(19)
(11)EP 0 001 709 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
02.06.1982 Bulletin 1982/22

(21)Application number: 78300514.3

(22)Date of filing:  17.10.1978
(51)International Patent Classification (IPC)3C07D 493/20, C12N 1/26, C12P 17/02, A23K 1/17
// (C07D493/20, 311:00, 311:00, 307:00)

(54)

Deoxynarasin antibiotics, their production and use

Deoxynarasin Antibiotika, ihre Herstellung und Verwendung

Antibiotiques du groupe de la déoxynarasine, leur procédé de préparation et leur utilisation


(84)Designated Contracting States:
DE GB NL SE

(30)Priority: 20.10.1977 US 844087

(43)Date of publication of application:
02.05.1979 Bulletin 1979/09

(71)Applicant: ELI LILLY AND COMPANY
Indianapolis Indiana 46285 (US)

(72)Inventors:
  • Nakatsukasa, Walter Mitsuo
    Indianapolis Indiana 46227 (US)
  • Marconi, Gary G.
    Indianapolis Indiana 46217 (US)
  • Neuss, Norbert
    Indianapolis Indiana 46260 (US)
  • Hamill, Robert L.
    Greenwood Indiana 46142 (US)

(74)Representative: Crowther, Terence Roger et al
Lilly Industries Limited European Patent Operations Erl Wood Manor
Windlesham Surrey GU20 6PH
Windlesham Surrey GU20 6PH (GB)

  
Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


Description


[0001] The invention relates to Deoxynarasin antibiotics, their use as an antibacterial and anticoccidial agent and in increasing feed utilisation in ruminants.

[0002] New improved antibiotics continue to be needed in veterinary medicine. For example, coccidiosis continues to be a wide-spread problem in the poultry industry. Coccidiosis results from infection by one or more species of Eimeria or Isospora (for a summary see Lung and Farr in "Diseases of Poultry," 5th ed, Biester and Schwarte, Eds., Iowa State University Press, Ames, Iowa, 1965, pp. 1056-1096). Economic losses due to coccidiosis are great, creating a demand for better anticoccidial agents.

[0003] Promotion of growth in ruminants, such as cattle and sheep, is another economically desirable objective of veterinary science. Of particular interest is growth promotion achieved by increasing feed-utilization efficiency. The mechanism for utilization of the major nutritive portion (carbohydrates) of ruminant feeds is well known. Microorganisms in the rumen of the animal degrade carbohydrates to produce monosaccharides and then convert these monosaccharides to pyruvate compounds. Pyruvates are metabolized by microbiological processes to form acetates, butyrates or propionates, collectively known as volatile fatty acids (VFA). For a more detailed discussion, see Leng in "Physiology of Digestion and Metabolism in the Ruminant," Phillipson et al., Eds., Oriel Press, Newcastle-upon-Tyne, England, 1970, pp. 408-410.

[0004] The relative efficiency of VFA utilization is discussed by McCullough in Feedstuffs, June 19, 1971, page 19; Eskeland et al. in J. An. Sci. 33, 282 (1971); and Church et al. in "Digestive Physiology and Nutrition of Ruminants," Vol. 2, 1.971 pp. 622 and 625. Although acetates and butyrates are utilized, propionates are utilized with greater efficiency. Furthermore, when too little propionate is available, animals may develop ketosis. A beneficial compound, therefore, stimulates animals to produce a higher proportion of propionates from carbohydrates, thereby increasing carbohydrate-utilization efficiency and also reducing the incidence of ketosis.

[0005] 20-Deoxynarasin and 20-deoxy-epi-1 7-narasin are new polyether antibiotics; they are most closely related to the prior art polyether antibiotic narasin (antibiotic A-28086 factor A; U.S. Patents 4,035,481 and 4,038,384). The structure of narasin proposed in these patents and by Occolowitz et al. [Biomed Mass Spectrometry 3, 272―277 (1976)] was recently confirmed by H. Seto et al. J. Antibiotics 30 (6) 530-532 (1977)] to be as shown;



[0006] As Seto et al. report, narasin is closely related to salinomycin (salinomycin = 4-demethyinarasin). More recently, J. W. Westley et al. reported on the C-17 epimers of deoxy-(0-8)-salinomycin [J. Antibiotics 30 (7) 610-612 (1977)]. Although the epimers of deoxysalinomycin are analogous to the epimers of deoxynarasin of this invention, there is no known chemical procedure by which the deoxynarasin epimers could be prepared from the deoxysalinomycin epimers.

[0007] This invention relates to the deoxynarasin antibiotic complex comprising at least two individual factors, 20-deoxynarasin and 20-deoxy-epi-17-narasin. The complex is produced by culturing a strain of the organism Streptomyces aureofaciens Duggar, NRRL 11181.

[0008] The term "antibiotic complex" as used in the fermentation art and in this document does not refer to a chemical complex, but to a mixture of co-produced individual antibiotic factors. As will be recognized by those familiar antibiotic production by fermentation, the ratio of individual factors produced in an antibiotic complex will vary, depending on the fermentation conditions used.

[0009] The pharmaceutically-acceptable salts of 20-deoxynarasin and 20-deoxy-epi-1 7-narasin are also part of this invention. To simplify discussions of utility, the term "deoxynarasin antibiotic" is used and refers to a member selected from the group consisting of deoxynarasin antibiotic complex, 20-deoxy- narasin, 20-deoxy-epi-1 7-narasin, and the pharmaceutically-acceptable salts of 20-deoxynarasin and 20-deoxy-epi-17-narasin.

[0010] The deoxynarasin antibiotics of this invention inhibit the growth of organisms which are pathogenic to animal and plant life. In one aspect of this activity, the deoxynarasin antibiotics are anti- coccidial agents. In addition, the deoxynarasin antibiotics increase feed-utilization efficiency in ruminants.

[0011] The deoxynarasin antibiotic complex comprises 20-deoxynarasin and 20-deoxy-epi-17-narasin which are obtained from the fermentation as a mixture. 20-Deoxynarasin and 20-deoxy-epi-17-narasin are separated from the deoxynarasin complex and isolated as individual compounds as hereinafter described. The deoxynarasin complex also contains minor factors which are removed by the procedures described. The deoxynarasin anti-biotic complex is soluble in most organic solvents, but is insoluble in water.

20-Deoxynarasin



[0012] 20-Deoxynarasin, one of the factors of this invention, has the same absolute configuration as narasin. The structure of 20-deoxynarasin is shown in Formula 1:


20-Deoxy-epi-1 7-narasin



[0013] The structure of 20-deoxy-epi-17-narasin, the other factor of this invention, is shown in Formula 2.



