Cultivation of a strain of the microorganism Nocardia sp. 11,340, which has been deposited in the American Type Culture Collection as A.T.C.C. No. 31531, yields a novel antibiotic substance EM 4940, having activity against a range of gram-positive and gram-negative bacteria, yeasts, fungi, acholeplasma, and the protozoan Trichomanas vaginalis.
Description
SUMMARY OF THE INVENTION Cultivation of a strain of the microorganism Nocardia sp. 11,340, which has been deposited in the American Type Culture Collection as A.T.C.C. No. 31531, yields a novel antibiotic substance EM 4940, having activity against a range of gram-positive and gram-negative bacteria, yeasts, fungi, acholeplasma, and the protozoan Trichomonas vaginalis. The chemical structure of EM 4940, the antibiotic of this invention, has been elucidated through the use of x-ray crystallography and is as follows: ##STR1## i.e., 3,4-dihydro-4-hydroxy-5-(3-hydroxy-2-pyridinyl)-4-methyl-2H-pyrrole-2-carboxamide. EM4940 is a mixture of two antibiotics, a 2,4-trans isomer and a 2,4-cis isomer, which have been designated EM 4940A and EM 4940B respectively.
DESCRIPTION OF THE DRAWINGS FIG. 1 shows the ultraviolet spectrum for EM 4940A and EM 4940B in methanol. FIG. 2 shows the infrared spectrum for EM 4940A and EM 4940B in potassium bromide. FIG. 3 shows the nuclear magnetic resonance of EM 4940A in deuterated chloroform containing two drops of deuterated methanol. FIG. 4 shows the nuclear magnetic resonance of EM 4940B in deuterated chloroform containing two drops of deuterated methanol.
DETAILED DESCRIPTION OF THE INVENTION The Microorganism The microorganism used for the production of EM 4940 is a strain of Nocardia sp. SC 11,340. A subculture of the organism can be obtained from the permanent collection of the American Type Culture Collection, Rockville, Maryland. Its accession number in this repository is A.T.C.C. No. 31531. In addition to the specific microorganism described and characterized herein, it should be understood that mutants of the microorganism (e.g., mutants produced through the use of x-rays, ultraviolet radiation or nitrogen mustards) can also be cultivated to produce EM 4940. Nocardia sp. 11,340, A.T.C.C. No. 31531, can be isolated from a moist soil sample containing the microorganism by first stamping the soil sample on a medium containing: KNO.sub.3 : 1 g. K.sub.2 HPO.sub.4 : 0.5 g. MgSO.sub.4.7H.sub.2 O: 0.5 g. NaCl: 0.5 g. FeSO.sub.4.7H.sub.2 O: 0.01 g. Glucose: 5 g. Agar: 20 g. Distilled water: 1 liter The medium is sterilized in an autoclave at 121.degree. C. for 20 minutes. After 14 days incubation at 28.degree. C., colonies of the Nocardia sp. SC 11,340 are isolated from the plates soil. These isolated colonies are then grown on a medium containing: Yeast extract: 1 g. Beef extract: 1 g. NZ Amine A: (a casein hydrolysate): 2 g. Glucose: 10 g. Agar: 15 g. Distilled water 1 liter The medium is adjusted to pH 7.3 and autoclaved at 121.degree. C. for 30 minutes. Nocardia sp. SC 11,340 produces a vegetative mycelium which fragments into rod and coccal forms within 5 days. The cells are nonacid fast and gram-positive. Colonies growing on a solid medium are smooth to doughy in consistency and are whitish gray in color. On glycerol asparagine agar there are no distinguishing characteristics; on oatmeal tomato paste agar, a soluble purple pigment is produced that permeates throughout the solid medium. No aerial mycelium is formed. Acid hydrolysates of whole cell walls analyzed by the method of Becker et al, Applied Microbiology, 12:421 (1964), indicate the presence of mesodiaminopimelic acid, galactose and arabinose as the major sugar components found. There is some ribose present but no madurose. This cell wall analysis represents a Type IV A pattern (Lechevalier et al, In: The Actionmycetales, H. Pransen (Ed.), VEB Guster Fisher Verlag, pgs. 398-400,402 (1970)) and is diagnostic for the genus Nocardia. To determine whether acid