ライフサイエンスコーパス: Micrococcus luteus

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1 nonpathogenic bacteria (Escherichia coli and Micrococcus luteus).

2 d yeast and interacts with peptidoglycan and Micrococcus luteus.

3 , H2B, and H4, for growth inhibition against Micrococcus luteus.

4 a means to distinguish Escherichia coli from Micrococcus luteus.

5 ium tuberculosis, Neisseria gonorrhoeae, and Micrococcus luteus.

6 d prophenoloxidase activation in response to Micrococcus luteus.

7 y from hemolymph activated by treatment with Micrococcus luteus.

8 the resuscitation-promoting factor (Rpf) of Micrococcus luteus.

9 enic and highly lysozyme-sensitive bacterium Micrococcus luteus.

10 s whose predicted products resemble Rpf from Micrococcus luteus.

11 the most common erroneous identification was Micrococcus luteus.

12 studies using gram-positive model bacterium Micrococcus luteus.

13 Four genomic DNAs of differing GC content (Micrococcus luteus, 72% GC; Escherichia coli, 50% GC; ca

14 Micrococcus luteus , a Gram-positive bacterium, is incap

15 Transcription termination factor Rho from Micrococcus luteus, a high G + C Gram-positive bacterium

16 The growth of Micrococcus luteus, a soil microorganism that belongs to

17 al activity of dendrigraft poly-L-lysines on Micrococcus luteus and Erwinia carotovora.

18 After the intraperitoneal injection of Micrococcus luteus and Escherichia coli, the peptide was

19 opin A gene was induced by the G(+) bacteria Micrococcus luteus and Staphylococcus aureus, but not by

20 Escherichia coli, Staphylococcus aureus, and Micrococcus luteus and the yeast, Candida albicans.

21 , Escherichia coli, Lactobacillus plantarum, Micrococcus luteus, and Staphylococcus aureus support th

22 as purified from the Gram-positive bacterium Micrococcus luteus, and the complete gene sequence was d

23 ssessed by qualitative agar plate test using Micrococcus luteus as substrate showing that both the un

24 y against Bacillus subtilis (but not against Micrococcus luteus), as well as against the parental and

25 te inhibited the growth of Escherichia coli, Micrococcus luteus, Bacillus subtilis, and Klebsiella pn

26 Staphylococcus epidermidis, Micrococcus luteus, Brevibacterium linens, Pseudomonas f

27 exhibit biphasic kinetics in the clearing of Micrococcus luteus cell suspensions, suggesting preferen

28 the biosynthesis of the teichuronic acid of Micrococcus luteus cell walls.

29 the D52A and D52A/N46A ChEWL complexes with Micrococcus luteus cells are 3- and 4-fold higher, respe

30 nging from 45% identity for the homolog from Micrococcus luteus (FtsZ[Ml]) to 91% identity for the ho

31 The best ligand was Micrococcus luteus lipomannan, followed by Enterococcus

32 lf thymus, salmon testes, and the bacterium, micrococcus luteus (lysodeikticus) containing different

33 Micrococcus luteus (NCTC2665, "Fleming strain") has one

34 Micrococcus luteus secretes a small protein called Rpf,

35 In contrast, against Micrococcus luteus the TA(-) mutant exhibited no defect

36 Rpf from Micrococcus luteus, the founder member of this protein f

37 In contrast to Uvr(A)BC, the Micrococcus luteus UV endonuclease efficiently incises u

38 uence similarity to the Escherichia coli and Micrococcus luteus UvrA proteins involved in excision re

39 of resuscitation-promoting factor (Rpf) from Micrococcus luteus, which is an extremely potent anti-do

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