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Monday, January 30, 2012

PowerPoint Presentation On Lakshmi Niwas Mittal

PPT On Lakshmi Niwas Mittal

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Presentation Transcript:
1. LAKSHMI NIWAS MITTAL
MAN OF STEEL

2. Few Points On Mittal Status
He is the Chairman and Chief Executive Officer of AECELOR MITTAL
Mr. Mittal is the richest man in INDIA,ASIA and THE U.K and Second in Europe
He is presently 6th Richest individuals in the world with a personal wealth of US$31.1 billion

3. EARLY LIFE
Lakshmi Niwas Mittal was born in to a Marwadi Business Family in churu district of Rajasthan, India.
He married with USHA, the daughter of a well-to-do moneylender.

4. education
He graduated from St. Xaviers Collage Calcutta with a Bachelor of Commerce Degree in Business and Accounting with First class.

5. UNIVERSITY EDUCTION FORMATION
In year 2002,Lakshmi Niwas mittal and Usha mittal foundation and the government of Rajasthan partnered together to established a university named the LNM INSTITUTE OF INFORMATION TECHNOLOGY(LNMIIT) in Jaipur. As an autonomous non-profit organization.

6. CARRER
Mr. Mittal Started his carrier working in families steel making business in India in 1976.
He set out established its international division beginning with the buying of run-down plant in Indonesia
Mittal steel is the largest steel maker in the world, with shipment of 50 million tones of steel and profit of an $22 billion in 2007

7. MITTAL SIBLINGS
PROMOD MITTAL
VINOD MITTAL

8. ADITYA MITTAL
Mr.Mittal bought No.6 palace Greens Kensington Garden at ₤117 Million for his son ADITY MITTAL.

Aditya Mittal Owner and director of the Board of the GERMAN FASHION LUXURY BRAND ESCADA

9. VANISHA MITTAL BHATIA
Mr.Mittal bought No.9 A palace Greens Kensington Garden at ₤70 Million for his Daughter VANISHA MITTAL BHATIA.

VANISHA MITTAL married to AMIT BHATIA a Businessman and a Philanthropist

Vanisha Mittal's wedding was the most expensive in the recorded history of the world

10. THANK YOU..!!
By:-
Nigam Raj
Delhi Business School

PowerPoint Presentation On Regulation of Gene Expression

PPT On Regulation of Gene Expression

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Presentation Transcript:
1. REGULATION OF GENE EXPRESSION IN PROKARYOTES

2. INTRODUCTION
Although Gregor John Mendel for the first time use the term Factor for hereditary units.
This mystery of hereditary unit reveled till 1900s. In 1909 W. Johanson coined the term Gene.
The earlier workers proposed various hypothesis to explain exact nature of gene.
At present we all know that, ‘Genes are made of DNA’.
Now we can define gene as, “Gene is a nucleic acid sequence that carries the information representing a particular polypeptide”.

3. Gene expressed itself through a series of steps involved in a sequential synthesis of products.
This can be summarized as follows-
DNA………… RNA…………PROTEIN
During the course of evolution cell have evolved control mechanism to insure that proteins are synthesized in the required amount at a specific time.
Thus we can say that organisms have evolved the ability to regulate the expression of a specific gene in response to environmental signal.

4. GENE EXPRESSION
Gene expression means synthesis of a particular product due to gene action.
Some of the gene product required by the cell under all growth conditions are called House keeping gene. These include constitutive gene & their expression is called constitutive gene expression.
Some gene are expressed only when their product is needed for growth & development under a given environment their expression is turn off when product is not needed such genes are called Regulatory gene.
Regulatory Genes includes-
Inducible Gene
Repressible Gene

5. REGULATION OF GENE EXPRESSION
Regulation of gene expression may be defined as, set of mechanism controlling the activation or inactivation of a particular gene.
The exhaustive mechanism/investigation have been established on the basis of study of gene expression in bacteria and viruses, that regulation of gene expression in prokaryotes occur mostly at two levels-
Transcriptional level
Translational level
Some time RNA degradation & protein modification also play major role in regulating but most of the prokaryotic genes that are regulated are controlled at transcriptional level.

6. THE REGULATION OF GENE EXPRESSION IS OF TWO TYPES:
Positive Regulation:- When the expression of genetic information is quantitatively increased by the presence of a specific regulatory element it is called positive regulation. It is regulated by inducible gene.
Negative Regulation:- When the expression of genetic information diminished by the presence of specific regulatory element it is called Negative regulation .It is done by repressible gene.
There are some mechanism have been given to explain the regulation of gene expression in prokaryotes.

7. OPERON MODEL
This is the model for transcriptional regulation of gene expression firstly F. Jacobs and J. monad in [1961] on the basis of there study on inducible system for the synthesis of the β- galactosidase enzymes in E. Coli proposed a model in order explain the induction & repression of gene expression. They got Nobel prized for this in [1965].
According to Jacob & Monad an operon (Unit of Gene Expression & Regulation) includes-
regulator gene
Promoter gene
Operator gene
Structural genes..

8. LAC OPERON
The lac operon is proposed by-Jacob & Monod (1961). Based on their study on regulation of lactose, metabolism of E. Coli.
This operon is consists of 3-contigeous structural genes (Lac Z, Lac Y & Lac A), a promoter & a regulator & an operator gene.
Lac Z Codes for β-galactosidase; an intracellular enzyme that cleaves the disaccharide lactose into glucose & galactose.
Lac Y codes for the - β galctosidase preameese; a membrane bound transport protein that pumps lactose into the cell.
Lac A code for β- galactosidase transacetylase; that transfers an acetyl group from Co-A to - β galactosidase.

9. NEGATIVE REGULATION OF LAC OPERON:-
The lac genes are controlled by negative regulation. In the absence of lactose (inducer) the repression occur on the operator binding site & very low level of transcription of loc Z, Y & A occurs.
When the lactose is available to the cell the low level of permease allow the up take of lactose & galactosidase catalyses the conversion of some lactose to allotactose.
Allolactose acts as an inducer & binds to the lac repressor. This causes a change in conformation of repressor reducing its affinity for the lac operon. The removal of lac-repressor from operator site allow the RNAP to bind at the promoter site (P lac) to begin the transcription of lac Z, Y, A gene.
The lac operon is an example of negative control of gene expression because bound repressor prevents the transcription of structural gene.

10. POSITIVE REGULATION OF LAC OPERON:
The P-lac promoter is not a strong promoter. It requires the presence of specific proteins called cAMP receptor protein (CRP) or some time called as catabolic activator protein (CAP).
When glucose is present in environment E-coli does not need any alternate carbon source such as lactose. There for lac operon is not normally activated. Glucose reduces the level of c-AMP in the cell. CRP (catabolic) receptor protein) which exist as a dimmer, can not bind to DNA in the absence of cAMP.

11. When glucose is absent level of cAMP in the cell is increases & CRP binds to cAMP. The CRP-cAMP complex then binds to the lactose operon promoter just upstream from site of RNAP.
It is believed that CRP-cAMP complex increases the binding of RNAP to the promoter & thus increasing the transcription rate 5o times. This type of gene regulation is an example of positive control of gene regulation.
As a fact we can say that the lac operon is subject to both positive & regulation.

12. TRYPTOPHAN OPERON
The trp operon is an example of biosynthetic operon also called as repressible operon.
The organization of five structural gene (trp E, trp D, trp C, trp B & trp A) & adjacent regulatory sequence of trp operon has been studied in details by Charles Yanofsky et;al in 1976.
The five structural genes coding for the enzymes needed for tryptophan biosynthesis from chorismate. These structural gene codes for 3 enzymes required for the biosynthesis of tryptophan from chorismic acid.
Anthranilate synthetase – Encoded by trp E & trp D
Tryptophan synthetase- Encoded by trp B & trp A.
N-(5’phosphoribosyl)–anthranilate isomerase Indole -3 glycerol phosphate synthetase- Encoded by the trp C.
These structural gene are contiguous with promoter operator.

13. For more please refer PPT.
Thanks.
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