products are formed from various carbohydrates in the presence of Nocardia sp. SC 11,340, the microorganism is cultured for 10 days on the basal medium of Ayers, Rupp and Johnson, Bull. U.S. Dept. Agri., No. 782 (1919), in the presence of each of the following carbohydrates, with the following results: ______________________________________Basal medium (control) - Glycerol +Adonitol - Inositol +Arabinose + Lactose -Cellobiose - Maltose +Erythritol - Mannitol +Glucose + Mannose -Melezitose - Xylose -Melibose - Fructose +Raffinose - Sucrose -Rhamnose - Sorbitol -Trehalose -______________________________________ Legend: +: acids formed -: acids not formed Nocardia sp, SC 11,340 decomposes casein and hypoxanthine, but not tyrosine, xanthine and quanine. There is hydrolysis of gelatin, but not starch. The Antibiotic The antibiotic EM 4940 can be produced by cultivating Nocardia sp. SC 11,340 A.T.C.C. No. 31531 at, or about, 28.degree. C. under submerged aerobic conditions on an aqueous nutrient medium containing an assimilable carbohydrate and nitrogen source. The fermentation is carried out until substantial antibiotic activity is imparted to the medium, usually about 120 to 144 hours, preferably about 144 hours. EM 4940 can be separated from the fermentation medium and purified using art-recognized techniques. For example, the broth can be centrifuged to remove the mycelium and then concentrated under reduced pressure. (Alternatively, filtration can be used to remove the mycelium from the broth). Inactive material can be precipitated from the concentrate using, for example, methanol, and then discarded. Extraction of the concentrate with ethyl acetate, removes most of the activity. The extract can be concentrated, applied to a chromatography column, e.g., one comprising silicic acid and cellulose, and the antibiotic EM 4940 eluted with chloroform. EM 4940 can be crystallized from acetontrile. The crystals consist of two forms, (A) platelets and (B) needles. Biologically, the A form is more active than the B form. The two forms are diastereoisomers and cannot usually be distinguished by UV, I.R., mass spectrometry or elemental analysis. One way to distinguish between the two isomers, is by proton N.M.R. where the A form has a C-CH.sub.3 peak at 1.75 ppm, while the B form has a C-CH.sub.3 peak at 1.65 ppm. A mixture of A+B forms has both peaks and from integration of the peaks, one can estimate the percentage of each in the sample. Separation of the two forms can be achieved by fractional crystallization from acetontrile. EM 4940 (3,4-dihydro-4-hydroxy-5-(3-hydroxy-2-pyrridinyl)-4-methyl-2H-pyrrole-2-carboxamide) has two assymetric carbon atoms--the carbon atom bearing the carboxamide group and the carbon atom bearing the methyl and hydroxyl groups. Accordingly, 3,4-dihydro-4-hydroxy-5-(3-hydroxy-2-pyridinyl)-4-methyl-2H-pyrrole-2-carboxamide exists in diastereoisomeric forms, or in racemic mixtures thereof. These are all within the scope of this invention. Detection of EM 4940 is based on a biological diffusion assay utilizing the following medium: BBL Seed Agar: 30.5 g. NaCl: 5 g. Distilled Water: 1 liter The medium is sterilized at 121.degree. C. for 20 minutes. Agar plates containing sub-inhibitory concentrations of diumycin are seeded with E. coli SC 10,888. Under these conditions, EM 4940 is inhibitory to E. coli SC 10,888. The following examples further illustrate this invention. EXAMPLE 1 A 250 liter batch of Nocardia sp. SC 11,340 A.T.C.C. No. 31531 is fermented in a 100 gallon stainless steel vessel with the media and operating conditions as described below: Stage 1 Nocardia sp. SC 11,340 is maintained on the following sterilized agar medium (A): Oatmeal: 20 g. Tomato paste: 20 g. Agar: 15 g. Tap water to 1 liter The medium is adjusted to pH 7.0 and sterilized at 121.degree. C. for 15 minutes. A loopful of surface growth from an agar slant (Medium A) of Nocardia sp. SC 11,340 A.T.C.C. No. 31531 is