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Cloning and expression analysis of superoxide dismutase SmMSD2 gene from Salvia miltiorrhiza
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Jia-ming PENG1, 2, Ren-jun QU2, Shi-wei WANG2, Xin-xin WANG2, Liang-ping ZHA1, Hua-sheng PENG1, 2, *, Ye SHEN2, *
Acta Pharmaceutica Sinica | 2023, 58(2) : 454 - 464
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Acta Pharmaceutica Sinica | 2023, 58(2): 454-464
Original Articles
Cloning and expression analysis of superoxide dismutase SmMSD2 gene from Salvia miltiorrhiza
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Jia-ming PENG1, 2, Ren-jun QU2, Shi-wei WANG2, Xin-xin WANG2, Liang-ping ZHA1, Hua-sheng PENG1, 2, *, Ye SHEN2, *
Affiliations
  • 1. School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
  • 2. State Key Laboratory of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, China
Published: 2023-02-12 doi: 10.16438/j.0513-4870.2022-0764
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Superoxide dismutase (SOD) is a key enzyme that scavenge superoxide anion free radical (O2·-) in vivo, and plays an important role in plant growth and development and stress. In this study, according to the genome and transcriptome data of Salvia miltiorrhizae, 9 SOD genes were identified and the expression patterns of SOD family genes were further analyzed, including 5 Cu/Zn-SOD, 2 Fe-SOD and 2 Mn-SOD. On the basis of proteomic analysis, combined with transcriptome data, one full-length cDNA of Mn-SOD gene, namely SmMSD2 was cloned from Salvia miltiorrhizae. The results of amino acid sequence alignment and phylogenetic analysis showed that SmMSD2 protein belongs to the manganese superoxide dismutase (Mn-SOD) subfamily, and SmMSD2 protein shares high sequence identity with the Mn-SOD proteins of various plants that all contain a C-terminal conserved metal-binding domain "DVWEHAYY". The prokaryotic expression vector pMAL-c2X-SmMSD2 was constructed and transformed into E. coli BL21 expressing strain, and the target recombinant protein was successfully induced and its enzymatic properties were analyzed. Spatiotemporal expression analysis showed that SmMSD2 gene was expressed in all tissues, indicating that SmMSD2 gene was constitutively expressed at a stable level. Real-time quantitative PCR indicated that drought (15% PEG6000), abscisic acid (ABA) and indole-3-acetic acid (IAA) could induce the expression of SmMSD2 gene, suggesting that SmMSD2 may be involved in the response of Salvia miltiorrhizae to abiotic stress such as drought, as well as the signaling pathways of phytohormone ABA and IAA. These results lay the foundation for further elucidating the involvement of superoxide dismutase in the stress response and accumulation of active components of Salvia miltiorrhiza.

Salvia miltiorrhiza  /  superoxide dismutase  /  multiple omics analysis  /  expression analysis  /  abiotic stress
Jia-ming PENG, Ren-jun QU, Shi-wei WANG, Xin-xin WANG, Liang-ping ZHA, Hua-sheng PENG, Ye SHEN. Cloning and expression analysis of superoxide dismutase SmMSD2 gene from Salvia miltiorrhiza[J]. Acta Pharmaceutica Sinica, 2023 , 58 (2) : 454 -464 . DOI: 10.16438/j.0513-4870.2022-0764
Year 2023 volume 58 Issue 2
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Article Info
doi: 10.16438/j.0513-4870.2022-0764
  • Receive Date:2022-06-23
  • Online Date:2025-11-21
  • Published:2023-02-12
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  • Received:2022-06-23
  • Revised:2022-07-28
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Affiliations
    1. School of Pharmacy, Anhui University of Chinese Medicine, Hefei 230012, China
    2. State Key Laboratory of Dao-di Herbs, National Resource Center for Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing 100700, 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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