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1 her species do not oxidize iron at all (e.g. Sulfolobus acidocaldarius).
2 onents during starvation-induced motility in Sulfolobus acidocaldarius.
3 in-like modification pathway in the archaeon Sulfolobus acidocaldarius.
4 of a shuttle plasmid (pJlacS) propagated in Sulfolobus acidocaldarius.
5 ave used previously to characterize Dbh from Sulfolobus acidocaldarius.
6 ated from the thermoacidophilic crenarchaeon Sulfolobus acidocaldarius.
7 and inhibitor binding to CYP119, a P450 from Sulfolobus acidocaldarius.
8 degrees C) is near the growth temperature of Sulfolobus acidocaldarius.
9 ions are met by the extreme thermoacidophile Sulfolobus acidocaldarius.
10 nd the archaeal chromatin protein Sac7d from Sulfolobus acidocaldarius.
11 atomic model of the two-component S-layer of Sulfolobus acidocaldarius.
12 re of the Aap of the archaeal model organism Sulfolobus acidocaldarius.
13 CYTH ortholog, SaTTM, from the crenarchaeote Sulfolobus acidocaldarius.
14 egrees C) and pH (2 to 4) on the motility of Sulfolobus acidocaldarius, a thermoacidophilic archaeon.
15 onucleotide-mediated transformation (OMT) in Sulfolobus acidocaldarius and Escherichia coli as a func
16 al structures of the XPD catalytic core from Sulfolobus acidocaldarius and measured mutant enzyme act
17 l context, we used ECT to image the archaeon Sulfolobus acidocaldarius and observed a distinct protei
18 bacterial cells (Methanosarcina acetivorans, Sulfolobus acidocaldarius and Pseudomonas putida) enrich
19 NA polymerases from the extreme thermophiles Sulfolobus acidocaldarius and Pyrodictium occultum (54%
20 proteins from the hyperthermophilic archaeon Sulfolobus acidocaldarius and S. solfactaricus, respecti
21 milar to the 7-kDa DNA binding proteins from Sulfolobus acidocaldarius and Sulfolobus solfataricus in
22 When cells of two auxotrophic mutants of Sulfolobus acidocaldarius are mixed and incubated on sol
24 extremely high temperature was developed for Sulfolobus acidocaldarius, based on the selection of pyr
25 kably, the ortholog of L30 from the archaeon Sulfolobus acidocaldarius binds specifically to the same
27 d GrsB, essential for GDGT ring formation in Sulfolobus acidocaldarius Both proteins are radical S-ad
29 ther with this system, we were able to image Sulfolobus acidocaldarius cells live to reveal tight cou
32 bled those of the thermoacidophilic archaeon Sulfolobus acidocaldarius, despite important molecular d
34 ganism, we cultivated the model Crenarchaeon Sulfolobus acidocaldarius DSM639 at different combinatio
35 aii 'restored' sulphur oxidation capacity in Sulfolobus acidocaldarius DSM639, but not autotrophy, al
37 mber of independent pyrimidine auxotrophs of Sulfolobus acidocaldarius for deletions and sequenced th
39 isolated from the thermoacidophilic archaeon Sulfolobus acidocaldarius grown at different temperature
40 hese and previously available sequences from Sulfolobus acidocaldarius, Haloferax volcanii and Methan
42 ) from the thermoacidophilic archaebacterium Sulfolobus acidocaldarius have been studied by perylene
43 E) from the thermoacidophilic archaebacteria Sulfolobus acidocaldarius have been studied using two-ph
44 hnique to show that both S. solfataricus and Sulfolobus acidocaldarius have three functional origins.
45 o that of the adenylate kinase from archaeal Sulfolobus acidocaldarius in many respects such as the e
46 we show that the integrity of the S-layer in Sulfolobus acidocaldarius is maintained as cells grow vi
47 recombinant Sac7d from the hyperthermophile Sulfolobus acidocaldarius is mapped using multi-dimensio
48 nant Sac7d protein from the thermoacidophile Sulfolobus acidocaldarius is shown to be stable towards
50 genes grsA and grsB in thermophilic archaeon Sulfolobus acidocaldarius is temperature- and pH-depende
52 shibatae, while no homologs were evident in Sulfolobus acidocaldarius, lending further support to th
53 317H variant of the thermostable CYP119 from Sulfolobus acidocaldarius maintains heme iron coordinati
54 f the ESCRT-III-dependent division system in Sulfolobus acidocaldarius, one of the closest experiment
56 i reverse gyrase (48% overall identity), the Sulfolobus acidocaldarius reverse gyrase (41% identity),
57 rize prototypical superfamily ATPase FlaI in Sulfolobus acidocaldarius, showing FlaI activities in ar
58 efore, we determine the crystal structure of Sulfolobus acidocaldarius soluble FlaG (sFlaG), which re
59 y dynamic and TBP from the archaeal organism Sulfolobus acidocaldarius strictly requires TFB for DNA
60 ochondrial aa3-type proton pump functions in Sulfolobus acidocaldarius terminal oxidase complexes.
62 on of strains of Sulfolobus solfataricus and Sulfolobus acidocaldarius that allow the incorporation o
63 tify saci_0568 and saci_0748, two genes from Sulfolobus acidocaldarius that are highly induced upon U
64 chromatin protein from the hyperthermophile Sulfolobus acidocaldarius that severely kinks duplex DNA
65 he relevance of this threat for the archaeon Sulfolobus acidocaldarius, the mode of GGCC methylation
66 of the extremely thermoacidophilic archaeon Sulfolobus acidocaldarius to assess genetic and physiolo
67 amics of the binding of the Sac7d protein of Sulfolobus acidocaldarius to double-stranded DNA has bee
68 e thermostable M/R complex from the archaeon Sulfolobus acidocaldarius using atomic force microscopy
71 Attempts to generate a tes-deleted mutant in Sulfolobus acidocaldarius were unsuccessful, suggesting
72 and ArnB, in the thermoacidophilic archaeon Sulfolobus acidocaldarius, where they act synergisticall
74 chromatin protein from the hyperthermophile Sulfolobus acidocaldarius which kinks duplex DNA by appr
75 The genomic mutation rate of the archaeon Sulfolobus acidocaldarius, which inhabits a harsh and po