Abstract
The transformation of Bacillus subtilis by homologous deoxyribonucleic acid (DNA) made available by gently lysing a stable L-form or protoplast suspension was 3 to 10-fold more efficient than DNA isolated by conventional procedures. This increased transformation was not influenced by digestion with pronase, trypsin, or ribonuclease. Preincubation of isolated DNA with L-form lysates did not increase the transformation efficiency above that achieved with untreated, isolated DNA. In addition to displaying a higher efficiency of transformation, the DNA found in these gently prepared lysates was also able to co-transform heretofore unlinked markers at frequencies in excess of those found by congression. Comparison of the frequency of multiple marker transformations to single marker events as a function of DNA dilution conclusively proves that these markers originated from the same continuous strand of DNA.
MeSH Terms
Bacillus subtilis/metabolism
Bacteriolysis
DNA, Bacterial/metabolism
Deoxyribonucleases/metabolism
Genes
L Forms
Mutation
Pronase/metabolism
Protoplasts
Ribonucleases/metabolism
Thymidine/metabolism
Transformation, Genetic
Tritium
Trypsin/metabolism
Chemicals
DNA, Bacterial
Tritium
Deoxyribonucleases
Ribonucleases
Trypsin
Pronase
Thymidine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Bettinger G E
Young F E
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27 references, click to expand
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