ライフサイエンスコーパス: Leuconostoc

1 ith the divergence away from the neighboring Leuconostoc branch.

2 ained by hydrolysis of Weissella confusa and Leuconostoc citreum dextrans.

3 Focusing on the alternansucrase (ASR) from Leuconostoc citreum NRRL B-1355, a well-known glucansucr

4 Lactococcus piscium, Lactococcus plantarum, Leuconostoc citreum, Leuconostoc gelidum, Zymomonas mobi

5 Leuconostoc citreumNRRL B-742 has been known for years t

6 aphylococcus, Lactobacillus, Lactococcus and Leuconostoc do not have P450s, with the exception of a h

7 Lactococcus plantarum, Leuconostoc citreum, Leuconostoc gelidum, Zymomonas mobilis and Saccharomyces

8 worse overall survival were associated with Leuconostoc inhae, Streptococcus salivarius, Collinsella

9 f 6,081.44 Da, and is produced by the strain Leuconostoc lactis APC 3969.

10 tococcus lactis subsp. lactis and 25% CFS of Leuconostoc lactis. subsp. cremoris.

11 llus composti, Lacticaseibacillus paracasei, Leuconostoc mesenteroides and Weissella confusa.

12 s equilibrated to NADH and pyruvate (Pyr) by Leuconostoc mesenteroides D-lactate dehydrogenase (DLDH)

13 haromyces cerevisiae, Zymomonas mobilis, and Leuconostoc mesenteroides exploit, respectively, the Emb

14 Leuconostoc mesenteroides G6PDH-mediated oxidation and L

15 (delta2) protons of His-240 from the 109 kDa Leuconostoc mesenteroides glucose 6-phosphate dehydrogen

16 ase, based on the structure of the bacterial Leuconostoc mesenteroides glucose-6-phosphate dehydrogen

17 ad of glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroides has been investigated by a str

18 dextransucrases) from oral streptococci and Leuconostoc mesenteroides has shown them to share a well

19 ysis of glucose-6-phosphate dehydrogenase of Leuconostoc mesenteroides have been investigated by site

20 of the bifunctional glucansucrase DSR-E from Leuconostoc mesenteroides NRRL B-1299.

21 d Lactobacillus plantarum were dominant, but Leuconostoc mesenteroides subsp.

22 enes, following Lc. lactis subsp. lactis and Leuconostoc mesenteroides subsp. cremoris (20%) whilst 2

23 d Lactobacillus plantarum were dominant, but Leuconostoc mesenteroides subsp. jonggajibkimchii, Lacto

24 sm of glucose 6-phosphate dehydrogenase from Leuconostoc mesenteroides was investigated by replacing

25 e (GS40) was identified within the genome of Leuconostoc mesenteroides YTU 40 that was further cloned

26 lostridium perfringens, Oenococcus oeni, and Leuconostoc mesenteroides) and no eukaryotic genomes.

27 c acid bacteria (Enteroccocus gallinarum and Leuconostoc mesenteroides).

28 cilli, certain strains of Weissella cibaria, Leuconostoc mesenteroides, and Enterococcus faecalis eme

29 The Gram-positive bacterium Leuconostoc mesenteroides, ATCC 8293, is intrinsically r

30 Staphylococcus aureus, Leuconostoc mesenteroides, Bacillus cereus and Enterococ

31 erococcus faecium-LR9 and to compare it with Leuconostoc mesenteroides-18C6 and enzymatic hydrolysis

32 eighboring taxa, Pediococcus pentosaceus and Leuconostoc mesenteroides.

33 m utilizing a mesophilic G6PDH (mG6PDH) from Leuconostoc mesenteroides.

34 atural substrates for G6P dehydrogenase from Leuconostoc mesenteroides.

35 ree-dimensional structure of the enzyme from Leuconostoc mesenteroides.

36 properties of a novel EPS (named EPS_O) from Leuconostoc mesenteroides.

37 flammation (HAM56+ cells), and Lactobacillus/Leuconostoc/Pediococcus numbers in fecal samples.

38 nsis, Companilactobacillus alimentarius, and Leuconostoc pseudomesenteroides were assayed as sourdoug

39 (Acinetobacter, Lactobacillus, Lactococcus, Leuconostoc, Saccharomyces and Zymomonas) and 10 species

40 ly correlated with Lactobacillus/Pediococcus/Leuconostoc spp. (P = 0.001).GOS consumption by infants

41 p. (P = 0.008) and Lactobacillus/Pediococcus/Leuconostoc spp. (P = 0.018); Lactobacillus/Pediococcus/

42 bulgaricus 1932, Leuconostoc spp. 4454, and Lacticaseibacillus casei 4339

43 spp. (P = 0.018); Lactobacillus/Pediococcus/Leuconostoc spp. decreased in the Fe group (P = 0.013),

44 Weisella, Leuconostoc, Staphylococcus, Streptococcus, and Lactococ

45 nt with higher abundance of Bifidobacterium, Leuconostoc, Stenotrophomonas, and Staphylococcus, which

46 HoPS from different species of Weisella and Leuconostoc were identified as thermally stable dextrans

47 icrobial counts (Lactobacillus, Lactococcus, Leuconostoc, yeast), antagonistic activity against foodb