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1 re 20-25 deg.C higher than the corresponding mesophile.
2 s of Bacteria, including microbes related to mesophiles.
3 egrees C, roughly the thermal death point of mesophiles.
4 arison with genes of other psychrophiles and mesophiles.
5 s of higher contact trace when compared with mesophiles.
6 rmophiles, and neither hyperthermophiles nor mesophiles.
7  thermophiles when compared to proteins from mesophiles.
8 ratures which rapidly denature proteins from mesophiles.
9             Here, we addressed this issue in mesophiles.
10 done on the mechanism of protein splicing in mesophiles.
11 ructure and of function in biomolecules from mesophiles.
12 andard motifs evident in all homologues from mesophiles.
13 ted deiodinases (IYDs) from humans and other mesophiles.
14 bial growth remained low at around 3-log for mesophiles, 4.5-log for yeasts and molds and 2-log for e
15 e thermophile Moorella thermoacetica and the mesophile Acetobacterium woodii, two acetogenic bacteria
16 approximately 29 known to occur in bacterial mesophiles and 24 to 31 known to occur in the archaeal h
17 s in A. cellulolyticus orthologs compared to mesophiles and inverse preferences for G and A at the fi
18 led to significantly lower counts of aerobic mesophiles and psychrotrophic bacteria in anchovy muscle
19 ain differences in properties of proteins in mesophiles and thermophiles, and the likely structural a
20                                Total aerobic mesophiles and total fungi counts were below 10(6) CFU/m
21 ive from the cold-loving psychrophiles, from mesophiles, and from thermophiles.
22 f helix-rich proteins found in thermophiles, mesophiles, and organisms that flourish near 0 degrees C
23      Although the growth temperatures of the mesophiles are about 50 degrees C below that of M. janna
24 he psychrophile Bacillus globisporus and the mesophile Bacillus subtilis have been solved and compare
25  silico mutants of adenylate kinase from the mesophile Bacillus subtilis were generated, and their mo
26  lysC aptamer's ligand-free structure in the mesophile Bacillus subtilis.
27 ch a study with our model protein HPr from a mesophile, Bacillus subtilis, and a thermophile, Bacillu
28     Alternatively, organisms that evolved as mesophiles but later recolonized a hot environment (Ther
29 uantitatively compare hyperthermophiles with mesophiles by the rRNA method.
30 ein fragments that cooperatively function in mesophiles can be aided by the use of thermophilic enzym
31 logous domain of the cellulase CenA from the mesophile Cellulomonas fimi.
32 thermophile Pyrococcus furiosus (Pf) and the mesophile Clostridium pasteurianum (Cp) are monitored vi
33 ermophile Pyrococcus furiosus (RdPf) and the mesophile Clostridium pasteurianum (RdCp) has been studi
34 his structure with its counterparts from the mesophiles Clostridium symbiosum and Escherichia coli ha
35 r and more sensitive to antimycin A than the mesophile control, Chlamydomonas raudensis SAG 49.72.
36  primary difference between CYP175A1 and its mesophile counterparts is the investment of charged resi
37 dihydrouridine, on average, than that of the mesophile E. coli or the psychrotroph L. bavaricus.
38 lar or lower microbial counts (total aerobic mesophiles, enterobacteriaceae, and yeasts/moulds) while
39 olding for two ribonucleases H, one from the mesophile Escherichia coli and one from the thermophile
40                             We show that the mesophile Escherichia coli and the extremophile Shewanel
41                   For CheA proteins from the mesophile Escherichia coli and the thermophile Thermotog
42 rs was compared for RNA polymerases from the mesophile Escherichia coli and the thermophile Thermus a
43 hilic bacterium Thermus thermophilus and the mesophile Escherichia coli demonstrate a dramatic and su
44 e-adapted bacterial species such as SS9, the mesophile Escherichia coli did not regulate its fatty ac
45                      RNA polymerase from the mesophile Escherichia coli exists in two forms, the core
46 the thermophile Thermus thermophilus and the mesophile Escherichia coli revealed that the thermostabi
47 ntal data (metabolomics and 13C-MFA) for the mesophile Escherichia coli.
