食品科学 ›› 2025, Vol. 46 ›› Issue (20): 162-169.doi: 10.7506/spkx1002-6630-20250509-041

• 生物工程 • 上一篇    下一篇

过氧化物还原酶OsPrx3抑制DNA氧化损伤的功能

汪海洋,赵玉楠,卢延克,黄卉,王智勇,方庆   

  1. (湖北民族大学生物与食品工程学院,湖北 恩施 445000)
  • 出版日期:2025-10-25 发布日期:2025-09-17
  • 基金资助:
    硒食品营养与健康智能技术湖北省工程中心开放基金项目(PT082209);湖北民族大学横向项目(H24176); 湖北民族大学高阶科研培育项目(PY20019)

Peroxiredoxin 3 (OsPrx3) from Oryza sativa L. Functions to Inhibit Oxidative Damage to DNA

WANG Haiyang, ZHAO Yunan, LU Yanke, HUANG Hui, WANG Zhiyong, FANG Qing   

  1. (College of Biological and Food Engineering, Hubei Minzu University, Enshi 445000, China)
  • Online:2025-10-25 Published:2025-09-17

摘要: 目的:探究红米稻过氧化物还原酶OsPrx3基因原核细胞表达产物体外抑制DNA氧化损伤的功能。方法:分子重组构建大红谷OsPrx3基因及其定点突变体OsPrx3mC51A的原核表达载体,转化至大肠杆菌表达目的蛋白,体外鉴定其羟自由基清除活性;采用超螺旋形态(supercoiled form,SF)pMD18质粒为底物进行DNA缺刻实验,鉴定OsPrx3抑制DNA氧化损伤的功能。结果:成功在大肠杆菌细胞中表达红米稻OsPrx3;当OsPrx3质量浓度1.0 mg/mL、反应2 h时对羟自由基清除率为40%;构建目的基因OsPrx3定点突变体,通过测定羟自由基清除率发现OsPrx3mC51A近100%失活,证实第51位半胱氨酸残基是该酶参与过氧化反应的关键位点;以0.06 μg/μL pMD18质粒进行DNA缺刻实验,结果显示OsPrx3在相对较低质量浓度范围内(0.06~0.18 μg/μL)对目标DNA氧化损伤的抑制效应具有明显的量效关系,此范围内0.18 μg/μL OsPrx3的氧化损伤抑制率最高(88.9%),为最小酶质量浓度作用效应的1.7 倍;OsPrx3的最适反应质量浓度为0.15 μg/μL,此条件下抑制质粒DNA氧化损伤的效率为77.5%;若设定SF-DNA/缺刻形态DNA比值达1.0为氧化还原平衡点,则最适质量浓度作用下OsPrx3的较高抑制效应至少可维持180 min,并且此时体系中2 种DNA比值仍达1.5。以上结果表明,红米稻过氧化物还原酶OsPrx3原核表达产物体外具有较强抑制DNA氧化损伤的功能,本研究可为发现和运用红米稻有益蛋白资源提供理论依据。

关键词: 过氧化物还原酶;氧化损伤;DNA;红米稻;衰老

Abstract: Objective: To investigate the function of the prokaryotic expression product of the peroxiredoxin 3 gene (OsPrx3) from Oryza sativa L. in inhibiting DNA oxidative damage in vitro. Methods: Molecular recombination was used to construct a prokaryotic expression vector for OsPrx3 from ‘Dahonggu’ red rice and its site-directed mutant OsPrx3mC51A. The target protein was expressed in Escherichia coli and its in vitro hydroxyl radical scavenging activity was determined. Using the supercoiled form (SF) of the pMD18 plasmid as the substrate, DNA nicking experiments were conducted to identify the function of OsPrx3 in inhibiting DNA oxidative damage. Results: OsPrx3 was successfully expressed in E. coli. The scavenging rate of hydroxyl radical by OsPrx3 at 1.0 mg/mL was nearly 40% after 2 h of reaction. The results of hydroxyl radical scavenging assay revealed that OsPrx3mC51A was almost completely inactivated, confirming that cysteine residue at position 51 was the key catalytic site of this enzyme activity. The DNA nicking experiments using the pMD18 plasmid at 0.06 μg/μL showed that OsPrx3 at low concentrations (0.06–0.18 μg/μL) inhibited oxidative damage to the target DNA in a concentration-dependent manner. The highest inhibition rate of 88.9% was found at an OsPrx3 concentration of 0.18 μg/μL, which was 1.7-fold higher than that at 0.06 μg/μL. At optimal OsPrx3 concentration of 0.15 μg/μL, the inhibition rate of DNA oxidative damage was 77.5%. When a SF-DNA/nicked DNA (NF-DNA) ratio of 1.0 was set as the redox equilibrium point, the inhibitory effect of OsPrx3 at the optimal concentration could be maintained for at least 180 min, and the SF-DNA/NF-DNA ratio in the system still reached 1.5 after 180 min. Taken together, the prokaryotically expressed OsPrx3 could potently inhibit DNA oxidative damage in vitro. This study provides an experimental basis for the discovery and utilization of beneficial protein resources from red rice.

Key words: peroxiredoxin; oxidative damage; DNA; red rice; aging

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