suspended in 11 ml of 0.01% dupanol solution and is used as the source of inoculum to inoculate the following sterilized medium (B). Yeast extract: 4 g. Malt extract: 10 g. Dextrose: 4 g. Distilled water to 1 liter The medium is adjusted to pH 7.3 and sterilized at 121.degree. C. for 15 minutes. One thousand five hundred ml of this medium in a 4 liter flask is incubated 72 hours on a rotary shaker at 28.degree. C. (300 rpm, 2 inch stroke). Stage 2 Inoculum: 1.5 liters from stage 1. Medium B (28.5 liters, as described above) is adjusted to pH 7.3 and sterilized at 121.degree. C. for 15 minutes. To the sterilized medium is added 1.5 liters from stage 1 and the 30 liters of material is incubated for 72 hours. During incubation, the broth is aerated at the rate of 2.3 cubic feet per minute with agitation at 220 rpm. Stage 3 Inoculum: 12.5 liters from stage 2 Medium B (237.5 liters, as described above) is prepared as in stage 2 and then combined with 12.5 liters of inoculum from stage 2. The resulting 250 liters of material is incubated for 144 hours. During incubation the broth is agitated at 155 rpm and aerated at the rate of 10 cubic feet per minute. Removal of the mycelium by centrifugation leaves 185 liters of broth. The clear broth is concentrated under reduced pressure at or below 45.degree. C. to about 3.25 liters. The concentrate is poured slowly into 25 liters of methanol with stirring for 30 minutes, the mixture is centrifuged, and the inactive precipitate is discarded. The supernatant is concentrated under reduced pressure at or below 45.degree. C. to approximately 1.8 liters at which point most of the methanol is removed. The concentrate is then extracted four times with 1/2 volume ethyl acetate. The ethyl acetate extracts are combined and concentrated under reduced pressure at or below 45.degree. C. to approximately 100 ml, which contains more than 90% of the activity. The ethyl acetate concentrate is loaded onto a silicic acid/cellulose (2:1 by weight) column (43.times.70 cm), packed in chloroform. The column is eluted with chloroform. Approximately 3 liters of active material is collected from the column which after concentrating to dryness gives a dry weight of 11-12 g. This material is crystallized from acetonitrile to yield 4.1 g of crystalline EM 4940. The crystals of EM 4940 consist of two forms, (A) platelets and (B) needles. Biologically, the A form is more active than the B form. The two forms are diastereoisomers and cannot be distinguished by UV, I.R., mass spectrometry or elemental analysis. One way to distinguish between the two isomers, is by proton N.M.R. where the A form has a C-CH.sub.3 peak at 1.75 ppm, while the B form has a C-CH.sub.3 peak at 1.65 ppm. A mixture of A+B forms has both peaks and from integration of the peaks, one can estimate the percentage of each in the sample. The 4.1 g of EM 4940 obtained above, contains 80% A form and 20% B form. Separation of the two forms is achieved by dissolving the sample in acetonitrile. The B form is more soluble and the A form, therefore, precipitates first; 1.8 g of 97% pure A form is isolated from the sample. The A form of EM 4940 (platelets) has been determined to be an isomer of 2,4-trans-3,4-dihydro-4-hydroxy-5-(3-hydroxy-2-pyridinyl)-4-methyl-2H-pyrrole-2-carboxamide, and has the following characteristics: (1) melting point 165.degree.-168.degree. C. (2) soluble in methanol, ethanol, ethyl acetate, acetone and chloroform Insoluble in hexane and water (3) Ultraviolet spectrum shown in FIG. 1 .lambda.max--206 nm (E.sub.1 cm.sup.1% --480) .lambda.max--315 nm (E.sub.1 cm.sup.1% =220) (4) infrared spectrum shown in FIG. 2 (5) nuclear magnetic resonance shown in FIG. 3 (6) mass spectrometry--molecular ion=235 empirical formula=C.sub.11 H.sub.13 N.sub.3 O.sub.3 (7) elemental analysis ______________________________________Element Found Calculated for C.sub.11 H.sub.13 N.sub.3 O.sub.3______________________________________C 56.14% 56.22H 5.44% 5.58N 17.66% 17.88ash 0______________________________________ (8) optical rotation .alpha..sub.D =+20.degree. in methanol The B form of EM 4940 (needles) has been determined to be an isomer of 2,4-cis-3,4-dihydro-4-hydroxy-5-(3-hydroxy-2-pyridinyl)-4-methyl-2H-pyrrole-2-carboxamide, and has the following characteristics: (1) melting point 200.degree.