## Abstract We localized the gene for resistance to phage SPO1 relatively to the markers __pur B 34__ and __ura__ by means of the polyethylene‐glycol induced fusion of bacterial protoplasts of three‐fold auxotrophic __Bacillus subtilis__ strains S3 and S13. By this same method, the site of some aux
Fluorometric in vivo determination of Bacillus subtilis and phage 2C DNA
✍ Scribed by Guy A. Daxhelet; Marianne M. Kohnen; Marc M. Coene; Philippe P. Hoet
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 391 KB
- Volume
- 190
- Category
- Article
- ISSN
- 0003-2697
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✦ Synopsis
The validity of in vivo fluorometric assays was ascertained for phage and bacterial DNA measurements. The following parameters were determined by this simple technique. The DNA content of dividing cells of Bacillus subtilis 168/2 was 2.65 times higher than in resting cells. Assuming that resting cells harbor 1 genomic equivalent, its Mr was estimated to be 4.4 x 10(9) Da. A polymerization rate during growth of 788,000 bp min-1/cell is accounted for by a multifork replication mechanism. Both phage and host DNA could be measured accurately during the lytic cycle. Phage 2C DNA synthesis proceeded at a linear rate of 5.2 genome equivalents min-1.
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