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B A Fry

Publications and source records attributed to B A Fry.

7 recordsLinked to original sources

Structure and properties of the rapidly sedimenting replicating complex of staphylococcal phage K DNA.

Rapidly sedimenting complexes (RSCs) of replicating phage K DNA, isolated by rate zonal centrifugation in sucrose gradients, contain bacterial membrane lipids and protein. During the first half of the latent period the number of DNA molecules in a RSC increased from 1 to about 27. Digestion by Pronase caused the complexes to dissociate and release virion lengths of DNA which sedimented slowly like free mature DNA. RSCs treated with SDS disintegrated and released tangled DNA molecules, each about one virion length in size, but these structures retained their fast sedimentation characteristic. Chloramphenicol (CM) at 100 micrograms/ml did not completely inhibit complex formation or DNA replication, indicating that pre-existing host proteins were involved in these processes. CM reduced DNA replication by 50 to 80%. It is concluded that phage K DNA replicates attached to the cytoplasmic membrane of the host.

Bacterial Proteins↗

The morphology of staphylococcal bacteriophage K and DNA metabolism in infected Staphylococcus aureus.

The morphology and dimensions of bacteriophage K particles were determined by electron microscopy. This virus had an icosahedral head (approx. 70 nm diam.) and a long (210 nm) thin (15 nm) contractile tail which terminated in a complex basal appendage. The precise dimensions of the particles were dependent on the negative stain employed. The buoyant densities of the K virus particle and its DNA were 1 X 479 g/ml and 1 X 689 g/ml respectively. The DNA had a base composition of 30% G + C, a contour length of 16 X 1 micron and a calculated mol. wt. of 33 X 10(6). With Staphylococcus aureus (NCTC 9318) as host, the latent period was 25 min, the eclipse period 14 min and the average burst size 60 p.f.u./bacterium. Infection resulted in inhibition of host DNA synthesis and degradation of the bacterial DNA: the products were used for tee synthesis of phage DNA. The kinetics of DNA synthesis is infected and uninfected bacteria were examined. There was no initial cessation of DNA synthesis in the infected bacteria.

Base Composition↗