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Partial FI gene-independence of lambda-21 hybrid phages specifying chimeric terminases
M Feiss1, S Frackman, T Momany
1Department of Microbiology, University of Iowa, Iowa City 52242.
Virology
|November 1, 1988
Summary
The FI gene product (gpFI) is crucial for the growth of most lambda-21 hybrid phages producing chimeric terminases. Some phages show limited growth without gpFI, indicating partial dependence.
Area of Science:
- Molecular Biology
- Virology
- Bacteriophage Genetics
Background:
- Bacteriophages, such as lambda-21, possess genes essential for their replication and life cycle.
- Terminases are key enzymes involved in phage DNA packaging.
- The FI gene product (gpFI) is known to influence the life cycle of certain phages.
Purpose of the Study:
- To investigate the role of the FI gene in the life cycle of lambda-21 hybrid phages.
- To determine the dependence of chimeric lambda-21 terminases on the FI gene product.
- To compare the growth characteristics of FI-positive and FI-negative hybrid phages.
Main Methods:
- Construction of isogenic series of FI-positive (FI+) and FI-negative (FI-) derivatives of lambda-21 hybrid phages.
- Examination of plaque formation and burst size for different hybrid phage derivatives.
- Comparative analysis of phage growth in the presence and absence of the FI gene product.
Main Results:
- Three of the four lambda-21 hybrid phages (51, 67, 33) exhibited plaque formation and small burst sizes in the absence of gpFI, but grew significantly better with gpFI.
- All three chimeric terminases showed dependence on gpFI.
- The FI- hybrid phages grew better than lambda FI-, suggesting differences in chimeric terminases.
- Hybrid 54, producing an infirm terminase, showed greater dependence on gpFI than other hybrids and lambda.
Conclusions:
- The FI gene product (gpFI) is essential for optimal growth of most lambda-21 hybrid phages with chimeric terminases.
- Chimeric terminases exhibit varying degrees of dependence on gpFI.
- Differences in chimeric terminase structure or function may explain their altered dependence on gpFI compared to wild-type lambda terminase.