[0014] One of the best methods for differentiating narasin (A-28086 factor A), 20-deoxynarasin, and 20-deoxy-epi-1 7-narasin is by the use of 13C nuclear magnetic resonance (nmr) spectrometry. Table I summarizes the 13C nmr spectra of these compounds, each as the free acid, run in deuterochloroform (data in ppm).







[0015] Other good methods for differentiating 20-deoxynarasin from 20-deoxy-epi-narasin and from the known A-28086 factors include paper and thin-layer chromatography. For example, the Rf values of narasin (A-28086 factor A), A-28086 factor D, 20-deoxynarasin and 20-deoxy-epi-17-narasin in various paper-chromatographic systems, using Bacillus subtilis ATCC 6633 as a detection organism are given in Table II.



[0016] The Rf values of these antibiotics in a typical thin-layer chromatographic (TLC) system using silica gel are given in Table III.



[0017] The deoxynarasin antibiotics (20-deoxynarasin and 20-deoxy-epi-17-narasin) are soluble in a variety of organic solvents such as, for example, methanol, ethanol, dimethylformamide, dimethyl sulfoxide, ethyl acetate, chloroform, acetone and benzene; but are only slightly soluble in nonpolar organic solvents such as hexane; and are insoluble in water. It should be noted, however, that 20-deoxynarasin free acid is unstable in alcohols, converting to 20-deoxy-epi-17-narasin free acid. For example, 20-deoxynarasin acid (435.1 mg) was dissolved in methanol (40 ml) and allowed to stand at room temperature for four hours. The solution was then evaporated to dryness under vacuum; the residue was redissolved in dioxane and lyophilized to give 417.8 mg of 20-deoxy-epi-1 7-narasin acid.

[0018] Another substance, chromatographically coincident with A-28086-1 which is described in U.S. Patent 4,038,384, is co-produced with the deoxynarasin complex. Although this substance initially co- precipitates with the deoxynarasin antibiotics, it is readily separated from them by silica-gel chromatography. On silica-gel thin-layer chromatography this substance is less polar than either 20-deoxynarasin or 20-deoxy-epi-17-narasin when ethyl acetate is the developing solvent. Vanillin spray reagent (3% vanillin in methanol + 0.5 ml conc HZSOQ per 100 ml of solution) is convenient for detection. After spraying with vanillin and heating, this substance, like A-28086-1, gives a blue spot while the deoxynarasin antibiotics give bright yellow spots which darken later.

[0019] 20-Deoxynarasin and 20-deoxy-epi-17-narasin are capable of forming salts. The pharmaceutically-acceptable alkali-metal, alkaline-earth-metal and amine salts of 20-deoxynarasin and 20-deoxy-ep/'-17-narasin are also part of this invention. "Pharmaceutically acceptable" salts are salts in which the toxicity of the compound as a whole toward warm-blooded animals is not increased relative to the non-salt form. Representative and suitable alkali-metal and alkaline-earth-metal salts of 20-deoxynarasin and 20-deoxy-epi-1 7-narasin include the sodium, potassium, lithium, cesium, rubidium, barium, calcium, and magnesium salts. Suitable amine salts of 20-deoxynarasin and 20-deoxy-epi-17- narasin include the ammonium and the primary, secondary and tertiary Cl-c4-alkylammonium and hydroxy-C2-C4-alkylammonium salts. Illustrative amine salts include those formed by reaction of 20-deoxynarasin and 20-deoxy-epi-17-narasin with ammonium hydroxide, methylamine, sec-butylamine, isopropylamine, diethylamine, diisopropylamine, ethanolamine, triethylamine, 3-amino-1-propanol and the like.

[0020] The alkali-metal and alkaline-earth-metal cationic salts of 20-deoxynarasin and 20-deoxy-epi-17- narasin are prepared according to procedures commonly employed for the preparation of cationic salts. For example, the free acid form of the antibiotic is dissolved in a suitable solvent such as acetone or dioxane-water; a solution containing the stoichiometric quantity of the desired inorganic base is added to this solution. The salt thus formed can be isolated by routine methods, such as filtration or evaporation of the solvent.

[0021] The salts formed with organic amines can be prepared in a similar manner. For example, the gaseous or liquid amine can be added to a solution of the antibiotic factor in a suitable solution such as acetone, and the solvent and excess amine can be removed by evaporation.

[0022] A preferred method for the preparation of a desired salt of one of the deoxynarasin antibiotics is an appropriate initial choice of isolation procedure, such as, for example, adjusting the pH of the broth with an appropriate base or adding an appropriate cationic salt to the extracting solvent.

[0023] It is well known in the veterinary pharmaceutical art that the form of an antibiotic is not significant when treating an animal with the antibiotic. In most cases, conditions within the animal change the drug to forms other than the form in which it was administered. The salt form in which it may be administered is, therefore, insignificant to the method of treatment. The salt form may, however, be chosen for reasons of economics, convenience, and toxicity.

[0024] The novel antibiotics of this invention are produced by culturing a deoxynarasin-producing strain of Streptomyces aureofaciens under submerged aerobic conditions in a suitable culture medium until substantial antibiotic activity is produced. The antibiotics are recovered by using various isolation and purification procedures commonly used and understood in the art.

[0025] The organism useful for the preparation of the deoxynarasin antibiotics was obtained by N-methyl-N'-nitro-N-nitrosoguanidine-induced mutation of Streptomyces aureofaciens NRRL 8092. The taxonomic basis on which S. aureofaciens NRRL 8092 was classified as a strain of Streptomyces aureofaciens Duggar, is described in U.S. Patent 4,038,384.

[0026] The Streptomyces aureofaciens culture useful for production of the deoxynarasin antibiotics has been deposited and made a part of the stock culture collection of the Northern Regional Research Center, U.S. Dept. of Agriculture, Agricultural Research Service, Peoria, Illinois, 61604, from which it is available to the public under the number NRRL 11181.

[0027] The culture, which is here identified as NRRL 11181, has been isolated and mutated from a culture of Streptomyces aureofaciens which was originally isolated from a soil sample obtained from Mount Ararat in Turkey. The original soil isolate was cultured on agar plates, and sub-cultures were obtained by removing individual colonies of the microorganism from the surface of the agar plate. One of the single isolates obtained from a culture of the original soil isolate was the culture which is identified herein as NRRL 5758.

[0028] The above naturally selected culture was plated again, and a single colony was chosen from it. This process of natural selection was repeated eight times, and a ninth-generation single-colony isolate was chosen for further selection.

