食品科学 ›› 2025, Vol. 46 ›› Issue (11): 146-153.doi: 10.7506/spkx1002-6630-20241024-162

• 生物工程 • 上一篇    

红米稻血红素结合蛋白rHBP2抗氧化的功能

黄卉,汪海洋,张彩云,李志作,安建辉,曾智,卢延克,方庆   

  1. (1.湖北民族大学,湖北 恩施 445000;2.生物资源保护与利用湖北省重点实验室,湖北 恩施 445000)
  • 发布日期:2025-05-14
  • 基金资助:
    湖北省自然科学基金计划项目(2023AFB1109)

Antioxidant Function of rHBP2, a Heme-Binding Protein from Red Rice

HUANG Hui, WANG Haiyang, ZHANG Caiyun, LI Zhizuo, AN Jianhui, ZENG Zhi, LU Yanke, FANG Qing   

  1. (1. Hubei Minzu University, Enshi 445000, China; 2. Hubei Key Laboratory of Biological Resources Protection and Utilization, Enshi 445000, China)
  • Published:2025-05-14

摘要: 目的:探究从红米稻中克隆的血红素结合蛋白(heme-binding protein,HBP)基因rHBP2的原核表达产物的抗氧化功能。方法:分子克隆目标基因并构建表达载体,大肠杆菌转化、表达进而分离目标蛋白rHBP2,鉴别其体外结合血红素与抗氧化活性;进一步采用rHBP2蛋白饲喂秀丽隐杆线虫N2,而后鉴别线虫对氧化、高温应激能力,以及线虫氧化调控相关基因的表达水平。结果:序列和分子结构分析显示,rHBP2的全长编码DNA序列为651 bp,编码一个含216 个氨基酸的蛋白质,其氨基酸序列在稻属植物中保守性超过90%;rHBP2分子结构具“内外兼容”特征,数个折叠片形成的“口袋”可能为血红素结合提供了重要位点;而典型的α螺旋位于外围,可能为其他潜在分子互作提供了条件。大肠杆菌成功表达了rHBP2蛋白,大小近25 kDa。rHBP2对1.0 mmol/L氯化血红素亲和性极强,并具有较高的羟自由基清除活性,1 mg/mL rHBP2对羟自由基相对清除率接近30%。饲喂rHBP2的线虫在H2O2氧化和35 ℃高温处理条件下的存活率分别可达对照组的5.7 倍(1.5 h)和2.4 倍(8 h),表明rHBP2具有显著增强线虫耐受氧化、高温的功能。此外,与对照组相比,饲喂rHBP2的线虫内源活性氧含量较对照显著降低,且氧化调控基因如SOD-3、CAT-1等表达水平显著提升。以上结果表明,rHBP2具有相对较强的抗氧化功能,本研究为发现和利用红米稻抗氧化蛋白质资源提供了实验基础。

关键词: 红米稻;抗氧化;血红素结合蛋白;秀丽隐杆线虫

Abstract: Objective: To investigate the antioxidant function of the prokaryotic expression product of the heme-binding protein (HBP) gene, rHBP2, cloned from red rice. Methods: We conducted molecular cloning of target genes and construction of expression vectors, transformation and expression in Escherichia coli, followed by isolation of the target protein rHBP2 and identification of its heme binding capacity and antioxidant activity in vitro. Additionally, we assessed the effect of feeding rHBP2 on oxidative and heat stress responses and oxidative stress-responsive gene expression in Caenorhabditis elegans N2. Results: Sequence and molecular structure analysis showed that the full-length coding sequence (CDS) of rHBP2 was 651 bp, encoding a protein containing 216 amino acid residues. The conservativeness of its amino acid sequence exceeded 90% among the compared rice plants. The molecular structure of rHBP2 exhibited both internal and external compatibility, and the pocket formed by several folded sheets might provide an important site for heme binding. The typical alpha helix was located on the periphery, potentially facilitating other potential interactions. rHBP2 was successfully expressed in E. coli, with a molecular weight of approximately 25 kDa. RHBP2 demonstrated a strong binding affinity for 1.0 mmol/L hemin and high hydroxyl radical scavenging activity, which scavenged nearly 30% of hydroxyl radical at a concentration of 1 mg/mL rHBP2. After 1.5 h exposure to H2O2 and 8 h exposure to 35 ℃, the survival rates of nematodes fed rHBP2 were 5.7 and 2.4 times higher than those of the control group, respectively, indicating that rHBP2 significantly enhanced nematode tolerance to oxidative and thermal stress. Moreover, nematodes fed rHBP2 exhibited significantly lower endogenous reactive oxygen species (ROS) levels and higher expression levels of oxidative stress-responsive genes such as SOD-3 and CAT-1. These results suggested that rHBP2 had potent antioxidant function. This study provides an experimental basis for discovering and utilizing antioxidant proteins from red rice.

Key words: red rice; antioxidant; heme-binding protein; Caenorhabditis elegans

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