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GB621469A - Improvements in or relating to process for recovering riboflavin - Google Patents

Improvements in or relating to process for recovering riboflavin

Info

Publication number
GB621469A
GB621469A GB25467/44A GB2546744A GB621469A GB 621469 A GB621469 A GB 621469A GB 25467/44 A GB25467/44 A GB 25467/44A GB 2546744 A GB2546744 A GB 2546744A GB 621469 A GB621469 A GB 621469A
Authority
GB
United Kingdom
Prior art keywords
riboflavin
mash
liquefaciens
bacteria
nutrient
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
GB25467/44A
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.)
Commercial Solvents Corp
Original Assignee
Commercial Solvents Corp
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 Commercial Solvents Corp filed Critical Commercial Solvents Corp
Priority to GB25467/44A priority Critical patent/GB621469A/en
Publication of GB621469A publication Critical patent/GB621469A/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
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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

A material which on oxidation yields riboflavin and which is described as a riboflavin precursor is prepared by inoculating a nutrient riboflavin-containing mash having a riboflavin concentration of at least 65 m g per c.c. with an active culture of bacteria which synthesizes substantially no additional riboflavin in said mash and which is active to produce an Eh value of - 0.096 volt or less and to yield a precipitate of said riboflavin precursor. The preferred temperature of the insulation is in the range 8-47 DEG C. Bacteria which are mentioned as suitable for the process of the invention are streptococci f calis, liquefaciens, cremoris, zymogenes and lactis, Escherichia coli, Clostridium acetobutylicum, Clostridium saccharo-butyl-acetonicum-liquefaciens-delta, and serratia phymouthensis. The preferred nutrient mash is that obtained by fermenting a sterile mash containing as the substrate proteins and carbohydrates with an acetine culture of the fungus Eremothecium Ashbyii in the presence of abundant aeration. Specification 621,468 is referred to.
GB25467/44A 1944-12-19 1944-12-19 Improvements in or relating to process for recovering riboflavin Expired GB621469A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB25467/44A GB621469A (en) 1944-12-19 1944-12-19 Improvements in or relating to process for recovering riboflavin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB25467/44A GB621469A (en) 1944-12-19 1944-12-19 Improvements in or relating to process for recovering riboflavin

Publications (1)

Publication Number Publication Date
GB621469A true GB621469A (en) 1949-04-11

Family

ID=10228164

Family Applications (1)

Application Number Title Priority Date Filing Date
GB25467/44A Expired GB621469A (en) 1944-12-19 1944-12-19 Improvements in or relating to process for recovering riboflavin

Country Status (1)

Country Link
GB (1) GB621469A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2920592A1 (en) * 1975-08-29 1980-12-04 Merck & Co Inc METHOD FOR PURIFYING RIBOFLAVIN

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2920592A1 (en) * 1975-08-29 1980-12-04 Merck & Co Inc METHOD FOR PURIFYING RIBOFLAVIN

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