Plasmids useable as gene-cloning vectors in an in vitro packaging by coliphage λ: “cosmids” |
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Authors: | John Collins Heinrich J Brüning |
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Institution: | Gesellschaft für Biotechnologische Forschung, Mascheroder Weg 1, D-3300 Braunschweig W.-Germany |
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Abstract: | A plasmid which contains a cos site of λ and can be packaged into lambda bacteriophage particles is termed a “cosmid”. Such plasmids can be used as gene cloning vectors in conjunction with an in vitro packaging system. The properties of a new series of cosmids based on the ColE1 replicon are described, including small temperature-sensitive plasmids which have lost mobilisation functions and carry no IS sequences. Amongst these plasmids are vectors for XmaI, BglII, BamHI, HindIII, PstI, KpnI, SalI and EcoRI. It is demonstrated that by using cosmids in particular size ranges these plasmids provide a high efficiency cloning system which yields essentially only hybrid clones without resort to a second selection or screening step, and without prior modification (e.g. phosphatase) treatment of the DNA.Attempts were made to optimise the cloning properties of the cosmid system. An Escherichia coli “gene bank” was obtained with an efficiency of 5·105 clones per μg of E. coli DNA, and in which any particular unselected marker may be found in about one out of every 400 clones.It was demonstrated that deletion of mobilisation functions leads to loss of ability to form relaxation-complex without affecting copy number or segregation properties of the temperature-sensitive derivatives. The vectors are amplifiable in chloramphenicol to make up about 50% of the total cellular DNA. |
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Keywords: | Gene banks packaging DNA in λ bacteriophage mapping ColE1 mutants recombinant DNA restriction endonucleases SDS sodium dodecyl sulphate TCA trichloroacetic acid |
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