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THE lac OPERON
Rudrakshi B.Raut
The Institute Of Science,Mumbai
M.sc-2 (sem:3)
Paper-2
Roll no.17
CONTENT
Introduction
Concept of lac operon
Operon model
Functioning of lac operon
Different Scenarios
Lac mutations :
 Structural Mutation
 Operator Mutation
 Promoter Mutation
Positive and Negative control
References
INTRODUCTION
• Operon is operating units which can be
defined as the cluster of genes located
together on the chromosomes &
transcribed together.
• It is group of closely linked structure
genes & associated control gene which
regulate the metabolic activity.
• All the genes of an operon are
coordinately controlled by a mechanism
1st described in 1961 by Francois Jacob
& Jaques Monod of the Pasture institute
of Paris.
Jacob, Monod & Lwoff
The lac operon
• The lactose operon designated as lac operon.
• The lac operon codes for enzymes involved in
the catabolism (degradation) of lactose.
• lactose is the disaccharide which is made up
of glucose & galactose.
• It is the inducible operon since the presence
of lactose induce the operon to switched on.
Operon model
Designation
of gene
Codes for
enzyme
Function of the enzyme
lac Z β-galactosidase Breaks down lactose into
glucose & galactose.
lac y galactose
permease
This protein, found in the
E.coli cytoplasmic membrane,
actively transports lactose
into the cells
lac a Thio-galactoside
trans acetylase
The function of this
enzyme is not known. It is
coded for by the gene
lacA.
Element Purpose
Operator (lacO) Binding site for repressor
Promoter (lacP) Binding site for RNA Polymerase
Repressor Gene encoding the lac repressor
protein. Binds to DNA at the
operator & blocks binding of RNA
Polymerase at the promoter.
lacI Controls production of the
repressor protein
FUNCTIONING OF LAC OPERON
• In the absence of lactose(inducer), the
regulator gene produce a repressor protein
which bind to the operator site & prevent the
transcription as a result, the structural gene
do not produce mRNA & the proteins are not
formed.
• When lactose(inducer), introduce in the
medium, binds to the repressor the repressor
now fails to binds to the operator.
• Therefore the operoter is made free &
induces the RNA polymerase to bind to the
initiation site on promoter which results in
the synthesis of lac mRNA.
• This mRNA codes for three enzyme necessary
for lactose catabolism.
A simplified E. coli
bacterial cell.
The lac operon gene
sequence.
The repressor
molecule, bound to
the controlling
region.
Lactose molecules added to
the environment outside of
the cell.
Lactose molecules bound
to the repressor.
This releases the
repressor from the DNA.
RNA polymerase
transcribing the genes in
the lac operon into mRNA.
Ribosomes translating
the mRNA into proteins.
One of the proteins
(yellow) encoded by the
lac operon allows
lactose to enter the cell
at a high rate.
A second protein
(orange) digests the
lactose as it enters the
cell.
The lactose molecules
bound to the repressor
are released.
s
Repressor again binds to the controlling
region of the DNA.
Different Scenarios
1. Lactose (-)
2. Lactose (+)
3. Lactose (+) and glucose (+)
4. Lactose (+) and glucose (-)
1. When lactose is absent
• A repressor protein is continuously synthesised. It
sits on a sequence of DNA just in front of the lac
operon, the Operator site
• The repressor protein blocks the Promoter site
where the RNA polymerase settles before it starts
transcribing
Regulator
gene
lac operonOperator
site
z y a
DNA
I
O
Repressor
protein
RNA
polymeraseBlocked
2. When lactose is present
• A small amount of a sugar allolactose is
formed within the bacterial cell. This fits onto
the repressor protein at another active site
(allosteric site)
• This causes the repressor protein to change its
shape (a conformational change). It can no
longer sit on the operator site. RNA
polymerase can now reach its promoter site
z y a
DNA
I O
2. When lactose is present
• A small amount of a sugar allolactose is
formed within the bacterial cell. This fits onto
the repressor protein at another active site
(allosteric site)
• This causes the repressor protein to change its
shape (a conformational change). It can no
longer sit on the operator site. RNA
polymerase can now reach its
promoter site
Promotor site
z y a
DNA
I O
3. When both glucose and lactose are present
• When glucose and lactose are present RNA
polymerase can sit on the promoter site but it
is unstable and it keeps falling off.
Promotor site
z y a
DNA
I O
Repressor
protein removed
RNA polymerase
4. When glucose is absent and lactose is present
• Another protein is needed, an activator protein.
