A rapid and safe plasmid isolation method for efficient engineering of recombinant lactobacilli expressing immunogenic or tolerogenic epitopes for oral administration.

C B Maassen

doi:10.1016/s0022-1759(98)00206-3

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A rapid and safe plasmid isolation method for efficient engineering of recombinant lactobacilli expressing immunogenic or tolerogenic epitopes for oral administration.

C B Maassen

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Abstract

Recombinant lactobacilli are being developed which can be used as expression and delivery vectors of heterologous antigens in oral vaccination and other therapeutic applications. Because most Lactobacillus strains do not accept ligation mixtures, sufficiently pure plasmid DNA needs to be isolated from Lactobacillus casei to transform other Lactobacillus strains. The isolation of plasmid DNA from Gram-positive lactobacilli is complicated by the resilience of the peptidoglycan layer. Here a rapid, safe and efficient method is described that combines enzymatic breakdown of the cell wall and purification of the plasmid by commercially available DNA-binding columns. For the lysis-resistant L. casei strain, this method yields high levels of pure plasmid DNA that can be used for common molecular techniques, such as digestion and transformation, with high efficiency.

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Administration, Oral Bacterial Proteins DNA, Bacterial Deoxyribonuclease BamHI Deoxyribonucleases, Type II Site-Specific Genetic Engineering Immune Tolerance Immunodominant Epitopes Lactobacillus Lacticaseibacillus casei Plasmids Recombination, Genetic Transformation, Genetic Journal Article Research Support, Non-U.S. Gov't

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C B Maassen. 1999-02-01. A rapid and safe plasmid isolation method for efficient engineering of recombinant lactobacilli expressing immunogenic or tolerogenic epitopes for oral administration.. https://doi.org/10.1016/s0022-1759(98)00206-3

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