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5 s equilibrated to NADH and pyruvate (Pyr) by Leuconostoc mesenteroides D-lactate dehydrogenase (DLDH)
6 haromyces cerevisiae, Zymomonas mobilis, and Leuconostoc mesenteroides exploit, respectively, the Emb
8 (delta2) protons of His-240 from the 109 kDa Leuconostoc mesenteroides glucose 6-phosphate dehydrogen
9 ase, based on the structure of the bacterial Leuconostoc mesenteroides glucose-6-phosphate dehydrogen
10 ad of glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroides has been investigated by a str
11 dextransucrases) from oral streptococci and Leuconostoc mesenteroides has shown them to share a well
12 ysis of glucose-6-phosphate dehydrogenase of Leuconostoc mesenteroides have been investigated by site
14 enes, following Lc. lactis subsp. lactis and Leuconostoc mesenteroides subsp. cremoris (20%) whilst 2
15 sm of glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroides was investigated by replacing
16 lostridium perfringens, Oenococcus oeni, and Leuconostoc mesenteroides) and no eukaryotic genomes.
24 ly correlated with Lactobacillus/Pediococcus/Leuconostoc spp. (P = 0.001).GOS consumption by infants
25 p. (P = 0.008) and Lactobacillus/Pediococcus/Leuconostoc spp. (P = 0.018); Lactobacillus/Pediococcus/
26 spp. (P = 0.018); Lactobacillus/Pediococcus/Leuconostoc spp. decreased in the Fe group (P = 0.013),
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