GB593953A - Improvements in or relating to the production of riboflavin in an aqueous medium - Google Patents

Improvements in or relating to the production of riboflavin in an aqueous medium

Info

Publication number
GB593953A
GB593953A GB17548/43A GB1754843A GB593953A GB 593953 A GB593953 A GB 593953A GB 17548/43 A GB17548/43 A GB 17548/43A GB 1754843 A GB1754843 A GB 1754843A GB 593953 A GB593953 A GB 593953A
Authority
GB
United Kingdom
Prior art keywords
molasses
medium
peptone
neopeptone
riboflavin
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
GB17548/43A
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.)
Pfizer Inc
Original Assignee
Pfizer Inc
Charles Pfizer 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 Pfizer Inc, Charles Pfizer and Co Inc filed Critical Pfizer Inc
Publication of GB593953A publication Critical patent/GB593953A/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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/525Isoalloxazines, e.g. riboflavins, vitamin B2

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)

Abstract

Riboflavin - producing mycetes, especially Eremothecium Ashbyii, when grown at 22-34 DEG C. in a medium containing carbohydrates not exceeding 5 per cent, and proteins or their non-toxic degradation-products together with a minor quantity of wheat germ, the liquor being subjected to vigorous agitation in a continuous current of sterile humidified air during the fermentation, afford increased yields of the vitamin. Advantageously, glucose, sucrose including brown sugar, malt syrup molasses including black strap molasses, and hydrolysed starch or a starch-containing material may be used as carbohydrates, while peptones, crude or refined, are suitable proteins. Stock cultures of E. Ashbyii are carried on a molasses-peptone agar medium adjusted to pH 6.0, incubated at 28 DEG C. and transferred every week to a fresh medium, from which inocula for large-volume fermentations are prepared by incubating at 28 DEG C. for about 3 days, a portion of the stock culture on fresh molasses-peptone "slants." In examples: (1) brown sugar, neopeptone, wheat germ, beef extract, monobasic potassium dihydrogenphosphate, sodium chloride and distilled water medium at pH 6.0 is sterilized and a current of air is led into the cooled fermenter, prior to inoculation with "starter" culture; (2) a fermentation conducted exactly as in (1), substituting a medium comprising cane molasses syrup, neopeptone, peptone, tryptone, beef extract, potassium dihydrogen phosphate, sodium chloride and distilled water, at pH 6.0 and using sterile cane molasses solution as carbohydrate.
GB17548/43A 1942-09-29 1943-10-25 Improvements in or relating to the production of riboflavin in an aqueous medium Expired GB593953A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US593953XA 1942-09-29 1942-09-29

Publications (1)

Publication Number Publication Date
GB593953A true GB593953A (en) 1947-10-30

Family

ID=22022671

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17548/43A Expired GB593953A (en) 1942-09-29 1943-10-25 Improvements in or relating to the production of riboflavin in an aqueous medium

Country Status (1)

Country Link
GB (1) GB593953A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2493274A (en) * 1947-07-16 1950-01-03 Hoffmann La Roche Production of riboflavin by fermentation process
US2578738A (en) * 1949-11-04 1951-12-18 Thomas G Pridham Biological production of riboflavin
US2973305A (en) * 1954-07-08 1961-02-28 Takeda Pharmaceutical Process for preparing flavinadenine dinucleotide and reduced-form thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2493274A (en) * 1947-07-16 1950-01-03 Hoffmann La Roche Production of riboflavin by fermentation process
US2578738A (en) * 1949-11-04 1951-12-18 Thomas G Pridham Biological production of riboflavin
US2973305A (en) * 1954-07-08 1961-02-28 Takeda Pharmaceutical Process for preparing flavinadenine dinucleotide and reduced-form thereof

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