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1 moproteota are predicted or were shown to be methylotrophic.
2 ing isotopic signatures of hydrogenotrophic, methylotrophic, acetoclastic, and methoxydotrophic metha
3 ences in (13)CH(3)D compositions between the methylotrophic, acetoclastic, and methoxydotrophic pathw
4 rine-isocitrate lyase pathway common to many methylotrophic anaerobes, in which formaldehyde produced
5 ates were S-layer-deficient, non-motile, non-methylotrophic and devoid of iron-oxidation despite the
6 thanol and may exhibit adaptability in using methylotrophic and hydrogenotrophic pathways based on te
7 ndent activities were detected in all of the methylotrophic and methanotrophic proteobacteria tested
8                 Pink-pigmented facultatively methylotrophic bacteria (PPFMs), classified as Methyloba
9  in vivo and in vitro results establish that methylotrophic bacteria can utilize actinides instead of
10 endent enzyme activities in cell extracts of methylotrophic bacteria from 13 different genera are rep
11                                              Methylotrophic bacteria have evolved pathways for lantha
12                            Most serine cycle methylotrophic bacteria lack isocitrate lyase and conver
13                                              Methylotrophic bacteria such as Methylorubrum extorquens
14  the electron-transfer flavoprotein from the methylotrophic bacteria W3A1 (wETF) in solution.
15  the electron-transfer flavoprotein from the methylotrophic bacteria W3A1 (wETF) were used to advanta
16          Thirty-nine distinct populations of methylotrophic bacteria were observed.
17  key roles in the central metabolism of many methylotrophic bacteria, acting as redox-active cofactor
18  spiders farm and feed on methanotrophic and methylotrophic bacteria, expanding the realm of animals
19               LanM is produced abundantly by methylotrophic bacteria, including Methylorubrum extorqu
20 sole carbon and energy source by specialised methylotrophic bacteria, isolated from a variety of envi
21 are also known in other plants, animals, and methylotrophic bacteria, suggesting an ancient evolution
22 nethiol oxidase (MTO), related to the MTO in methylotrophic bacteria, that converts methanethiol to H
23                             In Gram-negative methylotrophic bacteria, the first step in methylotrophi
24 contained homologs of genes present in known methylotrophic bacteria.
25 -have biological relevance in the context of methylotrophic bacteria.
26 d technology as well as in the metabolism of methylotrophic bacteria.
27 al for the oxidation of formaldehyde in most methylotrophic bacteria.
28 ethanopterin, a C1 transfer coenzyme used by methylotrophic bacteria.
29 vide a comprehensive review of metabolism of methylotrophic bacteria.
30 n methanol dehydrogenase in the periplasm of methylotrophic bacteria.
31 -ribulose 5-phosphate in formaldehyde-fixing methylotrophic bacteria.
32 on has not yet been experimentally tested in methylotrophic bacteria.
33 genic archaea, sulfate-reducing archaea, and methylotrophic bacteria.
34 occurs during oxidation of methyl halides by methylotrophic bacteria.
35 hic alpha-proteobacteria or in gram-positive methylotrophic bacteria.
36                               The mesophilic methylotrophic bacterium Methylobacterium extorquens AM1
37  for normal levels of Ln accumulation in the methylotrophic bacterium Methylobacterium extorquens AM1
38 lism of one- and two-carbon compounds by the methylotrophic bacterium Methylobacterium extorquens AM1
39    Previous complementation studies with the methylotrophic bacterium Methylobacterium extorquens hav
40 ically involved in methanol oxidation in the methylotrophic bacterium Methylobacterium extorquens hav
41         Here, using XoxF1 MDH from the model methylotrophic bacterium Methylorubrum extorquens AM1, w
42 versatilis universalis FAM5 is a facultative methylotrophic bacterium that has been found in a variet
43                                   An aerobic methylotrophic bacterium, Methylobacterium extorquens AM
44 ts to control acetyl-CoA flux to PHB in this methylotrophic bacterium.
45 tion of the N-methylglutamate pathway in the methylotrophic beta-proteobacterium Methyloversatilis un
46                                          The methylotrophic capabilities of Methylobacterium/Methylor
47 MttB superfamily member; MthC, homologous to methylotrophic cobalamin-binding proteins; MthA, homolog
48 was further supported by the presence of the methylotrophic genus Methanococcoides.
