Dunaliella salina - Overview

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                 Dunaliella salina Dunaliella salina is a unicellular microalgae belong to division Chlorophyta . It is found in salinity environments such as salted brines, salt evaporation ponds, and hypersaline lakes  .It is able to tolerate varying NaCl concentrations, ranging from 0.2% to approximately 35% . Thus, Dunaliella salina is a hyper-halotolerant organism found in high densities in saline lakes.  The ability to tolerate high salt concentrations is advantageous, since competition is minimal in high salt concentration areas.  How D.salina   tolerate high salt concentration? D. salina has adapted to survive in high salinity environments by accumulating glycerol to balance osmotic pressure. Note :  D. salina is also adapted to solar radiation using β-carotene to protect against ionizing energy.                 Red Colour of Salt Brines  Dunaliella salina...

biotech , what is biotechnology

**Eugenics:  Branch dealing with genetic engineering.
  Euphenics:   Improvement of human                phenotypic characters .
  Euthenics: Improvement of human                   functional and well being.

**Feature of plamsid:  EXtrachromosomal DNA material found in bacterial cell, independent restriction,circular, double stranded ,transferable.When extracellular material added to the plasmid ,then it is called vector.

**Retrovirus have the ability to transform normal cells into cancerous cell in animals; ssRNA.

**linking of antibiotic resistance gene with the plasmid vector became possible with DNA ligase.

**Har  Govind Khorana : 1st time synthesize artificial gene in 1969.

**1st recombinant DNA (rDNA) molecules were generated in 1973 by Paul Berg,Herbert Boyer,Annie Chang and Stanley Cohen   of Stanford university and university of California San Francisco.

**Father of Genetic Engineering: Paul Berg
Father of Biotechnology            :  Karoly Ereky
Father of Indian Biotechnology:  Kiran Mazumdar Shaw

**Fruitfly widely used in genetic engineering.
**AIU1,Hind111,EcoRI: restriction endonuclease .
**pBR 32: Plasmid in E .colu,firstly widely user E.coli cloning vectors.Created in 1977 in the laboratory of Herbert Boyer at the university of California .

**Agrobacterium tumefaciens, a gram -ve soil bacterium which can cause crown gall tumors at wound sites or infected dicotyledons plants,used as a vector .

**1st biochemical to be produced commercially by microbial cloning and genetic engineering is human insulin.

**Experimental manipulation of DNA of different species producing recombinant DNA is known as rDNA technology. Restriction endonuclease are most widely used in rDNA technology.

**Selectable marker :A gene whose expression helps to identify transformed cell.

**Exonuclease catalyse the removal of nucleotide from the ends of DNA while endonuclease   catalyse the removal of DNA from mid.

**Ques: While isolating DNA from  bacteria enzymes that not required??
(a)Lysozyme
(b)protease
(c) ribonuclease
(d)deoxyribonuclease
Ans- deoxyribonuclease(this digest DNA hence DNA not isolated instead of digested.)

**Ques- In preparation of rDNA molecule which is not required?
(a)Restriction endonuclease
(b)DNA ligase
(c)E.coli
(d)DNA fragment
AnsE.coli

**Stirred tank reactor is usually cylindrical.
**Golden rice is rich in-Beta carotene and ferritin.(beta carotene is precursor of vitamin A.

**A single strand of  nucleic acid tagged with a radioactive molecule is called probe.

**Agarose extracted from sea weeds used in Gel electrophoresis,a method of separation of macromolecules and their fragments based on their size and charge.

**DNA polymerase enzyme is isolated from Thermus  aquatics.

**For rapid production of alcohol, immobilized yeast cells kept in calcium alginate beds.

*Vector:  The DNA molecule to which the gebe of interest is integrates for cloning called vector.

*Source of EcoR1 : Escherichia coli RY13.

**Lal Bahadur Shastri biotechnological centre is in Delhi.

**In plant biotechnology, root tumors are induced in plant using the bacterium Agrobacterium rhizogenes.


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