This stabilises RNA polymerase.
• The activator protein only works when glucose is
absent
• In this way E. coli only makes enzymes to
metabolise other sugars in the absence of glucose
Promotor site
z y a
DNA
I O
Transcription
Activator
protein steadies
the RNA
polymerase
Summary
Carbohydrates Activator
protein
Repressor
protein
RNA
polymerase
lac Operon
+ GLUCOSE
+ LACTOSE
Not bound
to DNA
Lifted off
operator site
Keeps falling
off promoter
site
No transcription
+ GLUCOSE
- LACTOSE
Not bound
to DNA
Bound to
operator site
Blocked by the
repressor
No transcription
- GLUCOSE
- LACTOSE
Bound to
DNA
Bound to
operator site
Blocked by the
repressor
No transcription
- GLUCOSE
+ LACTOSE
Bound to
DNA
Lifted off
operator site
Sits on the
promoter site
Transcription
LAC MUTATIONS
• Jacob & Monod workout the structure &
function of lac operon by analyzing mutations
that affects lactose metabolism.
• To help define the role of the different
components of the operon, they use partial
diploid stain of E.coli.
• They determine that some part of the lac
operon are cis acting where other are trans
acting.
STRUCTURAL-GENE MUTATION
• Jacob and Monod first discovered some
mutant strains that had lost the ability to
synthesize either β-galactosidase or
permease.
• The mutation which occurred on lacZ and LacY
structural genes altered the amino acid
sequences of the proteins encoded by the
genes.
a) In the absence of inducer, the lacO+ operon is
turned off, whereas the lacOc operon produces
functional β-galactosidase from the lacZ+ gene and
nonfunctional permease molecules from the lacY-
gene with missense mutation.
b) In the presence of inducer the functional β-
galactosidase and defective permease are produce
from the lacOc operon, whereas the lacO+ operon
produces nonfunctional β-galactosidase from the
lacZ- gene & functional permease from lacY+ gene.
OPERATOR MUTATIONS
• Jacob & Monod find another constitutive mutants to a
site adjacent to lacZ.
• This mutations occurred at the operator site & were
referred to as lacOc.
• The lacOc mutations altered the sequence of DNA at
the operator so that the repressor protein was no
longer able to bind.
• A partial diploid with genotype lacI+ lacOc lacz+ /lacI+
lacO + lacz+ exhibited constitutive synthesis of β-
galactosidase, indicating that lacOc is dominant over
lacO +.
PROMOTER MUTATION:
• Mutations affecting lactose metabolism have also been
isolated at the promoter site; these mutations are
designated lacP- ,and they interfere with the binding of
RNA polymerase to the promoter.
• This binding is essential for the transcription of the
structural gene.
• E.coli strain with lacP- mutation does not produce lac
proteins either in a presence or absence of lactose.
• lacP- mutations are cis acting.
• The lac operon is under two forms of
control; positive and negative control.
• Negative control occurs when the binding
of a protein prevents an event.
• Positive control is when the binding
causes the event.
POSITIVE CONTROL
• When glucose is available, gene that participate in the
metabolism other sugars are repressed, in a
phenomenon known as catabolite repression.
• Catabolite repression Is a type of +ve control in the lac
operon.
• The catabolite activator protein(CAP), complex cAMP,
binds to a site near the promoter & stimulates the
binding of RNA polymerase.
• A cellular level of cAMP are controlled by glucose;
allolactose level increases the abundance of cAMP &
enhance the transcription of the lac structural genes.
NEGATIVE CONTROL
• The lac repressor bind to the operator.
• The DNA sequence cover by the repressor
overlaps the DNA sequence recognized by the
RNA polymerase.
• Therefore, when the repressor is bound to the
operator, RNA polymerase cannot bind to the
promoter & transcription can not occur, the lac
operon is said to be under –ve control.
