Week 2 Flashcards

(34 cards)

1
Q

Biomolecule

A

Found in living organisms and contain carbon atoms

  • The structure of the carbon atom allows it to form a large variety of complex molecules with other atoms, including hydrogen, oxygen and nitrogen.

Biomolecules are made up of smaller molecules that bond together to form a larger substance

Several monomers join together to form a large polymer

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2
Q

Carbohydrates

A

Made up of carbon, hydrogen and oxygen (1:2:1) (2 Hydrogen atoms for every carbon and oxygen atom)

Are a form of short-term energy storage molecules for out cells

Three Major Groups:
- Monosaccharides - simpel sugars (glucose, fructose, galactose)
- Disaccharides - formed when two monosaccharides bind together (e.g. 2 glucose -> maltose)
- Polysaccharides - Formed when several monosaccharides bind together. e.g. glycogen (several glucoses)

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3
Q

Lipids

A

Lipids are non-polar molecules that are insoluble in water

They are long term energy storage for our cells

Also insulates the body and cushions major organs against shock

Mostly made up of carbon and hydrogen sometimes oxygen

Five Classes -
- Triglycerides
- Phospholipids
- Eicosanoids
- Steroids
- Ketones

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4
Q

Nucleotides & Nucleic Acids

A

Nucleic acids are chains of nucleotides and store our genetic information

Deoxyribonucleic acid (DNA) found in the nucleus as a double helix of nucleotides

Ribonucleic acid (RNA) found in both the nucleus and cytoplasm as a single strand of nucleotides.

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5
Q

Amino Acids & Proteins

A

Amino acids will form peptide bonds with each other to form polypeptides.

Proteins are typically > 50 amino acids in length but most have 300 or more.

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6
Q

Triglycerides (Lipids)

A

Sub Classes:
Several Subtypes (Depending on bonds between fatty acid chains)

Saturated e.g. increase levels of ‘bad’ cholesterol in blood → heart disease

Unsaturated

Monounsaturated

Polyunsaturated

Different types have different effect on human health.

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7
Q

Metabolism +Main Purposes

A

The set of life-sustaining chemical reactions in organisms

These enzyme-catalysed reactions allow our cells to maintain homeostasis

Three Main Purposes
The conversion of food into energy to run cellular processes

The conversion of food to building blocks for proteins, lipids, nucleic acids and some carbohydrates.

The elimination of nitrogenous wastes.

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8
Q

Role of Enzymes

A

Enzymes: Proteins that bind substrates at an active site. The reaction occurs while bound to the enzyme, and the products are then released.

Each individual reaction consists of substrates that are transformed into products

A + B substrates —> C + D products
Substrates often need to be activated before a reaction will take place

Reactions in living things are catalysed (induced and sped up) by enzymes.
Enzymes work by lowering the energy required for activation of a reaction

Enzymes are not used up in the reaction and are free to catalyse more reactions.

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9
Q

Metabolic Reactions

A

Catabolic Reactions: Involve the breakdown of larger molecules into smaller ones

Anabolic Reactions: Involve the production of larger molecules from smaller ones.

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10
Q

Enzyme Activity (6)

A

Temperature: Enzymes have optimum temperatures that vary according to the enzyme and the organism that contains
the enzyme. Extreme temperatures denature (degrade) the enzyme

pH: Each enzyme has an optimum pH at which it functions best, suited to the environment it operates in. Denaturation of the protein occurs at non-optimal pH.

Substrate Concentration: Generation of product increases with increasing substrate concentration

Enzyme concentration: Increased availability of active enzyme increases generation of product

Cofactors: Many enzymes require vitamin-based coenzymes or metal ions to function
Inhibitors: Molecules that bind to the enzyme inhibit activity. Inhibition may be reversible or irreversible (poisoning)

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11
Q

ATP

A

A major role of metabolic reactions is to provide our body with energy necessary for survival

This energy is synthesised into a temporary form of energy storage called ATP. (in cells)

ATP: A complex organic chemical that provides energy to drive many processes into living cells. e.g. muscle contraction, nerve impulse propagation, cell division

ATP is synthesised by combining ADP (Adenosine diphosphate), inorganic phosphate and energy.