[0029] The ninth-generation isolate was grown in a chemically defined agar medium with one percent galactose as the sole carbon source. A spore suspension was prepared by ultrasonically agitating the agar medium to dislodge the spores, and hyphal fragments were minimized by filtering the suspension through a Whatman No. 1 filter paper.

[0030] The spore suspension was grown in a complex liquid medium, the pH of which was adjusted to 8.8, which contained 2 mg./ml. of N-methyl-N'-nitro-N-nitrosoguanidine, for 72 hours at 30°C. The cultures growing on the medium were then harvested and homogenized with a tissue grinder.

[0031] The homogenized culture was diluted and plated on agar plates and incubated at 30°C. until idividual colonies could be distinguished. One of the individual selected colonies was used to start a new culture which is here identified as NRRL 8092.

[0032] The culture identifies as NRRL 8092 was grown in a chemically defined agar medium with glucose as the sole carbon source. A suspension consisting of both spores and hyphal fragments was prepared by ultrasonically agitating the agar medium. The mixed spore and hyphal suspension was then exposed to 2 mg./ml. of N-methyl-N'-nitro-N-nitrosoguanidine in a complex liquid medium at pH 8.8 for 96 hours on a 30°C. shaker, and the culture was then harvested, homogenized, and plated as was described in the step immediately above. One of the individual colonies selected from these agar plates was grown to prepare the culture which is here identified as NRRL 11181.

[0033] It will be recognized by those skilled in the art that, given our invention, it should now be possible to generate additional strains which have essentially the same biosynthetic capabilities as S. aureofaciens NRRL 11181 (i.e. the ability to produce 20-deoxynarasin and 20-deoxy-epi-17-narasin) by subjecting S. aureofaciens NRRL 5758, NRRL 8092, or NRRL 11181, to mutagenic treatment. Although N-methyl-N'-nitro-N-nitrosoguanidine was used to obtain S. aureofaciens NRRL 11181, other known mutagens such as ultraviolet rays, X-rays, high-frequency waves, radioactive rays and other chemical agents could be used to induce a similar mutagenesis. Part of our invention, therefore, is the method of producing deoxynarasin antibiotic complex which comprises cultivating Streptomyces aureofaciens NRRL 11181 or a mutant thereof capable of producing the antibiotic complex.

[0034] The culture medium used to grow Streptomyces aureofaciens NRRL 11181 can be any one of a number of media. For economy in production, optimal yield, and ease of product isolation, however, certain culture media are preferred. Thus, for example, preferred carbohydrate sources in large-scale fermentation are tapioca dextrin and sucrose, although glucose, corn starch, fructose, mannose, maltose, lactose, and the like can also be employed. Corn oil, peanut oil, soybean oil and fish oil are other useful sources of carbon. A preferred nitrogen source is enzyme-hydrolyzed casein, although peptones, soybean meal, cotton-seed meal, amino acids such as glutamic acid, and the like are also useful. Among the nutrient inorganic salts which can be incorporated in the culture media are the customary soluble salts capable of yielding sodium, magnesium, calcium, ammonium, chloride, carbonate, sulfate, nitrate, and like ions.

[0035] Essential trace elements necessary for the growth and development of the organism should also be included in the culture medium. These trace elements commonly occur as impurities in other constituents of the medium in amounts sufficient to meet the growth requirements of the organism.

[0036] It may be necessary to add small amounts (i.e. 0.2 mt/1.) of an antifoam agent such as polypropylene glycol to large-scale fermentation media if foaming becomes a problem.

[0037] Although it is not essential, antibiotic production is enhanced by the addition of a small amount of oil such as soybean oil.

[0038] For production of substantial quantities of the deoxynarasin antibiotics, submerged aerobic fermentation in tanks is preferred. Smaller quantities may be obtained by shake-flask culture. Because of the time lag in antibiotic production commonly associated with inoculation of large tanks with the spore form of the organism, it is preferable to use a vegetative inoculum. The vegetative inoculum is prepared by inoculating a small volume of culture medium with the spore form or mycelial fragments of the organism to obtain a fresh, actively growing culture of the organism. The vegetative inoculum is then transferred to a larger tank. The medium used for the growth of the vegetative inoculum can be the same as that employed for larger fermentations, but other media can also be employed.

[0039] The deoxynarasin-producing organism can be grown at temperatures between about 20° and about 40°C. Optimum deoxynarasin production appears to occur at temperatures of about 27°-30°C.

[0040] As is customary in aerobic submerged culture processes, sterile air is blown through the culture medium. For efficient growth of the organism the volume of air used in tank production is preferably above 0.1 volume of air per volume of culture medium per minute. For efficient antibiotic production the volume of air used in tank production is preferably above 0.25 volume of air per volume of culture medium per minute. High levels of dissolved oxygen do not depress antibiotic production.

[0041] Production of the antibiotics can be followed during the fermentation by testing samples of the broth or of extracts of the mycelial solids for antibiotic activity against organisms known to be sensitive to the antibiotics. One assay organism useful in testing the antibiotics of the present invention is gacillus subtilis ATCC 6633. The bioassay is conveniently performed by paper-disc assay on agar states.

[0042] Another convenient monitoring method is by turbidometric assay on a semiautomated system (Autoturb@ microbiological assay system, Elanco) described by N. R. Kuzel and F. W. Kavanaugh in J. Pharmaceut. Sci. 60 (5), 764 and 767 (1971). In testing the deoxynarasin antibiotics, the following test parameters are used: Staphylococcus aureus (H-Heatley) NRRL B-314 in a nutrient broth medium (pH 7), incubated for four hours at 37°C. Test samples and standard are dissolved in methanol-water (1:1) The standard, A-28086 factor A, is presented to the Autoturb@ carrousel at concentrations of 1, 2, 3 4, and 5 mcg/ml.

[0043] The initial pH of the uninoculated culture medium varies with the medium used. In general, the pH should be in the range of 6.0 to 7.5. The harvest pH at the end of the fermentation is usually slightly higher, in the range of 6.5 to 8.0.

[0044] Generally, antibiotic activity is detectable as early as the second day of the fermentation. Maximum production of antibiotic activity usually occurs between about the fourth and the tenth days.

[0045] Following their production under submerged aerobic fermentation conditions, the deoxynarasin antibiotics previously described can be recovered from the fermentation medium by methods commonly used in the fermentation art. The antibiotics produced during the fermentation occur in both the mycelial mass and in the filtered broth. Maximum recovery of the deoxynarasin antibiotics is accomplished, therefore, by a combination of methods, including filtration, extraction, and adsorption chromatography. A preferred solvent for separating the deoxynarasin antibiotics from either whole or filtered fermentation broth is ethyl acetate, although other commonly used solvents are satisfactory.

