Manufacture of aminoglycoside antibiotics

This invention relates to a novel method of manufacturing aminoglycoside antibiotics by fermentation using a new variety of microorganisms of the genus Micromonospora. More particularly, this invention deals with methods of producing gentamicins with a new species Micromonospora scalabitana. Cultures of the living microorganism were deposited at the American Type Culture Collection, Rockville, Maryland, USA, and were assigned the number ATCC 31435.
In the course of screening for antibiotics soil samples of Portugal, a beautiful red microorganism was isolated from a soil sample from the plains of Santarem, a city that in Roman times was called Scalabis. It was clear from the first tests that this microorganism was an antibiotic producer and that the metabolite was active against gram positive and gram negative microorganisms. These observations lead to its extensive study.
Microscopic examination revealed long branched mycelium with a few spores. First, it was considered a strain of Streptomyces but later it was established that it was a strain of Micromonospora and named Micromonospora scalabitana. The antibiotic produced was found to be identical with components of the gentamicin group by thin layer chromatography.
Micromonospora scalabitana was carefully tested and compared with other micromonosporas, especially those producing gentamicin. Microscopic examination of cultures shows that the microorganism produces a long branched mycelium of 0.5-0.7.mu. in diameter. One week old or older cultures grown on special agar media contain round and ellipsoidal spores located on short or long sporophores. Some sporophores can be so short, that they seem to be sessile or almost sessile. Three day old cultures in broth grown in shake flasks contain many chlamydosphores. This microscopical picture and spore formation is very similar to that of young cultures of M. chalcea ATCC 12452 and M. sagamiensis ATCC 21803. Older cultures of M. chalcea and M. sagamiensis have overabundance of spores, while the number of spores produced by M. scalabitana remains modest and in characteristic configuration. A comparision with M. purpurea ATCC 15835 and N.R.R.L. 2953 was attempted, but both these strains are such poor spore formers that a meaningful comparison was not possible.
Growth on various culture media: Micromonospora scalabitana grows on many solid and in many liquid media. Growth and colony formation on solid media is quite characteristic. First there is a pin point size colony, which grows and changes into a small globule. The globule grows, increases in size and, when broken, it can be seen that it is a vesicle filled wih liquid. Additional growth and partial dessication cause flattening. In the center the growth stops but it continues growing on the bottom and edges, where the supply of nutrients is good. Growth, dessication and spreading cause: flattening, folding and cracking. These and other physical and metabolic processes cause formation of various colonial forms, some very bizzare or artistic: flat or plicate, tiny or giant, shaped as stars, flowers, etc. The growth is very slow.
Micromonospora scalabitana produces a red somatic pigment. It can be of various shades depending on composition of the media, pH, age of the culture, temperature of incubation and storage temperature. No agar-diffuseable pigment was observed. Like all other micromonosporas, M. scalabitana mutates very easily. Spontaneously, as well as after exposure to mutagenic agents, it can give mutants of many colors, ranging from colorless to black and of many colors and shades in-between. It also produces mutants with changed metabolism, requiring special nutrients and producing an altered antibiotic pattern. Some of these mutants have abundance of spores, others paucity of spores.
As mentioned above, the original strain of M. scalabitana was red, forming few spores. Following mutations and selective isolation many other characteristic strains were isolated. To eliminate confusion, just for practical reasons, that new characteristic was included into the name and hence not only M. scalabitana var. rubra (the type strain) exists, but also M. scalabitana var. pallida, var. aurantiaca, var. salmonicolor, var. coelicolor, var. ferruginosa, var. brunea, var. sporogenes and var. asporogenes.
Spore formation is very light or absent among colorless and light-colored strains, quite the opposite, darker or darkening strains have often, but not always, abundance of spores.
For the description of the pigments, standard color charts were not used. With all those variations such studies are, not only impractical, but often misleading. All those pigments are very changeable and they have different hues caused by small differences in media composition, pH, nutrients, temperature of incubation, age of culture, etc. In general, younger cultures, especially those grown at lower temperatures and pH below 7, are lighter and brighter. Cultures grown in alcaline conditions, at higher temperatures and with longer incubations, are of darker shade and often form dark pigments (brown, gray, purple, black and green).
M. scalabitana grows well under aerobic conditions in the temperature range 25.degree.-38.degree. C. It also grows under lower temperatures, but more slowly. It even continues growing in the refrigerator at 4.degree. C. For such cultures in a refrigerator it is necessary to initiate growth first. For example: inoculated agar plates are left overnight standing on a laboratory table at room temperature. Next day the growth is not visible but if the plates are then left standing in the refrigerator the growth very slowly develops. For a fullgrown culture 5-6 months incubation in the refrigerator is necessary. Dark pigments were never observed under those cold conditions, only light colored pigments develop.
Two strains of M. scalabitana were selected and deposited in the American Type Culture Collection. They are M. scalabitana var. rubra ATCC 31435 and M. scalabitana var. sporogenes. ATCC 31436.
