Plasmids as Vectors

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  Cloning and Expression Vectors

  Cloning Vectors for Recombinant DNA

  Plasmids as Vectors

 pBR322 and pBR327 Vectors

 pUC Vectors

  Yeast Plasmid Vectors

  Examples of Yeast Plasmid Vectors

  Retriever Vectors

  Cosmids as Vectors

  Phagemids as Vectors

  Bluescript II KS

  PI Cloning Vectors for Cloning Large DNA Segments

  F-factor Based Vectors

  Plant and Animal Viruses as Vectors

  Plant Viruses ( Cauliflower Mosaic Virus OR CaMV and Geminivirus

  Important Geminiviruses

  Animal Viruses

  Transposons as Vectors

  Artificial Chromosome ( YAC and MAC) Vectors for Cloning Large DNA Segments

 Expression Vectors for High Level of Expression of Cloned Genes

  Promoters

  Nopaline Synthase (nos) Promoter from T-DNA

  Dual Promoter of Mannopine Synthase (mas) Genes 1 and 2

  35S RNA Promoter of CaMV

  Polyhedrin Promoter from Baculovirus

  Expression Cassettes

  Baculovirus and Expression Vector System for Insect Cells

  Virus Expression Vector for Mammalian Cells

 Transforming Viruses Used as Vectors in Mammalian Cells

  Binary and Shuttle Vectors

 

Plasmids as Vectors

Plasmids as Vectors - Plasmids are defined as autonomous elements, whose genomes exist in the cell as extrachromosomal units. They are self replicating circular (only rarely linear) duplex DNA molecules, which are maintained in a characteristic number of copies in a bacterial cell, yeast cell or even in organelles found in eukaryotic cells.

These plasmids can be single copy plasmids that are maintained as one plasmid DNA per cell or multi copy plasmids, which are maintained as 10-20 genomes per cell. There are also plasmids, which are under relaxed replication control, thus permitting their accumulation in very large numbers (upto 1000 copies per cell).

These are the plasmids which are used as cloning vectors, due to their increased yield potential.Circular plasmid DNA which is used as a vector, can be cleaved at one site with the help of a restriction enzyme to give a linear DNA molecule.

A foreign DNA segment can now be inserted, by joining the ends of broken circular DNA to the two ends of foreign DNA, thus regenerating a bigger circular DNA molecule that can now be separated by gel electrophoresis on the basis of its size.Selection of chimeric DNA is also facilitated by the resistance genes, which the plasmid may carry against one or more antibiotics.

If a plasmid has two such genes conferring resistance against two antibiotics and if the foreign DNA insertion site lies within one of these two genes, then the chimeric vector loses resistance against one antibiotic, the gene for which has foreign DNA inserted within its structure.

In such a situation, the parent vector in bacterial cells can be selected by resistance against two antibiotics and the chimeric DNA can be selected by retention of resistance against only one of the two antibiotics.

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  Ti and Ri Plasmids as Vectors for Higher Plants

  Bacteriophage as Vectors

  Lambda Phage Vectors

  EMBL3 and EMBL4 (Replacement Vectors)

 Charon 34 and Charon 35

  M13 Phage as Vector for DNA Sequencing