (K(V)) channel from a hyperthermophilic archaebacterium from an oceanic thermal vent.

11 sion gene ftsZ from the extremely halophilic archaebacterium Halobacterium salinarium.

12 found in the extremely halophilic archaeum (archaebacterium) Halobacterium halobium.

13 iator tRNA gene from the moderate halophilic archaebacterium Haloferax volcanii and mutants derived f

14 Significantly, FtsZ from the archaebacterium Haloferax volcanii is a GTPase that is l

15 nome sequences for several eubacteria and an archaebacterium has had a great impact on the interpreta

16 nal domain of the related subunit I from the archaebacterium Meiothermus ruber was reported.

17 In the archaebacterium Methanocaldococcus jannaschii (M. jannas

18 X-ray structure of the Nep1 homolog from the archaebacterium Methanocaldococcus jannaschii in its fre

19 melanogaster, Saccharomyces cerevisiae, and archaebacterium Methanocaldococcus jannaschii, which enc

20 und in nonphotosynthetic organisms, viz. the archaebacterium Methanococcus jannaschii, the eubacteriu

21 29 such pumps, and with the exception of the archaebacterium Methanococcus jannaschii, the numbers of

22 of auxotrophs in the antibiotic-insensitive archaebacterium Methanococcus.

23 fic ADP-ribose pyrophosphatase gene from the archaebacterium, Methanococcus jannaschii, introduced in

24 G. lamblia were most similar to those of the archaebacterium Methanosarcina barkeri and the delta-pur

25 Monomethylamine methyltransferase of the archaebacterium Methanosarcina barkeri contains a novel

26 ntial subunit of the RNase P enzyme from the archaebacterium Methanothermobacter thermoautotrophicus

27 losuccinate lyase from the hyperthermophilic archaebacterium Pyrobaculum aerophilum has been determin

28 ubredoxin protein from the hyperthermophilic archaebacterium Pyrococcus furiosus was examined by a hy

29 terize the enzyme from the hyperthermophilic archaebacterium Pyrococcus furiosus.

30 ions of a glutamate transporter homolog from archaebacterium Pyrococcus horikoshii, sodium/aspartate

31 mblia and Entamoeba histolytica and from the archaebacterium, Pyrococcus furiosus.

32 a; and a protein of unknown function from an archaebacterium, reveals an apparently conserved core, a

33 globus fulgidus") reduces sulphate--the only archaebacterium so far known to do so--and makes very sm

34 fraction E (PLFE) from the thermoacidophilic archaebacterium Sulfolobus acidocaldarius has been inves

35 fraction E (PLFE) from the thermoacidophilic archaebacterium Sulfolobus acidocaldarius have been stud

36 synthase (sIGPS) from the thermoacidophilic archaebacterium Sulfolobus solfataricus were compared to

37 s furiosus is a strictly anaerobic archaeon (archaebacterium) that grows at temperatures up to 105 de

38 litoralis is a strictly anaerobic archaeon (archaebacterium) that grows at temperatures up to 98 deg

39 mal stability and structural simplicity, the archaebacterium Thermoplasma Acidophilum 20S proteasome

40 hanococcus voltae (a methanogenic, anaerobic archaebacterium) was shown to generate spontaneously 4.4

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