Metabolic reactions are regulated by negative feedback inhibition, where the end product of a pathway acts as a non-competitive inhibitor by binding to the allosteric site of an enzyme upstream, changing its shape to prevent substrate binding and further production of intermediates or the end product. This feedback loop prevents excess compounds from accumulating and tightly regulates metabolic pathways in response to cellular needs. Negative feedback inhibition of isoleucine biosynthesis from threonine is provided as an example of this important regulatory mechanism in metabolism.
Metabolic reactions are regulated by negative feedback inhibition, where the end product of a pathway acts as a non-competitive inhibitor by binding to the allosteric site of an enzyme upstream, changing its shape to prevent substrate binding and further production of intermediates or the end product. This feedback loop prevents excess compounds from accumulating and tightly regulates metabolic pathways in response to cellular needs. Negative feedback inhibition of isoleucine biosynthesis from threonine is provided as an example of this important regulatory mechanism in metabolism.
Metabolic reactions are regulated by negative feedback inhibition, where the end product of a pathway acts as a non-competitive inhibitor by binding to the allosteric site of an enzyme upstream, changing its shape to prevent substrate binding and further production of intermediates or the end product. This feedback loop prevents excess compounds from accumulating and tightly regulates metabolic pathways in response to cellular needs. Negative feedback inhibition of isoleucine biosynthesis from threonine is provided as an example of this important regulatory mechanism in metabolism.
Metabolic reactions are regulated by negative feedback inhibition, where the end product of a pathway acts as a non-competitive inhibitor by binding to the allosteric site of an enzyme upstream, changing its shape to prevent substrate binding and further production of intermediates or the end product. This feedback loop prevents excess compounds from accumulating and tightly regulates metabolic pathways in response to cellular needs. Negative feedback inhibition of isoleucine biosynthesis from threonine is provided as an example of this important regulatory mechanism in metabolism.
1 Metabolism (AHL) Essential idea: Metabolic reactions are
regulated in response to the cell’s needs.
Many elements of the metabolism are
controlled by negative feedback by end product inhibition. The end product acts as a non-competitive inhibitor binding the When the inhibitor binds to the enzyme this causes a allosteric site on an enzyme which controls change in the shape of the active site which prevents the the production of an intermediate substrate(s) binding. This results in the intermediate compound earlier in the pathway. compound not being produced, which ultimately means no end product can be produced. The more end product there is the more it inhibits it's own production, this prevents an By Chris Paine excess of unneeded compounds. https://bioknowledgy.weebly.com/ http://cnx.org/resources/44b414f98827125a5facb5f05c980dbd/Figure_04_01_10.jpg Understandings, Applications and Skills Statement Guidance 8.1.U1 Metabolic pathways consist of chains and cycles of enzyme-catalysed reactions. 8.1.U2 Enzymes lower the activation energy of the chemical reactions that they catalyse. 8.1.U3 Enzyme inhibitors can be competitive or non- Enzyme inhibition should be studied using one competitive. specific example for competitive and non- competitive inhibition. 8.1.U4 Metabolic pathways can be controlled by end- product inhibition. 8.1.A1 End-product inhibition of the pathway that converts threonine to isoleucine. 8.1.A2 Use of databases to identify potential new anti- malarial drugs. 8.1.S1 Calculating and plotting rates of reaction from raw experimental results. 8.1.S2 Distinguishing different types of inhibition from graphs at specified substrate concentration. 8.1.U1 Metabolic pathways consist of chains and cycles of enzyme-catalysed reactions.
Challenge: by changing just one letter at a time, get from
‘TREAD’ to ‘BLINK’. All intermediates must be real English words.
TREAD _____ _____ _____ _____ _____ BLINK 8.1.U1 Metabolic pathways consist of chains and cycles of enzyme-catalysed reactions.
Metabolism: the sum total of all chemical reactions that occur within an organism. Metabolic pathways*: cycles or chains of enzyme catalysed reactions. The chemical change from one molecule to another often does not happen not in one large jump, but in a sequence of small steps. The small steps together form what is called a metabolic pathway. * aka biochemical pathways TREAD Initial substrate
BREAD BREED BLEED intermediates
BLEND BLIND BLINK end product
http://highered.mheducation.com/sites/dl/free/0072437316/120070/bio09.swf 8.1.U1 Metabolic pathways consist of chains and cycles of enzyme-catalysed reactions.
Metabolic pathways*: cycles or chains of enzyme catalysed reactions.
Glycolysis, a part of The Calvin cycle, a part of photosynthesis, is an
respiration, is an example of a example of a metabolic cycle metabolic chain
http://www.ib.bioninja.com.au/higher-level/topic-8-cell-respiration/82-photosynthesis.html http://www.ib.bioninja.com.au/higher-level/topic-8-cell-respiration/81-cell-respiration.html 8.1.U2 Enzymes lower the activation energy of the chemical reactions that they catalyse.
Activation energy: the initial input of energy
that is required to trigger a chemical reaction. The key effect enzymes have upon reactions
Enzymes benefit organisms by speeding up the rate at which reactions occur,
they make them happen millions of times faster.
http://www.ib.bioninja.com.au/_Media/exergonic_reaction_med.jpeg 8.1.U2 Enzymes lower the activation energy of the chemical reactions that they catalyse.
How do enzymes lower the activation energy of a reaction?