-201.degree. C. (2) infrared spectrum shown in FIG. 2 (3) nuclear magnetic resonance shown in FIG. 4 (4) mass spectrometry=molecular ion=235 empirical formula --C.sub.11 H.sub.13 N.sub.3 O.sub.3 (5) elemental analysis ______________________________________Element Found Calculated for C.sub.11 H.sub.13 N.sub.3 O.sub.3______________________________________C 56.38 56.22H 5.60 5.58N 17.78 17.88ash 0______________________________________ EXAMPLE 2 Nocardia sp. SC 11,340 A.T.C.C. No. 31531 is maintained on the following sterilized agar medium (A): Oatmeal: 20 g. Tomato paste: 20 g. Agar: 15 g. Tap water to 1 liter The medium is adjusted to pH 7.0 and autoclaved at 121.degree. C. for 15 minutes. A loopful of surface growth from an agar slant (medium A) of Nocardia sp. SC 11,340, (ATCC 31531) is used to inoculate each of six 500 ml Erlenmeyer flasks each containing 100 ml of the following sterilized medium (B). Yeast extract: 4 g. Malt extract: 10 g. Dextrose: 4 g. Distilled water to 1 liter The medium is adjusted to pH 7.3 before sterilization at 121.degree. C. for 15 minutes. The flasks are then incubated at 28.degree. C. on a rotary shaker (300 rpm; 2 inch stroke) for approximately 72 hours. After the appropriate incubation as described above, 5% (vol/vol) transfers are made from the grown culture flasks to one hundred, 500 ml Erlenmeyer flasks each containing 100 ml of sterilized medium (B) as described above. After inoculation the flasks are incubated at 28.degree. C. on a rotary shaker (3000 rpm, 2 inch stroke) for approximately 120-144 hours. At this time, the contents of the flasks are pooled and the broth is centrifuged yielding approximately 9 liters of supernatant broth. The antibiotic is extracted using the procedure described in Example 1. In addition to the fermentation media utilized in the above examples, the following media are exemplary of others that can be used for the production of EM 4940 and can be substituted for medium B in the above examples: ______________________________________ Medium C Grams______________________________________Yeast Extract 4Malt Extract 10Dextrose 25Distilled H.sub.2 O to 1 liter______________________________________ pH adjusted to 7.3 before sterilization @ 121.degree. C. for 15 minutes. ______________________________________ Medium D Grams______________________________________Glycerol 30Pharmamedia 20Yeast Extract 20Glucose 20Distilled H.sub.2 O to 1 liter______________________________________ pH adjusted to 7.3 before sterilization @ 121.degree. C. for 15 minutes. ______________________________________ Medium E Grams______________________________________Yeast Extract 4Malt Extract 10Glucose 10Glycerol 2Distilled H.sub.2 O to 1 liter______________________________________ pH adjusted to 7.3 before sterilization @ 121.degree. C. for 15 minutes. ______________________________________ Medium F Grams______________________________________Glycerol 10L-Asparagine 5KH.sub.2 PO.sub.4 1Na.sub.2 HPO.sub.4 2Glucose 50Mg SO.sub.4 . 7H.sub.2 O 0.2Tap H.sub.2 O to 1 liter______________________________________ pH adjusted to 7.3 before sterilization @ 121.degree. C. for 15 minutes. ______________________________________ Medium G Grams______________________________________(NH.sub.4).sub.2 SO.sub.4 2L-Asparagine 5Glucose 50Glycerol 10KH.sub.2 PO.sub.4 7K.sub.2 HPO.sub.4 7Mg SO.sub.4 . 7H.sub.2 O 0.2Distilled H.sub.2 O to 1 liter______________________________________ pH adjusted to 7.3 before sterilization @ 121.degree. C. for 15 minutes. Biological Testing (A) Minimum Inhibitory Concentration (MIC) determination of EM 4940A and EM 4940B against organisms in an aerobic screen. 