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1 s the first rRNA operon to be sequenced from B. megaterium.
2 3PGA accumulation, as observed previously in B. megaterium.
3  glucose, glycerol, or acetate compared with B. megaterium and E. coli.
4 ter to be determined for the CbiXL from both B. megaterium and Synechocystis.
5 fied superdormant spores of Bacillus cereus, B. megaterium, and B. subtilis isolated after optimal he
6 he layer orders inferred for B. subtilis and B. megaterium are consistent with measurements in the li
7 constructed consisting of the E. coli or the B. megaterium beta subunit carrying the C-terminal 18% o
8 played the energy-coupling defect, while the B. megaterium beta subunit carrying the E. coli C-termin
9        The E. coli beta subunit carrying the B. megaterium C-terminal region displayed the energy-cou
10 enzyme was homologously produced in the host B. megaterium DSM319.
11 acis, the presence of anhydromuropeptides in B. megaterium germination exudates, which is indicative
12 rings early in spore germination, as did the B. megaterium homolog of the major B. subtilis chromosom
13                                     In vivo, B. megaterium inactivates AHLs by a CYP102A1 dependent m
14                                              B. megaterium is a commercially available, nonpathogenic
15                                              B. megaterium is able to synthesize vitamin B(12) throug
16 troduction of the gerU/gerVB gene cluster to B. megaterium KM extends the range of germinants recogni
17 idues and a highly conserved lysine onto the B. megaterium P46 crystal structure revealed a striking
18 elevating the pH of developing forespores of B. megaterium resulted in rapid utilization of the fores
19                                              B. megaterium sleB cwlJ double mutant strains complement
20 nce of either the N- or C-terminal domain of B. megaterium SleB is sufficient for initiation of corte
21                                              B. megaterium SleL appears to be associated with the epi
22 An in-frame fusion joining the 3' end of the B. megaterium spoIIE coding sequence to the 5' end of gf
23 ave exploited the physical dimensions of the B. megaterium sporangium, in conjunction with wide-field
24 ation, and these processes were increased in B. megaterium spores with a core pH of approximately 7.8
25 res and > or =20-fold lower in B. cereus and B. megaterium spores.
26 t complete genome sequences of two important B. megaterium strains, the plasmidless strain DSM319 and
27                                           In B. megaterium, the gvp region carries a cluster of 15 pu
28                        Whereas protection by B. megaterium was linked to impaired egg laying, corresp

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