ライフサイエンスコーパス: pellicle

1 erns of proteins present in whole saliva and pellicle.

2 novel proteins not previously identified in pellicle.

3 ant for the formation of the acquired enamel pellicle.

4 kely to be precursors of the acquired enamel pellicle.

5 ially influence the biological properties of pellicle.

6 tant in the formation of the acquired enamel pellicle.

7 bserved between slabs with and those without pellicle.

8 to be incorporated into the acquired enamel pellicle.

9 atite (sHA), an in vitro model of the enamel pellicle.

10 and contributes to the hydrophobicity of the pellicle.

11 equired to maintain a connective and elastic pellicle.

12 with salivary components within the salivary pellicle.

13 colony formation and the inability to form a pellicle.

14 d salivary components of the acquired enamel pellicle.

15 for the development of bacterial biofilms or pellicles.

16 film models but remain largely undefined for pellicles.

17 ted in cell-free supernatants from disrupted pellicles.

18 aces and at the air-liquid interface, termed pellicles.

19 onspindle ensembles nucleated by Tetrahymena pellicles.

20 P. aeruginosa PA14 that were unable to form pellicles.

21 In pure saliva- or serum-derived pellicles, 82 and 84 proteins were identified, respectiv

22 al saliva on tooth surfaces, acquired enamel pellicle (AEP), protects against erosive wear.

23 ously defined neutralization-sensitive zoite pellicle Ag.

24 arches, and confirm the protective effect of pellicle against dental erosion.

25 croscopy, 18.44 binding was localized to the pellicle and an intracytoplasmic tubulovesicular network

26 ce with in vivo-formed human acquired enamel pellicle and analyzed the serum immune responses.

27 y of structures associated with the membrane pellicle and is influenced by the kinetics of actin fila

28 cus mutans-derived exoenzymes present in the pellicle and on microbial surfaces (including non-mutans

29 PNAG was present in both pellicle and planktonic wild-type B. subtilis cells and

30 say reactivity with sporozoite and merozoite pellicles and the antigen (Ag) deposited on glass substr

31 types in culture, including the formation of pellicles and wrinkled colonies, in a syp-dependent mann

32 sitory for precursors of the acquired enamel pellicle, and a vehicle for modulation of the viscoelast

33 ns, such as the helical conformations of the pellicle, and identify previously unnoticed features of

34 gative phenotypes, namely wrinkled colonies, pellicles, and solid-surface-associated biofilms, led to

35 icular, the production of wrinkled colonies, pellicles, and the matrix on the colony surface was elim

36 gly, the triple mutant was competent to form pellicles, another biofilm phenotype, but they generally

37 that Bacillus subtilis biofilm colonies and pellicles are extremely nonwetting, greatly surpassing t

38 The most promising materials for pellicles are fluorinated polymers, but currently availa

39 We also experimentally demonstrate that the pellicles are soft elastic materials for small deformati

40 on, aggregation, and eventual formation of a pellicle at the air-liquid interface.

41 ll-scale transposon screen using an in vitro pellicle biofilm assay.

42 al attachment to agar surfaces and supported pellicle biofilm formation.

43 ein component of the extracellular matrix in pellicle biofilms formed by Bacteroidetes and Proteobact

44 n addition, we find that the ability to make pellicle biofilms is common among M. tuberculosis isolat

45 d interface just before the formation of the pellicle but only in strains that have flagella.

46 lulose is a component of the E. chrysanthemi pellicle but that pellicle formation still occurs in a s

47 inactive PKAc1 is maintained at the parasite pellicle by interacting with acylated PKAr.

48 or PelD that is critical to the formation of pellicles by Pseudomonas aeruginosa.

49 tion in adhesion of the bacteria to salivary pellicles, catabolism of dietary starches, and biofilm f

50 re involved in the formation of the salivary pellicle coating supragingival tooth surfaces.

51 proteins in whole saliva and in vivo formed pellicle components.

52 at emanate via this sulcus, which may impact pellicle composition locally.

53 Precursor proteins of the acquired enamel pellicle derive from glandular and non-glandular secreti

54 Pellicle developed on experimental slabs located on 8 in

55 icle formation was temperature dependent and pellicles did not form at 36 degrees C, even though TTSS

56 site-specificity of dental erosion, and that pellicle does protect the teeth from erosion.

57 rfacial rheology to compare the evolution of pellicle elasticity in real time to understand the molec

58 llum-based motility similarly contributes to pellicle formation and fitness in competition assays in

59 ment and detachment profiles to polystyrene, pellicle formation and stability at the air/medium inter

60 ed the development of colony corrugation and pellicle formation at the air-liquid interface.

61 Pellicle formation behavior requires production of extra

62 failed to produce CPS and were defective in pellicle formation in microtiter wells and in a biofilm

63 d motility, chemotaxis and oxygen sensing to pellicle formation in the Gram-positive Bacillus subtili

64 lcus, their ability to participate in dental pellicle formation is likely reduced in the presence of

65 ent of the E. chrysanthemi pellicle but that pellicle formation still occurs in a strain with an inse

66 Pellicle formation was temperature dependent and pellicl

67 p transcription, wrinkled colony morphology, pellicle formation, and surface adherence, while disrupt

68 enotypes such as wrinkled colony morphology, pellicle formation, and surface adherence.

69 Mutation of RemA or RemB impairs pellicle formation, complex colony architecture, and mot

70 In addition to being required for pellicle formation, the pel genes are also required for

71 ase subunit, is required for E. chrysanthemi pellicle formation, this inexpensive assay can be used a

72 or successful competition during B. subtilis pellicle formation.