Energy is stored in the ATP molecules as potential energy.

When needed, ATP is broken down into ADP and inorganic phosphate, and energy is released.

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12
Q

ATP & Mitochrondria

A

Most of the cell’s ATP is generated in the mitochondria (the ‘powerhouse’ of the cell)

Energy to make ATP is supplied by glucose and other nutrient molecules through specific reactions

Inner mitochondrial membrane forms folds called cristae, which is where ATP synthesis occurs

Inner membrane also contains the electron transport chain and ATP synthase, which are critical during ATP synthesis
Within the matrix are also important molecules involved in ATP synthesis

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13
Q

Cellular Respiration

A

Cellular Respiration: A type of metabolic reaction where biomolecules (carbohydrates, lipids, proteins) are broken down to synthesise ATP.
Glucose is the primary biomolecule broken down via cellular respiration.

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14
Q

Aerobic Respiration

A

Aerobic Respiration:
Uses oxygen and occurs mostly in the mitochondria (but can occur in cytoplasm)
A single glucose molecule can produce 30-32 ATP molecules

Will also produce carbon dioxide and water as by-products

Involves the interaction of glucose with oxygen, through a process called glucose oxidation, to produce energy.

Oxygen is obtained from our respiratory system when we breath and carbon dioxide is expelled as a waste product.

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15
Q

Anaerobic Respiration

A

Does not use oxygen and occurs only in the cytoplasm

A single glucose molecule can produce 2 ATP molecules

Will also produce lactic acid as a by product.

Occurs when the cell’s metabolic demand is too high that not enough oxygen can be supplied to the cell for glucose oxidation to occur. e.g. muscle cells during intense exercise.

Anaerobic respiration can be divided into two main stages:

  • Glycolysis
  • Pyruvate Fermentation
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16
Q

Examples of Anaerobic Respiration

A

Intense exercise: Body’s demand for ATP can exceed oxygen supply, especially in hardworking muscle cells. When oxygen supply is insufficient for demands of aerobic respiration — cells switch to anaerobic.

High-Altitude Conditions: At high altitudes, oxygen level is lower than at sea level — resulting in less oxygen available for aerobic respiration. People not acclimatised go through anaerobic exasperation → fatigued quicker

Medical Conditions: Certain conditions can impair oxygen delivery to tissue and lead to increased anaerobic respiration. e.g. respiratory diseases such as chronic obstructive pulmonary disease (COPD) or severe astham that limits oxygen intake.

17
Q

Leigh Syndrome

A

Caused by mutations in the proteins that make up the electron transport chain.
Electron transport chain: Located in the inner membrane of mitochondria and is involved in the process of oxidative phosphorylation (where ATP is mainly produced)

Mutations in mtDNA or nuclear genes encoding mitochondrial proteins can impair energy production

Affects organs that have high energy demand e.g. brain, muscle. Symptoms include:
Poor muscle tone
Movement disorders
Severe developmental delays
Seizures
Respiratory distress
Cardiac arrhythmias

18
Q

DNA

A

DNA is made up of four nucleotide bases
Adenine
Thymine
Guanine
Cytosine

Bases pair up and form strong hydrogen bonds to form the double helix structure of DNA.
A pairs with T
G pairs with C

19
Q

Template Strand

A

Template strand: Gene that codes for a specific protein
The template strand is used during transcription to synthesise RNA.

20
Q

Complementary Strand

A

Complementary strand: Opposite to the template strand

21
Q

Transcription

A

A process occurring in the nucleus where RNA is synthesised from DNA.

Controlled by an enzyme called RNA polymerase, which ‘reads’ the template strand of DNA and synthesises a single strand of RNA

22
Q

Gene Structure

A

Promoter region: The start of the gene where RNA polymerase binds to and begins transcription

Coding region: A sequence of nucleotides that are transcribed into the RNA strand.

