SU884574A3 - Method of preparing protein from microorganism suspension - Google Patents
Method of preparing protein from microorganism suspension Download PDFInfo
- Publication number
- SU884574A3 SU884574A3 SU772485597A SU2485597A SU884574A3 SU 884574 A3 SU884574 A3 SU 884574A3 SU 772485597 A SU772485597 A SU 772485597A SU 2485597 A SU2485597 A SU 2485597A SU 884574 A3 SU884574 A3 SU 884574A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- protein
- suspension
- content
- microorganisms
- nucleotides
- Prior art date
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- 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
- C12N1/08—Reducing the nucleic acid content
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- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Biotechnology (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Microbiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Medicinal Chemistry (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Peptides Or Proteins (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Abstract
Description
нов и колеблетс в основном от 20 мин до 20 ч.New and varies mainly from 20 minutes to 20 hours.
Способ предусматривает использование всех видов микроорганизмов, т.е. дрожжей, бактерий, грибов и т.д.Так, в качестве дрожжей используют Saccharomyces cerevlsiae, Candida boldinii , в качестве микробактёрий Nocardia erytropolis, Aspergillus niger дл плесневых грибов.The method involves the use of all types of microorganisms, i.e. yeast, bacteria, fungi, etc. So, Saccharomyces cerevlsiae, Candida boldinii, Nocardia erytropolis, Aspergillus niger microbacteria for mold fungi are used as yeasts.
Микроорганизмы используютс как обработанные, например высушенные в м гких услови х или лиофилизированные одноклеточные, либо необработанные . Согласно данному способу длительность нагрева снижают путем введени биологических препаратов, содержащих рибонуклеазу, например солодовые ростки трав и зерновых, в частности ростки солода или экстракты изMicroorganisms are used as treated, for example, dried under mild conditions or lyophilized single-cell or untreated. According to this method, the heating time is reduced by administering biological preparations containing ribonuclease, for example, malt sprouts of herbs and cereals, in particular malt sprouts or extracts from
них.of them.
1one
Снижение содержани RNA в одноклеточном протеине достигает до 0,2. вес. % потери протеина незначительны ивыход его практически достигает 90% и выше . Особое преимущество способа заключаетс в том, что рибонуклеинова кислота практически полностью расщепл етс до 5 -нуклеотидов, которые сами по себе вл ютс достаточно ценными веществами. Кроме того, фильтрат, используемый дл получени нуклеотидов после отделени протеина, можно снова использовать дл выращивани микроорганизмов с получением нуклеиновых кислот , т.е. таким образом, получаетс практически циркул ционный цикл нуклеотидов. Одновременно микроорганизмы дл нового роста используют имеющиес в растворе составные части клеток, остатйчный растворимый протеин, и т.п., что приводит к снижению используемых при выращивании микроорганизмов добавок биотина и лпожжевого экстракта.The decrease in the RNA content in the unicellular protein reaches 0.2. weight. % protein loss is insignificant and its output practically reaches 90% and more. A particular advantage of the method is that ribonucleic acid is almost completely decomposed into 5-nucleotides, which themselves are quite valuable substances. In addition, the filtrate used to obtain nucleotides after protein separation can be reused for growing microorganisms to produce nucleic acids, i.e. in this way, a practically circulating nucleotide cycle is obtained. At the same time, microorganisms for cell growth utilize the cell components present in the solution, residual soluble protein, etc., which leads to a decrease in the biotin and lactic acid additives used in the cultivation of microorganisms.
Получаемый протеин по предлагаемому способу более чистый,лучше усваиваетс , содержит детергенты солей или RNA, не имеет запаха и может быть использован в качестве пищевого продукта.The resulting protein according to the proposed method is cleaner, better digested, contains detergents of salts or RNA, has no odor and can be used as a food product.
Пример. 200 л водной суспензии приведенных в табл.1 микроорганизмов с содержанием сухой массы 15-20% нагревают до и 15 ч вып держивают при этой температуре при перемешивании. рН поддерживают между 7-8,5 путэм добавлени МаОН. Затем смесь кратковременно кип т т и сырой протеин отдел ют и сушат.Example. 200 l of an aqueous suspension of the microorganisms listed in Table 1, with a dry mass content of 15–20%, are heated and melted at this temperature for 15 hours while stirring. The pH is maintained between 7-8.5 by addition of NaOH. The mixture is then briefly boiled and the crude protein is separated and dried.
Выход составл ет 25-32 кг сырогоThe yield is 25-32 kg of raw.
э протеина. Табл.1 показывает содержание RNA в исходном материале и достигнутое при этом расщепление RNA. П р и м е р 2. а)3 кг солодовых ростков измельчают, добавл ют 30 л НлО и 40 мин выдерживают при . Полученную суспензию непосредственно или после отделени нерастворимьк элементов ростков солода на центрифуге примен ютe protein. Table 1 shows the RNA content of the starting material and the RNA cleavage achieved therewith. PRI mme R 2. a) 3 kg of malt sprouts are ground, 30 l of HlO are added and the mixture is kept for 40 min. The resulting suspension, either directly or after the separation of insoluble elements of malt sprouts, is applied in a centrifuge.
5 в следукадем процессе.5 in the following process.