1. Using BA-2 Agar The antibiotic is prepared in 0.1 M phosphate buffer pH 7.0 at a concentration of 1000 .mu.g/ml. Two-fold dilutions are made in Mueller Hinton broth resulting in a range from 1000 .mu.g/ml to 0.5 .mu.g/ml. One ml of each dilution is placed into individual 100.times.15 mm petri dishes to which 9.0 ml of BA-2 agar are added. The final drug concentration in the agar ranges from 100 .mu.g/ml to 0.05 .mu.g/ml. All organisms are grown in approximately 15-20 ml of antibiotic assay (AA) broth (Difco Bacto antibiotic medium No. 3) by inoculating the broth with a loopful of the organism from a BHI agar slant. The inoculated tubes are incubated at 37.degree. C. for 18-20 hours. Each incubated broth culture is checked for growth level by a visual turbimetric reading against a McFarland No. 5 standard and adjusted accordingly with AA broth (A McFarland No. 5 standard is equivalent to approximately 1.times.10.sup.9 CFU/ml CFU is colony forming units). The visual check is made immediately prior to use. The adjusted broth for each organism is then tested at the appropriated inoculum level. For this series of tests the inoculum level is 10.sup.4 CFU. The broth cultures were thus diluted 1:100 in AA broth to give 10.sup.7 CFU/ml. The organisms are then stamped onto the agar plates using a Denley Multi Point Innoculator which delivers 0.001 ml of culture producing an inoculum level of 10.sup.4 CFU. After stamping, the plates are incubated at 37.degree. C. for 18 hours. The MIC is recorded as the lowest concentration of antibiotic that inhibits the growth of 3 colonies or less. The results of this procedure are reported in Table I. TABLE I______________________________________ Number in collection Minimum Inhibitory of E. R. Squibb Concentration (.mu.g/ml)Organism and Sons, Inc. EM4940A______________________________________Acinetobactercalcoaceticus 8333 50.0Enterobactercloacae 10,459 >100.0Escherichiacoli 10,404 100.0Escherichiacoli 10,857 50.0Escherichiacoli 10,896 25.0Klebsiellaaerogenes 10,436 100.0Klebsiellapneumoniae 11,066 50.0Proteusmorganii 9774 50.0Pseudomonasaeruginosa 8754 >100.0Pseudomonasaeruginosa 9330 50.0Pseudomonasaeruginosa 9545 25.0Salmonellatyphimurium 9201 50.0Serratiamarcescens 9782 100.0Serratiamarcescens 1111 >100.0Shigellasonnei 8449 50.0Staphylococcusaureus 2400 >100.0Staphylococcusaureus 10,165 50.0Staphylococcusaureus 11,239 >100.0Streptococcusfaecalis 9011 >100.0______________________________________ Additional tests were run using the above methodology and the results of these tests are reported in Table II. TABLE II______________________________________ Number in collection Minimum Inhibitory of E. R. Squibb Concentration (.mu.g/ml)Organism and Sons, Inc. EM4940A 4940B______________________________________Staphylococcusaureus 2400 >200 >200Staphylococcusaureus 10,165 100 100Staphylococcusaureus 11,239 50 100Staphylococcusaureus 2661 >200 >200Streptococcusfaecalis 9011 >200 >200Escherichiacoli 10,404 50 50Escherichiacoli 10,857 50 50Salmonellatyphimurium 9201 50 50Klebsiellaaerogenes 10,436 50 50K. pneumoniae 11,066 50 50Proteus rettgeri 8217 50 50P. morganii 9774 100 100Serratiamarcescens 9782 50 50Serratiamarcescens 11,111 100 100Pseudomonasaeruginosa 9545 12.5 12.5Pseudomonasaeruginosa 8754 100 100Pseudomonasaeruginosa 9330 >200 >200Acinetobactercalcoaceticus 8333 100 100Enterobactercloacae 10,459 50 100Shigellasonnei 8449 50 50______________________________________ A. Using H-59 Synthetic Agar The method is as described above except that H-59 agar is substituted for BA-2 agar. The results of this procedure are described in Table III. TABLE III______________________________________ Number in collection Minimum Inhibitory of E. R. Squibb Concentration (.mu.g/ml)Organism and Sons, Inc. EM4940A______________________________________Acinetobactercalcoaceticus 8333 25.0Enterobactercloacae 10,459 100.0Escherichiacoli 