The media used for Micromonospora scalabitana studies were the following:
Bennett's agar
Emerson's agar
Czapek-Dox agar (Difco)
Gelatin (Difco)
Antibiotic agar no 11 (Difco)
Nutrient agar (Difco)
Glucose yeast extract agar
Glucose asparagine agar
NZ Amine glucose agar
Peptone iron agar (Difco)
Tryptose broth (Difco)
Tryptose agar
The precise composition of these media is generally well known and described in various manuals and text books as well as in the Media Section of the A.T.C.C. catalogue.
In addition, many other media prepared and described for micromonospora studies (see for instance G. M. Luedeman, U.S. Pat. No. 3091572) were used as for example:
Luedeman's micromonospora basal medium:
______________________________________Broth: Beef extract 0.3% Tryptose 0.5% Yeast extract 0.5% Dextrose 0.1% Soluble starch 2.4%______________________________________
They are dissolved in deionized water, the pH is adjusted to 7.2-7.3 and sterilized in autoclave at 121.degree. C.
Agar: To the composition described above is added agar 1.5% (Difco), the pH is adujsted to 7.2 and sterilized in the autoclave at 121.degree. C.
Medium for preparation of washed mycelium (Luedeman-Brodsky) (G. M. Luedeman and B. C. Brodsky, Antimicrob. Ag. and Chemoth. (1963), 116)
______________________________________NZ Amine type A (Sheffield) 0.5%Yeast extract (Difco) 0.5%Soluble starch (Difco) 2.0%Dextrose (Merck) 0.1%Calcium carbonate (Merck) 0.1%______________________________________
They are dissolved in deionized water, pH adjusted to 7.2 and sterilized in autoclave at 121.degree. C.
It should be noted that in this and other media NZ Amine is a trade mark of the Sheffield Chemical Co., Norwich, N.Y., U.S.A. and Difco and Merck mean, respectively, reagents of the Difco Laboratories Inc., Detroit, Mich., U.S.A. and of E. Merck, Darmstadt, German Federal Republic.
Basal medium for carbohydrate utilization studies (Luedeman) (G. M. Luedeman, Trans. N.Y. Acad. Sci. 33 (2), 207 (1971)
______________________________________Yeast extract (Difco) 0.5%Calcium carbonate (Merck) 0.1%Agar (Difco) 1.5%Distilled water up to 100%sterilized in autoclave at 121.degree. C.______________________________________
The carbohydrates are prepared separately, autoclaved separately in dry state and mixed with melted agar to obtain a final concentration of 1%.
Agar for spore formation studies:
______________________________________Dextrose (Merck) 1.0%Yeast extract (Difco) 0.5%Agar (Difco) 1.5%Calcium carbonate (Merck) 0.1%______________________________________
They are dissolved or suspended in deionized water, the pH adjusted to 7.2 and sterilized in autoclave at 121.degree. C.
Slightly less favorable results were obtained with the agar described as the A.T.C.C. Medium no 5.
Potato slices--They were prepared in the usual way using local white potatoes as the starting material. After autoclaving the pH of plain potatoes was 5.4, which is lower than the pH of the potatoes used by Luedeman. When the surface of the potatoes was slightly covered with calcium carbonate the pH on the surface was 6.8.
Micromonospora scalabitana was carefully studied using all the media described. Whenever and wherever it was possible, M. scalabitana was compared with known micromonosporas, especially those producing the gentamicin complex. Those strains most often used for comparison were the following: M. purpurea A.T.C.C. 15835, M. purpurea N.R.R.L. 2953, M. chalcea ATCC 12452, the red variant of the A.T.C.C. strain number 12452 isolated in our laboratory, M. sagamiensis, ATCC 21803 and a recently isolated strain of M. echinospora var. pallida. Comparison of growth and pigment formation of those strains are shown in Table I.
Sodium chloride tolerance was tested on Ludeman's micromonospora basal medium agar. Various concentrations of sodium chloride were added to the melted agar and after solidification various strains of micromonospora were inoculated on the surface and incubated at 32.degree. C. for 7 days. The results are shown in Table II.
Micromonospora chalcea was the most resistant with light growth even at 5% concentration. M. purpurea and M. echinospora were able to grow at 3% concentration of sodium chloride. M. scalabitana was the most sensitive. It tolerated well concentrations of NaCl of 1% or less. There was only a scant growth at 2% and absolutely no growth at higher concentrations.
Influence of pH was tested on the same Luedeman's basal medium and the pH was adjusted to desirable degrees with hydrochloric acid. Melted agar was poured in Petri dishes and, after solidification, the agar surface was inoculated with various strains of micromonospora. All plates were incubated for seven days at 32.degree. C. and the results are tabulated in the Table III.
Again M. chalcea was the most resistant and able to grow even at pH 5.8 and there was luxurious growth on plates at pH higher than 6. Both strains of M. purpurea and M. echinospora and both strains of M. sagamiensis tolerated a pH of 6.1. M. scalabitana was, again, the most sensitive. There was medium growth at pH 6.5 and no growth at lower pH.
