23 - Anabolism and regulation of metabolism Flashcards

1
Q

Macromolecule

A

a very large molecule important to biophysical processes (e.g. protein or nucleic acid)

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2
Q

Gluconeogenesis

A

generation of glucose from non-carbohydrate carbon substrates (esp. pyruvate and lactate)

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3
Q

Amphibolic

A

biochemical pathway that involves both catabolism and anabolism

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4
Q

Central metabolic pathways

A

pathways that generate the 12 precursor
metabolites. Includes the glycolytic pathways (i.e. Embden-Meyerhof, Entner-Doudoroff, pentose phosphate) and the TCA cycle

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5
Q

Metabolic channeling

A

regulation of metabolic pathway activity by localising metabolites and enzymes to specific parts of a cell

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6
Q

Allosteric

A

regulation of an enzyme by binding an effector molecule (allosteric effector) at a site other than the enzyme’s active site

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7
Q

Feedback inhibition

A

enzyme inhibition by the end products of a pathway

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8
Q

Level of organisation

A

Inorganic molecules + carbon source –> precursor metabolites –> Monomers or building blocks –> macromoleucles –> supramolecular systems –> organelles –> cells

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9
Q

Macromolecule examples

A

Nucleic acids, proteins, polysaccharides, lipids

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10
Q

Anabolism

A

Synthesis of complex molecules from simple ones.

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11
Q

Turnover

A

non-growing cells degrade and replace (resynthesise) cellular constituents, requiring ATP

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12
Q

first 3 principles governing biosynthesis

A
  1. Macromolecules are synthesised from a limited number of simple structural units (monomers)
  2. Many enzymes are used for both catabolism and anabolic processes
  3. Some enzymes function in only one direction in amphibolic pathways
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13
Q

last 3 principles governing biosynthesis

A
  1. Anabolism consumes energy (endogonic)
  2. Anabolic and catabolic reactions can be physically separated
  3. Anabolic and catabolic reactions use different cofactors
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14
Q

12 precursor metabolites

A

building blocks of all molecules in cells.

they make up the majority of the intermediates of glycolsis and TCA cycle

termed the central metabolic

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15
Q

Macromolecules are synthesized from a limited number of simple structural units (monomers)

A

Saves genetic storage capacity, biosynthetic raw material, and energy

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16
Q

Many enzymes are used for both catalytic and
anabolic processes

A

Most enzymes involved in the glycolysis pathway that produces ATP from glucose are also involved in the gluconeogenesis. Saves materials and energy.

17
Q

Some enzymes function in only one direction in amphibolic pathways

A

enables independent regulation of catabolism and anabolism by regulating the activity of pathway-specific enzymes

18
Q

Anabolic and catabolic reactions can be physically separated

A

Biosynthesis and catabolic functions are
located in separate organelles (e.g. mitochondria, lysosomes, ER).

Allows some pathways to operate simultaneously but independently

19
Q

Which cofactors do anabolic and catabolic pathways use

A
  • Catabolism produces NADH (acts as an electron acceptor)
  • Anabolism uses NADPH as an electron donor
20
Q

What does NADPH stand for

A

nicotinamide adenine dinucleotide phosphate

21
Q

name 3 Precursor metabolites

A

Glucose - 6, Ribose - 5, Pyruvate

22
Q

What is regulation of metabolism important for

A
  1. Efficiency (conservation of energy and materials) e.g. no synthesis of enzymes for which no substrate is available or no synthesis of enzymes to produce end products already in abundance
  2. Maintenance of metabolic balance in response to external changes
23
Q

3 major ways of metabolism regulation

A
  1. Metabolic channelling
  2. Regulation of gene expression
  3. Posttranslational regulation of enzyme activity
24
Q

Metabolic channelling

A
  • metabolic channeling is the physical separation of metabolic pathways in the cell
  • compartmentalisation
  • common way organisms separate and regulate pathways

-enables better control as key metabolites can be restricted or enhanced to affect the efficeint functioning of the pathway

25
Q

Advantages of metabolic channelling*

A
  • Facilitates separate operation and regulation of similar pathways
  • Enables enhanced pathway control by regulation of delivery of key metabolites to the various compartments.
26
Q

Regulation of gene expression

A
  • Controls the synthesis of a particular enzyme
  • Relatively slow, but conserves energy and the use of cellular materials
  • Can occur at transcription or translation
27
Q

Posttranslational regulation of enzyme activity

A
  • Following synthesis of the enzyme
  • Involves direct stimulation or inhibition of the activity of critical enzymes
28
Q

Three important mechanisms of Posttranslational regulation of enzyme activity

A
  1. Allosteric regulation
  2. Covalent modification of enzymes
  3. Feedback inhibition
29
Q

Allosteric regulation

A

Allosteric effector binds non-covalently at regulatory site changing the shape of the enzyme and alters activity of the catalytic site.

Can be:
- Positive effector increases enzyme activity
- Negative effector inhibits the enzyme

30
Q

Covalent modification of enzymes

A
  • Covalent bonding of a chemical group to the
    enzyme affects its activity
  • Allows more sophisticated control (Regulation of the enzymes that catalyse the covalent modification adds a second level of control)
31
Q

Feedback (end product) inhibition

A
  • End products inhibit one or more critical enzymes in a pathway
  • Each end product regulates its own branch of a branching pathway
  • involves the “pacemaker” enzyme which
    catalyses the slowest rate-limiting reaction