GB1432039A - Method of treating microorganisms - Google Patents
Method of treating microorganismsInfo
- Publication number
- GB1432039A GB1432039A GB5176473A GB5176473A GB1432039A GB 1432039 A GB1432039 A GB 1432039A GB 5176473 A GB5176473 A GB 5176473A GB 5176473 A GB5176473 A GB 5176473A GB 1432039 A GB1432039 A GB 1432039A
- Authority
- GB
- United Kingdom
- Prior art keywords
- treatment
- slurry
- rupturing
- cells
- mins
- 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
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, 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
- C12N1/06—Lysis of microorganisms
-
- A—HUMAN NECESSITIES
- A21—BAKING; EDIBLE DOUGHS
- A21D—TREATMENT, e.g. PRESERVATION, OF FLOUR OR DOUGH, e.g. BY ADDITION OF MATERIALS; BAKING; BAKERY PRODUCTS; PRESERVATION THEREOF
- A21D2/00—Treatment of flour or dough by adding materials thereto before or during baking
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J1/00—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites
- A23J1/18—Obtaining protein compositions for foodstuffs; Bulk opening of eggs and separation of yolks from whites from yeasts
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/22—Working-up of proteins for foodstuffs by texturising
- A23J3/225—Texturised simulated foods with high protein content
- A23J3/227—Meat-like textured foods
Abstract
1432039 Extracting contents of microorganism cells DAI NIPPON SUGAR MFG CO Ltd 7 Nov 1973 [10 Nov 1972 (2)] 51764/73 Headings A2B and C6F [Also in Division C6] An aqueous slurry of microorganisms containing 2-32% dry weight of living cells is treated with at least one agent to weaken' the cell walls, the agent being an acid, alkali, or hydrophilic organic solvent, for 20 mins-2 hrs at <70‹C for pH 0.5-4.0, for 10 mins- 16 hrs at 25-65‹C for pH 7.0-10.5 or for 4 mins-6 hrs at 0-30‹C for pH 10.5-12.0, and then the cells are mechanically ruptured using a grinder or roll mill. The microorganism may be a yeast (e.g. Candida utilis, Saccharomyces cerevisiae, Saccharomyces fragilis, Saccharomyces carlsbergensis, Candida tropicalis, Candida lipolytica, or Rodotorula glutinis), or a bacterium (e.g. Bacillus subtilis or Corynebacterium sp.) or an alga (e.g. Arthrospira, Spirulina, Scenedestius sp. and Chlorella vulgaris). The alkali for treatment at pH 7.0-10.5 may be ammonia or a hydroxide, carbonate or alkaline lactate, citrate, succinate, or acetate of Na, K, NH 3 , Mg or Ca, and for treatment at pH 10.5-12.9 NaOH or KOH may be used, whilst for acid treatment hydrochloric, phosphoric, acetic, lactic, or citric acid may be used. Treatment at pH 7.5-9.5 may be carried out in the presence of ethyl acetate, toluene, acetone, or an alcohol in an amount of 0.5-3% of the weight of the slurry. Treatment may be effected using acetone, methanol, ethanol, propanol or isopropanol preferably in an amount <2.4 times that of the cell moisture content at <30‹C till the intracellular moisture content is <30% w/w. Preferably the cells are separated from the residual waste liquor before rupturing. Preferred rupturing devices are a ball mill containing glass or ceramic beads, or Zr or Al balls having a size of 0.2-1.5 mm or a sand grinder containing 30-90% v/u sand. The rupturing may be carried out continuously with a slurry input rate of 1.8- 40 times the vessel volume portions. A threeroll, high-speed mill, may be used, the front roll being rotated at 120-350 m/min at 20-40 kg/cm<SP>2</SP> pressure with an input of slurry containing 45-65 wt% moisture. Prior to rupturing the slurry may be mixed with cereal flour, powdered gluten, soya bean protein, sodium alginate or starch. Waste liquor may be retained, adjusted to pH 1-7, and dried as an extract, possibly after treatment at pH 5.0-6.0 with activated carbon.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11202672A JPS4971186A (en) | 1972-11-10 | 1972-11-10 | |
JP11202772A JPS5530834B2 (en) | 1972-11-10 | 1972-11-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1432039A true GB1432039A (en) | 1976-04-14 |
Family
ID=26451284
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB5176473A Expired GB1432039A (en) | 1972-11-10 | 1973-11-07 | Method of treating microorganisms |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB1432039A (en) |
Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0008728A2 (en) * | 1978-08-26 | 1980-03-19 | Deutsche Hefewerke GmbH | Preparation of yeast autolysate |
EP0173924A2 (en) * | 1984-09-01 | 1986-03-12 | BOEHRINGER INGELHEIM INTERNATIONAL GmbH | Mechanical process for dislodging bacterial cells for the isolation of peptides prepared by recombinant techniques |
WO1988008881A1 (en) * | 1987-05-11 | 1988-11-17 | Schering Corporation | Extraction of granulocyte macrophage colony stimulating factor from bacteria |
EP0342892A1 (en) * | 1988-05-17 | 1989-11-23 | Schering Corporation | Extraction of human interleukin-4 from bacteria |
WO2005016024A1 (en) * | 2003-08-15 | 2005-02-24 | Grain Processing Corporation | Method for dissociation of cells |
WO2015001261A1 (en) * | 2013-07-04 | 2015-01-08 | Roquette Freres | Optimised method for breaking chlorella walls by mechanical crushing |
US9386774B2 (en) * | 2014-12-16 | 2016-07-12 | Heliae Development, Llc | Application of mixotrophic chlorella for the improved yield and quality of solanaceae plants |
US11102985B2 (en) | 2017-11-10 | 2021-08-31 | Heliae Development, Llc | Biomass compositions and methods for making the same |
CN114249409A (en) * | 2021-11-26 | 2022-03-29 | 河海大学 | Pre-oxidation coupling pressurizing device and method for river and lake blue algae treatment |
-
1973
- 1973-11-07 GB GB5176473A patent/GB1432039A/en not_active Expired
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0008728A2 (en) * | 1978-08-26 | 1980-03-19 | Deutsche Hefewerke GmbH | Preparation of yeast autolysate |
EP0008728A3 (en) * | 1978-08-26 | 1980-04-16 | Deutschen Hefewerke Gestellschaft Mit Beschrankter Haftung | Yeast autolysate, its preparation and its application in food and fodder |
EP0173924A2 (en) * | 1984-09-01 | 1986-03-12 | BOEHRINGER INGELHEIM INTERNATIONAL GmbH | Mechanical process for dislodging bacterial cells for the isolation of peptides prepared by recombinant techniques |
EP0173924A3 (en) * | 1984-09-01 | 1988-02-03 | Boehringer Ingelheim International G.M.B.H | Mechanical process for dislodging bacterial cells for the isolation of peptides prepared by recombinant techniques |
WO1988008881A1 (en) * | 1987-05-11 | 1988-11-17 | Schering Corporation | Extraction of granulocyte macrophage colony stimulating factor from bacteria |
EP0291294A1 (en) * | 1987-05-11 | 1988-11-17 | Schering Corporation | Extraction of granulocyte macrophage colony stimulating factor from bacteria |
US5136024A (en) * | 1987-05-11 | 1992-08-04 | Schering Corporation | Extraction of granulocyte macrophage colony stimulating factor from bacteria |
US4958007A (en) * | 1988-05-17 | 1990-09-18 | Schering-Plough Corp. | Extraction of human interleukin-4- from bacteria |
WO1989011541A1 (en) * | 1988-05-17 | 1989-11-30 | Schering Corporation | Extraction of human interleukin-4 from bacteria |
EP0342892A1 (en) * | 1988-05-17 | 1989-11-23 | Schering Corporation | Extraction of human interleukin-4 from bacteria |
WO2005016024A1 (en) * | 2003-08-15 | 2005-02-24 | Grain Processing Corporation | Method for dissociation of cells |
US7425439B2 (en) | 2003-08-15 | 2008-09-16 | Grain Processing Corporation | Method for dissociation of cells |
WO2015001261A1 (en) * | 2013-07-04 | 2015-01-08 | Roquette Freres | Optimised method for breaking chlorella walls by mechanical crushing |
FR3008001A1 (en) * | 2013-07-04 | 2015-01-09 | Roquette Freres | OPTIMIZED METHOD OF BREAKING CHLORELLA WALLS BY MECHANICAL MILLING |
US10465159B2 (en) | 2013-07-04 | 2019-11-05 | Corbion Biotech, Inc. | Optimised method for breaking chlorella walls by mechanical crushing |
US9386774B2 (en) * | 2014-12-16 | 2016-07-12 | Heliae Development, Llc | Application of mixotrophic chlorella for the improved yield and quality of solanaceae plants |
US11102985B2 (en) | 2017-11-10 | 2021-08-31 | Heliae Development, Llc | Biomass compositions and methods for making the same |
CN114249409A (en) * | 2021-11-26 | 2022-03-29 | 河海大学 | Pre-oxidation coupling pressurizing device and method for river and lake blue algae treatment |
Also Published As
Publication number | Publication date |
---|---|
AU6234573A (en) | 1975-05-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |