41 genes of SPP1 have been delineated by using complementation analyses of 75 conditionally lethal (ts and sus) mutations. The physical locations of these genes on the SPP1 chromosome have been determined by transfection/marker rescue experiments in which restriction endonuclease generated fragments
The genome of Bacillus subtilis phage SPP1:
β Scribed by Ratcliff, S. W. ;Luh, J. ;Ganesan, A. T. ;Behrens, B. ;Thompson, R. ;Montenegro, M. A. ;Morelli, G. ;Trautner, T. A.
- Publisher
- Springer
- Year
- 1979
- Tongue
- English
- Weight
- 639 KB
- Volume
- 168
- Category
- Article
- ISSN
- 0026-8925
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β¦ Synopsis
SPP1 DNA was cleaved by the restriction endonucleases, BglI, BglII, EcoRI, KpnI, SmaI, and SalI. The molecular weights of the DNA fragments obtained by single enzyme digestion or by consecutive digestion with two enzymes were determined by electron microscopic measurements of contour length and by gel electrophoresis. The major fragments from the six digests could be ordered to give a consistent restriction map of SPP1. The electropherograms of several digests indicated that certain fragments occurred in less than stoichiometric amounts or were heterogeneous in size. Such bands carried a major part of radioactivity, when SPP1 DNA was terminally labelled with P32 prior to degradation by restriction enzymes. These results, and studies of the effect of exonuclease III treatment on restriction enzyme patterns define the terminal restriction fragments. All data obtained support the conclusion drawn in the preceding paper (Morelli et al., 1978 b) that the SPP1 genome is terminally redundant and partially circularly permuted.
π SIMILAR VOLUMES
The left part of the SPP1 chromosome can be defined by the presence of dispensable DNA. With this definition, the polarities of the separable H and L strands of SPP1 DNA ar 5'--3' and 3'--5', respectively, from left to right.
The development of bacteriophages SPP1 and phi 29 has been studied in several B. sutilis mutants defective in host DNA replication, under non permissive conditions. Several gene products, involved in the synthesis of host DNA, are required for phi 29 replication, while SPP1 seems to require only the
## Abstract We localized the gene for resistance to phage SPO1 relatively to the markers __pur B 34__ and __ura__ by means of the polyethyleneβglycol induced fusion of bacterial protoplasts of threeβfold auxotrophic __Bacillus subtilis__ strains S3 and S13. By this same method, the site of some aux