ライフサイエンスコーパス: conjugal transfer

1 for the enhancement and repression of pLYL72 conjugal transfer.

2 d required for plasmid DNA processing during conjugal transfer.

3 lactone (AAI) to regulate genes required for conjugal transfer.

4 cation, and support efficient termination of conjugal transfer.

5 c DNA-binding protein required for efficient conjugal transfer.

6 n density-dependent regulation of Ti plasmid conjugal transfer.

7 raI abolished the production of AAI and also conjugal transfer.

8 , the quorum-sensing activator of Ti plasmid conjugal transfer.

9 in this system and are most consistent with conjugal transfer.

10 However, these mutants retained residual conjugal transfer activity when tested in strain NT1, wh

11 During conjugal transfer an essential factor, called the coupli

12 RP4 (TraG(RP4)) and TraG and VirD4 from the conjugal transfer and T-DNA transfer systems of Ti plasm

13 sing system, suggesting a connection between conjugal transfer and vegetative replication of these vi

14 nctions, including integration and excision, conjugal transfer, and regulation.

15 mids encode genes involved in pilus-mediated conjugal transfer, as well as pilL-V, which encodes a se

16 erobacteria by recognizing a plasmid-encoded conjugal transfer complex as a receptor.

17 For low numbers of sites, the efficiency of conjugal transfer decreased as an exponential function o

18 port that the Agrobacterium-to-Agrobacterium conjugal transfer efficiencies of RSF1010 increase drama

19 plasmid TiC58 or plasmid RSF1010 reduces the conjugal transfer efficiency of pAtC58 10- or 1,000-fold

20 he quorum-dependent activation of Ti plasmid conjugal transfer exhibited a lag of almost 8 h when the

21 Only the trbK mutant was unaffected in conjugal transfer from either donor.

22 ency of 10(-4) to 10(-5) per recipient after conjugal transfer from Escherichia coli.

23 bB, -C, -D, -E, -L, -F, -G, and -H abolished conjugal transfer from strain UIA5, which lacks the 450-

24 nosa and Erwinia spp., as well as T1 plasmid conjugal transfer in Agrobacterium tumefaciens, and many

25 After conjugal transfer into P. aeruginosa, plasmid integrants

26 ed may be used to increase the efficiency of conjugal transfer into restriction-competent bacteria.

27 lasmid gene markers: traA from the conserved conjugal transfer machinery and vapA and vapB, found in

28 uency of transposon loss is a consequence of conjugal transfer, making this loss a marker for that tr

29 The determinants responsible for conjugal transfer map to two regions, tra and trb, of th

30 ese proteins is required for the increase in conjugal transfer mediated by the recipient.

31 es (close to 100%) from the chromosome after conjugal transfer of a Flp recombinase-expressing plasmi

32 Conjugal transfer of Agrobacterium tumefaciens Ti plasmi

33 Conjugal transfer of Agrobacterium tumefaciens Ti plasmi

34 Conjugal transfer of Agrobacterium tumefaciens Ti plasmi

35 Conjugal transfer of Agrobacterium tumefaciens Ti plasmi

36 Conjugal transfer of bacterial plasmids requires a pore

37 Conjugal transfer of Bacteroides mobilizable transposon

38 s well as its own synthesis, can promote the conjugal transfer of both chromosomal and plasmid genes

39 Conjugal transfer of chromosomal DNA between strains of

40 hines, but present-day functions include (i) conjugal transfer of DNA by cell-to-cell contact, (ii) t

41 Sinorhizobium meliloti 1021 is required for conjugal transfer of DNA.

42 bium sp. strain NGR234, which is involved in conjugal transfer of DNA.

43 ysaccharides and components required for the conjugal transfer of DNA.

44 tudies did not detect replication delays for conjugal transfer of episomes containing PIT elements.

