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1 d), 0.10mgkg(-1) (natamycin) and 2mugkg(-1) (tylosin).
2 trend was only statistically significant for tylosin.
3 ession and changes in response to the use of tylosin.
4 and enrofloxacin, and 97% were sensitive to tylosin.
5 lycone precursor of the macrolide antibiotic tylosin.
6 ne, and low susceptibility to lincomycin and tylosin.
9 zed by the cleavage of the mycarose sugar of tylosin and subsequent modification of 4'-hydroxyl group
10 f three major use antibiotics (trimethoprim, tylosin, and lincomycin) to algal and cyanobacterial spe
11 macrolide antibiotics (such as erythromycin, tylosin, and narbomycin) depend ultimately on the glycos
12 tibiotic feed additives such as monensin and tylosin are added to the finishing diets of feedlot catt
19 es has led to the assignment of tylM1 in the tylosin biosynthetic gene cluster and desVI in the methy
20 , 2.2 kb of DNA from the tylLM region of the tylosin biosynthetic gene cluster of S. fradiae has been
22 ified by sequence analysis at one end of the tylosin biosynthetic gene cluster of Streptomyces fradia
24 specific activator that controls most of the tylosin-biosynthetic (tyl) genes that are subject to reg
27 in, valnemulin, doxycycline, lincomycin, and tylosin by broth microdilution and that to carbadox by a
29 acity of Streptomyces fradiae (a producer of tylosin) by importing genes from the narbomycin producer
31 ualitative analyses of sequences showed that tylosin caused microbial population shifts in both abund
32 mined the fecal microbiome of pigs receiving tylosin compared with untreated pigs using pyrosequencin
35 determination of sorbic acid, natamycin and tylosin in Dulce de leche, a traditional South American
36 ueous concentrations of chlortetracyline and tylosin in runoff decreased in consecutive rainfall even
37 nal PKS modules that produce the 16-membered tylosin macrocycle, using them as biocatalysts in the ch
39 housing pigs that were fed chlortetracyline, tylosin or bacitracin and were land applied via broadcas
40 ork, the biosynthesis of d-mycaminose in the tylosin pathway of Streptomyces fradiae was investigated
42 ion of the ole PKS loading module, or of the tylosin PKS loading module, for the erythromycin (ery) l
44 (RT-PCR) suggests that tylS is essential for tylosin production and controls the expression of tylR (
55 ncode the synthesis or addition of all three tylosin sugars, plus polyketide ring oxidation, and at l
60 omycin, apramycin, tiamulin, tilmicosin, and tylosin were tested by broth microdilution against vario
61 me resulted in the production of demycinosyl-tylosin, whereas other glycosyltransferase activities in
62 els of the commercially important antibiotic tylosin, with TylP occupying the top of this cascading n
63 Thus, targeted disruption of tylU reduced tylosin yields by about 80% and bioconversion analysis w
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