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1 acterioplankton, suggested it is an obligate methylotroph.
2 on: a methanotroph and two nonmethanotrophic methylotrophs.
3 enase, is found in all known proteobacterial methylotrophs.
4 and obligately or facultatively autotrophic methylotrophs.
5 ium extorquens AM1, the best-studied aerobic methylotroph, a periplasmic methylamine dehydrogenase th
6 m extorquens AM1, a serine cycle facultative methylotroph, accumulates poly-beta-hydroxybutyrate (PHB
8 he metabolic versatility of this facultative methylotroph and is a model for other metabolic networks
9 ial community and that type I methanotrophs, methylotrophs and actinomycetes are important organisms
10 boreal lakes, and that EET, particularly by methylotrophs and anoxygenic phototrophs, should be furt
13 ied as being related to a wide range of both methylotrophs and non-methylotrophs from Alphaproteobact
14 -glutamyl-methylamide pathway, found in both methylotrophs and non-methylotrophs, to metabolize methy
16 Recent studies of acetate assimilation in methylotrophs and purple phototrophs have revealed remar
18 date, MYFR has not been identified in other methylotrophs, and it is unknown whether its structural
19 netic similarities recently reported between methylotrophs, and methanogens with respect to their pat
20 ylobacterium extorquens AM1 is a facultative methylotroph capable of growth on both single-carbon and
22 distribution is highly complex in this model methylotroph during growth on acetate and is fundamental
25 to formaldehyde were speculated to exist in methylotrophs for decades but had never been discovered.
26 o a wide range of both methylotrophs and non-methylotrophs from Alphaproteobacteria, Betaproteobacter
28 xploration of the response to lanthanides in methylotrophs has revealed that the lanthanome is not co
29 re we show that yeasts in a third clade, the methylotrophs, have a simpler two-locus switching system
30 of growing at a rate comparable with natural methylotrophs in a wide range of methanol concentrations
34 has been characterized from the facultative methylotroph Methylobacterium extorquens AM1 and shown t
38 novel methylotrophy genes of the facultative methylotroph Methylobacterium extorquens AM1 were identi
39 ate dehydrogenase systems in the facultative methylotroph Methylobacterium extorquens AM1 whose expre
40 e analyzed the metabolism of the facultative methylotroph Methylobacterium extorquens AM1, which lack
44 to the previously sequenced genomes of three methylotrophs, Methylobacterium extorquens (an alphaprot
47 chemically characterized MYFR from the model methylotroph Methylorubrum extorquens and identified an
48 tracting a nearly complete genome of a novel methylotroph, Methylotenera mobilis, reconstructing its
51 tion in terms of discovery of novel types of methylotrophs, novel modes of methylotrophy, and novel m
53 d a transfer of carbon to methanol-oxidizing methylotrophs of the betaproteobacterial family Methylop
55 nly methanotrophs but also nonmethanotrophic methylotrophs play a significant role in global carbon c
56 ical fractionation with whole cells of three methylotrophs (strain IMB-1, strain CC495, and strain MB
57 omics to characterize an uncultivated marine methylotroph that actively incorporated carbon from (13)
58 a non-methylotrophic organism to a synthetic methylotroph that grows to a high cell density has been
59 egeneracy as it is beneficial to facultative methylotrophs that have to switch between using methylam
60 ribulose monophosphate (RuMP) cycle used by methylotrophs to assimilate methanol differs from the ty
61 eration cycle (GRC) operates in serine cycle methylotrophs to effect the net conversion of acetyl coe