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3种假单胞菌CaCl2法感受态细胞制备及转化条件

赵峰1,2,张颖1**,李慧1,史荣久1,韩斯琴1   

  1. (1中国科学院沈阳应用生态研究所污染生态与环境工程重点实验室, 沈阳 110016; 2中国科学院大学, 北京 100049)
  • 出版日期:2013-03-18 发布日期:2013-03-18

CaCl2heat shock preparation of  competent cells of three Pseudomonas strains and related transformation conditions.

ZHAO Feng1,2, ZHANG Ying1, LI Hui1, SHI Rong-jiu1, HAN Si-qin1   

  1. (1Key Laboratory of Pollution Ecology and Environmental Engineering, Institute of Applied Ecology, Chinese Academy of Sciences, Shenyang 110016, China; 2University of Chinese Academy of Sciences, Beijing 100049, China)
  • Online:2013-03-18 Published:2013-03-18

摘要: 假单胞菌因其生境和代谢类型的多样性,在污染环境修复、生物转化、生物防治等领域具有广阔的应用潜力;外源基因的导入是假单胞菌遗传改造的重要环节,而感受态细胞的制备和转化方法的建立是导入外源基因的重要方法学基础.本研究以从石油污染土壤中分离筛选的假单胞菌属的3个菌株Pseudomonas putida TS11、P. stutzeri DNB、P. mendocina JJ12为对象,通过3因素4水平正交实验设计,研究了不同CaCl2浓度、热激时间及复苏时间对不同假单胞菌感受态细胞制备及转化效率的影响.结果表明: CaCl2浓度是影响假单胞菌转化效率的最主要因素(P<0.05),且在制备感受态细胞之前用无菌蒸馏水多次洗涤菌体细胞,转化率明显提高.3种假单胞菌的CaCl2转化优化条件分别为:100 mmol·L-1 CaCl2,热激3 min,复苏1.5 h;50 mmol·L-1 CaCl2,热激6 min,复苏1.5 h;75 mmol·L-1 CaCl2,热激4.5 min,复苏0.5 h.在上述转化条件下,3种假单胞菌的外源质粒转化效率均达到10.5个转化子·μg-1 DNA水平.

Abstract:

Pseudomonas, due to its diversity in habitat and metabolic type, makes it have broad prospects applying in bioremediation, bioconversion, and biocontrol, while the introduction of exogenous gene is the key link to genetically modified Pseudomonas. The preparation and transformation of competent cells are the important methodological basis of the introduction of exogenous gene. In this paper, three Pseudomonas strains (P. putida TS11, P. stutzeri DNB, and P. mendocina JJ12) isolated from a petroleum-contaminated soil were taken as the recipient strains, and a three-factor and four-level orthogonal experiment was conducted to investigate the effects of CaCl2 concentration, heat shock duration, and recovery duration on the preparation and transformation efficiency of the strains competent cells. The results showed that CaCl2 concentration was the most important factor affecting the transformation efficiency (P<0.05), and the transformation efficiency was improved markedly when the Pseudomonas cells were repeatedly washed with sterile distilled water before the preparation of competent cells. When the P. putida TS11 cells were treated with 100 mmol·L-1 of CaCl2, heatshocked for 3 minutes at 42 ℃, and incubated for 1.5 hours at 30 ℃, the P. stutzeri DNB cells were treated with 50 mmol·L-1 of CaCl2, heatshocked for 6 minutes, and incubated for 1.5 hours, and the P. mendocina JJ12 cells were treated with 75 mmol·L-1 of CaCl2, heat shocked for 4.5 minutes, and incubated for 0.5 hours, the transformation efficiency of exogenous plasmids in the three strains all achieved 10.5 cells·μg-1 DNA.