Growth on potato plugs was slightly different from what was reported by Luedeman. The reason was very simple. Luedeman used American white potatoes that after sterilization had pH 5.8-6.2 on the surface. Those used here were of Portuguese origin and the pH was 5.4 on the surface after sterilization. When this acidity was eliminated with calcium carbonate
TABLE 1__________________________________________________________________________ M. M. chalcea M. scalabitana M. ATCO 12452 M. chalcea M. M. purpurea M. purpurea echinospora var. rubra scalabitana var. ATCO 12452 sagamiensisMedium: ATCO 15835 NRRL 2953 var. pallida ATCC 31435 var. pallida aurantiaca var. rubra ATCO__________________________________________________________________________ 21803Czapek- Gr. fair Gr. fair Gr. fair Gr. fair Gr. fair Gr. fair Gr. fair Gr. fairDox agar C. lt. orange C. Lt. brown C. Lt. orange C. lt. brown C. Colorless C. orange C. orange-red C. apricot D.p. O D.p. O D.p. O D.P. O D.p. O D.p. O D.p. O D.p. OGlucose- Gr. good Gr. good Gr. good Gr. good Gr. good gr. good Gr. good Gr. goodyeast C. purpleextract C. purplish later C. Lt orange C. Red-brown C. Colorless C. bright C. orange-red C. brightagar darkening black darkening orange orange D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. OGlucose- Gr. poor Gr. poor Gr. poor Gr. poor Gr. poor Gr. poor Gr. poor Gr. pooraspar- C. Bluish- C. reddish- C. bluish- C. brown C. colorless C. deep C. red C. brick redgine agar purple purple purple orange D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. OAntibiotic Gr. poor to Gr. poor to Gr. fair Gr. poor to Gr. poor Gr. poor Gr. poor Gr. pooragar fair fair fair C. Lt. orange C.Lt. orange C.Lt. orange C. Red brown C. colorless C.orange C. red O. orange# 11 later gray graying D.p. O D.p. O D.p. lt. gray- D.p. O D.p. O D.p. O D.p. O D.p. O brownish Gr. poor to Gr. poor to gr. poor Gr. poor to Gr. poor Gr. poor Gr. poor Gr. poorPepton-iron fair fair fair C. lt. orange C. colorless C. Colorless C. reddish- C. Colorless C. Lt. orange C. Lt. red C. Lt. orangeagar brown Dp. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O Gr. fair Gr. fair Gr. fair to Gr. fair Gr. fair Gr. fair Gr. fair Gr. fairAmine- redglucose C. orange- C. brown dar- C. brown C. dark red- C. Colorless C. brown-red C. dark C. colorless lateragar brown edge kening purplish brown brown D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. OTryptose Gr. fair Gr. fair Gr. fair Gr. fair Gr. fair Gr. fair Gr. fair Gr. fairagar C. bright C. orange C. orange C. raspberry C. Colorless C. orange C. red C. orange orange red greenish D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O Gr. good Gr. good Gr. good Gr. good Gr. good Gr. good Gr. good Gr. goodEmerson'sagar C. reddish C. reddish C. brown C. Raspberry C. Colorless C. lt. brown C. darkening C. orange orange orange red red D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O Gr. good Gr. good Gr. good Gr. good Gr. good Gr. good Gr. good Gr. goodBennett's C. dusty C. reddish C. brown C. raspberry C. colorless C. terra C. red C. orangeagar orange orange red cotta D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. O D.p. OLuedeman's Gr. luxurious Gr. luxurious Gr. luxurious Gr. luxurious Gr. luxurious Gr. very Gr. very Gr. verybasal C. orange good good goodagar C. reddish later C. orange C. darkening C. colorless C. darker C. darkening C. orange orange purple later brown red terra cotta red brown D.p. O D.p. O D.p. lt.brown D.p. O D.p. O D.p. O D.p. O D.p. OGelatin liquefied liquefied liquefied liquefied liquefied liquefied liquefied liquefied__________________________________________________________________________ NOTE: Abreviations: Gr. = growth C. = color D.p. = difusible pigment lt. = light
TABLE II__________________________________________________________________________NaCl tolerance (on agar)Comparison of six strains of various MicromonosporasSodium M. scalabitana M. scalabitanachloride M. purpurea M. purpurea var. rubra var. sporogenes M. chalcea M. echinospora1% ATCC 15835 NRRL 2953 ATCC 31435 ATCC 31436 ATCC 12452 var. pallida__________________________________________________________________________0 +++ +++ +++ +++ +++ +++1 +++ +++ +++ +++ +++ +++2 +++ +++ + + +++ +++3 ++ + 0 0 +++ ++4 0 0 0 0 +++ 05 0 0 0 0 + 06 0 0 0 0 0 07 0 0 0 0 0 0__________________________________________________________________________
TABLE III__________________________________________________________________________Influence of the pH upon growth on agar plates M. scalabitana M. scalabitana M. purpurea M. purpurea var. rubra var. sporogenes M. chalcea M. echinospora M. sagamiensis M. sagamiensispH ATCC 15835 NRRL 2953 ATCC 31435 ATCC 31436 ATCC 12452 var. pallida ATCC 21803 ATCC__________________________________________________________________________ 219497.6 +++ +++ +++ +++ +++ +++ +++ +++7.2 +++ +++ +++ +++ +++ +++ +++ +++6.8 +++ +++ +++ +++ +++ +++ +++ +++6.5 +++ +++ ++ ++ +++ +++ +++ +++6.1 + + 0 0 +++ ++ ++ ++5.8 0 0 0 0 + 0 0 05.4 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0__________________________________________________________________________
