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1 lmost equal numbers in biofilms that produce transconjugants.
2 o donors showed no difference in recoverable transconjugants.
3 verage of 103 antibiotic-resistant Y. pestis transconjugants.
4 he respective donors are carried over to the transconjugants.
5 ning higher cell densities produced very few transconjugants.
8 nd dehII genes in about 10% of transposition transconjugants and provided a genetic link between tran
9 h includes the lag time of newly formed F(+) transconjugants and the recovery time between successive
14 erred the Ti plasmid to recipients, yielding transconjugants by 14 to 21 days following infection.
18 (49,763 bp), isolated from Escherichia coli transconjugant D7-3, which was obtained through pRA1 tra
21 m1 transfers at a frequency of 1.35 x 10(-5) transconjugants/donor to ICEPm1-deficient P. mirabilis u
24 ses and DNA hybridizations revealed that the transconjugant harbored a single plasmid of approx. 92 k
27 rs mutationally derepressed for blcC yielded transconjugants in planta at numbers 10-fold lower than
33 (4.5 x 10(-3)) was observed in all of the 23 transconjugants obtained, and the direction of tetracycl
34 tween virulence and avirulence by generating transconjugants of a virulent race harbouring plasmids e
36 DNA transfer at a frequency of about 10(-3) transconjugants per donor and that this process is depen
37 id transfer rates can reach or exceed 10(-1) transconjugants per donor in vivo and under laboratory c
39 ned the genome sequences of 22 F1-generation transconjugants, providing the first genome-wide view of
42 valent to that of UPEC strain HE300, and the transconjugant showed significantly increased growth com
43 ion site in a P. gingivalis Tn4351-generated transconjugant showed that a complete copy of the previo
47 ulated M-type 3 GAS strain DLS003 produced a transconjugant that exhibited a mucoid colony morphology
48 tibiotic screening revealed only one type of transconjugant that was resistant to ampicillin and tetr
52 as used as a donor, a highly conjugative VmR transconjugant was isolated that formed constitutive cel
53 rtion into the recipient chromosome in these transconjugants was recombination across flanking region
54 -Tet(s)) were resistant to erythromycin, the transconjugants were initially picked up as ampicillin-
55 s 1 week earlier, but by the following week, transconjugants were recovered at numbers indistinguisha
56 ESBL-producing strains (17 Escherichia coli transconjugants) were studied to define "sensitive" inte
57 sive genome-wide mosaicism within individual transconjugants, which generated large-scale sibling div
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