8.1 - metabolism Flashcards

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1
Q

what are metabolic reactions?

A
  • a complex network of chemical reactions within cells
  • a series of smaller steps with specific enzymes that catalyse each step of the reaction
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2
Q

what is a metabolic pathway?

A
  • a series of steps of a metabolic reaction
  • involve a chain of reactions in a linear path but some form a cycle as the end product of reaction starts the rest of the pathway.
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3
Q

how are substraits converted into products?

A

with metabolic reactions with a specific enzyme

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4
Q

what is activation energy? (BIO)

A
  • a molecule has to gain enough energy to reach the transition state
  • needed to break or bonds in the substrates
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5
Q

how do enzymes effect activation energy?

A
  • enzymes speed up the rate of biochemical reactions by lowering the activation energy
  • the active site of enzyme stresses and destabilises the bonds to reach the transition state faster
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6
Q

what is exergonic?

A
  • when reactants have more energy than the products the free energy is released into the system
  • usually a catabolic reaction
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6
Q

what is Endergonic?

A
  • when the reactants have less energy than the products the free energy is lost to the system
  • usually an anabolic reaction
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7
Q

how to calculate rate of reaction?

A

rate of reaction (S-1) =
1/time taken(s)

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8
Q

what is an inhibitor?

A
  • molecule that can bind to enzymes and reduce the activity of an enzyme
  • competitive and non-competitive
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9
Q

what is a competitive inhibition?

A
  • substrate and competitive inhibitors are structurally and chemically similar and compete for the same active site on enzyme
  • when binded it occupies active site of enzyme and prevents substrate from binding
  • eg. Relenza
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10
Q

what is Relenza?

A
  • antivirus drug designed to treat Flu A virus
  • Relenza is synthesised to completely bind to the NA active site and prevents HA from binding, so less spread of Flu in body
  • also prevents new virions forming
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11
Q

what is non-competitive inhibition?

A
  • substate and inhibitor are not structurally or chemically similar so do not bind to active site
  • binds to other sites called allosteric site
  • when binded it changes shape of active site and prevents the substrate from binding to enzyme
  • eg. cyanide
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12
Q

how can the effect of competitve inhibitors be reversed?

A
  • when a substrate concentration begins to exceed the concentration of inhibitor
    -however, it requires a much higher substrate concentration
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13
Q

how can the effect of non-competitive inhibitors be reversed?

A

it cant.

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14
Q

what is an end-product inhibition?

A
  • the product of the last reaction in the pathway inhibits the enzyme that catalyses the first reaction
  • forms negative feedback
  • end-product binds to an allosteric site and is a type of temporary non-competitive inhibition.
  • is reversible
  • excess end-product switches pathway off so intermediate products dont build up
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15
Q

what is chemogenomics?

A
  • a bioinformatics technique used to develop a new drug
  • when chemical binds to active site it can change metabolic activity, they test drugs on range of related organisims.
16
Q

what is malaria?

A
  • malaria is a mosquito-borne infectious disease caused by protist pathogens, common in tropical areas
  • symptoms are fever, fatigue, nausea, headaches, seizures, coma or death
  • there is a resistance to the malaria drug containing chloroquine
17
Q

chemogenomics and malaria.

A
  • resistance to chloroquine
  • using genomes from mosquitos they can screen new chemicals to see if they inhibit metabolic reactions
  • using chemogenomics scientists can chemically modify identified compounds to improve binding affinity and lower any toxicity