http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1071027-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_91bb7948041db2ff6ac70900397ae8fa
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N9-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N1-063
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A23L33-145
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A23L33-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-16
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N9-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A23L1-30
filingDate 1963-11-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1967-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1071027-A
titleOfInvention A method for the manufacture of seasoning material by the decomposition of whole yeast cells
abstract A method for the manufacture of a seasoning material by the enzymatic decomposition of whole yeast cells involves culturing Streptomyces satsumaensis ATCC 19242 in a broth medium containing inorganic phosphate material to produce a culture broth comprising a solution of enzymes, adding the culture broth, or the solution of enzymes adding the culture broth, or the solution of enzymes separated from it, to a suspension of yeast cells in an aqueous medium containing antiseptic material (toluene, ethyl acetate, or nitrofurazone), and allowing the enzymes to digest the yeast cells to produce a digest solution containing various 5'-nucleotides, organic acids, sugars (acetic, adenyl, cytidylic, glutamic, guanylic, inosinic and uridylic acids and glucose) and other seasoning components. The inorganic phosphate is added in sufficient amount, between 0.1 - 0.6%, to inhibit or repress the production of phosphatase. 5'-nucleotidase produced is inactivated by heating the cultured broth or the separated solution of enzymes to 50 DEG -60 DEG C. for 5 - 20 minutes. The solution obtained by the digestion is regulated to pH 5.0, extracted with ethyl acetate, and regulated to pH 6.5, the solution is distilled off under reduced pressure until one-fifth has been removed or, alternatively, the solution is kept for 20 minutes at 100 DEG C. for the removal of the remaining solvent, and finally the solution is spray-dried at between 90 DEG and 120 DEG C. to yield a powdery material. Other seasoning materials such as sodium chloride, sugars, spices vinegar, soya sauce, miso (soya bean mash), amino acids, and meat, poultry and fish extracts, may be added to the digest solution or to the spray-dried powdery material. The cultural and morphological characteristics of Streptomyces satsumaensis are disclosed. According to the detailed procedure described in the Examples the Streptomyces satsumaensis micro-organisms were initially cultivated in a medium consisting of baker's yeast, soluble starch, potassium hydrogen phosphate, magnesium sulphate or chloride, sodium chloride or corn steep liquor, and water to produce the solution of enzymes, which solution was then digested with a 20-40% solution of baker's yeast.ALSO:A method for the manufacture of a seasoning material by the enzymatic decomposition of whole yeast cells involves culturing Streptomyces satsumaensis ATCC 19242 in a broth medium containing inorganic phosphate material to produce a culture broth comprising a solution of enzymes, adding the culture broth, or the solution of enzymes separated from it, to a suspension of yeast cells in an aqueous medium containing antiseptic material (toluene, ethyl acetate, or nitrofurazone), and allowing the enzymes to digest the yeast cells to produce a digest solution containing various 51-nucleotides, organic acids, sugars (acetic, adenyl, cytidylic, glutamic, guanylic, inosinic and uridylic acids and glucose) and other seasoning components. The inorganic phosphate is added in a sufficient amount, between 0.1-0.6%, to inhibit or repress the production of phosphatase. 51-nucleotidase produced is inactivated by heating the cultured broth or the separated solution of enzymes to 50 DEG -60 DEG C. for 5-20 minutes. The solution obtained by the digestion is regulated to pH 5.0, extracted with ethyl acetate, and regulated to pH 6.5, the solution is distilled off under reduced pressure until one-fifth has been removed or, alternatively, the solution is kept for 20 minutes at 100 DEG C. for the removal of the remaining solvent, and finally the solution is spray-dried at between 90 DEG and 120 DEG C. to yield a powdery material. Other seasoning materials such as sodium chloride, sugars, spices, vinegar, soya sauce, miso (soya bean mash), amino acids, and meat, poultry and fish extracts, may be added to the digest solution or to the spray-dried powdery material. The cultural and morphological characteristics of Streptomyces satsumaensis are disclosed. According to the detailed procedure described in the Examples the Streptomyces satsumaensis micro-organisms were initially cultivated in a medium consisting of baker's yeast, soluble starch, potassium hydrogen phosphate, magnesium sulphate or chloride, sodium chloride or corn steep liquor, and water to produce the solution of enzymes, which solution was then digested with a 20-40% solution of baker's yeast.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-100426988-C
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115530351-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0299078-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014505485-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-9192184-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103369976-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103369976-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1479299-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0299078-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1479299-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1080645-A4
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1080645-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5288509-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2012110534-A1
priorityDate 1962-11-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP15309
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID1521027
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID878495
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID24450
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID962
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID4907
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID56318
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID452899714
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP21588
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID454620584
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ05927
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID986721
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419588682
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448670727
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4577
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID4932
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5353356
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID190
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5793
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4932
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID3847
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID916883
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID4577
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ61503
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8DFG4
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538408
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID213308
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP20646
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP22848
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID1521027
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9KQ30
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8CE08
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP21589
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID178457
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID58813
http://rdf.ncbi.nlm.nih.gov/pubchem/gene/GID23959
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1140
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419508054
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ1YDF6
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ7CT96
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID456922693
http://rdf.ncbi.nlm.nih.gov/pubchem/taxonomy/TAXID213308
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5234
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID448277656
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCP29240
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ9I767
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419512635
http://rdf.ncbi.nlm.nih.gov/pubchem/protein/ACCQ8A507
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8857
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5360315
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID409298605
http://rdf.ncbi.nlm.nih.gov/pubchem/anatomy/ANATOMYID3847

Total number of triples: 84.