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1 ort the plant glucosides arbutin, fraxin and esculin.
2  nitrate or nitrite, or hydrolyze gelatin or esculin.
3 ept that it grows in 20% bile and hydrolyzes esculin.
4 y occurring fluorescent coumarin glucosides (esculin and fraxin) were phloem loaded and transported i
5                                              Esculin and oligochitosaccharides induced genes in one o
6 p IIc produced acid from sucrose, hydrolyzed esculin, and usually reduced nitrate.
7 to 2 days; were oxidase positive; hydrolyzed esculin; and grew on Campylobacter selective medium.
8                   Utilization of arbutin and esculin, aryl-beta-glucosides, was defective in some mut
9 th and compared it to direct plating on bile esculin azide (BEA) agar for the isolation of VRE from f
10             This medium was compared to bile esculin azide agar (BEAV) and was 98.2% sensitive and 99
11 HROMagar VanRE (CVRE) was compared with bile esculin azide agar plus vancomycin to screen for vancomy
12 ompared the performance of VRE-BMX with bile esculin azide agar supplemented with vancomycin (BEAV).
13       In this study, a commercial agar (bile esculin azide agar with 6 microg of vancomycin per ml [B
14 cus faecium, VRESelect, was compared to bile esculin azide agar with 6 mug/ml vancomycin (BEAV) for t
15 n sensitivity (range, 89.9 to 93.9%) to bile esculin azide agar with vancomycin (BEAV) agar (84.8%) f
16 ar (Remel, Lenexa, KS), 86% and 92% for bile esculin azide with vancomycin (BEAV; Remel), and 96.5% a
17  compared to culture consisting of both bile-esculin-azide agar with 6 mug/ml vancomycin (BEAV agar)
18  Compared to BBL Enterococcosel agar, a bile-esculin-azide-vancomycin (BEAV) agar, the initial overal
19 ), Spectra VRE (Remel, Lenexa, KS), and bile-esculin-azide-vancomycin (BEAV; Remel) agars were compar
20     In wild-type plants, the fluorescence of esculin decayed to background levels about 2 h after phl
21                                    Rutin and esculin have been polymerised by laccase.
22 illin resistance, zwittermicin A resistance, esculin hydrolysis, hemolysis, orange pigment production
23 ucrose, maltose, and 20 other carbohydrates, esculin hydrolysis, indole production, arginine dihydrol
24 five previously recommended tests (tests for esculin hydrolysis, production of acid from salicin, L-r
25 ansporter (HvSUT1), which does not transport esculin in oocytes, failed to load esculin into the phlo
26 transport esculin in oocytes, failed to load esculin into the phloem.
27                                         Bile esculin-positive colonies from the direct and broth subc
28 od also resulted in significantly fewer bile esculin-positive, non-VRE isolates requiring further wor
29 increased expression of specific CYPs, while esculin showed no effect.
30 5% positive), positive reaction for the bile esculin test (100%), growth at 45 degrees C (96%), varia
31 ty (> 99%) and specificity (97%) of the bile-esculin test can be obtained with a bile concentration o
32                                     The bile-esculin test is used to differentiate enterococci and gr
33 zed hippurate, and were variable in the bile-esculin test.
34  helicin, salicin, arbutin, maltose, fraxin, esculin, turanose, and alpha-methyl-d-glucose.
35  OsSUT1 was found to be sufficient to confer esculin uptake activity.
36 damine, a red fluorescent probe that, unlike esculin, was stable for several hours after phloem unloa
37 port the fluorescent coumarin beta-glucoside esculin when expressed in yeast.

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