73 ignificant carbohydrate factor essential for pellicle formation.

74 ur genes, epsHIJK, known to be essential for pellicle formation.

75 is not absolutely essential for, B. subtilis pellicle formation.

76 ed colony formation, adherence to glass, and pellicle formation.

77 not carry curli genes, requires the TTSS for pellicle formation.

78 dies have demonstrated that whole saliva and pellicle formed in vitro from oral fluid contain covalen

79 Tooth protection from erosion by salivary pellicle has been shown in vitro, but the hypothesis tha

80 The results showed that whole saliva and pellicle have more complex protein patterns than those o

81 d during the maturation of Bacillus subtilis pellicles in relation to their mechanical response.

82 Components identified in pellicle included histatins, lysozyme, statherin, cytoke

83 ensity, the bacteria present on the salivary pellicle incorporated low levels of radiolabeled nucleos

84 lar basis of matrix protein contributions to pellicle integrity and elasticity.

85 mes found in saliva can be incorporated into pellicle, interact with host-derived molecules on the su

86 The acquired enamel pellicle is an oral, fluid-derived protein layer that fo

87 Human acquired enamel pellicle is composed of molecules that selectively adsor

88 biofilms at air-liquid interfaces, that is, pellicles, is much less complete.

89 an acid-resistant protein in acquired enamel pellicle; it could therefore be included in oral product

90 bservations in the light of a theory for the pellicle kinematics, providing a precise understanding o

91 teins, particularly gp340, from the salivary pellicle leads to biofilm attachment, which accelerates

92 ic clusters of cells, followed by spreading (pellicle-like) growth to cover the entire surface.

93 been shown in vitro, but the hypothesis that pellicle may differ quantitatively at sites of erosion h

94 y history of euglenids, and suggest that the pellicle may serve as a model for engineered active surf

95 A plastic cell envelope called pellicle mediates these deformations.

96 liminary evidence in an in vivo saliva/serum pellicle model.

97 inct contributions of the matrix proteins to pellicle morphology, microscale architecture, and mechan

98 Neither salivary protein pellicles nor salivary proteins in solution significantl

99 ossible that bacterial adherence to salivary pellicle occurs as a cumulative effect of multiple prote

100 The mitotic spindle and the pellicle of the forming daughter cells appear to generat

101 nt of Streptococcus gordonii to the acquired pellicle of the tooth surface involves specific interact

102 ease-associated enzymes may destroy salivary pellicles on pathogenic bacteria to hinder their clearan

103 ination and the ability to aggregate to form pellicles on the broth surface.

104 lticellular behavior, which is manifested as pellicles on the culture surface and biofilms at the sur

105 e presence of salivary proteins, either as a pellicle or in solution.

106 Experiments on pellicles, or floating biofilms, of Bacillus subtilis sh

107 aintenance of the mechanical strength of the pellicle over time and contributes to the hydrophobicity

108 The pellicle (PEL) polysaccharide is synthesized by the oppo

109 lieved to recognize and bind specifically to pellicle polysaccharides covering the entire bacterium.

110 ived from oral epithelial cells, crosslinked pellicle precursor proteins which may be important in th

111 These results demonstrate that primary pellicle precursor proteins, acidic proline-rich protein

112 Statherin is an enamel pellicle protein that inhibits hydroxyapatite (HAP) nucl

113 ful method for the identification of various pellicle proteins, including some which show mineral hom

114 ppear to be involved in the formation of the pellicle's extracellular matrix.

115 The pellicle screen also identified mutants with lesions in

116 nding of the link between local actuation by pellicle shear and shape control.

117 We find that the active pellicle shear deformations causing shape changes can re

118 yeast extract-Casamino Acids)-PVC, and YESCA-pellicle that are dependent on type 1 pili (LB) and curl

119 otein, a constituent of the salivary film or pellicle that coats the tooth.

120 One such biofilm is the pellicle that forms at the air-liquid interface in stand

121 Pellicles that formed under conditions that upregulate c

122 d radiation-durable polymers for use in soft pellicles, the polymer films which protect the chip from

123 Slabs were then visualized, and pellicle thickness measured, by confocal laser scanning

124 Pellicle thickness varied significantly within the denta

125 s observed between the degree of erosion and pellicle thickness.

126 al triple-membrane structure of the parasite pellicle to the plasma membrane remain largely unknown.

127 hown that the thickness of acquired salivary pellicle varies within the dental arches, which may be r

128 until ca. 12 to 32% of the enamel's salivary pellicle was saturated (ca. 2.5 x 10(5) to 6.3 x 10(5) c

129 y the micro-amounts of components present in pellicle, we immunized mice with in vivo-formed human ac

130 ction, and contact angle measurements of the pellicles, we defined distinct contributions of the matr

131 ular/sublingual secretion, whole saliva, and pellicle were subjected to isoelectric focusing followed

132 l environment for 0 min, 30 min and 2 h, the pellicles were analyzed by SDS-PAGE.

133 Motility and formation of biofilms and pellicles were observed only when bacterial cells were i

134 The pellicle, which is a cohesive mat of cells, was exploite

135 al cavity are coated with a salivary film or pellicle, which lacks apparent intermolecular organizati

136 itochondrion outer membrane and the parasite pellicle, whose features suggest the presence of membran

137 functional properties of the acquired enamel pellicle will therefore be mostly dictated by the saliva

138 and carbonic anhydrase II by probing in vivo pellicle with specific polyclonal anti-sera.

139 determine the thickness of acquired salivary pellicle within the dental arches, investigate the possi