10,404 50.0Escherichiacoli 10,857 25.0Klebsiellaaerogenes 10,436 50.0Klebsiellapenumoniae 11,066 50.0Pseudomonasaeruginosa 8754 >100.0Pseudomonasaeruginosa 9330 50.0Pesudomonasaeruginosa 9545 25.0Salmonellatyphimurium 9201 50.0Serratiamarcescens 9782 100.0Serratiamarcescens 11,111 100.0Shigellasonnei 8449 50.0Streptococcusfaecalis 9011 >100.0______________________________________ (B) Minimum Inhibitory Concentration (MIC) determination of EM4940A against organisms in an anaerobic screen. The antibiotic is prepared as described above for the aerobic screen. All organisms are maintained in a tube of chopped meat broth with glucose supplied by Scott Laboratories in Rhode Island. Two days prior to running the test 0.1 ml of the maintained culture is transferred to a fresh tube of chopped meat broth, and the tube is incubated at 37.degree. C. for 48 hours. After 48 hours incubation each culture is assumed to have grown to 1.times.10.sup.8 CFU/ml. The organisms are stamped onto antibiotic containing agar plates (Mueller Hinton Agar BBL+5% whole sheep blood+0.2% lysed sheep blood) to give an inoculum level of 10.sup.5 CFU. After stamping, the plates are placed in an anaerobic gas pack system (BBL) and incubated at 37.degree. C. for 18 hours. The MIC is recorded as the lowest concentration of antibiotic that inhibits the growth of 3 colonies or less. The results of this procedure are reported in Table IV. TABLE IV______________________________________ Number in collection Minimum Inhibitory of E. R. Squibb Concentration (.mu. g/ml)Organism and Sons, Inc. EM4940A______________________________________Bacteroidesfragilis 9005 50.00Bacteroidesfragilis 9844 12.50Bacteroidesfragilis 10,277 50.00Bacteroidesfragilis 10,278 50.00Bacteroidesfragilis 10,279 50.00Bacteroidesfragilis 10,281 50.00Bacteroidesfragilis 11,085 100.00Bacteroidesfragilis 11,086 50.00Bifidobacteriumdentium 11,260 >100.00Clostridiumhistolyticum 8572 12.50Clostridiumperfringens 11,256 50.00Clostridiumsepticum 1780 12.50Clostridiumsporogenes 2372 12.50Eubacteriumlentum 11,261 12.50Fusobacteriumnecrophorum 11,338 12.50Hemophilusvaginalis 8568 100.00Hemophilusvaginalis 9640 100.00Peptococcusvariabilis 11,264 50.00Peptostreptococcusanaerobius 11,263 50.00Propionibacteriumacnes 4020 50.00______________________________________ (C) Minimum Inhibitory Concentration determination of EM4940A against Candida albicans. The day previous to running the test, an overnight broth culture of Candida albicans in both F4 broth and yeast nitrogen broth (YNB) is prepared. The overnight broth culture contains approximately 1.0.times.10.sup.7 CFU/ml. Both broth cultures are diluted 10.sup.-3 in the respective broths; the antibiotic is prepared at a concentration of 2 mg/ml in 0.1 M phosphate buffer pH 7.0. A 1:8 dilution is of Solution A yields a 1:64 dilution (Solution B). The test compounds are distributed in 13.times.100 mm sterile test tubes procedure, using Kahn pipettes (0.2 ml) according to the following schedule: ______________________________________Tube Addition Concentration______________________________________1 0.2 ml Stock Solution 100 .mu.g/ml2 0.1 ml Stock Solution 50 .mu.g/ml3 0.05 ml Stock Solution 25 .mu.g/ml4 0.2 ml Solution A (1:8 of stock) 12.5 .mu.g/ml5 0.0 ml Solution A (1:8 of stock) 6.3 .mu.g/ml6 0.05 ml Solution A (1:8 of stock) 3.1 .mu.g/ml7 0.2 ml Solution B (1:64 of stock) 1.6 .mu.g/ml8 0.1 ml Solution B (1:64 of stock) 0.8 .mu.g/ml9 0.05 ml Solution B (1:64 of stock) 0.4 .mu.g/ml10 Positive Growth Control (no compound) --______________________________________ To each of the above tubes add 4.0 ml of the 10.sup.-3 dilution of the broth culture to give a final inoculum of 10.sup.4 CFU/ml. The tubes are incubated at 37.degree. C. for 18 hours. After this time the results are recorded as: + growth comparable to growth in the control tube; .