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作 者:匡逢春[1] 郑重谊[1] 谭周进[1,2] 谢达平[1] 肖冰梅[3] 谢丙炎[4]
机构地区:[1]湖南农业大学 [2]湖南中医药大学基础医学院,湖南长沙410208 [3]湖南中医药大学基础医学院 [4]中国农业科学院蔬菜花卉研究所
出 处:《生物技术通讯》2008年第5期704-707,共4页Letters in Biotechnology
基 金:科技部支撑计划(2006BAD08A08);湖南省教育厅青年基金(05B029)
摘 要:目的:为了提高再生率,对影响革兰阳性菌枯草芽胞杆菌KR株和革兰阴性菌荧光假单胞菌B13株原生质体再生的因素进行研究。方法:研究了酶解时间,再生方式,再生培养基中稳定剂的种类,Ca2+、Mg2+、琥珀酸钠、L-色氨酸的浓度及培养基的放置时间对KR和B13株原生质体再生的影响。结果:对KR株酶解20min,采用夹层培养,再生培养基中加入0.6mol/L蔗糖、0.03mol/L Ca2+、0.02mol/L Mg2+、0.3mol/L琥珀酸钠、0.2mol/L L-色氨酸,培养基在37℃放置72h,原生质体再生率可达42.7%;对B13酶解15min,采用夹层培养,培养基中加入0.6mol/L NaCl、0.02mol/L Ca2+、0.01mol/LMg2+、0.3mol/L琥珀酸钠、0.1mol/L L-色氨酸,培养基在37℃放置48h,原生质体再生率可达15.3%。结论:影响革兰阳性菌枯草芽胞杆菌KR株和革兰阴性菌荧光假单胞菌B13株原生质体再生的因素是不同的。Objective: In order to improve the regeneration rate, the effects of different factors on the regeneration of Gram-positive Bacillus subtilis KR strain and Gram-negative Pseudomonas fluorescent B13 strain were conducted. Meth. otis: The experiments were designed for pretoplast regeneration of KR and B13 strains as the following factors: lysozyme treatment time, regeneration mode, stabler in culture medium, and the concentration of Ca^2+, Mg^2+, sodium succinate acid, L-tryptophan, and culture medium placed time. Results: The optimal protoplast regeneration conditions for KR strain were lysozyme treatment 20 min, interlayer, 0.6 mol/L sucrose, 0.03 mol/L Ca^2+, 0.02 mol/L Mg^2+, 0.3 mol/L sodium succinate acid, 0.2 mol/L L-tryptophan and culture medium placed 72 h under 37℃. The optimal protoplast regeneration conditions for B13 strain were lysozyme treatment 15 min, interlayer, 0.6 mol/L NaC1, 0.02 mol/L Ca^2+, 0.01 mol/L Mg^2+, 0.3 mol/L sodium succinate acid, 0.1 mol/L L-tryptophan and culture medium placed 48 h under 37℃. The highest protoplast regeneration rates of KR strain and B13 strain were 42.7% and 15.3% respectively. Conclusion: The factors which affected Gram-positive bacterium's protoplast regeneration were different from which affected Gram-negative bacterium.
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