POSITIVE VS NEGATIVE CONTROL
Regulatory
protein is
present
Mutate
regulatory
gene to lose
function
Positive control
Negative control
Example of
regulatory
protein
Operon ON
Operon OFF
Operon OFF
Operon ON
Activator
Repressor
REFERENCE
Books :
• Genetics by Benjamin Pierce
• iGenetics by Peter J.Russell
Internet :
• Www.google.com
• https://www.google.co.in/search?q=The+lac+operon
+in+e.coli.ppt&client=opera&hs=OtG&biw=1366&bih
=586&source=lnms&tbm=isch&sa=X&ei=OzQ0VJu1N4
2xuATqjIH4BQ&ved=0CAYQ_AUoAQ
The Lac operon

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The Lac operon

  • 1. THE lac OPERON Rudrakshi B.Raut The Institute Of Science,Mumbai M.sc-2 (sem:3) Paper-2 Roll no.17
  • 2. CONTENT Introduction Concept of lac operon Operon model Functioning of lac operon Different Scenarios Lac mutations :  Structural Mutation  Operator Mutation  Promoter Mutation Positive and Negative control References
  • 3. INTRODUCTION • Operon is operating units which can be defined as the cluster of genes located together on the chromosomes & transcribed together. • It is group of closely linked structure genes & associated control gene which regulate the metabolic activity. • All the genes of an operon are coordinately controlled by a mechanism 1st described in 1961 by Francois Jacob & Jaques Monod of the Pasture institute of Paris. Jacob, Monod & Lwoff
  • 4. The lac operon • The lactose operon designated as lac operon. • The lac operon codes for enzymes involved in the catabolism (degradation) of lactose. • lactose is the disaccharide which is made up of glucose & galactose. • It is the inducible operon since the presence of lactose induce the operon to switched on.
  • 6. Designation of gene Codes for enzyme Function of the enzyme lac Z β-galactosidase Breaks down lactose into glucose & galactose. lac y galactose permease This protein, found in the E.coli cytoplasmic membrane, actively transports lactose into the cells lac a Thio-galactoside trans acetylase The function of this enzyme is not known. It is coded for by the gene lacA.
  • 7. Element Purpose Operator (lacO) Binding site for repressor Promoter (lacP) Binding site for RNA Polymerase Repressor Gene encoding the lac repressor protein. Binds to DNA at the operator & blocks binding of RNA Polymerase at the promoter. lacI Controls production of the repressor protein
  • 8. FUNCTIONING OF LAC OPERON • In the absence of lactose(inducer), the regulator gene produce a repressor protein which bind to the operator site & prevent the transcription as a result, the structural gene do not produce mRNA & the proteins are not formed.
  • 9.
  • 10. • When lactose(inducer), introduce in the medium, binds to the repressor the repressor now fails to binds to the operator. • Therefore the operoter is made free & induces the RNA polymerase to bind to the initiation site on promoter which results in the synthesis of lac mRNA. • This mRNA codes for three enzyme necessary for lactose catabolism.
  • 11.
  • 12. A simplified E. coli bacterial cell. The lac operon gene sequence.
  • 13. The repressor molecule, bound to the controlling region. Lactose molecules added to the environment outside of the cell.
  • 14. Lactose molecules bound to the repressor. This releases the repressor from the DNA. RNA polymerase transcribing the genes in the lac operon into mRNA.
  • 15. Ribosomes translating the mRNA into proteins. One of the proteins (yellow) encoded by the lac operon allows lactose to enter the cell at a high rate.
  • 16. A second protein (orange) digests the lactose as it enters the cell. The lactose molecules bound to the repressor are released.
  • 17. s Repressor again binds to the controlling region of the DNA.
  • 18. Different Scenarios 1. Lactose (-) 2. Lactose (+) 3. Lactose (+) and glucose (+) 4. Lactose (+) and glucose (-)
  • 19. 1. When lactose is absent • A repressor protein is continuously synthesised. It sits on a sequence of DNA just in front of the lac operon, the Operator site • The repressor protein blocks the Promoter site where the RNA polymerase settles before it starts transcribing Regulator gene lac operonOperator site z y a DNA I O Repressor protein RNA polymeraseBlocked
  • 20. 2. When lactose is present • A small amount of a sugar allolactose is formed within the bacterial cell. This fits onto the repressor protein at another active site (allosteric site) • This causes the repressor protein to change its shape (a conformational change). It can no longer sit on the operator site. RNA polymerase can now reach its promoter site z y a DNA I O
  • 21. 2. When lactose is present • A small amount of a sugar allolactose is formed within the bacterial cell. This fits onto the repressor protein at another active site (allosteric site) • This causes the repressor protein to change its shape (a conformational change). It can no longer sit on the operator site. RNA polymerase can now reach its promoter site Promotor site z y a DNA I O
  • 22. 3. When both glucose and lactose are present • When glucose and lactose are present RNA polymerase can sit on the promoter site but it is unstable and it keeps falling off. Promotor site z y a DNA I O Repressor protein removed RNA polymerase
  • 23. 4. When glucose is absent and lactose is present • Another protein is needed, an activator protein. This stabilises RNA polymerase. • The activator protein only works when glucose is absent • In this way E. coli only makes enzymes to metabolise other sugars in the absence of glucose Promotor site z y a DNA I O Transcription Activator protein steadies the RNA polymerase
  • 24. Summary Carbohydrates Activator protein Repressor protein RNA polymerase lac Operon + GLUCOSE + LACTOSE Not bound to DNA Lifted off operator site Keeps falling off promoter site No transcription + GLUCOSE - LACTOSE Not bound to DNA Bound to operator site Blocked by the repressor No transcription - GLUCOSE - LACTOSE Bound to DNA Bound to operator site Blocked by the repressor No transcription - GLUCOSE + LACTOSE Bound to DNA Lifted off operator site Sits on the promoter site Transcription
  • 25. LAC MUTATIONS • Jacob & Monod workout the structure & function of lac operon by analyzing mutations that affects lactose metabolism. • To help define the role of the different components of the operon, they use partial diploid stain of E.coli. • They determine that some part of the lac operon are cis acting where other are trans acting.
