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PMID: 137989 Published · ppublish English Journal Article

SP-10 bacteriophage-specific nucleic acid and enzyme synthesis in Bacillus subtilis W23.

Journal of virology ·Vol. 21 ·No. 1 ·1977-01-00 ·Pages 84-95

Markewych O, Boghosian A, Dosmar M, Ende D, Witmer H

Abstract

Bacillus subtilis W23 was infected with a clear-plaque variant of SP-10 phage, namely, SP-10c. Exogenous thymidine was not incorporated into phage DNA (even in the presence of deoxyadenosine), nor was there any transfer of thymidine nucleotides from bacterial to viral DNA. The lytic program was unaffected by concentrations of 5-fluorodeoxyuridine sufficient to reduce bacterial DNA synthesis by greater than 95%. Although these data are consistent with the interpretation that thymidine nucleotides are excluded from phage DNA, formic acid digests of SP-10c DNA contained what appeared to be the four conventional bases; however, adenine and thymine were not recovered in equimolar yields. DNA-RNA hybridization and hybridization competition experiments were done. Synthesis of host RNA started to wane moments postinfection and stopped completely by 36 min. SP-10c coded for discrete classes of early and late RNA. The possibility of discrete subclasses of early RNA exists. Replication of the bacterial genome appeared to terminate 12 min postinfection. Degradation of the host DNA to acid-soluble material started at 36 min and, by the end of the latent period, greater than 90% of the host chromosome was hydrolyzed. Four apparent phage-coded enzymes have been identified. A di- and triphosphatase degraded dUTP, dUDP, dTTP, and dTDP (and, to a lesser extent, dCDP and d CTP) to the corresponding monophosphates; the enzyme had no apparent activity on dATP and dGTP. SP10c also coded for a DNA-dependent DNA polymerase, lysozyme, and a nuclease that degrades native bacterial DNA. Judging from the dependence of enzyme synthesis on the time of addition of rifampin (an inhibitor of the initiation of RNA synthesis), messengers for the di- and triphosphatase, as well as the nuclease, are transcribed from promoters that start to function 6 min postinfection. Promoters for polymerase and lysozyme did not become functional until 8 and 16 min postinfection, respectively.

MeSH Terms
Aminoglycosides Anti-Bacterial Agents/pharmacology Bacillus subtilis/metabolism Bacteriophages/enzymology,metabolism DNA Replication DNA, Bacterial/metabolism DNA, Viral/biosynthesis DNA-Directed DNA Polymerase/biosynthesis Deoxyribonucleases/biosynthesis Floxuridine/pharmacology Hydrolysis Muramidase/biosynthesis Nucleic Acid Hybridization Nucleotidases/biosynthesis RNA, Bacterial/biosynthesis RNA, Viral/biosynthesis Rifampin/pharmacology Viral Proteins/biosynthesis
Chemicals
Aminoglycosides Anti-Bacterial Agents DNA, Bacterial DNA, Viral RNA, Bacterial RNA, Viral Viral Proteins Floxuridine DNA-Directed DNA Polymerase Deoxyribonucleases Nucleotidases Muramidase Rifampin
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Markewych O
Boghosian A
Dosmar M
Ende D
Witmer H
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35 references, click to expand
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Article Info
Journal
Journal of virology
Abbr.
J Virol
ISSN
0022-538X
Published
1977-01-00
Pages
84-95
Language
English
Region
United States
NLM ID
0113724
PMCID
PMC353793
Subset
IM
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