ライフサイエンスコーパス: restriction-modification system

1 /absence of insertion sequences and a type I restriction modification system.

2 ular lactate, and modification of the type I restriction-modification system.

3 and C.BclI, a controller protein of the BclI restriction-modification system.

4 to be the endonuclease component of a novel restriction-modification system.

5 eria, it does not appear to be part of a DNA restriction-modification system.

6 , but it does not appear to be part of a DNA restriction-modification system.

7 ompetitive inhibitor of the bacterial type I restriction/modification system.

8 for a methyltransferase from a model type I restriction/modification system.

9 ases, those whose function lies outside of a restriction/modification system.

10 methyltransferase that is not part of a DNA restriction/modification system.

11 clude blocking phage attachment, CRISPR, and restriction modification systems.

12 at are now termed Type I, II, III and IV DNA restriction-modification systems.

13 CCWGG motifs as a marker of self DNA akin to restriction-modification systems.

14 tions such as those observed with the Type I Restriction-Modification systems.

15 ors, called C proteins, controls a subset of restriction-modification systems.

16 d disease processes, as well as in bacterial restriction-modification systems.

17 strains in nature vary dramatically in their restriction-modification systems.

18 in because of their sensitivity to bacterial restriction-modification systems.

19 15 nucleotides in the TfiTok6A1I and Tsp32IR restriction-modification systems.

20 which in turn, are rarely incorporated into restriction/modification systems.

21 is, cell-surface-associated proteins and DNA restriction/modification systems.

22 VPI-2 encodes a P4-like integrase, a restriction modification system, a Mu phage-like region,

23 ; these include a previously uncharacterized restriction-modification system, a nuclease-helicase com

24 ic DNA in cells carrying the wild-type EcoRI restriction-modification system: (a) binding to EcoRI* s

25 Correspondingly, two loci encoding Type I restriction-modification systems able to change their sp

26 The Restriction-modification system AhdI contains two conver

27 For the hpyV and hpyAIV restriction-modification systems, an in-depth analysis o

28 ound on plasmids, including those encoding a restriction-modification system and arsenic resistance,

29 ned and expressed the ahdIC gene of the AhdI restriction-modification system and have purified the re

30 oth systems are closely related to the PvuII restriction-modification system and share its target spe

31 re are barriers to genetic transfer, such as restriction-modification systems and CRISPR loci, that l

32 may contribute to genetic variability, i.e., restriction-modification systems and integrases.

33 ches in DNA is key for maintaining bacterial restriction/modification systems and gene silencing in h

34 mology to DNA methyltransferases of type III restriction/modification systems and has 40 tetranucleot

35 rast to M. jannaschii, A. fulgidus has fewer restriction-modification systems, and none of its genes

36 lleviation may be a characteristic of Type I restriction-modification systems, and that it can be ach

37 Phase-variable restriction-modification systems are a feature of a dive

38 Type I DNA restriction/modification systems are oligomeric enzymes

39 tes, SfiI displays all of the hallmarks of a restriction-modification system as opposed to a recombin

40 We also identified a number of putative restriction-modification systems, bacteriophage genes an

41 er of MTase genes, presumably with the whole restriction-modification systems, between Bacteria and A

42 However, if type I restriction-modification systems bind to unmodified targ

43 tal role in shaping bacterial evolution, and restriction-modification systems can modulate this flow.

44 We conclude that PV of a Type IIG restriction-modification system causes changes in site-s

45 Type II restriction-modification systems cleave and methylate DN

46 The BcgI restriction-modification system consists of two subunits

47 Most bacterial genomes harbor restriction-modification systems, encoding a REase and i

48 striction (R) and methylase (M) genes of the Restriction-Modification system Esp1396I are tightly reg

49 sm is proposed for the evolution of the NaeI restriction-modification system from a topoisomerase/lig

50 The BslI restriction-modification system from Bacillus species wa

51 ave isolated and characterized the genes for restriction-modification systems from two species of Sal

52 DNA modification, mediated by restriction-modification systems, functions as an immune

53 The cloning and sequencing of BsoBI restriction-modification system has been described by Ru

54 sporters, cryptic phages, and three types of restriction-modification systems have been identified in

55 Restriction-modification systems have been identified in

56 Two restriction-modification systems have been previously di

57 Restriction-modification systems have to distinguish bet

58 ch systems, which include the CRISPR-Cas and restriction-modification systems, have proven to be inva

59 A type IIs restriction-modification system, hpyIIRM, was active in

60 ion efficiencies suggested the presence of a restriction-modification system in F. nucleatum.

61 which recognizes GAATTC and is a member of a restriction-modification system in Rhodobacter sphaeroid

62 i encodes a homologue of an unusual Type IIG restriction-modification system in which the endonucleas

63 We conclude that the type II restriction-modification systems in H. pylori are highly

64 transformation are numerous strain-specific restriction-modification systems in H. pylori.

65 ng the inner barriers to transformation were restriction-modification systems in M. xanthus, which co

66 We conclude that restriction-modification systems inhibit the genomic int

67 The PvuII restriction-modification system is a type II system, whi

68 Therefore, the thermophilic Tsp45I restriction-modification system is plasmid-borne within

69 ole of facilitated diffusion in this type II restriction-modification system is proposed.

70 ion sequence (IS) elements, that encodes the restriction/modification system LlaI and carries an abor

71 bits low %G+C and encodes proteins of phage, restriction modification systems, mobile elements, and o

72 However, unlike restriction-modification systems, phage DNA does not app

73 rial genomes (Labrie et al, 2010), including restriction-modification systems (R-M) (Tock & Dryden, 2

74 n identified in bacterial genomes, including restriction-modification systems (R-M), abortive infecti

75 The PspGI restriction-modification system recognizes the sequence

76 e systems, in particular toxin-antitoxin and restriction-modification systems, show nonrandom cluster

77 nsists of genetic rearrangements in a Type I restriction-modification system (SpnD39III).

78 ldarius, the mode of GGCC methylation by its restriction-modification system, SuaI, was investigated.

79 Type IIB restriction-modification systems, such as BcgI, feature

80 An extensive analysis is included of the restriction-modification systems that are predicted to b

81 Finally, we describe examples of Type II restriction-modification systems that have features in c

82 toxA flanking DNA contained a homologue of a restriction/modification system that was shown to be fun

83 spite the pronounced similarity of the three restriction-modification systems, the flanking sequences

84 known about the distribution and movement of restriction-modification systems themselves.

85 lts support generalization of the concept of restriction-modification system to the concept of self-r

86 g frames with homology to enterotoxin genes, restriction-modification systems, transposases, and seve

87 cificity subunit of hetero-oligomeric type I restriction-modification systems) was significantly high

88 ains of Escherichia coli expressing the SfiI restriction-modification system were transformed with pl

89 nes encoding surface-associated proteins and restriction-modification systems were especially diverse

90 These type I restriction-modification systems were originally identif

91 epresents a minimal approach to assembling a restriction-modification system wherein a single DNA rec

92 involvement of PT modifications in a type of restriction-modification system with wide distribution i

93 ided the starting point for the evolution of restriction-modification systems with novel sequence spe