Titlebook: Biosynthesis; John W. Corcoran Book 1981 Springer-Verlag Berlin · Heidelberg 1981 Biosynthese.Biosynthesis.Tetracycline.antibiotic.antibio

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Youngwha Kee,Yunji Kim,Rhonda Phillips followed by the discovery of neomycin, paromomycin, kanamycin, gentamicin, sisomicin, butirosin, ribostamycin, spectinomycin, fortimicin, validamycin, minosaminomycin, and hygromycin, to name but some of the naturally occurring members of this class of compounds.

GROSS

https://doi.org/10.1007/978-94-011-1016-7es 6-APA, isopenicillin N (Fig. 2) (which has a δ-linked L-α-aminoadipyl side chain . and a number of penicillins with non-polar side chains [RCO in (II)] derived from mono substituted acetic acids whose nature depends on the precursors present in the fermentation medium. For example, when phenoxyac

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https://doi.org/10.1007/978-3-031-01582-3 in a more detailed account of macrolides. et al., 1977) as well as in an annual report on the subject of antibiotics., 1977. A detailed discussion of the 16-membered group of macrolides appears in Chapter 8 of this volume. Of all the other possible models, the family of the erythromycins has been t

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Bayesian Preference Elicitation,). Some of the macrolide antibiotics, including leucomycin, spiramycin, and acetylspiramycin have clinical applications and/or are used as supplements in animal feeds. The currently known macrolides can be classified biosynthetically into four groups, on the basis of the pattern of glycosidation of

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Suggestions for Research and Practice,, the 12-, 14-, or 16-member macrolides, the ansamycins or the polyene antibiotics. The biosynthesis of these classes of compounds is discussed in several other chapters. There are also a few rather unusual macrolides which do not fit into any of these major categories. The biosynthesis of three of

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RACE

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