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[从乳酸杆菌中分离微量质粒DNA方法的优化]

[Optimization of the method of isolation of microamounts of plasmid DNA from lactobacilli].

作者信息

Tiurin M V

出版信息

Mol Gen Mikrobiol Virusol. 1990 Mar(3):29-31.

PMID:2362600
Abstract

Modification of the alkaline lysis at elevated temperature technique is proposed isolation of plasmid DNA from lactobacilli. Modification consists of colorimetric control of culture phase during the biomass growth, pH control at the probes treatment with lysozyme and alkaline solution of natrium dodecylsulfate by adding the indicator bromcrezolpurple into the medium for biomass growth. The high concentration of lysozyme is used (10 mkg.ml-1). Lactobacilli are lysed at 2 min incubations of the probes with the lytic solution in the boiling water bath. The treatment of the probes by proteinase K, by the mixture of chloroform:phenol:isoamyl spirit (25:24:1 vol/vol/vol) and by diethylpirocarbonate increased considerably the quality of the obtained DNA preparations. The modified technique is suitable for isolation of the plasmid DNA from lactobacilli of different species, enterococci, streptococci and other lactic bacteria. The connection of antibiotic resistance marker and the plasmid profile of lactobacilli under different conditions with the presence of the plasmid DNA- protein complex is discussed.

摘要

提出了在高温下对碱裂解法进行改进,用于从乳酸杆菌中分离质粒DNA。改进包括在生物量生长过程中通过比色法控制培养阶段,在用溶菌酶和十二烷基硫酸钠碱性溶液处理样品时通过向生物量生长培养基中添加溴甲酚紫指示剂来控制pH值。使用高浓度的溶菌酶(10μg/ml)。将样品与裂解液在沸水浴中孵育2分钟以使乳酸杆菌裂解。用蛋白酶K、氯仿:苯酚:异戊醇混合物(25:24:1体积/体积/体积)和焦碳酸二乙酯处理样品,显著提高了所得DNA制剂的质量。改进后的技术适用于从不同种类的乳酸杆菌、肠球菌、链球菌和其他乳酸菌中分离质粒DNA。讨论了在不同条件下抗生素抗性标记与乳酸杆菌质粒图谱以及质粒DNA - 蛋白质复合物存在之间的关系。

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