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The ITS2 sequences’ characters study of imported Arnebiae Radix based on DNA barcoding and PCR-RFLP technologies*
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Jie LIU1, Sheng-yun DAI1, Hai-yuan GU1, 2, Fei QIAO1, Chao-jie LIAN1, Li-nong GUO1, Jian ZHENG1, **, Shuang-cheng MA1, **, Jia MI3
Chinese Journal of Pharmaceutical Analysis | 2024, 44(5) : 750 - 755
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Chinese Journal of Pharmaceutical Analysis | 2024, 44(5): 750-755
Column on Quality Evaluation of Arnebiae Radix
The ITS2 sequences’ characters study of imported Arnebiae Radix based on DNA barcoding and PCR-RFLP technologies*
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Jie LIU1, Sheng-yun DAI1, Hai-yuan GU1, 2, Fei QIAO1, Chao-jie LIAN1, Li-nong GUO1, Jian ZHENG1, **, Shuang-cheng MA1, **, Jia MI3
Affiliations
  • 1.National Institutes for Food and Drug Control, Beijing 102629, China
  • 2.Shenyang Pharmaceutical University, Shenyang 110016, China
  • 3.Yili Institute of Inspection, Testing and Certification, Yili 835000, China
Published: 2024-05-31 doi: 10.16155/j.0254-1793.2024.05.02
Outline
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Objective:

To provide reference for quality control and authenticity identification of Arnebiae Radix medicinal materials and decoction pieces in the market. By studied on the ITS2 sequences’ characters of imported Arnebiae Radix,based on DNA barcoding and PCR-RFLP technologies.

Methods:

The ITS2 region was selected as the DNA barcode sequence for comparison and identification of imported Arnebiae Radix and reference medicinal materials. The ITS2 sequences of imported Arnebiae Radix from different sources with reference medicinal materials were compared based on DNA barcoding and PCR-RFLP technologies.

Results:

After the restriction endonucliase AluI enzyme digestion,the agarose-gel electrophoresis results of 39 imported Arnebiae Radix samples showed that,only DH3 had bands at around 500 bp,and none bands between 100 bp and 300 bp. And the results of other imported Arnebiae Radix samples had two or three obvious bands between 100 bp and 300 bp. The ITS2 sequences of imported Arnebiae Radix samples were compared with the reference medicinal materials,among which DH3 had the largest differences of 15 bases compared to the reference medicinal materials,the ITS2 sequence of F2 was same to the reference medicinal materials,and other imported Arnebiae Radix samples had 1-9 bases difference compared to the reference medicinal materials. The clustering results showed that the imported Arnebiae Radix sample DH3 was clearly distinguished from other imported Arnebiae Radix samples and reference medicinal materials which was in a single branch. There were 14 samples,which were clustered together with the reference medicinal materials in one branch with support rate ≥50%.

Conclusion:

The ITS2 region is selected to compare the similarities and differences of ITS2 sequences between imported Arnebiae Radix samples and reference medicinal materials based on DNA barcode and PCR-RFLP technologies,which provids a reference for effective identification of Arnebiae Radix medicinal materials and decoction pieces,and a strong guarantee for market supervision of Arnebiae Radix medicinal materials.

imported Arnebiae Radix  /  internal transcribed spacer 2(ITS2)  /  DNA barcoding  /  restriction endonuclease  /  polymerase chain reaction-restriction fragment length polymorphism(PCR-RFLP)
Jie LIU, Sheng-yun DAI, Hai-yuan GU, Fei QIAO, Chao-jie LIAN, Li-nong GUO, Jian ZHENG, Shuang-cheng MA, Jia MI. The ITS2 sequences’ characters study of imported Arnebiae Radix based on DNA barcoding and PCR-RFLP technologies*[J]. Chinese Journal of Pharmaceutical Analysis, 2024 , 44 (5) : 750 -755 . DOI: 10.16155/j.0254-1793.2024.05.02
Year 2024 volume 44 Issue 5
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Article Info
doi: 10.16155/j.0254-1793.2024.05.02
  • Receive Date:2023-04-12
  • Online Date:2026-03-20
  • Published:2024-05-31
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  • Received:2023-04-12
Funding
Affiliations
    1.National Institutes for Food and Drug Control, Beijing 102629, China
    2.Shenyang Pharmaceutical University, Shenyang 110016, China
    3.Yili Institute of Inspection, Testing and Certification, Yili 835000, 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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