ライフサイエンスコーパス: Escherichia coli K12

1 I-E CRISPR/Cas system of the model bacterium Escherichia coli K12.

2 (the Rut pathway) was recently discovered in Escherichia coli K12.

3 y running it over 2390 promoter sequences of Escherichia coli K12.

4 and transcriptional control of metabolism in Escherichia coli K12.

5 on, we identified recently formed operons in Escherichia coli K12.

6 e biology of the prototypical model organism Escherichia coli K12.

7 rovar Typhi (S. typhi), and 29% missing from Escherichia coli K12.

8 y against Listeria monocytogenes Scott A and Escherichia coli K12.

9 approximately 4.5% of Yersinia pestis, 5% of Escherichia coli K12, 6% of Archaeoglobus fulgidus, 8% o

10 Using Escherichia coli K12 and Bacillus subtilis, linkage pred

11 For Escherichia coli K12 and Bacillus subtilis, our method i

12 he CE column for separation and detection of Escherichia coli K12 and E. coli O157 targets.

13 arly, we examined a wild-type (WT) strain of Escherichia coli K12 and mutant strains with lesions aff

14 from a well-characterized list of operons in Escherichia coli K12 and perform comparative analysis of

15 ing the preponderance of LRCs in the GRNs of Escherichia coli K12 and several other organisms, we fin

16 PS to characterize the chemical stability of Escherichia coli K12 antibodies on the surfaces of diamo

17 d biosensor that can reliably detect a model Escherichia coli K12 bacterium using EIS, positioning th

18 s can escape type I-E CRISPR-Cas immunity in Escherichia coli K12 by making point mutations in the se

19 -A+/+ mice increased the permeability of the Escherichia coli K12 cell membrane to a greater extent t

20 yte cells and of the gyr B gene in bacterial Escherichia coli K12 cells establishes that SCGA will al

21 me-scale study of HU- and IHF binding to the Escherichia coli K12 chromosome using ChIP-seq.

22 Periodicity was quantified in 4289 Escherichia coli K12 confirmed and putative protein sequ

23 particular, we predicted 158 uber-operons in Escherichia coli K12 covering 1830 genes, and found that

24 Induction of antibacterial activity against Escherichia coli K12 D31 was 7.5 times greater in pupal

25 ular mass with bactericidal activity against Escherichia coli K12 D31.

26 mulated reads from real genomes and a PacBio Escherichia coli K12 dataset demonstrate that Not-So-Gre

27 The basolateral addition of LPS (ultrapure Escherichia coli K12) decreased HCO(3)(-) absorption in

28 -SIGN) specifically binds to the core LPS of Escherichia coli K12 (E. coli), promoting bacterial adhe

29 Campylobacter jejuni, Enterococcus faecalis, Escherichia coli K12, E. coli O157:H7, Salmonella enteri

30 The comparison results on Escherichia coli K12 genome and the human genome show th

31 Our dream of determining the entire Escherichia coli K12 genome sequence has been realized.

32 of almost all SlyA-activated genes from the Escherichia coli K12 genome suggests that the functional

33 to 94% of known cis-regulatory motifs in the Escherichia coli K12 genome, while achieving high predic

34 s and then applied to the well-characterized Escherichia coli K12 genome.

35 ization (SIDD) in a complete chromosome, the Escherichia coli K12 genome.

36 our prediction, we have tested the method on Escherichia coli K12, in which operon structures have be

37 Strains of Escherichia coli K12, including MG-1655, accumulate meth

38 Two-thirds of the lipid A in wild-type Escherichia coli K12 is a hexa-acylated disaccharide of

39 The CspE protein from Escherichia coli K12 is a single-stranded nucleic acid-b

40 teria tested, including both Gram-negatives (Escherichia coli K12, K1 and Salmonella typhimurium) and

41 1, and a nonmotile (with paralyzed flagella) Escherichia coli K12 MG1655 DeltamotA that is incapable

42 ity were selected, including a highly motile Escherichia coli K12 MG1655, an environmental strain Sph

43 rophage is one of the 10 prophage regions in Escherichia coli K12 MG1655.

44 mutations conferring rifampin resistance in Escherichia coli K12 (MG1655) and explores the nature of

45 s, phagocytosed PLA-expressing Y. pestis and Escherichia coli K12 more efficiently than PLA-negative

46 ated products of each of the 4,290 predicted Escherichia coli K12 open reading frames (ORFs) to measu

47 Here, the percent cell viability loss of Escherichia coli K12 resulting from the interaction with

48 ans, Bacillus globigii, and three strains of Escherichia coli (K12, SM10, ATCC 25922).

49 Escherichia coli K12 solutions (10(1)-10(8) CFU/mL) were

50 d us to purify 4,256 proteins encoded by the Escherichia coli K12 strain within 10 h.

51 are encoded in both the 16S and 23S rRNAs of Escherichia coli K12; that nucleotide sequences that cou

52 encing of bisulfite-treated genomic DNA from Escherichia coli K12 to describe, for the first time, th

53 pplied to gene expression data obtained from Escherichia coli K12 undergoing a carbon source transiti

54 igned and constructed a synthetic circuit in Escherichia coli K12, using glycolytic flux to generate

55 rB), lpxM(msbB), and lpxP, were generated in Escherichia coli K12 W3110.

56 inding periplasmic binding protein (LivK) of Escherichia coli K12 was flanked with CFP (cyan fluoresc

57 The pulmonary clearance of Escherichia coli K12 was reduced in SP-A-null mice and w

58 By applying this method to Escherichia coli K12, we have predicted 185 functional m

59 of colonic epithelial cells challenged with Escherichia coli K12, we showed that inhibition of histo

60 odalis glossinidius, whereas infections with Escherichia coli K12 were lethal.

61 if to an F(+), alpha-complementing strain of Escherichia coli K12, which expresses the omega-domain o