б)По 200 л суспензии таких же микроорганизмов, как и в примере 1 с таким же содержанием сухих веществ, нагревают до , добавл ют пригод товленную суспензию солодовых ростков или экстракт (пример 2а) и затем смесь нагревают 2-15 ч при 65с. Затем обработку провод т как в примере 1. Выход составл ет 25-35 кг сы . рого протеина, среднее содержание чистого протеина около 70%.b) 200 l of a suspension of the same microorganisms as in example 1 with the same solids content is heated to, a suitable suspension of malt sprouts or extract is added (example 2a) and then the mixture is heated for 2-15 h at 65 s. The treatment is then carried out as in Example 1. The output is 25-35 kg of sulfur. royal protein, the average pure protein content of about 70%.
Табл.2 показывает достигнутое расщепление RNA. Выход 5 -нуклеотидов при примерном 10%-ном содержании RNA в сухом продукте 7-800 г каждого изTable 2 shows the achieved RNA cleavage. The output of 5-nucleotides with an approximate 10% RNA content in the dry product 7-800 g each of
0 четырех различных 5 -нуклео-идов, при меньшем содержании RNA в исходном материале они были соответственно ниже.0 of four different 5-nucleosides, with a lower RNA content in the starting material, they were respectively lower.
Биомасса по примеру 2Biomass for example 2
Saccharomyces cerevisiaeSaccharomyces cerevisiae
carlsbergensis carlsbergensis
Candida boidihii (примерно возраст Candida boidihii (approximately age
Nocardia erytropolisNocardia erytropolis
Bacillus cereus (возраст 1 год)Bacillus cereus (age 1 year)
Streptococcus faccalisStreptococcus faccalis
Pseudomonas fluoreszensФормула изобретени Способ получени протеина из суспензии микроорганизмов путем ее нагревани при определенных значени х рН с последугацим вьаделением целевого продукта и 5 -нуклеотидов, отличающийс тем, что, с целью сни жени содержани нуклеиновых кислот в протеине с одновременным повышением выхода 5-нуклеотидов, нагреваниеPseudomonas fluoreszens Formula of the Invention A method of obtaining protein from a suspension of microorganisms by heating it at certain pH values with subsequent injection of the target product and 5-nucleotides, characterized in that in order to reduce the content of nucleic acids in the protein with simultaneous increase in the yield of 5-nucleotides, heating
Таблица 2table 2
Разложение RNA экстрактом ростков солодаDecomposition of RNA extract of malt sprouts
100% 90%100% 90%
26%26%
100%100%
30%thirty%
100%100%
70% супензии осуществл ют в течение 215 ч при температуре 63-67°С и рН 7-8,5, после чего в нее ввод т суспензию солодовых ростков или их экстракт и смесь кип т т в течение 0,5-5 мин. Источники информации, прин тые во внимание при экспертизе 1,Патент США 3720585,кл. 260-112, опублик.1973. 2.Патент Великобритании 1372870, кл. С 6 F, опублик.1974 (прототип).70% of the suspension is carried out for 215 hours at a temperature of 63-67 ° C and a pH of 7-8.5, after which a suspension of malt sprouts or their extract is introduced into it and the mixture is boiled for 0.5-5 minutes. Sources of information taken into account in examination 1, US Patent 3,720,585, cl. 260-112, published 1973. 2. The UK patent 1372870, cl. C 6 F, publish 1974 (prototype).
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2622982A DE2622982B1 (en) | 1976-05-21 | 1976-05-21 | Process for the production of protein with a low nucleic acid content from microorganisms |
Publications (1)
Publication Number | Publication Date |
---|---|
SU884574A3 true SU884574A3 (en) | 1981-11-23 |
Family
ID=5978741
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU772485597A SU884574A3 (en) | 1976-05-21 | 1977-05-20 | Method of preparing protein from microorganism suspension |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPS52143290A (en) |
CA (1) | CA1077772A (en) |
FI (1) | FI58156C (en) |
SE (1) | SE433501B (en) |
SU (1) | SU884574A3 (en) |
YU (1) | YU125877A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2616662B1 (en) * | 1987-06-16 | 1994-02-18 | Guyomarch Sa Ets | FOOD ADDITIVE FOR ANIMALS, FOOD COMPRISING SUCH AN ADDITIVE AND METHOD FOR IMPROVING THE GROWTH OF ANIMALS |
MY186172A (en) * | 2011-09-22 | 2021-06-30 | Danisco Us Inc | Endogenous dnase activity to reduce dna content |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1440642A (en) * | 1973-09-24 | 1976-06-23 | Ranks Hovis Mcdougall Ltd | Production of edible protein containing substances |
GB1466078A (en) * | 1973-09-26 | 1977-03-02 | British Petroleum Co | Treatment of proteinaceous material |
SE7401668L (en) * | 1974-02-07 | 1975-08-08 | Scp Exploatering Ab |
-
1977
- 1977-05-06 CA CA277,828A patent/CA1077772A/en not_active Expired
- 1977-05-16 SE SE7705701A patent/SE433501B/en not_active IP Right Cessation
- 1977-05-19 YU YU125877A patent/YU125877A/en unknown
- 1977-05-20 FI FI771621A patent/FI58156C/en not_active IP Right Cessation
- 1977-05-20 SU SU772485597A patent/SU884574A3/en active
- 1977-05-20 JP JP5862677A patent/JPS52143290A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
SE433501B (en) | 1984-05-28 |
FI771621A (en) | 1977-11-22 |
JPS52143290A (en) | 1977-11-29 |
FI58156C (en) | 1980-12-10 |
CA1077772A (en) | 1980-05-20 |
FI58156B (en) | 1980-08-29 |
JPS5637799B2 (en) | 1981-09-02 |
YU125877A (en) | 1982-10-31 |
SE7705701L (en) | 1977-11-22 |
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