Conjugative transfer of IncI1 plasmid DNA primase
β Scribed by Chatfield, Lee K. ;Wilkins, Brian M.
- Book ID
- 104724807
- Publisher
- Springer
- Year
- 1984
- Tongue
- English
- Weight
- 680 KB
- Volume
- 197
- Category
- Article
- ISSN
- 0026-8925
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β¦ Synopsis
DNA primase of ColIb-P9drd-1 generates RNA primers that are thought to initiate DNA synthesis on the conjugatively transferred strand of the plasmid. To examine whether plasmid-specified primase is transferred during conjugation, we exploited the property of the enzyme to promote bacterial DNA replication in dnaG (primase-defective) mutants of Escherichia coli. It was found that dnaG3 recipient cells, treated with rifampicin to inhibit transcription, recovered ability to synthesise bacterial DNA by a process requiring an active plasmid primase gene in donor cells and a functional conjugation system. A non-transferable primase gene in the donor strain complemented a primase-negative derivative of ColIb-P9drd-1, confirming that the enzyme responsible for recovery was supplied by donor cells. The implication is that certain proteins are transmitted from donor cells to promote conjugative metabolism of plasmid DNA in the recipients.
π SIMILAR VOLUMES
We demonstrated the conjugative transfer of plasmid pTO1 from Eschetichia colt S17-1 to different Rhodococcus spp. The plasmid contains the oriT fragment from RK2 and a fragment of Streptomyces (~C31 actinophage with the attachment site and the integration genes. Experiments on hybridization showed
The pri gene locus of the conjugative broad host range plasmid RP4 maps between coordinates 40.3 and 43.5 and encodes two antigenically related forms of a DNA primase with a molecular mass of 118 and 80 kDa (kilodalton). Genesis of these two products has been examined using Pri +-recombinant plasmid