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Establishment and application of a rapid authentication test method based on enzymatic recombinase amplification technology for the identification of Gastrodiae Rhizoma*
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Qiu-he MA1, Yu-he MA1, Tao LI1, Yue LIU1, Jin-jun CHAI1, Zi-qiang XU1, Ang LIU1, Li-jun GAO1, **, Wei XIA1, Ming-cheng LI1, 2, Yong-mei QU3
Chinese Journal of Pharmaceutical Analysis | 2024, 44(4) : 729 - 736
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Chinese Journal of Pharmaceutical Analysis | 2024, 44(4): 729-736
Rapid Analysis
Establishment and application of a rapid authentication test method based on enzymatic recombinase amplification technology for the identification of Gastrodiae Rhizoma*
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Qiu-he MA1, Yu-he MA1, Tao LI1, Yue LIU1, Jin-jun CHAI1, Zi-qiang XU1, Ang LIU1, Li-jun GAO1, **, Wei XIA1, Ming-cheng LI1, 2, Yong-mei QU3
Affiliations
  • 1.School of Medical Technology, Beihua Universsity, Jilin 132013, China
  • 2. Innovation Center for Detection on DNA Fingerprint of Traditional Chinese Medicine, Jilin 132013, China
  • 3.Jilin Guoan Pharmaceutical Limited Company, Jilin 132013, China
Published: 2024-04-30 doi: 10.16155/j.0254-1793.2024.04.20
Outline
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Objective:

To establish a method for the rapid identification of the authenticity of Gastrodiae Rhizoma herbs based on enzymatic recombinase amplification (ERA) technique.

Methods:

Following the principle of ERA primer design, Oligo 7.0 software was applied to screen and optimize the ERA-specific primers of Tianma based on the ITS2 genome sequences of Gastrodia elata and its common artifacts. Primer Premier 5.0 software was applied to design the specific PCR primers for the identification of Gastrodia elata, and through the optimization of ERA and PCR reaction system, the optimal reaction time for ERA was finally determined to be 17 min, the optimal reaction temperature was 40 ℃, the optimal annealing temperature for PCR was 57 ℃, and the cycle was 32 times, and the established method was verified for sensitivity and specificity, and the samples of asparagus available in the traditional Chinese medicine The sensitivity and specificity of the established method were verified, and the commercially available asparagus samples in the market were selected for testing.

Results:

The designed primers for the specific identification of ERA in Gastrodia elata did not cross-react with its common forgeries, and the specificity was good, a repeatability results showed that the three repeatability tests were consistent, with no false positives or false negatives;the sensitivity of this method for Gastrodia elata genomic DNA was 1 pg·μL-1, which was higher than that of conventional PCR;the ERA technique can be used for the rapid identification of commercially available samples of Gastrodia elata and the results of the assay are the same as those of the PCR method.

Conclusion:

The established detection method is simple, rapid, with high specificity and sensitivity, and provides a new means for the authentication of the Gastrodiae Rhizoma.

enzymatic recombinase amplification  /  polymerase chain reaction  /  Gastrodia elata  /  qualitative  /  authentication  /  rapid detection
Qiu-he MA, Yu-he MA, Tao LI, Yue LIU, Jin-jun CHAI, Zi-qiang XU, Ang LIU, Li-jun GAO, Wei XIA, Ming-cheng LI, Yong-mei QU. Establishment and application of a rapid authentication test method based on enzymatic recombinase amplification technology for the identification of Gastrodiae Rhizoma*[J]. Chinese Journal of Pharmaceutical Analysis, 2024 , 44 (4) : 729 -736 . DOI: 10.16155/j.0254-1793.2024.04.20
Year 2024 volume 44 Issue 4
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Article Info
doi: 10.16155/j.0254-1793.2024.04.20
  • Receive Date:2023-07-14
  • Online Date:2026-03-13
  • Published:2024-04-30
Article Data
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History
  • Received:2023-07-14
Funding
Affiliations
    1.School of Medical Technology, Beihua Universsity, Jilin 132013, China
    2. Innovation Center for Detection on DNA Fingerprint of Traditional Chinese Medicine, Jilin 132013, China
    3.Jilin Guoan Pharmaceutical Limited Company, Jilin 132013, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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