[0046] An especially advantageous method of separating the deoxynarasin antibiotics is to lower the pH of the whole fermentation broth to about pH 3.0. At this pH the deoxynarasin antibiotics are conveniently separated with the mycelial mass by filtration. This method is described for recovery of the related antibiotics, A-28086 factors A, B, and D and salinomycin, by Boeck and Berg in U.S. 4,009,262. Another advantageous aspect of this method involves adding a bicarbonate such as, for example, sodium bicarbonate, to the whole broth in amounts of approximately one gram per liter. Using this method, the doexynarasin antibiotics are conveniently separated with the mycelial mass in salt form. Methanol is a preferred solvent for separating the antibiotics from the mycelial mass, but other lower alcohols and ketones are also suitable.

[0047] Azeotropic distillation can also be advantageously used in recovery of the deoxynarasin antibiotics. In this method an organic solvent which forms an appropriate azeotrope with water is added to the aqueous fermentation broth. This solvent-broth mixture is subjected to azeotropic distillation in order to remove at least half the water from the broth, leaving a water-solvent mixture in which the deoxynarasin antibiotics are in solution in the organic solvent. Insoluble by-products can be separated by suitable means such as filtration or centrifugation. The deoxynarasin antibiotics can then be recovered from the organic solution by well-known procedures such as evaporation of solvent, precipitation by adding a nonsolvent, or extraction.

[0048] Organic solvents which form appropriate azeotropes with water in order to carry out such a re- covery procedure include, illustratively, butyl alcohol, amyl alcohol, hexyl alcohol, benzyl alcohol, butyl acetate, amyl acetate, 1,2-dichloroethane, 3-pentanone, 2-hexanone, benzene, cyclohexanone, toluene, the xylenes and the like.

[0049] There is special advantage in recovery by azeotropic distillation on large-scale fermentation processes. Both water and solvent taken overhead in the azeotrope can be separated by known techniques and thereafter recycled for further use. The water thus removed is free of contaminants and does not require a waste disposal process.

[0050] Further purification of the deoxynarasin antibiotics includes additional extraction and adsorption procedures. Adsorptive materials such as silica gel, carbon, Florisil® (magnesium silicate, Floridin Co., P.O. Box 989, Tallahassee, Fla.) and the like can be advantageously used.

[0051] Alternatively, the culture solids, including medium constituents and mycelium can be used without extraction or separation, but preferably after removal of water, as a source of the deoxynarasin antibiotic complex. For example, after production of deoxynarasin antibiotic activity, the culture medium can be dried by lyophilizing or drum drying and mixed directly into feed premix.

[0052] In another aspect, after production of deoxynarasin activity in the culture medium, the mycelium can be separated and dried to give a product which can be used directly in a feed premix. When separating the mycelium for such use, the addition of calcium carbonate (about 10 g/L) aids in filtration and gives an improved dried product.

[0053] Under the conditions used thus far, 20-deoxynarasin and 20-deoxy-epi-1 7-narasin are recovered as the major factors from the Streptomyces aureofaciens strain described previously and designated as NRRL 11181. Some minor factors are also recovered from S. aureofaciens NRRL 11181 in amounts too small to permit characterization. Although the ratio of factors varies depending on the fermentation and isolation conditions used, in general more 20-deoxy-epi-17-narasin than 20-deoxynarasin is recovered.

[0054] 20-Deoxynarasin and 20-deoxy-epi-17-narasin are separated from each other and isolated as individual compounds by the use of well-known methods such as column chromatography, thin-layer chromatography, counter-current distribution and the like. For example, column chromatography over silica gel is used to separate 20-deoxynarasin and 20-deoxy-epi-1 7-narasin by eluting the column with varying solvent mixtures. For example, using benzene-ethyl acetate solvent mixtures over a silica-gel column, 20-deoxy-epi-1 7-narasin is eluted first, and 20-deoxynarasin is eluted later. Thin-layer chromatography on silica gel, using a 100% ethyl acetate solvent, is a convenient method for monitoring elution progress.

[0055] The deoxynarasin antibiotics of this invention are antibacterial agents. For example, the relative microbiological activity of 20-deoxy-epi-17-narasin (free acid) is described in Table IV. The conventional disc-diffusion method was used.



[0056] In one aspect, the deoxynarasin antibiotics inhibit the growth of anaerobic bacteria. The minimal inhibitory concentrations (MIC) at which 20-deoxy-epi-17-narasin (free acid) inhibits various anaerobic bacteria, determined by standard agar-dilution assay, are summarized in Table V. End points were read after 24-hour incubation period.



[0057] Activity against Mycoplasma is another useful aspect of the antimicrobial activity of the deoxynarasin antibiotics. Mycoplasma species, also known as pleuropneumonia-like (PPLO) organisms, are pathogenic to man and various animals. Agents active against PPLO organisms are especially needed by the poultry industry. The minimal inhibitory concentrations (MIC) of 20-deoxy-epi-17- narasin (free acid) against illustrative Mycoplasma species, as determined by in vitro broth-dilution studies, are summarized in Table VI.



[0058] The deoxynarasin antibiotics are also antiviral agents. For example, 20-deoxy-epi-1 7-narasin is active against rhinovirus type 3, vaccinia virus, herpesvirus and influenza A virus, as demonstrated by in vitro plaque suppression tests, similar to that described by Siminoff, Applied Microbiology 9 [1], 66-72 (1961).

[0059] A deoxynarasin antibiotic of this invention can therefore be administered orally, topically or parenterally to mammals for the control of viruses. Useful dosage levels for prevention or treatment of viral disease vary from about 1 to about 5 mg/kg of mammalian body weight, depending upon the virus and upon whether the drug is to be used prophylactically or therapeutically.

[0060] Furthermore, solutions containing a deoxynarasin antibiotic, preferably together with a surfactant, can be used to decontaminate the in vitro habitat on which viruses, such as polio or herpes, are present. Solutions containing from about 1 to about 1500 mcg/ml of a deoxynarasin antibiotic are effective in the control of viruses.

[0061] The acute toxicities of 20-deoxy-epi-17-narasin (free acid) and 20-deoxynarasin (Na salt), when administered intraperitoneally to mice and expressed as LD50, are 201 mg/kg and 5 mg/kg, respectively.

