戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (1語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
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
7                               This synthetic methylotroph alleviated a so far uncharacterized hurdle,
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
11           The MEDS domain is present in both methylotrophs and complex methanogens, and both the MEDS
12          Viruses infecting nonmethanotrophic methylotrophs and heterotrophic predatory bacteria were
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
15 success of mutualistic relationships between methylotrophs and plants.
16    Recent studies of acetate assimilation in methylotrophs and purple phototrophs have revealed remar
17 ay that converts acetyl-CoA to glyoxylate in methylotrophs and Streptomyces spp.
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
21          Methylibium petroleiphilum PM1 is a methylotroph distinguished by its ability to completely
22 distribution is highly complex in this model methylotroph during growth on acetate and is fundamental
23             We also review new directions in methylotroph ecology that improve our understanding of t
24 dies and provides increased understanding of methylotroph ecophysiology.
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
27                                              Methylotrophs grow on reduced single-carbon compounds li
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
31                                              Methylotrophs mainly occurred attached to sediment parti
32                              In serine cycle methylotrophs, methylene tetrahydrofolate (H4F) is the e
33 tigated the lanthanome in the obligate model methylotroph Methylobacillus flagellatus.
34  has been characterized from the facultative methylotroph Methylobacterium extorquens AM1 and shown t
35                             The serine cycle methylotroph Methylobacterium extorquens AM1 contains tw
36                                          The methylotroph Methylobacterium extorquens AM1 oxidizes me
37                              The facultative methylotroph Methylobacterium extorquens AM1 possesses 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
41 h parameters was assessed in the facultative methylotroph Methylobacterium extorquens AM1.
42 haracterized in the serine cycle facultative methylotroph Methylobacterium extorquens AM1.
43 n a chromosomal fragment of the serine cycle methylotroph Methylobacterium extorquens AM1.
44 to the previously sequenced genomes of three methylotrophs, Methylobacterium extorquens (an alphaprot
45 se (DL-FalDH) was isolated from the obligate methylotroph Methylococcus capsulatus Bath.
46 Cytochrome c' was isolated from the obligate methylotroph Methylococcus capsulatus Bath.
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
49                            Various groups of methylotrophs, microorganisms that can grow on one-carbo
50                                         Many methylotrophs-microorganisms that grow on reduced single
51 tion in terms of discovery of novel types of methylotrophs, novel modes of methylotrophy, and novel m
52                                 Methano- and methylotrophs of the bacterial families Methylomonadacea
53 d a transfer of carbon to methanol-oxidizing methylotrophs of the betaproteobacterial family Methylop
54                                              Methylotrophs persisted for weeks in the absence of meth
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
62 pathway, found in both methylotrophs and non-methylotrophs, to metabolize methylamine.
63        Abundances of methanotrophs and other methylotrophs were roughly similar across all samples, p
64                  In several newly discovered methylotrophs, XoxF is the active methanol dehydrogenase