ライフサイエンスコーパス: N. europaea

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1 N. europaea was not able to grow with fructose as an ene

2 P460 cytochromes from M. capsulatus Bath and N. europaea was low (24.3% of residues identical), altho

3 anagement in the ammonia-oxidizing bacterium N. europaea.

4 s pathway, the enzyme isolated directly from N. europaea (NeNIR) was biochemically and structurally c

5 The protein was isolated from N. europaea with Cu(II) bound but was found to be capabl

6 sembled native cytochrome P460 purified from N. europaea in its UV-visible spectroscopic, ligand bind

7 With this in mind, we tested if N. europaea could utilize fructose and other compounds a

8 and one ammonia monooxygenase gene (amoA) in N. europaea was up-regulated upon exposure to 1 nM QD-PE

9 tween cytochromes P460 and cytochromes c' in N. europaea and M. capsulatus, confirm the importance of

10 Modelling of the electron flow in N. europaea demonstrated low electron flow to denitrific

11 may be important during ammonia oxidation in N. europaea at low oxygen concentrations to detoxify NO

12 l poststarvation cellular response system in N. europaea.

13 Several AOB, including N. europaea, also possess a divergent monocistronic copy

14 Provision of TBP with Eu increased N. europaea inhibition, although TBP alone did not subst

15 and Eu additions at 50 and 100 ppm inhibited N. europaea, even when virtually all of the REE was inso

16 d has been reported to support the growth of N. europaea.

17 Mutant versions of cytochrome P460 of N. europaea in which Lys70 70 was replaced by Arg, Ala,

18 ress response regulon during the recovery of N. europaea from extended ammonia starvation, thus indic

19 ignificant role in mediating the recovery of N. europaea from starvation.

20 The transcriptional response of N. europaea to ammonia addition following short- and lon

21 The recently completed genomic sequence of N. europaea revealed a potential permease for fructose.

22 The strategy of N. europaea to accumulate Fe from the environment involv

23 rong Ag(+) ligands and was unable to protect N. europaea from Ag(+) toxicity.

24 ionic IC supply to excess gaseous IC supply, N. europaea chemostat cultures demonstrated an acclimati

25 Together, the results indicated that N. europaea mobilized enhanced IC scavenging pathways fo

26 These results show that N. europaea can be grown in CO(2)-free medium by using f

27 Previous studies have shown that N. europaea can utilize limited amounts of certain organ

28 The experiments suggested that N. europaea cells may be able to use different promoters

29 cussed in terms of a catalytic model for the N. europaea enzyme and compared with other cytochrome c

30 ove 5.4, which is a typical pH limit for the N. europaea lineage.

31 e data show that the electrochemistry of the N. europaea cytochrome c peroxidase is unlike other pero

32 here we find that the catalytic waves of the N. europaea enzyme have a midpoint potential of >500 mV

33 Under these conditions, interrogation of the N. europaea proteome revealed increased levels of carbon

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