TABLE IV______________________________________Growth on potato plugs Potato alone Potato - CaCO.sub.3Microorganism: pH 5.4 pH 6.9______________________________________M. purpurea Growth: 0 Growth: +++ATCC 15835 Pigment: 0 Pigment: orange later brownM. purpurea Growth: 0 Growth: +++NRRL 2953 Pigment: 0 Pigment: orange, purple spotsM. scalabitana Growth: 0 Growth: +++var. rubra Pigment: 0 Pigment: dark rasp-ATCC 31435 berry redM. scalabitana Growth: 0 Growth: +++var. sporgenes Pigment: 0 Pigment: yellow toATCC 31436 light orangeM. chalcea Growth: ++ Growth: +++ATCC 12452 Pigment: orange- Pigment: strawberry red redM. echinospora Growth: 0 Growth: +++var. pallida Pigment: 0 Pigment: orange turning purpleM. sagamiensis Growth: 0 Growth: +++ATCC 21803 Pigment: 0 Pigment: orange______________________________________
the surface pH became 5.8 and all micromonosporas were able to grow if heavier inoculum was inoculated on the surface. The data resulted are given in Table IV.
Carbohydrate utilization is the most important group of tests necessary for the classification of micromonosporas. They were performed according to the description published by Luedeman. Washed mycelia of all cultures were prepared first and used for inoculation of appropriate sugar agars. Agar medium containing only 0.5% yeast extract and calcium carbonate was used as control.
A single test does not give a completely reliable result. For that reason all tests were repeated in six consecutive generations. For example: glucose agar was inoculated with washed mycelium of M. chalcea. After seven days of incubation at 32.degree. C. the result was recorded and the growing culture was used as inoculum for the second generation on glucose agar. After incubation at 32.degree. C. for seven days the result was recorded and this culture used again as inoculum for the third generation and so on until obtaining the record of six generations of growth on glucose agar. The results obtained are shown in Table V.
Carbohydrate utilization tests are not exactly ideal. There is not a completely negative culture. Even the negative controls represent a scant growth and positive utilization tests represent only increase in size and volume of growth in comparison to the scant growth of the controls. This fact can seriously affect the record because of the personal and highly individual reading that is the basis of evaluation.
Adaptation of strains to certain sugars was noticeable and in some cases the emergence of mutants with different degrees of utilization was observed.
The lactose and d-ribose tests were especially fitting for demonstration of such dissociation of cultures. Other sugars may act similarly but at a lower rate if sufficient number of transfer to transfer to transfer are performed.
Utilization of melibiose is the most important test for classification of micromonosporas. According to the latest (1973) edition of Bergey's Manual (published by the Williams & Wilkins Co., Baltimore, Maryland, USA) all strains utilizing melibiose belong to group A. Micromonospora scalabitana utilizes melibiose.
The next step is raffinose; M. scalabitana does not utilize raffinose.
Spore formation is also used for the classification. M. scalabitana forms spores on longer as well as on shorter monopodial sporophores.
TABLE V__________________________________________________________________________Utilization of Carbohydrates M. scalabitana M. scalabitana M. purpurea M. purpurea var. rubra var. sporogenes M. chalcea M. echinospora M. sagamiensisCarbohydrate: ATCC 15835 NRRL 2953 ATCC 31435 ATCC 31436 ATCC 12452 var. pallida ATCC__________________________________________________________________________ 21803Dextrose (Difco) +++ +++ ++ ++ +++ +++ +++Sucrose (Difco) +++ +++ +++ ++ +++ +++ +++Lactose (E.Merck) + + ++ +++ +++ + +++Melibiose (Difco) 0 0 ++ ++ +++ 0 +++Raffinose (Difco) 0 0 0 0 ++ 0 ++d-Ribose (E.Merck) + + ++ ++ + + +Rhamnose (Difco) 0 0 0 0 0 +++ +Inosital (Difco) 0 0 0 0 0 0 0Mannitol (Difco) 0 0 0 0 0 0 0Glycerol (E.Merck) 0 0 0 0 0 0 0Soluble starch(Difco) +++ +++ +++ +++ +++ +++ +++Potato dextrin (Staley) +++ +++ + + +++ +++ +++Control 0 0 0 0 0 0 0__________________________________________________________________________
All these tests would suggest that M. scalabitana is a strain of M. narashinoensis. Since a culture of this last microorganism was not available, a direct laboratory comparison under controled conditions was not possible.
On table VI the published data on M. narashinoensis (Bergey's Manual of Determinative Bacteriology, 1973 Edition) and the laboratory results on M. scalabitana are summarized side by side.
There are considerable similarities but also considerable difference between M. narashinoensis and M. scalabitana and therefore they cannot be considered identical but clearly different, related species.
