GB691786A - Recovery of streptomycin from solutions thereof - Google Patents

Recovery of streptomycin from solutions thereof

Info

Publication number
GB691786A
GB691786A GB19430/49A GB1943049A GB691786A GB 691786 A GB691786 A GB 691786A GB 19430/49 A GB19430/49 A GB 19430/49A GB 1943049 A GB1943049 A GB 1943049A GB 691786 A GB691786 A GB 691786A
Authority
GB
United Kingdom
Prior art keywords
resin
streptomycin
eluted
acid
column
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
GB19430/49A
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.)
Merck and Co Inc
Original Assignee
Merck and Co Inc
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 Merck and Co Inc filed Critical Merck and Co Inc
Publication of GB691786A publication Critical patent/GB691786A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
    • C12N1/20Bacteria; Culture media therefor
    • C12N1/205Bacterial isolates

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • Medicinal Chemistry (AREA)
  • Biomedical Technology (AREA)
  • Virology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

Abstract

In the process of the parent Specification, the carboxylic type ion-exchange resin employed for adsorption of streptomycin is one formed by the copolymerization of a divinyl compound (e.g. divinyl benzene) and a polymerizable acid (e.g. acrylic or methacrylic acid). Advantageously a column of resin in the form of a salt (e.g. its sodium salt) is used, e.g. in a three-step cycle consisting of passing a clarified streptomycin-containing broth through the column, eluting the adsorbed streptomycin with a solution of acid, and regenerating the resin by passing a solution of a base (e.g. sodium hydroxide) through the column, followed by washing with water. It is also possible to use the resin otherwise than in a column, to use it in its hydrogen form, and to use calcium chloride solution as eluting material. The resin should preferably contain only 2.5-5.0 per cent of the divinylbenzene component in order that it may have a high porosity. The broth treated should desirably have a pH above 4.5 (preferably about neutral point) and be freed from calcium and other ions liable to interfere with the process. The streptomycin may be recovered from the eluate (which also contains metal salts) by evaporating (preferably under reduced pressure) to small volume or to dryness, taking up the residue in methanol or other solvent for streptomycin in which the salts are insoluble, filtering, precipitating streptomycin from the filtrate (e.g. with acetone), filtering and drying, and, if desired, converting the product to its crystalline calcium chloride complex salt by dissolving it in methanol and adding calcium chloride. In examples, a copolymer of 95 per cent of methacrylic acid and 5 per cent of divinylbenzene is used in the form of (1) its ammonium salt, and (2) its sodium salt, elution being effected with dilute hydrochloric acid. Example (3) gives comparative results with this resin, one containing 10 per cent of divinyl benzene and a carboxylic resin believed to be of the phenolformaldehyde type (all eluted with hydrochloric acid), a sulphonated phenol-formaldehyde resin and a sulphonated coal resin (both eluted with sodium chloride solution or aqueous sulphuric acid), a silicate exchange resin (eluted with sodium chloride solution), carbon (eluted with acidified aqueous methanol) and fuller's earth (eluted with an aqueous solution of pyridine hydrochloride). Specification 638,664 also is referred to.
GB19430/49A 1949-01-08 1949-07-23 Recovery of streptomycin from solutions thereof Expired GB691786A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US691786XA 1949-01-08 1949-01-08

Publications (1)

Publication Number Publication Date
GB691786A true GB691786A (en) 1953-05-20

Family

ID=22087235

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19430/49A Expired GB691786A (en) 1949-01-08 1949-07-23 Recovery of streptomycin from solutions thereof

Country Status (1)

Country Link
GB (1) GB691786A (en)

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