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Cloning and enzymatic function characterization of a novel tropinone reductase Ⅰ (DaTRI 2) in Datura arborea
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Wei QIANG1, Ke XIA2, Xu-peng ZHAO3, Wei FU1, Jian-min MAN1, Ming-sheng ZHANG1, *
Acta Pharmaceutica Sinica | 2019, 54(3) : 574 - 581
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Acta Pharmaceutica Sinica | 2019, 54(3): 574-581
Original Articles
Cloning and enzymatic function characterization of a novel tropinone reductase Ⅰ (DaTRI 2) in Datura arborea
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Wei QIANG1, Ke XIA2, Xu-peng ZHAO3, Wei FU1, Jian-min MAN1, Ming-sheng ZHANG1, *
Affiliations
  • 1. School of Life Sciences/Resources Conservation and Germplasm Innovation in Mountainous Region Ministry of Education, Guizhou University, Guiyang 550025, China
  • 2. Guangxi Institute of Botany, Chinese Academy of Sciences, Guilin 541006, China
  • 3. Guiyang University, Guiyang 550005, China
Published: 2019-03-12 doi: 10.16438/j.0513-4870.2018-0994
Outline
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Tropinone reductase Ⅰ (TRI) is a key branch point enzyme in the midstream of tropane alkaloids (TAs) biosynthesis pathway and represents an important target for TAs metabolic engineering, which can lead to metabolic flux of substrate tropinone to TAs. A novel TRI gene was isolated from Datura arborea, a woody resource plant, and designated as DaTRI2 (GenBank accession number is MH705164). The full-length cDNA of DaTRI2 with 1 135 bp exhibits a high sequence homology (96.8%) with DaTRI, and is predicted to encode a protein of 347 amino acids. Deduced DaTRI2 protein contain a conserved TGXXXGXG motif involved in NADPH binding, the catalytic N-S-Y-K tetrad motif and eleven amino acid residues important for binding to its substrate tropinone. The phylogenetic analysis revealed that DaTRI2 and other TRIs from Solanaceous plants belong to the same cluster and DaTRI2 exhibited closest phylogenetic proximity to TRIs from Datura. DaTRI2 was expressed in E. coli and the purified recombinant protein can catalyze both tropinone reduction and tropine oxidation with an optimum pH value of 8.0 and 9.6, respectively. When tropinone was used as the substrate, the Km and Vmax values of DaTRI2 at pH 6.4 were 210.05 μmol·L-1 and 69.6 nkat·mg-1 protein respectively, while the Km and Vmax values for tropine as the substrate were 188.03 μmol·L-1 and 114 nkat·mg-1 protein respectively, at pH 9.6. DaTRI2 transcript was most abundant in the young leaf, followed by the root. Cloning of DaTRI2 gene and biochemical analysis of recombinant DaTRI2 facilitate further research on the molecular mechanism on TAs biosynthesis in woody plants and provide a more potent candidate for TAs metabolic engineering.

tropinone reductase  /  Datura arborea  /  tropane alkaloid  /  enzymatic kinetics
Wei QIANG, Ke XIA, Xu-peng ZHAO, Wei FU, Jian-min MAN, Ming-sheng ZHANG. Cloning and enzymatic function characterization of a novel tropinone reductase Ⅰ (DaTRI 2) in Datura arborea[J]. Acta Pharmaceutica Sinica, 2019 , 54 (3) : 574 -581 . DOI: 10.16438/j.0513-4870.2018-0994
Year 2019 volume 54 Issue 3
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Article Info
doi: 10.16438/j.0513-4870.2018-0994
  • Receive Date:2018-11-05
  • Online Date:2026-01-26
  • Published:2019-03-12
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  • Received:2018-11-05
  • Revised:2018-12-06
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Affiliations
    1. School of Life Sciences/Resources Conservation and Germplasm Innovation in Mountainous Region Ministry of Education, Guizhou University, Guiyang 550025, China
    2. Guangxi Institute of Botany, Chinese Academy of Sciences, Guilin 541006, China
    3. Guiyang University, Guiyang 550005, 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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