Monday, August 9, 2021

BIOTECHNOLOGY- CLONING VECTORS / VEHICLE DNA

 CLONING VECTORS are DNA molecules that carry a foreign DNA segment and replicate inside the host cell. The most commonly used vectors are plasmids and bacteriophages.

PROPERTIES OF A GOOD VECTOR: 

1. IT SHOULD HAVE AN ORIGIN OF REPLICATION [ ORI ]- It is required for replication of vector during cell division.

2. IT SHOULD HAVE SELECTABLE MARKER GENES- It is required for the identification of transformed cells from non-transformed cells. Usually, antibiotic resistance genes such as ampicillin and tetracycline resistance genes are used as selectable markers.

3. CLONING SITES- At least one unique restriction site is present on the marker gene, which can be used to insert the alien DNA.

4. CONTROL ELEMENTS- It should have control elements like PROMOTER, OPERATOR, RIBOSOMAL BINDING SITE.

Naturally occurring plasmids do not have all these properties, so Artificial plasmids are constructed.

eg. pBR-322, pBR-320, pACYC-177.



VECTORS FOR CLONING IN PLANTS AND ANIMALS:

Agrobacterium tumefaciens is a pathogen causing CROWN GALL disease in dicot plants. These bacteria possess Ti plasmid [ Ti - tumor-inducing ] containing T DNA ... T DNA is a piece of DNA required for insertion of plasmid in plant DNA.

Ti plasmid can be used as a vector to insert ALIEN DNA in plant cells.

RETROVIRUSES can be used to transfer ALIEN DNA in animal cells.


BIOTECHNOLOGY- RESTRICTION ENDONUCLEASES

 The European Federation of Biotechnology [EFB] has defined biotechnology as The integration of natural science and organisms. Cells, parts, and molecular analogues for products and services.

BIOTECHNOLOGY deals with techniques of using organisms or enzymes from organisms to produce products and processes useful for human welfare.    

TWO CORE TECHNIQUES ARE INCLUDED IN MODERN BIOTECHNOLOGY:

1. GENETIC ENGINEERING

2. MAINTENANCE OF STERILE AMBIENCE / CONDITIONS

1. GENETIC ENGINEERING: 

This includes modification of genetic material of organism using alien or foreign DNA. Recombinant DNA technology has made it possible to transfer gene or piece of DNA from one organism to another.

RDT uses RESTRICTION ENDONUCLEASE ENZYMES which cut the DNA at a specific sequence called recognition sequence or restriction site.

BELOW IS A LIST OF SOME RESTRICTION ENDONUCLEASE WITH THEIR RECOGNITION SITE:




Today we know more than 900 restriction enzymes that has been isolated from over 230 strains of bacteria each with different restriction site. RESTRICTION or RECOGNITION SITES are PALINDROMIC NUCLEOTIDE SEQUENCE IN DNA. PALINDROMES are sequences in which first half is the mirror image of second half. Restriction enzymes cut the phosphodiester linkage in the recognition site. Recognition sites are 4 to 8 nucleotide long sequences.

These enzymes are named restriction endonuclease because they restrict the growth of viral DNA that might enter the cell, during infection. Thus, R.E. serves as a defence mechanism and bacteria protects its own DNA from nucleolytic attack by methylation of its own chromosome. 

When cut by a restriction endonuclease, TWO TYPES of sequences are formed.

1. sticky ends or staggered cuts or cohesive ends 

2. blunts ends


Sunday, July 18, 2021

PYQ- NEET- PRINCIPLES OF INHERITANCE AND VARIATION

NEET- PYQ- PRINCIPLES OF INHERITANCE AND VARIATION

NEET- PYQ- PRINCIPLES OF INHERITANCE AND VARIATION

MCQ TEST - NEET

 

Saturday, July 17, 2021

NEET- P.Y.Q. ANIMAL KINGDOM- PRACTICE ONLINE

P.Y.Q. NEET - ANIMAL KINGDOM

P.Y.Q. NEET - ANIMAL KINGDOM

MCQ TEST - NEET

 

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BIOTECHNOLOGY- CLONING VECTORS / VEHICLE DNA

  CLONING VECTORS are DNA molecules that carry a foreign DNA segment and replicate inside the host cell. The most commonly used vectors are...