您的位置:山东大学 -> 科技期刊社 -> 《山东大学学报(理学版)》

J4

• 论文 • 上一篇    下一篇

Lp-1643蛋白单一结构域的黏附功能研究

刘 芳,都立辉,杨丽杰,杜 鹏,霍贵成*   

  1. 东北农业大学乳品科学教育部重点实验室, 黑龙江 哈尔滨 150030
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2006-10-24 发布日期:2006-10-24
  • 通讯作者: 霍贵成

Adhesion capacity of the single domain of Lp-1643 protein

LIU Fang, DU Li-hui, YANG Li-jie, DU Peng, HUO Gui-cheng*   

  1. Key Laboratory of Dairy Science,Ministry of Education, Northeast Agricultural University, Harbin 150030, Heilongjiang, China

  • Received:1900-01-01 Revised:1900-01-01 Online:2006-10-24 Published:2006-10-24
  • Contact: HUO Gui-cheng

摘要:

从植物乳杆菌KLDS 1.0320中克隆出Lp-1643蛋白N端的第一个结构域基因,与表达载体pET30a连接后成功构建重组质粒pET30a/N1。重组质粒转化大肠杆菌BL21后,以IPTG进行诱导,重组蛋白以可溶形式成功获得表达。通过亲和色谱技术用HisTrap FF柱对重组蛋白进行了分离纯化。以BSA作为对照,研究了重组蛋白His-N1对KLDS 1.0320菌株黏附Caco-2细胞的影响,现用该重组蛋白预处理Caco-2细胞之后,其上黏附的KLDS 1.0320数量显著减少(P<0.05)。这说明Lp-1643蛋白N端的第一个结构域具有黏附Caco-2细胞的功能。

关键词: 植物乳杆菌, Caco-2细胞, 黏附, Lp-1643蛋白

Abstract:

The gene coding for the first domain of the N terminus of Lp-1643 protein was amplified from KLDS 1.0320 genome. An expression vector designated pET30a/N1 was constructed. The recombinant protein was highly expressed in the strain E. coli BL21 induced by IPTG. Affinity chromatography with HisTrap FF column was used to separate and purify the recombinant protein of His-N1. Influences of the recombinant protein His-N1 on adhesion capacity of strain KLDS 1.0320 toCaco-2 cells were studied with BSA as a negative control. It was found that the numbers of KLDS 1.0320 adhering to Caco-2 cells pretreated by His-N1 dramatically decreased. This result indicates the single domain of Lp-1643 protein can adhere to Caco-2 cells.

Key words: Caco-2 cell

, adherence, Lp-1643 protein,

Lactobacillus plantarum

中图分类号: 

  • Q786
[1] 陆文伟,孔文涛,孙芝兰,孔 健*,季明杰 . Paenibacillus sp. K1 β-半乳糖苷酶基因的克隆及在大肠杆菌中的表达[J]. J4, 2008, 43(7): 69-73 .
[2]

孙芝兰,孔文涛,孔 健*

. Paenibacillus sp. K1 乳糖酶基因bga在乳酸乳球菌中的表达[J]. J4, 2008, 43(7): 74-77 .
[3] 王绍花,孔 健*,陈福坤 . 可控性自裂解乳球菌的构建[J]. J4, 2008, 43(7): 10-13 .
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!