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Cloning and expression analysis of S-adenosylmethionine synthetase gene from Aquilaria sinensis
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Xian-juan DONG1, Ying-ying FENG1, Xiao LIU1, Bo-wen QI1, Ya-ru YAN1, Ning DING1, Yun WU1, Bo-wen GAO2, *, Xiao-hui WANG1, *
Acta Pharmaceutica Sinica | 2018, 53(10) : 1743 - 1752
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Acta Pharmaceutica Sinica | 2018, 53(10): 1743-1752
Pharmacognosy
Cloning and expression analysis of S-adenosylmethionine synthetase gene from Aquilaria sinensis
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Xian-juan DONG1, Ying-ying FENG1, Xiao LIU1, Bo-wen QI1, Ya-ru YAN1, Ning DING1, Yun WU1, Bo-wen GAO2, *, Xiao-hui WANG1, *
Affiliations
  • 1. Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China
  • 2. School of Pharmacy, Baotou Medical College, Baotou 014060, China
Published: 2018-10-12 doi: 10.16438/j.0513-4870.2018-0591
Outline
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S-adenosylmethionine synthetase, a key enzyme in plant metabolism, plays an essential role in the plant defence system. In present study, a full length cDNA sequence of AsSAMS1 gene was cloned by RACE and reverse transcription PCR from Aquilaria sinensis calli. Meanwhile, the bioinformatics, prokaryotic expression, tissue-specific expression analysis, and expression analysis under different abiotic stresses and hormone treatments were performed. The open reading frame (ORF) of AsSAMS1 gene was 1 183 bp, encoding a protein of 393 amino acids with a calculated molecular mass (MW) of 43.13 kDa. Bioinformatic analysis indicated that AsSAMS1 contained 3 SAMS characteristic sequences. The phylogenetic analysis indicated that AsSAMS1 protein had the highest level of homology with SAMS protein from Glycine soja. The recombinant AsSAMS1 protein was successfully expressed in Escherichia coli BL21 (DE3) cells using the prokaryotic expression vector pET28a-AsSAMS1 and the recombinant AsSAMS1 was purified by Ni2+ affinity chromatography. Expression analysis results in different tissues indicated that AsSAMS1 was primarily observed in stems, and then stem tips and leaves, following by roots. The transcript level of AsSAMS1 and the content of S-adenosylmethionine (SAM) were induced by various abiotic stresses including salt, drought, cold, and heavy metal stress. Furthermore, AsSAMS1 expression level was enhanced upon methyl jasmonate (MeJA), salicylic acid (SA), gibberellin (GA3), and abscisic acid (ABA) treatment. These results provided valuable insights for further study on the role of SAMS in the mechanism of agarwood formation and plant resistance.

Aquilaria sinensis  /  S-adenosylmethionine synthetase  /  bioinformatics analysis  /  prokaryotic expression  /  expression analysis
Xian-juan DONG, Ying-ying FENG, Xiao LIU, Bo-wen QI, Ya-ru YAN, Ning DING, Yun WU, Bo-wen GAO, Xiao-hui WANG. Cloning and expression analysis of S-adenosylmethionine synthetase gene from Aquilaria sinensis[J]. Acta Pharmaceutica Sinica, 2018 , 53 (10) : 1743 -1752 . DOI: 10.16438/j.0513-4870.2018-0591
Year 2018 volume 53 Issue 10
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Article Info
doi: 10.16438/j.0513-4870.2018-0591
  • Receive Date:2018-06-27
  • Online Date:2026-01-15
  • Published:2018-10-12
Article Data
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History
  • Received:2018-06-27
  • Revised:2018-09-04
Funding
Affiliations
    1. Modern Research Center for Traditional Chinese Medicine, School of Chinese Materia Medica, Beijing University of Chinese Medicine, Beijing 100029, China
    2. School of Pharmacy, Baotou Medical College, Baotou 014060, 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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