食品科学

• 生物工程 • 上一篇    下一篇

抗瓜类细菌性果斑病菌单克隆抗体的制备及特性鉴定

曾海娟1,王广彬2,郭慧琴3,邱 实1,李建武1,翟绪昭1,丁承超1,宋春美1,刘 箐1,*   

  1. 1.上海理工大学医疗器械与食品学院,上海 200093;2.徐州绿健乳品饮料有限公司,江苏 徐州 221006;
    3.上海慧耘生物科技有限公司,上海 200433
  • 出版日期:2015-12-15 发布日期:2015-12-24

Preparation and Characterization of Monoclonal Antibody against Acidovorax avenae subsp. citrulli in Melons

ZENG Haijuan1, WANG Guangbin2, GUO Huiqin3, QIU Shi1, LI Jianwu1, ZHAI Xuzhao1, DING Chengchao1, SONG Chunmei1, LIU Qing1,*   

  1. 1. School of Medical Instrument and Food Engineering, University of Shanghai for Science and Technology, Shanghai 200093, China;
    2. Xuzhou Lüjian-Dairy Beverage Co. Ltd., Xuzhou 221006, China;
    3. Shanghai Prajna Biology Technique Ltd., Shanghai 200433, China
  • Online:2015-12-15 Published:2015-12-24

摘要:

以瓜类细菌性果斑病菌燕麦嗜酸菌西瓜亚种(Acidovorax avenae subsp. citrulli,Aac)野生型菌株SD01免疫BALB/c小鼠,间接酶联免疫吸附(enzyme-linked immunosorbent assay,ELISA)法筛选获得4 株稳定分泌抗SD01菌株的单克隆杂交瘤细胞株6F、6D、7E、4F,腹水抗体效价分别为1∶102 400、1∶102 400、1∶25 600、1∶51 200。采用饱和硫酸铵沉淀及Protein-G亲和层析法纯化腹水,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(sodiumdodecyl sulfate-polyacrylamide gelelectrophoresis,SDS-PAGE)显示纯化后的单克隆抗体(mAb)纯度较高,纯化后单克隆抗体(2 mg/mL)效价分别为1∶12 800、1∶6 400、1∶3 200、1∶6 400,亚型鉴定结果表明4 种单克隆抗体均为IgG2 a。间接ELISA结果表明,4 种单克隆抗体对8 种果斑病菌结合能力不同:6F可以结合6 种,6D、4F可以结合8 种,7E可以结合5 种。与3 种非Aac近源种植物病原菌交叉反应情况为:6F、4F与2 种非Aac近源种植物病原菌存在交叉反应,6D、7E与3 种非Aac近源种植物病原菌均无交叉反应。

关键词: 细菌性果斑病菌, 单克隆抗体, 制备, 特性鉴定

Abstract:

Four hybridoma cell lines secreting monoclonal antibodies (mAbs) against SD01, namely 6F, 6D, 7E and 4F,
were generated by immunizing BALB/c mice using wild-type strain SD01 of Acidovorax avenae subsp. citrulli (Aac) as
the immunogen. Ascites antibody titers were 1:102 400, 1:102 400, 1:25 600, and 1:51 200, respectively. Ascites were
purified using saturated ammonium sulfate precipitation and Protein-G affinity chromatography. Sodium dodecyl sulfatepolyacrylamide
gelelectrophoresis (SDS-PAGE) analysis showed high antibody purity. The titers of purified mAbs
(2 mg/mL) were 1:12 800, 1:6 400, 1:3 200, and 1:6 400, respectively. The subclass of mAbs was IgG2 a. Indirect enzymelinked
immunosorbent assay (ELISA) showed that four hybridoma cell lines had different binding capacity to eight strains
of Aac and three species of non-Aac plant pathogens. 6F could bind six strains of Aac, 6D and 4F could bind eight strains
of Aac, 7E could bind five strains of Aac. 6F and 4F had cross-reaction with two of the three species of non-Aac plant
pathogens, and 6D and 7E had no cross-reaction with all the three species of non-Aac plant pathogens.

Key words: bacterial fruit blotch, monoclonal antibody, preparation, characterization

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