ANTIBIOTIC PRODUCTION
As pointed out, Micromonospora scalabitana grows very well in many culture media. Such media must contain certain assimilable substances as sources of carbon and nitrogen and there must be an adequate supply of oxygen.
Suitable sources of nitrogen are soy proteins, soybean meal, bean meal, pea meal, corn steep liquor, peptones, meat extracts, yeast extracts, casein hydrolysate, nitrate salts, ammonium salts, etc. Many of these substances can serve simultaneously as sources of carbohydrates except, of course, pure chemical salts, as for instance, nitrates and ammonium salts. Many natural carbohydrates can be used as sources of carbon, such as dextrose, sucrose, maltose, lactose, all materials containing starches and dextrines, brewer's malt and many others.
The selected components are dissolved or suspended in deionized water and sterilized in the autoclave. The length of exposure to heat is important to prevent as much as possible the undesirable hydrolysis of the carbohydrates. The pH is also very important and the maintenance of sterility and the purity of the culture used are crucial for good results.
The range of fermentation temperature is wide but the best results for production are between 30.degree. and 35.degree. C. M. scalabitana produces gentamicin in the media referred above.
Under the term gentamicin all possible variations of gentamicin are possible, such as gentamicin A, B, the whole group of gentamicins C, antibiotics JI-20A and JI-20B, sisomicin and all others so far described gentamicin-related substances. Since there are great morphological and physiological variations among variants and mutants of N. scalabitana there are also great variations in the number, quality and potency of the substances produced. This can be easily demonstrated by paper chromatography or thin layer chromatography. Figure number 1 represents the thin layer chromatography of the gentamicins produced by a few strains tested.
TABLE VI__________________________________________________________________________Comparison of M. narashinoensis with M. scalabitanaTest M. narashinoensis M. scalabitana__________________________________________________________________________Spore formation: Spores spherical or elon- Spores spherical or gate oblongate 0.6-1 by 0.9-1.8 0.8-1.2 by 1.-1.4 Spores develop on branched Spores develop on bran- mycelium within 48 hours, ched mycelium, sometimes mature spores may be re- in 3-4 days, usually in leased into medium within 1-2 weeks and only 72 hours. occasionally we found a few released into medium.Yeast extract- abundant growth, deep good growth of manyglucose agar: orange color later covered colors depending on the with dark brown spore layer. variant tested No soluble pigment Spore formation of strain with dark hues No soluble pigmentNutrient agar: Minute orange to tan Minute colonies, color colored colonies later depending on the variant turning dark when spore used. No spore formation formation took place.Potato plug: Abundant folded growth, No growth on potato plug orange at first later turning alone. brown as spore formation When CaCO.sub.3 is put on the occurs. surface, good growth de- velops. Color and shade develops, or not develops depending on strain tested No spore formation.Gelatin: liquified liquified slowlyMilk: digested digestedNitrates not reduced not reducedAmmonium sulfate utilized moderately utilizied moderatelyNaCl tolerance good 5% poor -2% good 1% or lessAntibioticproduced: No cardorubin Gentamicin__________________________________________________________________________
Silica gel plates, type 60, were used and the solvent system was composed of the lower layer of a mixture of methanol-chloroform-28% ammonia (1:1:1). The zones were detected by spraying with a solution of 1 gm of ninhydrin in a mixture of 95% ethanol (50 ml) and glacial acetic acid (10 ml).
Trace elements play an important role in all biological processes because they are essential for some of the enzymatic systems involved in them. Therefore, they are very important in the fermentation process. The importance of half a dozen trace elements in the production of the tetracycline antibiotics by Streptomyces species has been well established by M. A. Petty and T.R.D. McCormick and beneficial effect of cobalt chloride upon the production of Micromonospora purpurea was described by W. Charney in U.S. Pat. No. 3,136,704. Various trace elements were tested with M. scalabitana using always the same basic medium to reduce to a minimum variations due to the influence of the oligoelements contained in the raw materials used. The most important oligoelement is calcium present as calcium carbonate. All the other elements, when used alone, are beneficial but to a much inferior degree. However, when they are used in combination with calcium carbonate and cobalt chloride the y gave a very favourable synergistic effect (see Examples number 4 and 5).
The antibiotic production process consists of several stages. Of those, the most important are: germination stage, preparation of the inoculum, submerged fermentation, one or more stages of extraction and purification and finally, the isolation of the crystalline antibiotic.

The following examples illustrate adequate methods for the production by fermentation of gentamicin according to this invention as well as some brief description of the extraction, purification and isolation stages.
EXAMPLE 1
Fermentation and antibiotic production in shake flasks Germination Stage: One vial of a lyophylized culture of M. scalabitana was opened and the content mixed under asseptic conditions with 60 ml of broth in an Erlenmeyer flask of 250 ml capacity. The composition of this broth was the following:
______________________________________Corn steep liquor 1.3%Soluble starch 2.5%Corn steep liquor 1.3%Soluble starch 2.5%Sucrose 0.1%Calcium carbonate 0.1%______________________________________
All these substances were dissolved or suspended in deionized water, the pH adjusted to 7.2 and distributed into the flasks 60 ml in each one. Sterilization in autoclave at 121.degree. C. for 15 minutes.