• The substrate binds to the enzymes’ active site and the active site is altered to reach the transition state. • Due to the binding the bonds in the substrate molecule are stressed/become less stable. • The binding lowers the overall energy level of the transition state. • The activation energy of the reaction is therefore reduced. • n.b. the net amount of energy released by the reaction is unchanged.
http://en.wikipedia.org/wiki/Image:Induced_fit_diagram.png 8.1.U3 Enzyme inhibitors can be competitive or non-competitive.
Inhibitor: a molecule that binds to an
enzyme and slows down or stops the enzyme’s function.
Use the animation to find out more about inhibitors.
A good alternative is Enzyme Inhibition from Wiley
http://www.northland.cc.mn.us/biology/biology1111/animations/enzyme.swf 8.1.U3 Enzyme inhibitors can be competitive or non-competitive.
http://www.northland.cc.mn.us/biology/biology1111/animations/enzyme.swf 8.1.U3 Enzyme inhibitors can be competitive or non-competitive. 8.1.U3 Enzyme inhibitors can be competitive or non-competitive. 8.1.U3 Enzyme inhibitors can be competitive or non-competitive. 8.1.U3 Enzyme inhibitors can be competitive or non-competitive. 8.1.S2 Distinguishing different types of inhibition from graphs at specified substrate concentration.
Features of competitive inhibitors
Rate of reaction is reduced
When the concentration of substrate
begins to exceed the amount of inhibitor, the maximum rate of the uninhibited enzyme can be achieved. However, it takes a much higher concentration of substrate to achieve this maximum rate.
https://wikispaces.psu.edu/download/attachments/46924781/image-6.jpg 8.1.S2 Distinguishing different types of inhibition from graphs at specified substrate concentration.
Features of non-competitive inhibitors
Rate of reaction is reduced
It takes approximately the same
concentration of enzyme to reach the • The binding of the non-competitive inhibitor prevents maximum rate, but the maximum some of the enzymes from being able to react regardless rate is lower than the uninhibited of substrate concentration. enzyme. • Those enzymes that do not bind inhibitors follow the same pattern as the normal enzyme. https://wikispaces.psu.edu/download/attachments/46924781/image-6.jpg 8.1.U3 Enzyme inhibitors can be competitive or non-competitive.
http://highered.mheducation.com/sites/dl/free/0072437316/ 120070/bio10.swf 8.1.A1 End-product inhibition of the pathway that converts threonine to isoleucine.
Isoleucine is an essential amino acid*
• Bacteria synthesize isoleucine from
threonine in a series of five enzyme- catalysed steps • As the concentration of isoleucine increases, some of it binds to the allosteric site of threonine deaminase • Isoleucine acts as a non-competitive inhibitor to threonine deaminase • The pathway is then turned off, regulating isoleucine production. • If the concentration of isoleucine later falls (as a result of its use) then the allosteric sites of threonine deaminase are emptied and the enzymes recommences the conversion of threonine to isoleucine takes place.
*Essential amino acids cannot be made by the
body, therefore they must come from food.
http://www.uic.edu/classes/bios/bios100/lecturesf04am/feedback-inh.gif 8.1.A2 Use of databases to identify potential new anti-malarial drugs.
Bioinformatics is an approach whereby
multiple research groups can add information to a database enabling other groups to query the database.
Bioinformatics has facilitated research into metabolic pathways is
referred to as chemogenomics.
• Sometimes when a chemical binds to a target site, it can significantly alter
metabolic activity. • Massive libraries of chemicals are tested individually on a range of related organisms. • For each organism a range of target sites are identified. • A range of chemicals which are known to work on those sites are tested.
http://upload.wikimedia.org/wikipedia/commons/0/02/Mosquito_bite4.jpg 8.1.A2 Use of databases to identify potential new anti-malarial drugs.
Malaria is a disease This protozoan uses mosquitoes as a host as well as
caused by the pathogen humans and hence can be passed on by mosquito bites Plasmodium falciparum.
Increasing drug resistance to anti-malarial drugs has lead to the use of bioinformatics and chemogenomics to try and identify new drugs.
• In one study, approx. 300,000 chemicals were screened against a chloroquine-
sensitive 3D7 strain and the chloroquine-resistant K1 strain of P. falciparum. • Other related and unrelated organisms, including human cell lines, were also screened. • (19) new chemicals that inhibit the enzymes normally targeted by anti-malarial drugs were identified • Additionally (15) chemicals that bind to malarial proteins were identified – this can help in the location of P. falciparum • These results indicate possible new directions for drug research.
http://upload.wikimedia.org/wikipedia/commons/0/02/Mosquito_bite4.jpg 8.1.S1 Calculating and plotting rates of reaction from raw experimental results.
Remember this lab? ing enzym e act iv ity. (Practical 3)
m ental invest igation of a factor affect 2.5.S2 Experi
Enzyme inhibition can be investigated using these two outlines by
Science & Plants for Schools: • The effect of end product, phosphate, upon the enzyme phosphatase • The inhibition of catechol oxidase by lead
Use the results from it or data from one of your enzyme inhibition labs to calculate the rate of reaction.
The rate of reaction can be calculated using the formula:
Rate of reaction (s-1) = 1 / time taken (s)
Time taken in enzyme experiments this is commonly the time to reach a measurable end point or when a standard event, caused by the enzyme reaction, has come to pass. This is usually measured by the effects of the accumulation of product, but can as easily be measured by the disappearance of substrates.