49 e methylotrophic bacteria, the first step in methylotrophic growth is the oxidation of methanol to fo
50 tely halophilic bacterium that is capable of methylotrophic growth on a range of one-carbon compounds
51 e activating enzyme (Fae) is required for Ln methylotrophic growth, demonstrating that XoxF1-mediated
52 genome of Methylobacillus flagellatus during methylotrophic growth.
53 ating methylene H4F from formaldehyde during methylotrophic growth: one involving the reaction of for
54 over, unnatural amino acid expression in the methylotrophic host was systematically optimized by modu
55               We sequenced the genomes of 19 methylotrophic isolates from Lake Washington, which belo
56 is universalis FAM5(T), the first cultivable methylotrophic member of the order.
57 icant overlap, confirming the commonality of methylotrophic metabolism downstream of the primary oxid
58 t formaldehyde, is the main branch point for methylotrophic metabolism in M. extorquens AM1.
59  serine cycle for carbon assimilation during methylotrophic metabolism.
60 ignificant role in biomass production during methylotrophic metabolism.
61 n is the main source of methylene H4F during methylotrophic metabolism.
62  produced (up to 24.9 +/- 0.3%) by a typical methylotrophic methanogen-Methanococcoides methylutens T
63 identified the erosion of genes required for methylotrophic methanogenesis along with horizontal acqu
64 hat mineral-OC interactions strongly control methylotrophic methanogenesis and potentially cryptic me
65 of corrinoid binding by proteins involved in methylotrophic methanogenesis are discussed.
66 bserved over sediment depth, indicating that methylotrophic methanogenesis could potentially fuel AOM
67                                          The methylotrophic methanogenesis found in the non-Euryarcha
68 se gas but the microbial diversity mediating methylotrophic methanogenesis is not well-characterized.
69     Our analysis raises the possibility that methylotrophic methanogenesis may have evolved from a me
70 ydrogenotrophic methanogenesis, suggest that methylotrophic methanogenesis might be a later adaptatio
71  how the transition from hydrogenotrophic to methylotrophic methanogenesis might have occurred.
72               Here, we present evidence that methylotrophic methanogenesis was the ancestral form of
73 tes from methylated compounds indicated that methylotrophic methanogenesis was the dominant methanoge
74 drABC appears to be specifically involved in methylotrophic methanogenesis, based on reduced growth a
75 t also displays the functional potential for methylotrophic methanogenesis, highlighting the importan
76 companied by a shift toward acetoclastic and methylotrophic methanogenesis.
77 ly correlated with the presence of genes for methylotrophic methanogenesis.
78 n/reduction pathway for hydrogenotrophic and methylotrophic methanogenesis.
79  These results provide new insights into the methylotrophic methanogenic pathway, confirming that met
80 rogenotrophic Methanomicrobiales, as well as methylotrophic Methanosarcinales, Methanococcales, Metha
81  of the first rare earth-dependent enzyme in methylotrophic Methylobacterium extorquens AM1 prompted
82 nzymes suggests evolutionary continuity from methylotrophic microbes to land plants, supporting micro
83                                          Non-methylotrophic microorganisms may also utilize methylami
84 ng an interaction between methanotrophic and methylotrophic microorganisms that allowed for rapid met
85 abolism by only three enzymes, turning a non-methylotrophic organism to a synthetic methylotroph that
86 ofactors in specific dehydrogenases found in methylotrophic organisms.
87 emperature-sensitive , with a preference for methylotrophic over hydrogenotrophic pathways when incub
88               The entry of methanol into the methylotrophic pathway of methanogenesis is mediated by
89  conditions are not limited to the classical methylotrophic pathway.
90 icrobes is limited, especially regarding the methylotrophic pathway.
91 rophic pathways for carbon assimilation, and methylotrophic pathways for energy conversion demonstrat
92                                          The methylotrophic Pichia angusta VKM Y-2559 and the oleagin
93 methanol dehydrogenase that is widespread in methylotrophic Proteobacteria.
94                                          The methylotrophic proteobacterium Methylobacterium extorque
95  predictions for this class, we cultivated a methylotrophic species, Candidatus Methanonezhaarchaeum
96 e of methanol concentrations, this synthetic methylotrophic strain illustrates genome editing and evo
97 thanogenesis rates of an hdrA1C1B1 mutant on methylotrophic substrates and downregulation of the gene
98 this strain was transitioning from growth on methylotrophic substrates to growth on acetate.