[0062] Anticoccidial activity is an important property of the deoxynarasin antibiotics of this invention. For example, in vitro experiments show that 20-deoxynarasin (Na salt) and 20-deoxy-epi-17-narasin (free acid) are active against Eimeria tenella, the protozoan organism most associated with coccidiosis, at levels as low as 0.2 ppm.

[0063] A feeding experiment in young chickens confirms that the deoxynarasin antibiotics have anticoccidial activity in vivo. In this experiment 20-deoxynarasin (Na salt), administered at a level of 100 ppm in the diet to chicks challenged with Eimeria tenella, prevented mortality, improved weight gains, and decreased the number of lesions in the chicks. The results of this experment are summarized in Table VII.



[0064] For the prevention or treatment of coccidiosis in poultry, an effective anticoccidial amount of deoxynarasin antibiotic is administered to birds, preferably orally on a daily basis. The deoxynarasin antibiotic can be supplied in many ways, but it is most conveniently supplied with a physiologically- acceptable carrier, preferably the feed ingested by the birds. Although a variety of factors must be considered in determining an appropriate concentration of deoxynarasin antibiotic, the rates of administration will be generally in the range of 0.003 to 0.03 percent by weight of unmedicated feed, and preferably in the range of 0.004 to 0.02 percent.

[0065] This invention also relates to anticoccidial feed compositions for poultry comprising poultry feed and from about 35 to about 180 grams per ton of a deoxynarasin antibiotic.

[0066] The ability to improve feed-utilization efficiency in animals is another important property of the deoxynarasin antibiotics. For example, deoxynarasin antibiotics improve feed-utilization efficiency in ruminants which have a development rumen function.

[0067] As discussed, efficiency of carbohydrate utilization in ruminants is increased by treatments which stimulate the animal's rumen flora to produce propionate compounds rather than acetate or butyrate compounds. The efficiency of feed use can be monitored by observing the production and concentration of propionate compounds in rumen fluid, using methods as described in U.S. 4,038,384.

[0068] Results in in vitro tests with 20-deoxynarasin (Na salt) and 20-deoxy-epi-17-narasin (free acid), showing the ratio of volatile-fatty-acid (VFA) concentrations in treated flasks to concentrations in control flasks, are shown in Table VIII.



[0069] The deoxynarasin antibiotics ot this invention are typically effective in increasing propionates and, thereby, the efficiency of feed-utilization when administered to ruminants orally at rates of from about 0.05 mg/kg/day to about 5.0 mg/kg/day. Most beneficial results are achieved at rates of from about 0.1 mg/kg/day to about 2.5 mg/kg/day. A preferred method of administration of an antibiotic of this invention is by mixing it with the animals' feed; however, it can be administered in other ways, for example, in tablets, drenches, boluses, or capsules. Formulation of these various dosage forms can be accomplished by methods well known in the veterinary pharmaceutical art. Each individual dosage unit should contain a quantity of a compound of this invention directly reJated to the proper daily dose for the animal to be treated.

[0070] This invention further relates to feed compositions adapted to fatten ruminants such as cattle and sheep. These feed compositions comprise cattle feed and from 1 to 30 grams per ton of a deoxynarasin antibiotic.

[0071] Swine dysentery is a common disease in the United States of other countries, annually causing losses in stock to swine growers world-wide. U.S. 3,947,586 teaches that polyether antibiotics are useful in the prevention and treatment of swine dysentery. Since the deoxynarasin antibiotics are new members of the class of polyether antibiotics, they should also be effective in the prevention and treatment of swine dysentery.

[0072] For the prevention or treatment (control) of dysentery in swine, it is preferable to incorporate an effective amount of a deoxynarasin antibiotic into the feed ration. The deoxynarasin antibiotics of this invention should be typically effective in preventing or controlling swine dysentery when administered to swine orally at rates of from about 35 to about 150 grams per ton of active compounds. An especially preferred rate should be about 100 grams of active compound per ton. Although the preferred method of administration is by mixing it with the animals' feed, it can also be administered in other ways, for example, in tablets drenches, boluses, or capsules. Each individual dosage unit should contain a quantity of an antibiotic of this invention directly related to the proper daily dose for the animal to be treated.

[0073] This invention further relates to feed compositions for swine comprising swine ration and an effective amount of a deoxynarasin antibiotic. As discussed, an effective amount is typically one in the range of from about 35 to about 150 grams of a deoxynarasin antibiotic per ton of feed.

[0074] The deoxynarasin antibiotics are antiviral agents and are also active against anaerobic bacteria, such as Clostridium perfringens. The deoxynarasin antibiotics are, therefore, beneficial in the treatment or prevention of enteritis in chickens, swine, cattle and sheep and in the treatment of enterotoxemia in ruminants.

[0075] Certain deoxynarasin compounds (20-deoxynarasin and its salts) exhibit ion-binding and ion- transport properties and are, therefore, ionophores (ion-bearers) (see B. C. Pressman, Alkali Metal Chelators- The lonophores, in "Inorganic Biochemistry," Volume 1, G. L. Eichhorn, Elsevier, 1973). These compounds can be used when the selective removal of a particular cation is desired. Examples of such uses include the removal and recovery of silver ions from solutions in photography, the removal of toxic cations from industrial waste steams before such streams are discharged to the environment, and desalinization of sea water. A deoxynarasin compound can be used as one component of an ion-specific electrode (see O. Kedem, et al., U.S. Patent 3,753,887). These compounds alter the cation permeability of both natural and artificial membranes. A deoxynarasin compound can be used, therefore, as a component in a membrane used for the selective transport of cations against a concentration gradient. One potential application of this property is in recovery of heavy and precious metals on a commercial basis [see E. L. Cussler, D. F. Evans, and Sister M. A. Matesick, Science 172, 377 (1971)].

[0076] In yet another aspect, 20-deoxynarasin and its salts are active as an inhibitor of the enzyme ATPase. ATPase, an alkali-metal-sensitive enzyme found in cell membranes, is involved in the energy necessary for active transport, "Active transport" refers to the energy-requiring series of operations whereby intracellular and extracellular fluids maintain their compostions. Inhibitors of ATPase reduce the energy required for active transport. In vitro tests have shown that 20-deoxynarasin (Na salt) inhibits cation transport ATPase in liver mitochondria at a half effective concentration of 0.065 mcg/ml.

[0077] 20-Deoxynarasin and its salts are also potential cardiotonic agents. In tests using isolated guinea- pig atria, for example, 20-deoxynarasin increased cardiac contractility. Response to this test is expressed as a percentage of the maximal contractile tension that could be elicited by a challenge dose of norepinephrine (10-4M). 20-Deoxynarasin (Na salt), at a 10-5 molar concentration, produced a mean (± standard error) increase in contractile tension of 43.8 t 1.4 (n=4) percent. For a more detailed description of this test, see U.S. 3,985,893.