The flasks were incubated on a rotary shaker at 32.degree. C. (280 r.p.m., 5 cm stroke) for 3 days. The quality and purity of the cultured flasks was checked. All contaminated or suspicious flasks are eliminated so that only the perfectly pure cultures can be used further.
For a small scale test the germination stage culture can be used as inoculum. For a larger fermentation another step is necessary.
Preparation of inoculum--Pure and well grown cultures of the germination stage are the basis of this step. This inoculum can be prepared in the same broth that was used in the germination stage but other media can be used as well. One such composition is as follows:
______________________________________Beef extract 0.3%Yeast extract 0.5%Tryptose 0.5%Soluble starch 2.5%Dextrose 0.1%Calcium carbonate 0.1%______________________________________
Proceed exactly as in the germination stage broth as to preparation, sterilization, etc.
The inoculated flasks are incubated on a rotary shaker (280 r.p.m. at 5 cm stroke) at 32.degree. C. for 3 days. All cultures are checked and only well grown cultures can be used.
Fermentation stage--The composition of the medium is the following:
______________________________________Soybean meal 3.5%Dextrin 3.0%Corn starch 2.0%Potato starch 0.5%Sucrose 1.0%Calcium carbonate 0.05%______________________________________
These products are dissolved and/or suspended in deionized water and antifoam (lard oil, for instance) and trace elements are added. The broth is distributed into series of 2 liter Erlenmeyer flasks, measuring 200 ml per flask and sterilized in autoclave at 121.degree. C.
Necessary trace elements: In addition to calcium carbonate, which is most important, only small doses of the following other trace elements are necessary per liter of broth:
______________________________________CoCl.sub.2 . 6H.sub.2 O 1 mgNi (CH.sub.3 CO.sub.2).sub.2 1 mgZnSO.sub.4 . 7H.sub.2 O 5 mgMnSO.sub.4 . H.sub.2 O 5 mgFeSO.sub.4 . 7H.sub.2 O 25 mgMgSO.sub.4 . 7H.sub.2 O 25 mg______________________________________
Small variations in the quantities necessary for the best results can be demonstrated when media are prepared from different sources of raw materials because there are variations in their content of trace elements.
For good growth of M. scalabitana it is necessary to prepare the broth in a way slightly different from general custom. M. scalabitana does not grow well if dextrin and starches are hydrolysed. Therefore, the pH of the fermentation medium before fermentation is not adjusted prior to sterilization but afterwards by pipetting 10% sodium hydroxide in adequate quantity. Ten percent volume is used as inoculum, i.e., 20 ml of prepared inoculum per 200 ml of fermentation broth in each flask.
All inoculated flasks are placed on a rotary shaker (150-180 r.p.m.) in an incubator room at 32.degree. C. for 5-7 days. Small samples can be occasionally removed asseptically.
Microscopical examination, pack cell volume and antibiotic titer are checked and recorded. At the end of incubation there was a titer between 400 and 500 micrograms of gentamicin activity per ml of broth produced.
Extraction: The pooled broth is acidified to pH 2.0 using 12 N sulfuric acid, stirring it for 30-40 minutes. After admixing a perlitic filter aid such as Dicalite 478R (a product of Dicalite Espanola, S.A., Barcelona, Spain), the mycelium is removed together with the filter aid by filtration and discarded. The pH of the filtered broth is adjusted to 8.0 with 6 N Sodium hydroxide and the broth passed through a glass column filled with a weak cationic ion exchange resin such as Amberlite IRC-50 (a product of the Rohm & Hass Co., Philadelphia, Pennsylvania, U.S.A.). The active antibiotics are adsorbed and the efluent can be discarded. The crude antibiotic may be eluted from the column with 1 N aqueous ammonia. Purification of the crude product may be carried out by adsorption on a silica gel column, elution with chloroform-methanol-ammonia and concentrating the various fractions in vacuum.
The final purified product conforms with the specifications of the U.S. Food and Drug Administration for gentamicin sulfate. The ratio of the various components may be determined by thin layer chromatography as described above. FIG. 1 shows the t.l.c. results of the crude antibiotic isolated from M. scalabitana var. rubra (number 2) and from M. scalabitana var. pallida (number 5).
EXAMPLE II
Fermentation in 10-liter laboratory fermentors
The germination stage is prepared exactly as described in Example I. One liter of inoculum is necessary for the inoculation of a ten-liter fermenter. Therefore, a sufficient number of Erlenmeyer flasks must be prepared with the composition of the germination broth shown in Example I, inoculated and incubated on a rotary shaker at 32.degree. C. for 3 days.
