ライフサイエンスコーパス: methanotrophic

1 hese compounds indicate episodes of vigorous methanotrophic activity in methane-laden water masses.

2 Overall, this study shows the importance of methanotrophic activity near the water table to attenuat

3 ne observed in the chamber are attributed to methanotrophic activity, which was highest in the capill

4 axonomic distribution of HpnR extends beyond methanotrophic and acetic acid bacteria.

5 For example, methanotrophic and nitrogen-fixing bacteria may benefit

6 by tight linkages between methane-utilizing (methanotrophic) and nonmethanotrophic bacteria.

7 2 biosynthesis was present in both anaerobic methanotrophic archaea (ANME) and sulphate-reducing bact

8 rocess is mediated by consortia of anaerobic methanotrophic archaea (ANME) that live in syntrophy wit

9 creased abundance of aggregates of anaerobic methanotrophic archaea (ANME-2) and sulfate-reducing bac

10 Yet only one association, between methanotrophic archaea and sulphate-reducing bacteria, h

11 rge multi-haem cytochromes in the genomes of methanotrophic archaea and the demonstration of redox-de

12 llaneous Crenarchaeotal Group, whereas known methanotrophic Archaea are not detectable.

13 Methanogenic and methanotrophic archaea play important roles in the globa

14 lative sequence abundance of ANME (anaerobic methanotrophic archaea), as well as aerobic Methylococca

15 found in strictly anaerobic methanogenic and methanotrophic archaea, catalyzes the reversible product

16 In nature, aerobic methanotrophic bacteria and anaerobic archaea are able t

17 s a small copper-binding peptide produced by methanotrophic bacteria and is intimately involved in bo

18 the soluble methane oxidation complex of the methanotrophic bacteria and the aromatic hydroxylation c

19 of methane monooxygenase (MMO) isolated from methanotrophic bacteria catalyzes the O2-dependent conve

20 cave-adapted shrimp suggest that carbon from methanotrophic bacteria comprises 21% of their diet, on

21 f potential biotechnological applications of methanotrophic bacteria has not been comprehensively dis

22 on discharge, was consumed quantitatively by methanotrophic bacteria in Gulf of Mexico deep waters ov

23 Methanotrophic bacteria oxidize methane to methanol in t

24 In nature, methanotrophic bacteria perform this reaction under ambi

25 d Methylomicrobium albus BG8, two species of methanotrophic bacteria that are of interest for monitor

26 Methanotrophic bacteria use methane, a potent greenhouse

27 acile conversion of methane into methanol in methanotrophic bacteria with high efficiency under ambie

28 ntings harbored significantly greater plant, methanotrophic bacteria, arthropod, and bird diversity t

29 take of (13)C into fatty acids indicative of methanotrophic bacteria, associated with increasing copy

30 Biofiltration, whereby CH(4) is oxidized by methanotrophic bacteria, is a potentially effective stra

31 genase (MMO) systems have been identified in methanotrophic bacteria, namely, a soluble or cytoplasmi

32 pendent conversion of methane to methanol in methanotrophic bacteria, thereby preventing the atmosphe

33 hat in the soluble methane monooxygenases of methanotrophic bacteria, to which AMO exhibits a signifi

34 ered the abundance of methanogens along with methanotrophic bacteria, which may have reduced CH4 cycl

35 ions and without significant intervention of methanotrophic bacteria.

36 yzes the oxidation of methane to methanol in methanotrophic bacteria.

37 oenzyme that oxidizes methane to methanol in methanotrophic bacteria.

38 oenzyme that converts methane to methanol in methanotrophic bacteria.

39 sed during thaw and subsequently consumed by methanotrophic bacteria.

40 suggesting that Cu-Mb uptake is specific to methanotrophic bacteria.

41 nd a residual microbial community containing methanotrophic bacteria.

42 oenzyme that oxidizes methane to methanol in methanotrophic bacteria.

43 lyze the oxidation of methane to methanol in methanotrophic bacteria.

44 rst step in the primary catabolic pathway of methanotrophic bacteria.

45 er, the first step of carbon assimilation in methanotrophic bacteria.

46 s are methane monooxygenases (MMOs) found in methanotrophic bacteria; however, these enzymes are not

47 s work opens the door to develop an array of methanotrophic bacterial strain-engineering strategies c

48 Delta(14)-sterol reductase (MaSR1) from the methanotrophic bacterium Methylomicrobium alcaliphilum 2

49 recent identification of a novel, tractable methanotrophic bacterium, Methylomicrobium buryatense, w

50 Here, we show that the linkage between methanotrophic carbon cycling and N2 fixation may consti

51 ents, and molecular diversity surveys reveal methanotrophic communities within protolithic nodules an

52 Using a methanotrophic enrichment culture incubated under differ

53 Here, we demonstrate that type II methanotrophic enrichments can mediate step two by coupl

54 MC09 is a mesophilic, halotolerant, aerobic, methanotrophic member of the Gammaproteobacteria, isolat

55 eir raw water and very high abundance of the methanotrophic Methylococcaceae.

56 n kinetics in soil infer the activity of two methanotrophic populations: one that is only active at h

57 o a lack of cultured representative deep-sea methanotrophic prokaryotes.

58 re detected in all of the methylotrophic and methanotrophic proteobacteria tested that assimilate for

59 an are likely to be met by a similarly rapid methanotrophic response.

60 This study provides new understanding of methanotrophic responses to methane starvation and recov