[0078] The contractile force of mammalian heart muscle in a warm-blooded mammal can be enhanced by administering an effective nontoxic dcse of 20-deoxynarasin or a pharmaceutically acceptable salt thereof. An effective nontoxic dose is a dose in the range of from about 30 to about 500 mcg/kg of body weight. A preferable dose range is from about 30 to about 100 mcg/kg of body weight. For this method, the antibiotic is administered parenterally, for example by intravenous infusion. A suitable method of administration is the drip method wherein the antibiotic is incorporated in a standard i.v. solution such as a dextrose solution.

[0079] 20-Deoxynarasin is preferably administered at doses below about 100 mcg/kg until the desired enhancement of the contractile force is observed. Thereafter the amount of 20-deoxynarasin administered can be regulated by the rate of infusion needed to maintain the desired response. As with the clinical administration of other inotropic agents, the dose of 20-deoxynarasin adminstered may be varied in a given clinical case according to such factors as the individual's tolerance of 20-deoxynarasin, the nature of the heart's affliction, e.g., the extent of damage to the heart muscle, and the age and general physical condition of the patient.

[0080] The positive inotropic agent 20-deoxynarasin can be used in a variety of clinical situations broadly classified as cardiogenic shock. Such conditions include, for example, myocardial infarction, congestive heart failure, and post-operative cardiogenic shock.

[0081] In order to illustrate more fully the operation of this invention the following examples are provided.

Example 1


A. Shake-flask fermentation



[0082] A culture of Streptomyces aureofaciens NRRL 11181 was prepared and maintained on a agar slant having the following composition:



[0083] The slant was inoculated with Streptomyces aureofaciens NRRL 11181, and the inoculated slant was incubated at 30°C. for up to 7 days. The mature slant culture was covered with sterile beef serum and scraped with a sterile loop to loosen the spores. The resulting beef-serum suspension of spores and mycelial fragments was lyophilized into a maximum of 6 pellets.

[0084] One lyophilized pellet thus prepared was used to inoculate 50 ml of a vegetative medium having the following composition:



[0085] The inoculated vegetative medium, in a 250-ml Erlenmeyer flask, was incubated at 30°C. foi some 24 to 48 hours on a shaker rotating through an arc 2 inches in diameter at 250 RPM.

[0086] The incubated vegetative medium above described (50 ml) was used to inoculate 250 ml of one of the following fermentation media:

Medium I:







[0087] The fermentation was incubated for a period of up to 10 days at 30°C. on a 250-RPM rotary shaker with a 2-inch arc.

B. Tank Fermentation



[0088] The tank fermentation is carried out using vegetative and fermentation media as described in Section A for shake-flask fermentation. For tank fermentation 10 ml of the vegetative medium are used to inoculate 400 ml of a second-stage vegetative medium in a 2-liter Erlenmeyer flask. After a 24-hour incubation at 30°C., 800 ml of the second-stage vegetative medium are used to inoculate 100 liters of fermentation medium in a 165-liter fermentation tank. The pH of the medium after sterilization at 121°C. for 45 minutes is approximately 6.8 ± 0.1. Fermentation is allowed to proceed for 10 days at 30 ± 1 °C. The tank is aerated with sterile air at a rate of 0.5 volumes of air per volume of culture medium per minute, stirring with conventional agitators at 300 RPM.

Example 2


Separation of the Deoxynarasin Complex



[0089] The pH of whole fermentation broth (4 I), obtained by the method described in Example 1 using medium II, was lowered to pH 3.0 by the addition of conc. HCI, stirring for 1 hour. The resulting solution was filtered with a filter aid (125 g Hyflo Super-Cel, a diatomaceous earth, Johns-Manville Corp.). The separated mycelial cake was extracted batchwise, using a blender, with a total of 2 liters of methanol which contained 50 g NaHC03 per liter. The methanol filtrate was evaporated under vacuum to a volume of approximately 450 ml; the pH of this solution was adjusted to pH 7.5 by the addition of conc. HCI. The resulting solution was extracted twice with CHCI3 (500 ml). The CHCI3 extracts were combined, dried over Na2SO4 and filtered. The filtrate was evaporated under vacuum to give 2.0 g of crude deoxynarasin complex.

Example 3


Isolation of Deoxynarasin and Epi-Deoxynarasin



[0090] Crude deoxynarasin complex (2 g), obtained as described in Example 2, was dissolved in a minimal amount of benzene and applied to a 1.5- x 22-cm column of silica gel (Merck 7729). The fractions isolated, solvents used, and amounts yielded are shown in the following table:





[0091] Fractions were monitored by TLC, using an ethyl acetate solvent system. Fractions 16-17 (126- mg) contained 20-deoxy-epi-17-narasin. Fractions 18-23 contained a mixture of 20-deoxynarasin and 20-deoxy-epi-1 7-narasin.

[0092] A mixture of 20-deoxynarasin and 20-deoxy-epi-17-narasin, obtained as above-described for fractions 18-23, was chromatographed by preparative TLC, using an ethyl acetate solvent system. The mixture (105 mg on one plate and 130 mg on another plate) was dissolved in a small amount of CH2CI2 and placed on a silica-gel (Merck) preparative plate. After the plate had been allowed to develop, the two separated materials were observed by ultraviolet light. Each of the areas representing the two materials were removed from the plate and extracted with CH2CI2:CH3OH (4:1). In this system deoxynarasin is the slower moving of the two components. From the plate containing 105 mg of material, 7.5 mg of 20-deoxy-epi-17-narasin and 27 mg of deoxynarasin were recovered. From the plate containing 130 mg of mixture, 4.0 mg of 20-deoxy-epi-1 7-narasin and 56 mg of 20-deoxynarasin were recovered.

Example 4


Alternate Isolation of 20-Deoxynarasin



[0093] Whole fermentation broth (95 1) was adjusted to about pH by the addition of HCI and then was stirred for 1 hour. Filter aid (Hyflo Supercel, 3%) was added, and the broth was filtered. The separated mycelial cake was extracted twice with about 45 I. of acetone which contained 50 g of NaHC03 per liter. The acetone extracts were combined and concentrated under vacuum to give about 10 liters of aqueous solution. The pH of this solution was adjusted to 8.0 by the addition of 5N HCI, and the resulting solution was extracted 3 times with 1/2 volumes of CH2CI2. The CH2CI2 extracts were combined and evaporated under vacuum to give an oily residue. This residue was taken up in 500 ml of upper phase of the solvent system hexane:methanol:water (10:7:1). The upper phase was extracted 6 times with 300-ml portions of lower phase. These extracts were combined and concentrated under vacuum to give a residue. This residue was dissolved in dioxane; the dioxane solution was lyophilized to give 19.4 g of deoxynarasin complex.