In the meantime a small laboratory fermenter of 10 l is prepared and filled with the following broth:
______________________________________Soybean meal 350 gmPotato dextrine 250 gmCorn starch 150 gmPotato starch 100 gmSucrose 100 gmCaCO.sub.3 5 gmCoCl.sub.2 . 6H.sub.2 O 8 mgNi (CH.sub.3 CO.sub.2).sub.2 8 mgZnSO.sub.4 . 7H.sub.2 O 50 mgMnSO.sub.4 . H.sub.2 O 50 mgMgSO.sub.4 . H.sub.2 O 250 mgFeSO.sub.4 . 7H.sub.2 O 250 mg______________________________________
All the ingredients are suspended and/or dissolved directly in the jar of the 10-liter fermenter, 20 ml of lard oil is added as antifoam, the cover closed tightly and sterilized in autoclave at 121.degree. C. for one hour. The pH is adjusted only after sterilization adding 25 ml of 10% sodium hydroxide. This way the hydrolysis of the ingredients will be minimal.
The loaded fermenter containing the sterile broth is placed in its water bath, the stirring mechansim is connected, aeration started and when the temperature reaches 34.degree. C., the fermenter is inoculated under asseptic conditions by adding one liter of the prepared inoculum.
The fermentation at 34.degree. C. is prolonged for 5 to 7 days checking occasionally the the quality of growth, microscopic examination, purity of culture and of course checking and recording the titer of produced antibiotics.
When the titer reached 450 .mu.gm per ml, the fermentation was terminated and the antibiotic extracted, purified and evaluated as it was described in Example I.
EXAMPLE III
Fermentation in 150-liter fermenters
The experiment was started as in the two previous examples.
A germination stage culture is prepared and after 3 days of incubation in the rotary shaker it is used to prepare the inoculum.
For the second stage, two steps will be needed. In the first step a volume of one liter of culture will be prepared as in Example II, using the following broth in skake flasks:
______________________________________Beef extract 0.3%Yeast extract 0.5%Tryptose 0.5%Soluble starch 2.5%Dextrose 0.1%Calcium carbonate 0.1%______________________________________
The pH is adjusted to 7.2, 20.degree. ml portions of the broth are distributed into 2-liter Erlenmeyer flasks and sterilized in the autoclave at 121.degree. C. for 25 minutes.
The inoculated flasks are incubated on a rotary shaker (150-180 r.p.m.) for 3 days. After checking for quality and purity the volume is pooled under asseptic conditions and is ready to be used for inoculation of a 10-liter fermentor in which the inoculum for the large fermentor will be prepared.
The medium for the 10-liter fermentor can be as follows:
______________________________________Sucrose 3.0%Solid corn steep 1.5 to 2.0%Calcium carbonate 0.7%Ammonium sulfate 0.2%Soybean meal 1.0%Lard oil 20 ml______________________________________
The preparation is carried out directly in the small fermentor using deionized water, adjusting the pH to 7.2 and sterilizingin autoclave at 121.degree. C. for one hour.
The fermentor is placed in its thermostated bath and, when the inside temperature is 34.degree. C., one liter of seed culture prepared in step number one is added under asseptic conditions. The incubation takes place at 34.degree. C. with constant stirring and aeration.
In the meantime the large fermentor is prepared, filled with fermentation broth and sterilized.
The composition of the fermentation broth, is as follows:
______________________________________Soybean meal 5.0 kgPotato dextrin 3.5 kgCorn starch 1.0 kgPotato starch 1.0 kgSucrose 1.5 kgCaCO.sub.3 0.8 kgCoCl.sub.2 6H.sub.2 O 120 mgNi (CH.sub.3 CO.sub.2).sub.2 100 mgZnSO.sub.4 . 7H.sub.2 O 750 mgMnSO.sub.4 . H.sub.2 O 750 mgMgSO.sub.4 . 7H.sub.2 O 3.75 gmFeSO.sub.4 . 7H.sub.2 O 3.75 gm______________________________________
The components are dissolved and/or suspended in 150 liters of deionized water, not more than 2% of antifoam is added and the contents sterilized under pressure. The pH is adjusted after sterilization adding enough 40% sodium hydroxide to reach pH 7.4-7.5.
The fermentor is cooled to 34.degree. C. and inoculated by adding at least 10 liters (preferably 15 liters) of the inoculum prepared in 10-liter fermentors.
The fermentation is continued for 5 to 7 days at 34.degree. C. Once a day a sample is taken under asseptic conditions for the necessary checking and evaluation of growth, purity and antibiotic potency. The fermentation was discontinued when the potency reached 475 .mu.gm/ml.
The broth was cooled to 20.degree. C., the pH adjusted to 1.5-2.5 with oxalic acid under constant stirring, 1.5-2.0% of Dicalite 478R added and the mycelium and filter aid removed by filtration. After neutralization of the filtered broth with 6 N sodium hydroxide at 15.degree. C. it was passed through a battery of ion exchange columns filled with Amberlite IRC-50 in the sodium cycle. After washing it with water the columns were eluted with 4 N sulfuric acid. Various fractions were combined, the pH adjusted to 5.0-5.5 with triethylamine, treated with activated carbon and poured into eight volumes of methanol. The crude gentamicin sulfate had a potency of 400 .mu.gm/mg and was purified by dissolving in water (100.000 .mu.gm/ml), treating with activated carbon and adsorbing the activity in a set of glass columns containing a finely ground weak cationic ion exchanger like Amberlite CG-50 in the ammonium cycle. Elution was carried out with 0.1-0.5 N ammonia and the fractions containing the C.sub.1 a, C.sub. 1 and C.sub.2 components combined, concentrated under vacuum to one tenth of the original volume, the pH adjusted to 5.0-5.5 with 5% sulfuric acid and precipitated with methanol. The dried product had an activity of 650 .mu.gm/mg.
