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1 rine-isocitrate lyase pathway common to many methylotrophic anaerobes, in which formaldehyde produced
2 ates were S-layer-deficient, non-motile, non-methylotrophic and devoid of iron-oxidation despite the
3 ndent activities were detected in all of the methylotrophic and methanotrophic proteobacteria tested
5 endent enzyme activities in cell extracts of methylotrophic bacteria from 13 different genera are rep
8 the electron-transfer flavoprotein from the methylotrophic bacteria W3A1 (wETF) were used to advanta
9 sole carbon and energy source by specialised methylotrophic bacteria, isolated from a variety of envi
10 are also known in other plants, animals, and methylotrophic bacteria, suggesting an ancient evolution
11 nethiol oxidase (MTO), related to the MTO in methylotrophic bacteria, that converts methanethiol to H
20 lism of one- and two-carbon compounds by the methylotrophic bacterium Methylobacterium extorquens AM1
21 Previous complementation studies with the methylotrophic bacterium Methylobacterium extorquens hav
22 ically involved in methanol oxidation in the methylotrophic bacterium Methylobacterium extorquens hav
23 versatilis universalis FAM5 is a facultative methylotrophic bacterium that has been found in a variet
26 tion of the N-methylglutamate pathway in the methylotrophic beta-proteobacterium Methyloversatilis un
27 e methylotrophic bacteria, the first step in methylotrophic growth is the oxidation of methanol to fo
28 tely halophilic bacterium that is capable of methylotrophic growth on a range of one-carbon compounds
30 ating methylene H4F from formaldehyde during methylotrophic growth: one involving the reaction of for
31 over, unnatural amino acid expression in the methylotrophic host was systematically optimized by modu
34 icant overlap, confirming the commonality of methylotrophic metabolism downstream of the primary oxid
40 drABC appears to be specifically involved in methylotrophic methanogenesis, based on reduced growth a
43 rogenotrophic Methanomicrobiales, as well as methylotrophic Methanosarcinales, Methanococcales, Metha
50 thanogenesis rates of an hdrA1C1B1 mutant on methylotrophic substrates and downregulation of the gene
52 ntous fungus (Aspergillus nidulans) and in a methylotrophic yeast (Pichia pastoris), the latter expre
53 isolated from the gene-engineered strain of methylotrophic yeast Hansenula polymorpha and commercial
54 belled protein, efficiently expressed in the methylotrophic yeast Komagataella (Pichia) pastoris.
56 oli (Ec) and then refolded (EcCSP) or in the methylotrophic yeast Pichia pastoris (PpCSP) for structu
57 P3;1, we overexpressed this aquaporin in the methylotrophic yeast Pichia pastoris and purified the he
58 ductase (NR; EC 1.6.6.1) was produced in the methylotrophic yeast Pichia pastoris and purified to nea
60 uman liver cDNA library and expressed in the methylotrophic yeast Pichia pastoris at a secretion yiel
61 s of the methanol utilization pathway in the methylotrophic yeast Pichia pastoris by binding to Mxr1p
65 pression of an algal phytochrome cDNA in the methylotrophic yeast Pichia pastoris led to time-depende
66 as a model glycoprotein and expressed in the methylotrophic yeast Pichia pastoris to obtain a post-tr
67 venom were constructed and expressed in the methylotrophic yeast Pichia pastoris to probe for the pr
68 ing the cDNA in frame into the genome of the methylotrophic yeast Pichia pastoris under the control o
76 enzymes were expressed in Pichia pastoris, a methylotrophic yeast strain, and their kinetic parameter
79 ble alcohol oxidase I (AOXI) promoter of the methylotrophic yeast, Pichia pastoris, is used widely fo
80 at greater than gram per liter levels in the methylotrophic yeast, Pichia pastoris, using the methano
82 ytosolically expressed in Pichia pastoris, a methylotrophic yeast, using spinach (Spinacia oleracea)
83 toris (Pp) and Hansenula polymorpha (Hp) are methylotrophic yeasts commonly used for industrial purpo
85 Unlike the intronless alcohol oxidases from methylotrophic yeasts, a genomic fragment of the Hv-p68
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