http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2005013146-A

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1a03734dc41d01be43c95c0b11f52430
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12R1-24
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12J1-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12J1-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N1-20
filingDate 2003-06-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_581e71fd4da75e44f4733168ebb0454a
publicationDate 2005-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2005013146-A
titleOfInvention GABA (γ-aminobutyric acid) -rich vinegar production method and lactic acid bacteria used therefor
abstract [Problem] To provide a method for producing vinegar with a high GABA content that has both the original functionality of vinegar and the functionality of GABA, and is highly desirable for the prevention of lifestyle-related diseases, and a lactic acid bacterium used therefor. The present invention is characterized in that lactic acid bacteria are inoculated into a saccharified cocoon having a glutamic acid content of 200 mg% or more and lactic acid fermentation is performed for 24 to 48 hours, and then alcoholic fermentation and acetic acid fermentation are sequentially performed using the obtained lactic acid fermentation broth. For producing vinegar having a GABA content of 60 mg% or more, and a glucose tolerance that is proliferated at a glucose concentration of 20% or more, and a conversion rate from glutamic acid to GABA of 80% or more in a fermentation period of 2 days, and high GABA production Sex Lactobacillus brevis. [Selection figure] None
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-101880239-B1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2014207891-A
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