+-. growth less than control tube; - no visible growth. The MIC is the least concentration of antibiotic giving a negative growth tube. The results of the procedure are reported in Table V. TABLE V______________________________________ Minimum Inhibitory Concentration (.mu.g/ml) Number in collection Medium: Yeast of E. R. Squibb Nitrogen BaseOrganism and Sons, Inc. Medium:F4 +Glucose______________________________________Candidaalbicans 5314 >100 >100______________________________________ (D) Minimum Inhibitory Concentration determination of EM4940A against dermatophytes. A 1 mg/ml solution of antibiotic is prepared in 0.1 M phosphate buffer pH 7.0. Two-fold dilutions are made in the broth resulting in a range of antibiotic concentrations from 1000 .mu.g/ml-0.5 .mu.g/ml. All organisms are grown from stock on F-4 agar slants. Each slant is washed with 10 ml of 0.1 H phosphate buffer pH 7.0. The spore suspension is transferred to a sterile 1.times.4 Morton cap tube and the suspension homogenized. The prepared agar plates are surface inoculated with 0.2 ml of the appropriate spore suspension. The organism is then streaked across the agar surface using a sterile swab. The inoculated plates are incubated at 26.degree. C. for 48 hours. The MIC is the highest dilution of each compound series showing no growth. The results of the procedure are reported in Table VI. TABLE VI______________________________________ Number in collection Minimum Inhibitory of E. R. Squibb Concentration(.mu.g/ml)Organism and Sons, Inc. EM4940A______________________________________T. mentagrophytes 2637 >100E. floccosum 9185 >100T. rubrum 9199 50M. canis 9237 100______________________________________ (E) Minimum Inhibitory Concentration determination of EM4940A against Trichomonas vaginalis. Compound preparation is carried out as described under (C). To each series of dilutions, 4 ml of a 1:100 dilution of T. vaginalis (grown in modified Diamond's Medium pH 6.0+10% rabbit serum) is made from a 40 hour culture. The tubes are incubated anaerobically at 37.degree. C. for 40 hours and the MIC's determined. The results of the procedure are reported in Table VIII. TABLE VII______________________________________ Number in collection Minimum Inhibitory of E. R. Squibb Concentration (.mu.g/ml)Organism and Sons, Inc. EM4940A______________________________________Trichomonasvaginalis 8560 12.5______________________________________ (F) Minimum Inhibitory Concentration determination of EM4940A against mycoplasmas. The antibiotic (1 mg) is dissolved in 200 microliters of dimethylsulfoxide (DMSO). Doubling dilutions are carried out in DMSO over twelve levels to give concentrations ranging from 5000-2.59 .mu.g/ml. To two sets of microtitration plates, 5 microliter aliquots of each concentration are transferred in triplicate. Each well of a triplicate set of dilutions is inoculated with 250 microliters of inoculated Channocks broth (10% of 48 hour culture of either M. mycoides or A. laidlawii). Plates are sealed and examined after 48 hours at 37.degree. C.-for phenol red color change red to yellow and the MIC recorded as the lowest concentration in which no color change occurs. The results of the procedure are reported in Table VIII. TABLE VIII______________________________________Organism MIC (.mu.g/ml) of EM4940A______________________________________Mycoplasma mycoides >100Acholeplasma laidlawii 100______________________________________ As shown by the above experiments the antibiotics of this invention have activity against a range of gram-positive and gram-negative bacteria, yeasts, fungi, acholeplasma, and the protozoan Tichomonas vaginalis. The antibiotics can, therefore, be used as (1) an environmental disinfectant, (e.g., as a spray or dust in a conventional carrier) and (2) an agent to combat infections due to the above-enumerated bacteria, yeasts, fungi, acholeplasma and Trichomonas vaginalis in various mammalian species (e.g., topically, orally or parenterally using pharmaceutically acceptable carriers, excipients, etc.).
Patent Grant
4249008
