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1  OmpR; the second contained mipA, encoding a murein hydrolase.
2 A and SarA both being negative regulators of murein hydrolases.
3 ation, and purified SspA cleaves Atl-derived murein hydrolases.
4 glycan amidases via its interaction with the murein hydrolase activator, EnvC.
5     Zymographic and quantitative analyses of murein hydrolase activity also revealed that disruption
6 nd lrgAB operons have been shown to regulate murein hydrolase activity and affect antibiotic toleranc
7 ous operons that have been shown to regulate murein hydrolase activity and affect sensitivity to peni
8                      The cid operon enhances murein hydrolase activity and antibiotic sensitivity, wh
9                The cid gene products enhance murein hydrolase activity and antibiotic tolerance where
10 d demonstrate that these operons, as well as murein hydrolase activity and antibiotic tolerance, are
11 operons have previously been shown to affect murein hydrolase activity and antibiotic tolerance.
12 ytSR two-component regulatory system affects murein hydrolase activity and autolysis.
13              Due to the growing link between murein hydrolase activity and biofilm maturation, autoly
14 hown to play a key role in the regulation of murein hydrolase activity and cell death in a manner tho
15 e wild-type gene restored expression of this murein hydrolase activity and cell separation levels to
16  of the B. anthracis cid and lrg homologues, murein hydrolase activity and cell viability in stationa
17  Staphylococcus aureus lrgAB operon inhibits murein hydrolase activity and decreases sensitivity to p
18 ence of 35 mM glucose and that this enhances murein hydrolase activity and decreases tolerance to van
19  was recently shown to inhibit extracellular murein hydrolase activity and increase tolerance to peni
20 om that of lrgAB by increasing extracellular murein hydrolase activity and increasing sensitivity to
21                         Cid proteins enhance murein hydrolase activity and penicillin sensitivity, wh
22 ologous proteins that regulate extracellular murein hydrolase activity and penicillin tolerance in a
23 teins that are involved in the regulation of murein hydrolase activity and penicillin tolerance.
24 -regulated operon, designated lrgAB, affects murein hydrolase activity and penicillin tolerance.
25 ysis in S. aureus by affecting the intrinsic murein hydrolase activity associated with the cell.
26  was also shown to have a positive impact on murein hydrolase activity but a negligible effect on sen
27 er resistance to lysis is due to a defect in murein hydrolase activity by using a zymogram analysis.
28 cidA gene results in decreased extracellular murein hydrolase activity compared to that of S. aureus
29 rgAB mutant produced increased extracellular murein hydrolase activity compared to that of the wild-t
30 sarV gene results in decreased extracellular murein hydrolase activity compared to that of wild-type
31 lts in significantly decreased extracellular murein hydrolase activity compared with that of the pare
32               Penicillin-induced killing and murein hydrolase activity in Staphylococcus aureus are d
33 r, neither mutation had a dramatic effect on murein hydrolase activity or autolysis.
34 , respectively, that function to control the murein hydrolase activity produced by the bacteria.
35 n of cidABC expression resulted in increased murein hydrolase activity produced by these cells.
36  increased autolysis and an altered level of murein hydrolase activity produced compared with the par
37 tracellular protease levels and altering the murein hydrolase activity profile.
38                      Zymographic analysis of murein hydrolase activity revealed that inactivation of
39     Zymographic and quantitative analyses of murein hydrolase activity revealed that mutation of the
40     Zymographic and quantitative analysis of murein hydrolase activity revealed that the lrgAB mutant
41      Rv2719c protein exhibited mycobacterial murein hydrolase activity that was localized to the N-te
42 , as well as its counterpart EA1, to exhibit murein hydrolase activity was confirmed by cloning their
43                     The effect of glucose on murein hydrolase activity was not observed in the cidA m
44 ncode a novel regulatory system that affects murein hydrolase activity, stationary-phase survival and
45 ion of the cid and lrg operons, which affect murein hydrolase activity, stationary-phase survival, an
46 n operon that encodes a positive effector of murein hydrolase activity, the upregulation of cidABC ex
47 Streptococcus mutans surface protein affects murein hydrolase activity.
48 enicillin, attributable in part to increased murein hydrolase activity.
49 on has a positive influence on extracellular murein hydrolase activity.
50 nes confer negative control on extracellular murein hydrolase activity.
51 ypothesized to be involved in the control of murein hydrolase activity.
52 g of S. aureus involves a novel regulator of murein hydrolase activity.
53 teins while lrgB may encode a protein having murein hydrolase activity.
54               Interestingly, the predominant murein hydrolase affected was an 85 kDa protein that was
55                                 Finally, two murein hydrolases, AmiC and EnvC, have been shown to loc
56  processes: increased expression of the AtlA murein hydrolase and decreased expression of wall-teicho
57               PCL is dependent upon the AtlA murein hydrolase and is regulated, in part, by the SrrAB
58 ere that Esp cleaves autolysin (Atl)-derived murein hydrolases and prevents staphylococcal release of
59                                              Murein hydrolases appear to be widespread in the virions
60 nvolved in the modification of substrates of murein hydrolases as well as in the regulation of expres
61 forms and perturb the deposition of the BslO murein hydrolase at cell division septa.
62  likely due to its inability to deposit BslO murein hydrolase at divisional septa.
63                  A model is proposed whereby murein hydrolases cleave the anchor structure of release
64                           LytN, a cross-wall murein hydrolase, contributes to the release of SpA by r
65 s of these genes suggest that lrgA encodes a murein hydrolase exporter similar to bacteriophage holin
66 effects on autolysis, in part, by modulating murein hydrolase expression and/or activity.
67                 In this report, we studied a murein hydrolase from the streptococcal bacteriophage C(
68 erns that provide protection from endogenous murein hydrolases governing cell division and from bacte
69      We show that bacteriophage N4 encodes a murein hydrolase (gp61) that is essential for N4 plaque-
70 drolase/peptidase) domain found in bacterial murein hydrolases; however, direct links between steps i
71 lular Listeria monocytogenes secretes p60, a murein hydrolase, into the host cell cytosol, where it i
72                            The regulation of murein hydrolases is a critical aspect of peptidoglycan
73     One such YSIRK-containing protein is the murein hydrolase LytN.
74 vidence for the enzymatic flexibility of the murein hydrolase NamA and demonstrate that bacterial sep
75 r to this N-terminal domain are found in the murein hydrolases of staphylococcal phages but not in th
76                                              Murein hydrolases of staphylococcal phages phi11, 80alph
77 nhibiting a putative holin from transporting murein hydrolases out of the cell.
78 217-225, which is derived from the bacterial murein hydrolase p60 and presented by the H-2Kd MHC clas
79                                   Lysins are murein hydrolases produced by bacteriophage that act on
80 y establish the existence of the cid and lrg murein hydrolase regulatory network in B. anthracis, but
81 from the bacterial surface by treatment with murein hydrolase, suggesting that the pilus fibres may b
82 ies are consistent with a role for PcsB as a murein hydrolase that balances the extent of cell wall s
83  studies show that lysin represents a unique murein hydrolase that has a rapid lethal effect both in
84 onger restricted the deposition of LysM-type murein hydrolases to cell division sites, which was asso
85 hat the LysM domains of Sle1 and LytN direct murein hydrolases to the staphylococcal envelope in the
86 of BslO, the S-layer-associated protein, and murein hydrolase, which cleaves septal peptidoglycan to
87 lation of expression and/or activity of some murein hydrolases, which, in turn, may play important ro
88 us aureus, a spherical microbe, secretes two murein hydrolases with LysM domains, Sle1 and LytN.