GB1072374A - Preparation of 6-aminopencillanic acid - Google Patents
Preparation of 6-aminopencillanic acidInfo
- Publication number
- GB1072374A GB1072374A GB4663363A GB4663363A GB1072374A GB 1072374 A GB1072374 A GB 1072374A GB 4663363 A GB4663363 A GB 4663363A GB 4663363 A GB4663363 A GB 4663363A GB 1072374 A GB1072374 A GB 1072374A
- Authority
- GB
- United Kingdom
- Prior art keywords
- penicillin
- preparation
- cells
- borate buffer
- acid
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D499/00—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
- C07D499/21—Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a nitrogen atom directly attached in position 6 and a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
- C07D499/42—Compounds with a free primary amino radical attached in position 6
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
6-Amino-penicillanic acid is produced by subjecting a penicillin to the action of enzymes present in or obtained from Streptomyces griseus, S. azureus, S. fradiae, S. olivaceus or Bacterium cyclo-oxydans. The penicillin may be penicillin G, penicillin V or a -phenoxyethyl penicillin. According to the example, a five day culture of the cells in a conventional medium is separated from the broth, resuspended in N/5 borate buffer at pH 8.5 and centrifuged. The cells are incubated with the penicillin in N/5 borate buffer at pH 8.5 and 45 DEG C. The 6-aminopenicillanic acid formed is recovered in the coventional manner.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4663363A GB1072374A (en) | 1963-11-26 | 1963-11-26 | Preparation of 6-aminopencillanic acid |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB4663363A GB1072374A (en) | 1963-11-26 | 1963-11-26 | Preparation of 6-aminopencillanic acid |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1072374A true GB1072374A (en) | 1967-06-14 |
Family
ID=10442000
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB4663363A Expired GB1072374A (en) | 1963-11-26 | 1963-11-26 | Preparation of 6-aminopencillanic acid |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1072374A (en) |
-
1963
- 1963-11-26 GB GB4663363A patent/GB1072374A/en not_active Expired
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