畜牧兽医学报 ›› 2010, Vol. 41 ›› Issue (6): 692-696.doi:

• 动物营养 • 上一篇    下一篇

荷斯坦奶牛瘤胃微生物脲酶的分离与鉴定

赵圣国1,2,王加启1*,刘开朗1,李旦1,2,于萍1,卜登攀1   

  1. 1. 中国农业科学院北京畜牧兽医研究所 动物营养学国家重点实验室,北京 100193;2. 甘肃农业大学 动物科学技术学院,兰州 730070
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2010-06-25 发布日期:2010-06-25
  • 通讯作者: 王加启

Isolation and Identification of Urease from the Rumen Content of Holstein Cows by a Culture-independent Strategy

ZHAO Sheng-guo1,2, WANG Jia-qi1*, LIU Kai-lang1, LI Dan1,2,YU Ping1, BU Deng-pan1   

  1. 1. State Key Laboratory of Animal Nutrition, Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China; 2. College of Animal Science and Technology, Gansu Agricultural University, Lanzhou 730070, China
  • Received:1900-01-01 Revised:1900-01-01 Online:2010-06-25 Published:2010-06-25

摘要: 本研究旨在从荷斯坦奶牛瘤胃中分离活性脲酶。从奶牛瘤胃中收集瘤胃内容物,通过离心和超声破碎的方法得到不含菌体细胞的瘤胃液(CFRF)和瘤胃菌体蛋白液(RCP),利用85%硫酸铵盐析,并透析后,用HiTrap Capto Q 离子交换层析柱纯化脲酶。将纯化后的脲酶用活性PAGE分离,并利用改良的Fishbein染色法,确定脲酶条带位置,切胶,经胰蛋白酶消化后,用LC-MS/MS分析,并用SEQUEST软件在NCBI数据库搜索与质谱信号相匹配的肽段和蛋白质。结果表明从CFRF和RCP中分离出较高活性的脲酶,但经染色后只有RCP脲酶显示活性条带。经质谱分析,最终鉴定出了3种微生物来源脲酶,分别与嗜热链球菌(Streptococcus thermophilus)、唾液链球菌(Streptococcus salivarius)和嗜碱芽孢杆菌(Bacillus halodurans)相似。这说明绕过纯培养微生物,直接从瘤胃中分离脲酶,来研究其性质和来源是可行的,尤其适合对未培养微生物的研究。

Abstract: This experiment was conducted to isolate urease active protein from cow rumen. Rumen contents were collected from Holstein cows via fistula. Cell free rumen fluid and ruminal cellular protein fluid were collected by centrifugation and ultrasonication. After precipitated by the addition of solid (NH4)2SO4 to 85% saturation and dialyzed, the fluid was applied to a HiTrap Capto Q ion exchange column. The fractions with urease activities were pooled, and concentrated by lyophilization. Then urease was separated by native-PAGE, and identified by modified Fishbein staining. The urease strap was excised from the gels, digested by trypsin and then analyzed by LCMS/MS. Searches of the peptide mass fingerprint data against NCBI databases were performed with the SEQUEST software. The results showed that higher activity urease was isolated and purified from cell free rumen fluid and ruminal cellular protein fluid. After staining, one brownish red strap containing urease from ruminal cellular protein fluid was observed. Three kinds of urease from Streptococcus thermophilus, Streptococcus salivarius and Bacillus halodurans were detected by mass spectrum. These results demonstrated the feasibility of isolating urease protein directly from rumen mixture without microorganism cultivation and this strategy could be expected to facilitate the research on uncultured microorganisms in rumen.