Termination sequence: Terminates the transcription process

23
Q

Transcription Steps (3)

A

Unzipping DNA
RNA polymerase binds to the promoter region of gene on the template strand
RNA polymerase causes the double-stranded DNA to ‘unzip’ (breaks hydrogen bonds’

RNA synthesis
RNA polymerase reads the template strand builds the RNA strand using free-floating nucleotides
Adenine (A) pairs with Uracil (U) — no thymine in RNA
Cytosine (C) with Guanine (G)

Termination
RNA polymerase reaches the termination sequence and the RNA is released as a single strand

24
Q

Types of RNA

A

messenger RNA (mRNA): A transcribed copy of the nucleotide sequence of a single gene for a specific protein.

ribosomal RNA (rRNA): Is a structural RNA that forms the ribosome, upon which proteins are synthesised.

transfer RNA (tRNA): A structural RNA involved in translation and protein synthesis

25
mRNA (Detailed)
Once fully transcribed, undergoes post-transcriptional modifications (e.g. splicing) Mature mRNA pass through nuclear pores, entering cytoplasm Not all DNA in a gene codes for the final protein. Exons: Coding parts of the gene may be interspersed with Introns: non-coding regions, that must be removed through exon splicing
26
RNA
Triplets of nucleotides in RNA called codons, code for specific amino acids. There are 64 possible codons that RNA can generate AUG — initiator codon, found at the beginning of every RNA strand.. Codes for methionine UUA, UAG, UGA — termination codon, found at the end of every RNA strand Do not code for amino acids Remaining 60 do. Most amino acids are encoded for by at least 2 codons.
27
Translation
The process where polypeptides (short sequences of amino acids) are synthesised from the mRNA script. Occurs on ribosomes, which bind to the mRNA tRNA reads mRNA transcript and carries the correct amino acid
28
tRNA (Transfer RNA)
Specific transfer RNAs (tRNA) bind to each type of amino acid One end has ‘Amino acid accepting end’ whereas the other contains the ‘anti-codon’ Anti-codon will have the opposite sequence to the codon on the mRNA strand. e.g. if the mRNA codon AUG for methionine, tRNA has anti-codon UAC.
29
Translation Steps
1. mRNA **binds to the small ribosomal unit** 2. **tRNA** specific to the start codon (AUG) will **bring a methionine** 3. Triggers the **large ribosomal unit to bind** 4. Another tRNA specific to the next amino acid in the sequence will bring the respective one 5. Two amino acids form a peptide bond 6. Ribosomes move along the mRNA strand and tRNA continue adding amino acids until it reaches a stop codon and the final protein is released.
30
Polyribosomes
Often there are several ribosomes translating a single mRNA strand at the same time. (Polyribosome) The length of completed polypeptides increases as the ribosomes move down the mRNA.
31
Post-Translational Processing
After translation, the protein must undergo further processing before it is fully functional and mature This can include: Cleavage of some amino acids Addition of lipids to form lipoproteins Addition of carbohydrates to form glycoproteins
32
Packaging Proteins
- Proteins are transported from the endoplasmic reticulum to the Golgi apparatus - In the Golgi, proteins are sorted and packaged into the vesicles that are targeted for their final destination - Protein destination can be to: - Stay within the cytoplasm of cell - Be part of specific organelles - Or to the plasma membrane for exocytosis
33
Cystic Fibrosis
Caused by mutations in the CFTR gene Normally responsible for regulating movement of chloride ions in and out the cell. Found everywhere but primarily maintains the consistency of mucus The most common mutation (Δ508) deletes three nucleotides, removing one amino acid (phenylalanine). This prevents proper protein folding, disrupting chloride ion transport and causing thick mucus in the lungs and other tissues, leading to breathing difficulties and increased infection risk.
34
Phospholipids
Phosphate group is polar and forms the hydrophilic head Fatty acid tails are non-polar and forms the hydrophobic tail