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Specialzied Restricted Genetic Transduction

Specialzied Restricted Genetic Transduction
In specialized transduction a particular bacteriophage strain can transfer only certain genes. In 1956 Morse and Lederberg found that in the lambda(λ) phage the transducing activity was restricted to the galactose locus. Only the gene loci adjacent to the site of insertion of the prophage are incorporated. Wild type bacterial prototrophs used as donors for lambda phage transduction affect recipient auxotrophs only by modifying gar to gal+. Other loci such as thr, trp, lac, etc., are never transduced. Restricted transduction is possible only with lysates produced by the induction of the prophage. In contrast to general tranduction, it is not possible with lysates produced by lytic infection.

All the gal+ transductants were found to be actively lysogenic (i. e. capable of liberating infective lambda phages on induction), or at least had immunity to infection from exogenous lambda. Most of the gal+ mutants were also found to be genetically unstable. About 1-10% of the individuals lost the gal + character and reverted to the gar phenotype.

When the lambda chromosome enters the bacterial host cells it either enters the lytic cycle, or is incorporated into the E. coli chromosome by recombination, and becomes a prophage. In the latter case the host survives integration and becomes a lysogen. In the lytic cycle the phage chromosome replicates and produces about a hundred progeny.

These are released by the lysing of the host. In the prophage condition, the phage DNA replicates each time the E.coli chromosome replicates. Under certain conditions, e. g exposure to ultra-violet light, the prophages enter the lytic cycle, turn into infectious viruses, and kill the hosts. The prophage is excised from the bacterial chromosome, and carries away with it pieces of the DNA of the host

The transduced genes are linked to the viral chromosome. Normal excision takes place in the vast majority of cells, giving rise to a circular viral chromosome and a nonlysogenic bacterial chromosome. The viral chromosome replicates by the rolling circle mechanism and produces several copies. Each unit length DNA is then packaged into infectious particles. When abnormal excision takes place (1 cell out of 100,000), a circular molecule containing some host DNA is formed. When this replicates, it gives rise to infectious particles containing a segment of bacterial DNA which has replaced a segment of viral DNA. Depending upon the site of abnormal excision, different virus variants are formed

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