[0094] Several samples, obtained in the same manner, were combined (40 g), dissolved in toluene and loaded onto a silica-gel column in a liquid chromatograph (Waters' Associates Prep. LC/System 500). The column was eluted with a toluene:ethyl acetate (9:1) solvent system at a flow rate of 250 ml/min, collecting fractions having a volume of 250 ml. Fraction content was monitored by TLC. Fractions 37-52 were combined and concentrated under vacuum to give a residue which was redissolved in dioxane and lyophilized to give 7.8 g of purified material rich in 20-deoxynarasin. This material was rechromatographed on the Waters' Prep LC/System 500 as above described. After eluting 50 fractions with the toluene:ethyl acetate (9:1) solvent system, the eluting soivent was changed to 100% ethyl acetate. Fractions 51-53 were combined and evaporated under vacuum to give a residue which was dissolved in dioxane and lyophilized to give 1.12 g of 20-deoxynarasin as its sodium salt.

Example 5


Preparation of 20-Deoxynarasin Free Acid



[0095] 20-Deoxynarasin sodium salt (200 mg) was dissolved in ethyl acetate (10 ml). This solution was washed with 0.1 N HCI (10 ml) and then twice with water (5 ml). The resulting organic layer was evaporated to dryness to give a residue which was redissolved in dioxane and lyophilized to give 139.6 mg of 20-deoxynarasin free acid as a white solid.

Example 6


Chick Ration for Coccidiosis Control



[0096] A balanced, high-energy ration adapted to feed chicks for rapid weight gain is prepared by the following recipe:



[0097] Deoxynarasin antibiotic complex, 20-deoxy-narasin or 20-deoxy-epi-17-narasin (about 0,01% by weight) is mixed with this ration in accordance with standard feed-mixing techniques. Chicks fed such a ration, with water ad libitum, are protected against exposure to coccidiosis.

Example 7


Improved Beef-Cattle Ration



[0098] A balanced high-grain beef-cattle ration is prepared as follows:





[0099] Deoxynarasin antibiotic complex, 20-deoxynarasin or 20-deoxy-epi-17-narasin (about 0.004% by weight) is mixed with this ration according to standard techniques. The mixed feed is compressed into pellets. At an average daily ingestion rate of 6.8 kg of feed per animal, this feed supplies approximately 300 mg of antibiotic per animal per day.

Example 8


Improved Swine Ration



[0100] A premix is prepared by standard methods using the following ingredients:

This premix is added to commercial swine ration, using standard feed-mixing techniques to give a final level of active compound of 100 grams/ton.


Claims

1. A deoxynarasin antibiotic complex comprising 20-deoxynarasin and 20-deoxy-epi-17-narasin or a pharmaceutically-acceptable salt thereof.
 
2. 20-Deoxynarasin of the formula

and its pharmaceutically acceptable salts.
 
3. 20-deoxy-epi-17-narasin of the formula

and its pharmaceutically acceptable salts.
 
4. A process of producing the deoxynarasin antibiotic complex as defined in claim 1 which comprises cultivating Streptomyces aureofaciens NRRL 11181, or a mutant thereof capable of producing the antibiotic complex of claim 1 in a culture medium containing assimilable sources of carbohydrate, nitrogen and inorganic salts under submerged aerobic fermentation conditions until a substantial amount of antibiotic activity is produced, and recovering the antibiotic complex in the form of the acids or their pharmaceutically-acceptable salts.
 
5. The process of claim 4 wherein the Streptomyces aureofaciens is the organism identified as NRRL 11181.
 
6. The process of either of claims 4 or 5 wherein the deoxynarasin antibiotic complex, or pharmaceutically-acceptable salts thereof, is isolated from the culture medium.
 
7. The process of claim 6 wherein 20-deoxynarasin, 20-deoxy-epi-17-narasin or a pharmaceutically acceptable salt thereof is isolated from the deoxynarasin antibiotic complex.
 
8. A method for increasing feed-utilization efficiency in ruminant animals which comprises orally administered to such animals an effective propionate increasing amount of deoxynarasin antibiotic complex, 20-deoxynarasin, 20-deoxy-epi-17-narasin, or a pharmaceutically acceptable salt thereof.
 
9. A feed composition comprising cattle feed and 20-deoxynarasin, 20-deoxy-epi-17-narasin, deoxynarasin antibiotic complex or a pharmaceutically acceptable salt thereof.
 
10. A feed composition comprising poultry feed and an anti-coccidial amount of 20-deoxynarasin, 20-deoxy-epi-17-narasin, deoxynarasin antibiotic complex or a pharmaceutically acceptable salt thereof.
 
11. A feed composition comprising swine feed and an amount effective to control swine dysentery of 20-deoxynarasin, 20-deoxy-epi-17-narasin, deoxynarasin antibiotic complex or a pharmaceutically acceptable salt thereof.
 
12. A biologically pure culture of the microorganism Streptomyces aureofaciens which is indentified as NRRL 11181, said culture having the ability to produce 20-deoxynarasin or 20-deoxy-epi-1 7-narasin upon fermentation in an aqueous nutrient medium containing assimilable sources of carbohydrate, nitrogen and inorganic salts.
 
13. A culture of the microorganism Streptomyces aureofaciens which is identified as NRRL 11181.
 


Revendications

1. Complexe antibiotique de déoxynarasine, caractérisé en ce qu'il comprend de la 20- déoxynarasine et de la 20-déoxy-epi-7-narasine ou un de leurs sels pharmaceutiquement acceptables.
 
2. 20-déoxynarasine de formule:

et ses sels pharmaceutiquement acceptables.
 
3. 20-déoxy-epi-7-narasine de formule:

et ses sels pharmaceutiquement acceptables.
 
4. Procédé de préparation du complexe antibiotique de déoxynarasine défini dans la revendication 1, caractérisé en ce qu'il consiste à cultiver Streptomyces aureofaciens NRRL 11181 ou une des ses souches mutantes capable de produire le complexe antibiotique de la revendication 1 dans un milieu de culture contenant des sources assimolables de carbohydrates, d'azote et de sels inorganiques dans des conditions de fermentation àrobie submergée jusqu'à ce qu'on obtienne une importante quantité d'activité antibiotique, puis récupérer le complexe antibiotique sous forme d'acides ou de leurs sels pharmaceutiquement acceptables.
 
