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1 yme A carboxylase, cause hypersensitivity to spectinomycin.
2 effective as selection on medium containing spectinomycin.
3 nfers bacterial resistance to the antibiotic spectinomycin.
4 ith some minor variations for ampicillin and spectinomycin.
5 rs that produce resistance to the antibiotic spectinomycin.
7 plastomic clones is ensured by selection for spectinomycin (aadA) or kanamycin (neo) resistance genes
9 findings also explain the mode of action of spectinomycin, an antibiotic that blocks translocation b
10 onses of different Arabidopsis accessions on spectinomycin, an inhibitor of chloroplast translation,
11 s without mutagenesis by a short exposure to spectinomycin, an inhibitor of plastid protein synthesis
12 , we generated a new semisynthetic series of spectinomycin analogs with selective ribosomal inhibitio
14 promoter-aadA cassette confers resistance to spectinomycin and streptomycin in both B. burgdorferi an
15 ch confers resistance to the aminoglycosides spectinomycin and streptomycin in Escherchia coli, can b
16 nt with FLARE-S vector DNA and selection for spectinomycin and streptomycin resistance, respectively.
17 ing the aadA gene that confers resistance to spectinomycin and streptomycin, has been considered crit
18 B8; and gene aadA1, conferring resistance to spectinomycin and streptomycin, was associated with an O
19 rase domain appears to be highly specific to spectinomycin and streptomycin, while the acetyltransfer
27 ies surviving on different concentrations of spectinomycin as well as the levels of transcriptional a
28 dium (MBM), which contains cycloheximide and spectinomycin at final concentrations of 0.5 mg/ml and 1
30 After identification of strains having the spectinomycin cassette inserted by a double-crossover ev
32 oramphenicol, erythromycin, fusidic acid and spectinomycin, do not induce the conformational changes
34 ransformation events per bombarded sample in spectinomycin-hypersensitive Slavice and Columbia acc2 k
35 Aminoglycoside-3''-adenylytransferase, the spectinomycin inactivating enzyme, is translationally fu
37 cloacae (conferring resistance to kanamycin, spectinomycin, lincomycin, and gentamycin/sisomycin, res
38 mbinase action at the loxP sites excised the spectinomycin marker, leaving a single loxP site within
40 (kanamycin, gentamycin, sisomycin, amikacin, spectinomycin, neomycin), macrolides-lincosamids (erythr
45 s leaves with a vector carrying a selectable spectinomycin resistance (aadA) gene and gfp, encoding t
46 e that confers a golden leaf phenotype and a spectinomycin resistance (aadA) gene that is necessary f
47 tid genome with the pCK2 vector in which the spectinomycin resistance (aadA) marker gene is flanked w
49 The transplastomic father lines carried a spectinomycin resistance (aadA) transgene incorporated i
51 Regenerated plants are homoplasmic for the spectinomycin resistance and the Pst I markers and heter
52 hat transplastomic clones can be selected by spectinomycin resistance and visually identified by fluo
55 new nonpolar mutagenesis method employing a spectinomycin resistance cassette was used to inactivate
56 four clinical isolates were disrupted with a spectinomycin resistance cassette, and the binding of is
58 in the N. tabacum nucleus was combined with spectinomycin resistance encoded in N. sylvestris plasti
59 ings with paternal plastids were selected by spectinomycin resistance encoded in the paternal plastid
63 tern blot analysis that insertion of a polar spectinomycin resistance gene in cheAY results in loss o
64 at of the GCN4 half-site in vivo, leading to spectinomycin resistance in the transcription interferen
66 d by direct selection for the transplastomic spectinomycin resistance marker in tissue culture; there
70 on of PSII, an aadA gene cassette conferring spectinomycin resistance was employed for mutagenesis.
71 nce of the eubacterial aadA gene (conferring spectinomycin resistance) fused to the 5' and 3' untrans
72 ssion of a eubacterial aadA gene, conferring spectinomycin resistance, is transcriptionally suppresse
73 athway and a selectable marker gene encoding spectinomycin resistance, was flanked at the 5' end by t
74 ng gene products despite the presence of the spectinomycin-resistance cassette, which was used to ina
75 and the N-terminal half, which contains the spectinomycin-resistance mutations, directly interacts w
77 st of natA and all of natB was replaced by a spectinomycin-resistance-gene cassette exhibited phenoty
78 nalysis of co-transformants selected using a spectinomycin-resistant 16S gene (16S(spec)) provided ev
79 veloped a cotransformation approach in which spectinomycin-resistant 16S rRNA-encoding DNA is the sel
84 imized construct into tobacco and subsequent spectinomycin selection of transgenic plants yielded T0
86 and viomycin inhibit INT formation, whereas spectinomycin selectively inhibits INT disappearance.
88 imparts resistance to kasugamycin (Ksm) and spectinomycin (Spc) and causes loss of one HpaI restrict
89 antibiotic binding, demonstrating a class of spectinomycin-specific functional molecular decoys built
90 ted with four-drug resistance (streptomycin, spectinomycin, sulfisoxazole, and tetracycline [St Spc S
91 acid as well as resistance to tetracycline, spectinomycin, sulfonamides, chloramphenicol, and gentam
93 ent of urease activity upon adding Ni(2+) to spectinomycin-treated Escherichia coli cells that expres
95 emcomitans SUNY 465 transiently resistant to spectinomycin was used with conjugation to generate an i
96 G-novobiocin, pirlimycin, premafloxacin, and spectinomycin, which are used in veterinary practice.
97 he antibiotics paromomycin, streptomycin and spectinomycin, which interfere with decoding and translo
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