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Along with chromosomal DNA, most bacteria also contain small independent pieces of DNA called plasmids that often encode advantageous traits but are not essential to their bacterial host. Plasmids can be easily gained or lost by a bacterium and can be transferred between bacteria as a form of horizontal gene transfer .
Bacteria that are growing logarithmically differ from stationary phase bacteria with regard to the number of genome copies present in the cell, and this has implications for the ability to carry out an important DNA repair process. During logarithmic growth, two or more copies of any particular region of the chromosome are ordinarily present in ...
Genetic transformation is the process by which a recipient bacterial cell takes up DNA from a neighboring cell and integrates this DNA into its genome by homologous recombination. In Neisseria meningitidis (also called meningococcus), DNA transformation requires the presence of short DNA uptake sequences (DUSs) which are 9-10 monomers residing ...
Naturally competent bacteria carry sets of genes that provide the protein machinery to bring DNA across the cell membrane(s). The transport of the exogenous DNA into the cells may require proteins that are involved in the assembly of type IV pili and type II secretion system, as well as DNA translocase complex at the cytoplasmic membrane. [20]
Bacterial conjugation is the transfer of genetic material (plasmid) between bacterial cells by direct cell-to-cell contact or by a bridge-like connection between two cells. [1] Discovered in 1946 by Joshua Lederberg and Edward Tatum, [ 2 ] conjugation is a mechanism of horizontal gene transfer as are transformation and transduction although ...
2.The Hfr cell forms a pilus and attaches to a recipient F- cell. 3.A nick in one strand of the Hfr cell's chromosome is created. 4.DNA begins to be transferred from the Hfr cell to the recipient cell while the second strand of its chromosome is being replicated. 5.The pilus detaches from the recipient cell and retracts.
Bacteria can be classified on the basis of cell structure, cellular metabolism or on differences in cell components, such as DNA, fatty acids, pigments, antigens and quinones. [116] While these schemes allowed the identification and classification of bacterial strains, it was unclear whether these differences represented variation between ...
DNA gyrase is not the sole enzyme responsible for decatenation. In an experiment by Zechiedrich, Khodursky and Cozzarelli in 1997, it was found that topoisomerase IV is the only important decatenase of DNA replication intermediates in bacteria. [20] When DNA gyrase alone was inhibited, most of the catenanes were unlinked.