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filingDate 2021-04-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f0382a14520df73b613cd014eff6334
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publicationDate 2021-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113174442-A
titleOfInvention A quantitative detection method for the expression of key genes in the synthesis of tetramethylpyrazine in Daqu
abstract The invention discloses a quantitative detection method for the expression of key genes in the synthesis of tetramethylpyrazine in Daqu, and belongs to the technical field of liquor detection. The invention adopts the real-time fluorescence quantitative method to detect the key genes (alsS gene and alsD gene) of tetramethylpyrazine synthesis in Daqu to detect the content change of tetramethylpyrazine. First, the genomic RNA in Daqu was extracted by the bacterial total RNA rapid extraction kit; then the RNA was converted into cDNA by the RevertAid First Strand cDNA Synthesis Kit (reverse transcription kit); and then real-time fluorescent PCR detection was performed to complete the tetramethyl Pyrazine content detection. The present invention utilizes molecular biology means to realize real-time quantitative detection of the alsS gene and alsD gene, which are key synthesis genes of tetramethylpyrazine, and evaluates the production of acetoin and tetramethylpyrazine by Bacillus. Compared with ordinary PCR methods, it has the advantages of simple operation, fast speed, and integration of product detection and quantitative analysis.
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