EXAMPLE IV
Influence of various trace elements upon gentamicin production in shake flasks
Various trace elements were tested with M. scalabitana var. rubra in a simple broth in which there was soybean meal 3%, dextrin 4%, dextrose 0.5% dissolved in deionized water. This composition was used as the basic medium to which various salts, singly and in combination were added. After sterilization in autoclave at 121.degree. C. for 15 minutes every flask was inoculated using one ml of a fresh broth culture of M. scalabitana var. rubra, incubated on a rotary shaker (280 r.p.m., 5 cm stroke) at 32.degree. C. for seven days. Then all flasks were evaluated, antibiotic titers established and the results tabulated in Table VII.
From these data it is concluded that really many salts in small amounts are important for gentamicin production by M. scalabitana var. rubra. The most important is calcium carbonate. All other chemicals, when used alone, were beneficial but their effect was much inferior. However, when they were used in combination with calcium carbonate and cobalt chloride they gave a very favourable synergistic effect.
EXAMPLE V
As a demonstration of the importance of multiple trace elements for the successful production of gentamicin, the following experiment was carried in 10 liter fermentors. One fermentor marked A was used as control and was filled with the following broth:
______________________________________Soybean meal 300 gmCorn starch 400 gmDextrose 50 gCalcium carbonate 5 gCobalt chloride 8 mgDeionized water 10 liters______________________________________
After adding antifoam, the whole fermentor was sterilized in autoclave for one hour at 121.degree. C. The pH was adjusted after sterilization adding asseptically 5 ml of 40% sodium hydroxyde.
A second fermentor, marked B, was prepared the same way with exactly the same ingredients in the same amounts. The only difference was the presence of additional trace elements which were added in the following amounts:
TABLE VII______________________________________Basal medium plus trace elements(per 100 ml of broth) PackedMe- celldium Trace elements: volume Titer:______________________________________1 0 1.6 222 50mg CaCO.sub.3 2.3 823 0.1mg COCl.sub.2 . 6H.sub.2 O 1.8 544 0.1mg Ni(CH.sub.3 CO.sub.2).sub.2 1.9 305 2.5mg NaCl 1.8 426 2.5mg MgSO.sub.4 . 7H.sub.2 O 1.7 487 2.5mg FeSO.sub.4 . 7H.sub.2 O 1.8 328 0.5mg ZnSO.sub.4 . 7H.sub.2 O 1.8 369 0.5mg MnSO.sub.4 . H.sub.2 O 1.9 3010 2.5mg Na.sub.2 S.sub.2 O.sub.4 1.8 3211 2.5mg K.sub.2 HPO.sub.4 1.8 4512 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O 2.4 15413 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O + +2.5mg FeSO.sub.4 . 7H.sub.2 O 2.7 25814 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O + +0.5mg ZnSO.sub.4 . 7H.sub.2 O 2.7 24515 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O + +0.5mg MnSO.sub.4 . H.sub.2 O 3.-- 23816 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O + +0.1mg Ni(CH.sub.3 CO.sub.2).sub.2 2.8 25817 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O + +0.1mg Ni(CH.sub.3 CO.sub.2).sub.2 + +2.5mg FeSO.sub.4 . 7H.sub.2 O 2.6 32818 50mg CaCO.sub.3 + 0.1mg CoCl.sub.2 . 6H.sub.2 O + +0.1mg Ni(CH.sub.3 CO.sub.2).sub.2 + 0.5mg MnSO.sub.4 . H.sub.2 O 2.5 293______________________________________Ni (CH.sub.3 CO.sub.2).sub.2 8 mgZnSO.sub.4 . 7H.sub.2 O 50 mgMnSO.sub.4 . H.sub.2 O 50 mgMgSO.sub.4 . 7H.sub.2 O 250 mgFeSO.sub.4 . 7H.sub.2 O 250 mg______________________________________
The addition of antifoam, sterilization and adjustment of the pH were done exactly as in the fermentor A.
Both fermentors were inoculated with the same volume of 500 ml of a 3-day old culture of M. scalabitana var. rubra and were incubated for 6 days at a temperature of 34.degree. C. with constant stirringd and aeration.
When the fermentation was terminated the control fermentor A (with calcium carbonate and cobalt chloride) had a titer of 358 .mu.gm while fermentor B (with calcium carbonate, cobalt chloride plus all other trace elements) had a titer of 488 .mu.gm/ml.

Manufacture of aminoglycoside antibiotics

Information

Patent Number

Date Filed

Date Issued

Inventors

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (1)

US Referenced Citations (1)