GB596847A - Process for producing yeast extract and food preparations made from yeast - Google Patents

Process for producing yeast extract and food preparations made from yeast

Info

Publication number
GB596847A
GB596847A GB391744A GB391744A GB596847A GB 596847 A GB596847 A GB 596847A GB 391744 A GB391744 A GB 391744A GB 391744 A GB391744 A GB 391744A GB 596847 A GB596847 A GB 596847A
Authority
GB
United Kingdom
Prior art keywords
mixture
cell residue
extract
yeast
per cent
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
GB391744A
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.)
Individual
Original Assignee
Individual
Filing date
Publication date
Application filed by Individual filed Critical Individual
Publication of GB596847A publication Critical patent/GB596847A/en
Expired legal-status Critical Current

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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
    • C12N1/06Lysis of microorganisms
    • C12N1/063Lysis of microorganisms of yeast

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Genetics & Genomics (AREA)
  • Mycology (AREA)
  • Biotechnology (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Microbiology (AREA)
  • Virology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)

Abstract

A yeast extract is prepared from compressed fresh baker's yeast containing about 75 per cent of water by mixing with 2-4 per cent of its wet weight of sodium chloride, heating to 57-67 DEG C., maintaining at that temperature for at least 40 hours and then separating the resulting extract from the yeast cell residue and evaporating to a desired consistency. The extract may be separated continuously by a centrifuge and the cell residue further centrifuged after adding wash water and if necessary heating by steam. A peeling or sedimentation centrifugal machine may be used with discontinuous separation of the cell residue. Separation may be effected also by filtration either by forcing the liquid up through a filter of compressed cellulose, e.g. by means of a saturated solution of sodium chloride, or by a suction pipe containing the filter being lowered in the liquid. The primary extract and all further extracts obtained by washing the cell residue are evaporated separately or together in open vessels at atmospheric pressure. If evaporation takes place in vacuo, fat is added to reduce foaming. The cell residue may be mixed with finely-divided vegetables e.g. mashed, boiled turnips after evaporating water, and mixing in lactic acid, lactic acid bacillus or Yoghurt-micro-organisms fermenting and, if desired, pasteurising. Beet juice, celery and small amounts of tomatoes may be added. The cell residue can also be utilized by plasmolysing it with sugar or malt and, if desired, proteolytic enzymes. Alternatively, the cell residue may be hydrolysed, e.g. with hydrochloric or sulphuric acid, and after neutralizing boiling the mixture with steam to assist the separation of the remaining cell walls from the mixture by centrifuging, sedimentation or filtering. A suitable method is to hydrolyse one half of the cell residue with acid and treat the other half with sodium hydroxide or lime at 50-60 DEG C. at such concentration that upon mixing the two portions a neutral mixture is obtained. In an example, to 50 kg. of fresh baker's yeast in narrow glass cylinders is added a saturated solution of NaCl at 100 DEG C. corresponding to 3 per cent NaCl on the total mixture and stirred, the temperature becoming 62 DEG C. at which the mixture is maintained for 60 hours. The mixture is raised to 90 DEG C. by steam and centrifuged. Hot water is added to the residue which is centrifuged. The extract and washing water are mixed and first evaporated at atmospheric pressure in a rapidly revolving evaporator and then in a vacuum evaporator. The cell residue is heated for about 24 hours with an amount of H2SO4 corresponding to 3 per cent of the mixture and then neutralized p with chalk and lime, filtered or centrifuged and then evaporated separately or together with the primary extract. 1 per cent of fat is added in portions during vacuum evaporation when foaming is worst.
GB391744A 1944-03-02 Process for producing yeast extract and food preparations made from yeast Expired GB596847A (en)

Publications (1)

Publication Number Publication Date
GB596847A true GB596847A (en) 1948-01-13

Family

ID=1627851

Family Applications (1)

Application Number Title Priority Date Filing Date
GB391744A Expired GB596847A (en) 1944-03-02 Process for producing yeast extract and food preparations made from yeast

Country Status (1)

Country Link
GB (1) GB596847A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3961080A (en) 1972-10-17 1976-06-01 Kikkoman Shoyu Co., Ltd. Process for autolysis of yeast
US3975553A (en) 1965-03-08 1976-08-17 Henri Griffon Deproteination of yeast cells
US4285976A (en) 1979-11-23 1981-08-25 Standard Oil Company (Indiana) Method for accelerating autolysis of yeast
WO1993024610A1 (en) * 1992-05-28 1993-12-09 Campina Melkunie B.V. Production of yeast product from lactose-containing substates
EP1498477A1 (en) * 2003-07-18 2005-01-19 B.F.L. Bakery Future Lines S.r.l. New active yeast in dry granular or powder form obtained through treatment of a mixture of known yeasts and its use in a pre-packed long-life preparation to be completed with the addition of water

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3975553A (en) 1965-03-08 1976-08-17 Henri Griffon Deproteination of yeast cells
US3961080A (en) 1972-10-17 1976-06-01 Kikkoman Shoyu Co., Ltd. Process for autolysis of yeast
US4285976A (en) 1979-11-23 1981-08-25 Standard Oil Company (Indiana) Method for accelerating autolysis of yeast
WO1993024610A1 (en) * 1992-05-28 1993-12-09 Campina Melkunie B.V. Production of yeast product from lactose-containing substates
EP1498477A1 (en) * 2003-07-18 2005-01-19 B.F.L. Bakery Future Lines S.r.l. New active yeast in dry granular or powder form obtained through treatment of a mixture of known yeasts and its use in a pre-packed long-life preparation to be completed with the addition of water

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