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Cloning and analysis of the DXR gene and its promoter in Morinda officinalis
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De-jin XIE1, You-jie YE1, De-ming YANG1, Ya-xin ZHANG1, Tian-you HE2, Li-guang CHEN1, Yu-shan ZHENG1, 2, *
Acta Pharmaceutica Sinica | 2020, 55(2) : 335 - 344
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Acta Pharmaceutica Sinica | 2020, 55(2): 335-344
Original Articles
Cloning and analysis of the DXR gene and its promoter in Morinda officinalis
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De-jin XIE1, You-jie YE1, De-ming YANG1, Ya-xin ZHANG1, Tian-you HE2, Li-guang CHEN1, Yu-shan ZHENG1, 2, *
Affiliations
  • 1. College of Forestry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
  • 2. College of Landscape, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
Published: 2020-02-12 doi: 10.16438/j.0513-4870.2019-0707
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The objective of this research was to clone 1-deoxy-D-xylulose 5-phosphate reductoisomerase gene (MoDXR) and its promoter sequence from Morinda officinalis and carry out bioinformatic analysis, cis-acting elements analysis, and prokaryotic expression. On the basis of the MoDXR gene sequence obtained from the M. officinalis transcriptome and with NCBI-ORFfinder analysis, a pair of specific primers were designed, and used for RT-PCR amplification. The promoter region sequence at the 5' end of MoDXR gene was isolated by the genome walking technique. Localization of MoDXR was carried out by subcellular analysis. The prokaryotic expression plasmid pET-28a-MoDXR was constructed and transfected into Escherichia coli BL21(DE3) chemically-competent cells; the recombiant plasmid expressed fusion protein after the induction by IPTG. The full-length cDNA of MoDXR was 2 015 bp, and open reading frame (ORF) size was 1 425 bp, and it encoded 474 amino acid residues and had a molecular mass of 51.27 kD. Sequence comparison with BlastP to the NCBI database revealed that MoDXR had high sequence similarity with many other DXRs, such as Coffea arabica DXR (CaDXR) and Rauvolfia verticillata DXR (RvDXR). A phylogenetic tree revealed that MoDXR had its closest relationship with DXR from Coffea arabica and Gardenia jasminoides. The subcellular localization revealed that MoDXR protein was located on the chloroplast. Plantcare analysis indicated that the promoter region sequence of MoDXR was 1 493 bp, covering multiple light, stress, and hormone-responsive cis-regulatory elements; protein electrophoresis showed that the expressed protein was the anticipated size. This research lays the foundation for further purification and structural and functional characterization of the MoDXR protein.

Morinda officinalis  /  1-deoxy-D-xylulose 5-phosphate reductoisomerase  /  promoter  /  bioinformatics analysis  /  prokaryotic expression
De-jin XIE, You-jie YE, De-ming YANG, Ya-xin ZHANG, Tian-you HE, Li-guang CHEN, Yu-shan ZHENG. Cloning and analysis of the DXR gene and its promoter in Morinda officinalis[J]. Acta Pharmaceutica Sinica, 2020 , 55 (2) : 335 -344 . DOI: 10.16438/j.0513-4870.2019-0707
Year 2020 volume 55 Issue 2
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Article Info
doi: 10.16438/j.0513-4870.2019-0707
  • Receive Date:2019-09-02
  • Online Date:2026-01-20
  • Published:2020-02-12
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History
  • Received:2019-09-02
  • Revised:2019-10-17
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Affiliations
    1. College of Forestry, Fujian Agriculture and Forestry University, Fuzhou, 350002, China
    2. College of Landscape, Fujian Agriculture and Forestry University, Fuzhou, 350002, 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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