GB830874A - A new antibiotic mitomycin c and its production by fermentation - Google Patents

A new antibiotic mitomycin c and its production by fermentation

Info

Publication number
GB830874A
GB830874A GB10987/58A GB1098758A GB830874A GB 830874 A GB830874 A GB 830874A GB 10987/58 A GB10987/58 A GB 10987/58A GB 1098758 A GB1098758 A GB 1098758A GB 830874 A GB830874 A GB 830874A
Authority
GB
United Kingdom
Prior art keywords
methanol
chloroform
antibiotic
solvent
mitomycin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB10987/58A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
KITASATO KENKYUSHO SH
KH Neochem Co Ltd
Original Assignee
KITASATO KENKYUSHO SH
Kyowa Hakko Kogyo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by KITASATO KENKYUSHO SH, Kyowa Hakko Kogyo Co Ltd filed Critical KITASATO KENKYUSHO SH
Publication of GB830874A publication Critical patent/GB830874A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

<PICT:0830874/IV (b)/1> <PICT:0830874/IV (b)/2> A new antibiotic, mitomycin C, active against pathogenic bacteria, is produced by growing Streptomyces calspitosus NRRL 2564 in a liquid nutrient medium under aerobic and preferably submerged conditions. The pH is 7.0, the temperature of cultivation is 26 DEG to 32 DEG C. and the duration 2 to 6 days. The medium contains a source of (a) nitrogen such as peptone, meat extract, corn steep liquor, soy bean meal, yeast, urea, ammonium sulphate and ammonium nitrate; (b) carbon, e.g. glucose, starch, glycerol, soybean oil, maltose and dextrin; and (c) inorganic salts such as sodium chloride, potassium chloride, calcium carbonate, potassium phosphate, ferrous sulphate, magnesium sulphate and zinc sulphate. Mitomycin C is recovered from the clarified broth by (a) adsorption, (b) solvent extraction. Adsorption is by means of carbon at pH 6 to 9, followed by elution with a solvent such as acetone, cyclohexanone, methyl isobutyl ketone, butanol, chloroform or a mixture thereof. Acetone is the preferred solvent and the carbon is washed with methanol to remove water. Extraction is at pH 6 to 9 by means of a water-immiscible solvent such as an alcohol, e.g. butanol, an ester, e.g. butyl acetate, a ketone, e.g. methyl isobutyl ketone and cyclohexanone, and chloroform. Extraction may be increased by the simultaneous utilization of salting-out agents such as sodium chloride and ammonium sulphate. Further purification is obtained by (A) chromatography on alumina and (B) countercurrent distribution. For (A), a solution of the crude antibiotic in chloroform is adsorbed on alumina and developed with chloroform containing increasing quantities of methanol up to 6%, the eluate containing 3 to 6% methanol being collected and the antibiotic recovered therefrom. Ethanol or butanol may be used in place of methanol. Alternatively, after developing with methanol containing 0.5% methanol, the purple alumina layer is removed and the antibiotic recovered by elution with methanol per se. For (B), the fixed phase is chloroform and the moving phase an aqueous phosphate buffer of pH 6.0 containing 10% sodium chloride. Mitomycin C occurs as purple coloured needle-shaped crystals which do not melt even at 360 DEG C.; it contains 53.84% carbon, 5.14% hydrogen and 15.49% nitrogen; it is soluble in water, methanol, ethanol and chloroform; slightly soluble in carbon tetrachloride, benzene and ethyl ether and insoluble in petroleum ether; stable in aqueous solution at pH 5 to 11 even on heating, less stable in organic solvent solution; peaks are observed in the ultra-violet absorption spectrum (Fig. 1) at <FORM:0830874/IV (b)/1> 742; infra-red absorption spectrum peaks are observed at the following frequencies (cm.-1) 2930, 2857, 1700, 1640, 1596, 1545, 1448, 1370, 1333, 1230, 1170, 1155, 1125, 1060, 1025, 1002, 969, 952, 919, 895, 854, 824, 780 and 701. It is active against many pathogenic micro-organisms including staphylococci and pneumoniae and is used medicinally (see Group VI).ALSO:A therapeutic composition comprises the antibiotic mitomycin C (see Group IV (b)) and a carrier which may be an ointment base, a solvent or an inert powder. The antibiotic may also be put up in tablet and capsule form.
GB10987/58A 1957-04-06 1958-04-08 A new antibiotic mitomycin c and its production by fermentation Expired GB830874A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP830874X 1957-04-06

Publications (1)

Publication Number Publication Date
GB830874A true GB830874A (en) 1960-03-23

Family

ID=13792384

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10987/58A Expired GB830874A (en) 1957-04-06 1958-04-08 A new antibiotic mitomycin c and its production by fermentation

Country Status (1)

Country Link
GB (1) GB830874A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2865391A1 (en) 2013-10-22 2015-04-29 medac Gesellschaft für klinische Spezialpräparate mbH Method for producing a freeze-dried pharmaceutical composition containing Mitomycin C

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2865391A1 (en) 2013-10-22 2015-04-29 medac Gesellschaft für klinische Spezialpräparate mbH Method for producing a freeze-dried pharmaceutical composition containing Mitomycin C
WO2015059023A1 (en) 2013-10-22 2015-04-30 Medac Gesellschaft für klinische Spezialpräparate mbH Method for producing a freeze-dried pharmaceutical composition having a mitomycin c content
EP3272361A1 (en) 2013-10-22 2018-01-24 medac Gesellschaft für klinische Spezialpräparate mbH Method for producing a freeze-dried pharmaceutical composition containing mitomycin c
US10688049B2 (en) 2013-10-22 2020-06-23 Medac Gesellschaft für klinische Spezialpräparate mbH Process for the preparation of a freeze-dried pharmaceutical composition containing mitomycin C
US11766405B2 (en) 2013-10-22 2023-09-26 Medac Gesellschaft Fur Klinische Spezialpraparate Mbh Process for the preparation of a freeze-dried pharmaceutical composition containing mitomycin C

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