45 nd proteins into plant cells, as well as the conjugal transfer of IncQ plasmids, such as RSF1010, bet

46 Conjugal transfer of plasmid DNA is terminated when the

47 ced stimulatory effect on the virB-dependent conjugal transfer of plasmid RSF1010 by agrobacterial do

48 The efficiency of conjugal transfer of plasmids from Escherichia coli to t

49 We conclude that conjugal transfer of pTiC58 is regulated in a quorum-dep

50 Conjugal transfer of pTiC58 requires two regions, tra wh

51 genes except trbI and trbK are essential for conjugal transfer of pTiC58.

52 cQ plasmid RSF1010 into plant cells, and the conjugal transfer of RSF1010 between Agrobacteria.

53 Genes required for replication and for conjugal transfer of the Agrobacterium tumefaciens Ti pl

54 the first time an oriT, which is involved in conjugal transfer of the circular form, has been implica

55 cell, while the other is responsible for the conjugal transfer of the entire Ti plasmid from one bact

56 ormation functions and are essential for the conjugal transfer of the IncP plasmid.

57 e the VirB system, AvhB products promote the conjugal transfer of the IncQ plasmid RSF1010, suggestin

58 for tumor formation; rather, it mediates the conjugal transfer of the pAtC58 cryptic plasmid between

59 e major type IV pilin subunit (pilS) reduced conjugal transfer of the plasmid by 4 orders of magnitud

60 um tumefaciens, activates genes required for conjugal transfer of the Ti plasmid and also enhances th

61 rb system encodes functions required for the conjugal transfer of the Ti plasmid between cells of Agr

62 Conjugal transfer of the Ti plasmid pTiC58 is regulated

63 Conjugal transfer of the Ti plasmids from Agrobacterium

64 specifically to a site within the origin of conjugal transfer of the transposon, oriT.

65 3-oxo-octanoyl-l-homoserine lactone control conjugal transfer of the tumor-inducing plasmid, the pri

66 iption factor TraR regulates replication and conjugal transfer of the tumour-inducing (Ti) plasmid in

67 efaciens, which controls the replication and conjugal transfer of the tumour-inducing (Ti) virulence

68 ine-type Ti plasmid pTiC58 are important for conjugal transfer of this element to recipient bacteria.

69 8 is one of three loci that are required for conjugal transfer of this Ti plasmid.

70 Conjugal transfer of Ti plasmids from Agrobacterium spp.

71 Conjugal transfer of Ti plasmids of Agrobacterium tumefa

72 genetic transformation of M. arthritidis and conjugal transfer of Tn916 from an enterococcal donor to

73 be part of a mechanism to prevent premature conjugal transfer of Tn916 prior to excision from the do

74 nical isolate R7 have been implicated in the conjugal transfer of VmR.

75 Distributive conjugal transfer offers a plausible mechanism for the p

76 cleaving both strands of the Tn916 origin of conjugal transfer (oriT) at several distinct sites and f

77 Mycobacterial distributive conjugal transfer permits innovative genetic approaches

78 on system (TFSS) proteins VirB9, VirB10, and conjugal transfer protein (CTP).

79 system enables A. tumefaciens to express its conjugal transfer regulon preferentially at high populat

80 ce and appears to constitute components of a conjugal transfer system that has been adopted to preven

81 teria and share extensive homology with many conjugal transfer systems.

82 bound secretion apparatus similar to type IV conjugal transfer systems.

83 P plasmid was cloned into pGNS-BAC to enable conjugal transfer, thereby allowing both electroporation

84 ring excision and nicking at the oriT during conjugal transfer, to prevent premature nicking at the o

85 egion encoding plasmid replication (rep) and conjugal transfer (tra) functions similar to those encod

86 taining a coresident conjugative transposon, conjugal transfer was repressed in the absence of tetrac

87 that a negative and a positive regulator of conjugal transfer were encoded outside the transfer regi

88 hat at least traG and traF are essential for conjugal transfer, while sequence analysis predicts that