  • 26. STRUCTURAL-GENE MUTATION • Jacob and Monod first discovered some mutant strains that had lost the ability to synthesize either β-galactosidase or permease. • The mutation which occurred on lacZ and LacY structural genes altered the amino acid sequences of the proteins encoded by the genes.
  • 27. a) In the absence of inducer, the lacO+ operon is turned off, whereas the lacOc operon produces functional β-galactosidase from the lacZ+ gene and nonfunctional permease molecules from the lacY- gene with missense mutation.
  • 28. b) In the presence of inducer the functional β- galactosidase and defective permease are produce from the lacOc operon, whereas the lacO+ operon produces nonfunctional β-galactosidase from the lacZ- gene & functional permease from lacY+ gene.
  • 29. OPERATOR MUTATIONS • Jacob & Monod find another constitutive mutants to a site adjacent to lacZ. • This mutations occurred at the operator site & were referred to as lacOc. • The lacOc mutations altered the sequence of DNA at the operator so that the repressor protein was no longer able to bind. • A partial diploid with genotype lacI+ lacOc lacz+ /lacI+ lacO + lacz+ exhibited constitutive synthesis of β- galactosidase, indicating that lacOc is dominant over lacO +.
  • 30.
  • 31. PROMOTER MUTATION: • Mutations affecting lactose metabolism have also been isolated at the promoter site; these mutations are designated lacP- ,and they interfere with the binding of RNA polymerase to the promoter. • This binding is essential for the transcription of the structural gene. • E.coli strain with lacP- mutation does not produce lac proteins either in a presence or absence of lactose. • lacP- mutations are cis acting.
  • 32. • The lac operon is under two forms of control; positive and negative control. • Negative control occurs when the binding of a protein prevents an event. • Positive control is when the binding causes the event.
  • 33. POSITIVE CONTROL • When glucose is available, gene that participate in the metabolism other sugars are repressed, in a phenomenon known as catabolite repression. • Catabolite repression Is a type of +ve control in the lac operon. • The catabolite activator protein(CAP), complex cAMP, binds to a site near the promoter & stimulates the binding of RNA polymerase. • A cellular level of cAMP are controlled by glucose; allolactose level increases the abundance of cAMP & enhance the transcription of the lac structural genes.
  • 34.
  • 35. NEGATIVE CONTROL • The lac repressor bind to the operator. • The DNA sequence cover by the repressor overlaps the DNA sequence recognized by the RNA polymerase. • Therefore, when the repressor is bound to the operator, RNA polymerase cannot bind to the promoter & transcription can not occur, the lac operon is said to be under –ve control.
  • 36.
  • 37. POSITIVE VS NEGATIVE CONTROL Regulatory protein is present Mutate regulatory gene to lose function Positive control Negative control Example of regulatory protein Operon ON Operon OFF Operon OFF Operon ON Activator Repressor
  • 38. REFERENCE Books : • Genetics by Benjamin Pierce • iGenetics by Peter J.Russell Internet : • Www.google.com • https://www.google.co.in/search?q=The+lac+operon +in+e.coli.ppt&client=opera&hs=OtG&biw=1366&bih =586&source=lnms&tbm=isch&sa=X&ei=OzQ0VJu1N4 2xuATqjIH4BQ&ved=0CAYQ_AUoAQ