5. Procédé suivant la revendication 4, caractérisé en ce que Streptomyces aureofaciens est l'organisme identifié sous le numéro NRRL 11181.
 
6. Procédé suivant l'une quelconque des revendications 4 et 5, caractérisé en ce que le complexe antibiotique de déoxynarasine ou ses sels pharmaceutiquement acceptables est ou sont isolé(s) du milieu de culture.
 
7. Procédé suivant la revendication 6, caractérisé en ce que la 20-déoxynarasine, la 20-déoxv- epi-7-narasine ou un de leurs sels pharmaceutiquement acceptables est isolé du complexe antibiotique de déoxynarasine.
 
8. Procédé en vue d'accroître l'efficacité de l'ingestion de nourriture chez les animaux ruminants, caractérisé en ce qu'il consiste à administrer, par voie orale, à ces animaux, un complexe antibiotique de déoxynarasine, la 20-déoxynarasine, la 20-déoxy-epi-7-narasine ou un de leurs sels pharmaceutiquement acceptables en une quantité augmentant efficacement la teneur en propionate.
 
9. Composition de nourriture comprenant un aliment pour bétail et de la 20-déoxynarasine, de la 20-déoxy-épi-17-narasine, un complexe antibiotique de déoxynarasine ou un de leurs sels pharmaceutiquement acceptables.
 
10. Composition de nourriture comprenant un aliment pour volaille et de la 20-déoxynarasine, de la 20-déoxy-epi-7-narasine, un complexe antibiotique de déoxynarasine ou un de leurs sels pharmaceutiquement acceptables en une quantité anticoccidienne.
 
11. Composition de nourriture comprenant un aliment pour porcs et de la 20-déoxynarasine, de la 20-déoxy-epi-7-narasine, un complexe antibiotique de déoxynarasine ou un de leurs sels pharmaceutiquement acceptables en une quantité permettant de combattre efficacement la dysenterie chez les porcs.
 
12. Culture biologiquement pure du microorganisme Streptomyces aureofaciens qui est identifié par le numéro NRRL 11181, cette culture ayant la capacité de produire la 20-déoxynarasine ou la 20- déoxy-epi-7-narasine par fermentation dans un milieu nutritif aqueux contenant des sources assimilables de carbohydrates, d'azote et de sels inorganiques.
 
13. Culture du micro-organisme Streptomyces aureofaciens qui est identifié par le numéro NRRL 11181.
 


Ansprüche

1. Deoxynarasin-Antibiotikumkomplex, bestehend aus 20-Deoxynarasin, und 20-Deoxy-epi-17- narasin oder einem pharmazeutisch unbedenkliches Salz hiervon.
 
2. 20-Deoxynarasin der Formel

und dessen pharmazeutisch unbedenkliche Salze.
 
3. 20-Deoxy-epi-17-narasin der Formel

und dessen pharmazeutisch unbedenkliche Salze.
 
4. Verfahren zur Herstellung des Deoxynarasin-Antibiotikumkomplexes gemäß Anspruch 1, dadurch gekennzeichnet, daß man Streptomyces aureofaciens NRRL 11181 oder eine Mutante hiervon, die zur Bildung des Antibiotikumkomplexes gemäß Anspruch 1 befähigt ist, in einem Kulturmedium, das assimilierbare Quellen für Kohlenhydrat, Stickstoff und anorganische Salze enthält, unter submersen aeroben Fermentationsbedingungen bis zur Bildung einer wesentlichen Menge an antibiotischer Aktivität züchtet und den Antibiotikumkomplex in Form de Säuren oder ihrer pharmazeutisch unbedenklichen Salze gewinnt.
 
5. Verfahren nach Anspruch 4, dadurch gekennzeichnet, daß man als Streptomyces aureofaciens den als NRRL 11181 identifizierten Organismus verwendet.
 
6. Verfahren nach einem der Ansprüche 4 oder 5, dadurch gekennzeichnet, daß man den Deoxynarasin-Antibiotikumkomplex oder pharmazeutisch unbedenkliche Salz hiervon aus dem Kulturmedium isoliert.
 
7. Verfahren nach Anspruch 6, dadurch gekennzeichnet daß man 20-Deoxynarasin, 20-Deoxy-epi-17-narasin oder ein pharmazeutisch unbedenkliches Salz hiervon aus dem Deoxynarasin-Antibiotikumkomplex isoliert.
 
8. Verfahren zur Erhöhung der Futterverwertung von Wiederkäuern, dadurch gekennzeichnet, daß man solchen Tieren oral eine eine Propionaterhöhung ergebende Menge an Deoxynarasin-Antibiotikumkomplex, 20-Deoxynarasin, 20-Deoxy-epi-17-narasin oder ein pharmazeutisch unbedenkliches Salz hiervon verabreicht.
 
9. Futtermittel, dadurch gekennzeichnet, daß es ein Rinderfutter und 20-Deoxynarasin, 20-Deoxy-epi-17-narasin, Deoxynarasin-Antibiotikumkomplex oder ein pharmazeutisch unbedenkliches Salz hiervon verabreicht..
 
10. Futtermittel, dadurch gekennzeichnet, daß es ein Geflügelfutter und eine anticoccidial wirksame Menge an 20-Deoxynarasin, 20-Deoxy-epi-17-narasin, Deoxynarasin-Antibiotikumkomplex oder einem pharmazeutisch unbedenklichen Salz hiervon enthält.
 
11. Futtermittel, dadurch gekennzeichnet, daß es ein Schweinefutter und eine zur Bekämpfung von Schweinedysenterie ausreichende Menge an 20-Deoxynarasin, 20-Deoxy-epi-17-narasin, Deoxynarasin-Antibiotikumkomplex oder einem pharmazeutisch unbedenkliches Salz hiervon enthält.
 
12. Biologisch reine Kultur des Mikroorganismus Streptomyces aureofaciens mit der Bezeichnung NRRL 11181, dadurch gekennzeichnet, daß diese Kultur bei Fermentation in einem Wässrigen Nährmedium, das assimilierbare Quellen für Kohlenhyrat, Stickstoff und anorganische Salz enthält, zur Bildung von 20-Deoxynarasin oder 20-Deoxy-epi-17-narasin befähigt ist.
 
13. Kultur des Mikroorganismus Streptomyces aureofaciens mit der Identitätsnummer NRRL11181.