48 opropylmalate dehydrogenase (IPMDH) from the mesophiles Escherichia coli and Salmonella typhimurium h
49 important for understanding the evolution of mesophiles from thermophiles.
50          In contrast, genetic studies of the mesophiles in the archaeal genus Methanococcus have beco
51      While dynamic modifications are rare in mesophiles, in extreme hyperthermophiles, ~50% of modifi
52 the hyperthermophile is obtained even if the mesophile is more stable at room temperature.
53           The calculations indicate that the mesophile is stabilized by the presence of salt while th
54 e structure and result in a return to a more mesophile-like DeltaC degrees (P).
55 binant (r) archaeal histones (rHFoB from the mesophile Methanobacterium formicicum, and rHMfA, rHMfB,
56 recombinant archaeal histone rHFoB, from the mesophile Methanobacterium formicicum, has been determin
57 rthermophile Methanothermus fervidus and the mesophile Methanobacterium formicicum, respectively, hav
58 ed for three archael histones: hFoB from the mesophile Methanobacterium formicicum; hMfB from the the
59         A closely related homologue from the mesophile Methanococcus maripaludis (Mma) is nearly iner
60 ted methanogenic members of the Archaea: the mesophile Methanococcus voltae (Mv), the thermophile M.
61 ted methanogenic members of the Archaea (the mesophile Methanococcus voltae (MVO), the thermopile Met
62 e Methanococcus thermolithotrophicus and the mesophile Methanococcus voltae have been solved to resol
63           Characterization of SepRS from the mesophile Methanosarcina mazei by gel filtration and non
64 ent of class II xylose isomerases (XIs) from mesophiles, moderate thermophiles, and hyperthermophiles
65 results observed for other psychrophiles and mesophiles, only clpB and hsp33 were upregulated at low
66           Vent samples have also yielded new mesophiles (optimal growth near 30 degreesC) that produc
67 ed with those of the citrate synthase from a mesophile, pig heart (PCS).
68         It is similar to values reported for mesophile proteins of comparable size, indicating that t
69 lues are similar to those observed for small mesophile proteins.
70 e native hyperthermophile protein from small mesophile proteins.
71 two features which differ significantly from mesophile proteins; (1) an unusually large proportion of
72 bacteriophage Pf1, both of which grow in the mesophile Pseudomonas aeruginosa.
73                           Lower increases in mesophile, psychrophile, Pseudomonas, Enterobacteriaceae
74                              Lower counts of mesophile, psychrophile, Pseudomonas, Enterobacteriaceae
75 three dominant strategies within the vibrio: mesophiles, psychrophiles and apparently generalist broa
76                               Success of the mesophile radiation is surprising given their highly red
77 ly adapted to cold temperatures stressful to mesophiles since little differential gene expression was
78                                           In mesophiles, single-stranded DNA binding proteins (SSBs)
79  III have focused mainly on the enzymes from mesophiles such as Escherichia coli.
80  to a greater extent in thermophiles than in mesophiles, suggesting that helical interaction based on
81 ermal optimum increases with temperature for mesophiles (temperature optima [Formula: see text]C), bu
82 arger than that of outer arm dynein from the mesophile Tetrahymena.
83 he loss in entropy upon folding is higher in mesophiles than in thermophiles.
84  previously reported for CPS from an enteric mesophile, the kinetic properties of the arginine-specif
85  to obtain recombinant proteins derived from mesophiles, the production of thermoacidophilic proteins
86 rved in all proteins, but in the case of the mesophile/thermophile comparison there is a directional
87 easing stability during the progression from mesophile to psychrophile, there is not a strict correla
88 iles use a mechanism similar to that used by mesophiles to deal with the large number of abasic sites
89 ferences in this measure of fluidity for the mesophile vs hyperthermophile protein interiors.
90 logenetic trees because they outcompeted the mesophiles when they adapted to lower temperatures, poss
91 pon folding is lower in thermophiles than in mesophiles, whereas the loss in entropy upon folding is
92 antly more favorable in thermophiles than in mesophiles, whereas the maximal stability temperature it
93 ty similar to that of histidine kinases from mesophiles, with maximum activity at 70 degreesC.