99 quens PA1 and is found almost exclusively in methylotrophic taxa.
100  characterization of the Rif1 homologue from methylotrophic thermotolerant budding yeast Hansenula po
101 ntous fungus (Aspergillus nidulans) and in a methylotrophic yeast (Pichia pastoris), the latter expre
102  isolated from the gene-engineered strain of methylotrophic yeast Hansenula polymorpha and commercial
103 belled protein, efficiently expressed in the methylotrophic yeast Komagataella (Pichia) pastoris.
104 xr1 (methanol expression regulator 1) of the methylotrophic yeast Komagataella phaffii (formerly Pich
105                                       In the methylotrophic yeast Komagataella phaffii, we identified
106 wo SREBP homologs, Hms1-1 and Hms1-2, in the methylotrophic yeast Komagataella phaffii.
107 revisiae (catT) have been co-produced in the methylotrophic yeast Pichia pastoris (Pp).
108 oli (Ec) and then refolded (EcCSP) or in the methylotrophic yeast Pichia pastoris (PpCSP) for structu
109 P3;1, we overexpressed this aquaporin in the methylotrophic yeast Pichia pastoris and purified the he
110 ductase (NR; EC 1.6.6.1) was produced in the methylotrophic yeast Pichia pastoris and purified to nea
111                                  We used the methylotrophic yeast Pichia pastoris as an expression ho
112 uman liver cDNA library and expressed in the methylotrophic yeast Pichia pastoris at a secretion yiel
113 s of the methanol utilization pathway in the methylotrophic yeast Pichia pastoris by binding to Mxr1p
114         Unlike Saccharomyces cerevisiae, the methylotrophic yeast Pichia pastoris can assimilate amin
115                                          The methylotrophic yeast Pichia pastoris is a popular host f
116                       The pas2 mutant of the methylotrophic yeast Pichia pastoris is characterized by
117 pression of an algal phytochrome cDNA in the methylotrophic yeast Pichia pastoris led to time-depende
118 as a model glycoprotein and expressed in the methylotrophic yeast Pichia pastoris to obtain a post-tr
119  venom were constructed and expressed in the methylotrophic yeast Pichia pastoris to probe for the pr
120 ing the cDNA in frame into the genome of the methylotrophic yeast Pichia pastoris under the control o
121 cids, a recombinant expression system in the methylotrophic yeast Pichia pastoris was developed.
122                                      For the methylotrophic yeast Pichia pastoris, a model organism t
123 e essential for peroxisome biogenesis in the methylotrophic yeast Pichia pastoris.
124 oduction of the catalytic domain of CA IX in methylotrophic yeast Pichia pastoris.
125 1) and the sunflower albumin 8 (SFA8) in the methylotrophic yeast Pichia pastoris.
126 ynthetic genes-ARG4, ADE1, and URA3-from the methylotrophic yeast Pichia pastoris.
127 me-biogenesis-defective (pex) mutants of the methylotrophic yeast Pichia pastoris.
128 ned and was expressed in and secreted by the methylotrophic yeast Pichia pastoris.
129 enzymes were expressed in Pichia pastoris, a methylotrophic yeast strain, and their kinetic parameter
130                         Pichia pastoris is a methylotrophic yeast that has been genetically engineere
131                                          The methylotrophic yeast, Pichia pastoris, has been genetica
132 ble alcohol oxidase I (AOXI) promoter of the methylotrophic yeast, Pichia pastoris, is used widely fo
133 at greater than gram per liter levels in the methylotrophic yeast, Pichia pastoris, using the methano
134 ation and peroxisome biogenesis genes in the methylotrophic yeast, Pichia pastoris.
135 ytosolically expressed in Pichia pastoris, a methylotrophic yeast, using spinach (Spinacia oleracea)
136 peroxisomes metabolize fatty acids (FA), and methylotrophic yeasts also metabolize methanol.
137 toris (Pp) and Hansenula polymorpha (Hp) are methylotrophic yeasts commonly used for industrial purpo
138                                          The methylotrophic yeasts Hansenula polymorpha and Pichia pa
139  Unlike the intronless alcohol oxidases from methylotrophic yeasts, a genomic fragment of the Hv-p68
140                                           In methylotrophic yeasts, glutathione-dependent formaldehyd
141 tity (>67%) with the alcohol oxidases of the methylotrophic yeasts.

 
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