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Questions and Answers
How does the arrangement of atoms within a biological molecule most significantly influence its function?
How does the arrangement of atoms within a biological molecule most significantly influence its function?
- By establishing the molecule's overall elemental composition.
- By dictating the molecule's specific shape and therefore its interactions. (correct)
- By determining the molecule's solubility in water.
- By influencing the molecule's color and light absorption properties.
How does the chemical process of hydrolysis facilitate the breakdown of disaccharides into monosaccharides?
How does the chemical process of hydrolysis facilitate the breakdown of disaccharides into monosaccharides?
- By rearranging the atoms within each monosaccharide, altering their properties.
- By adding a water molecule, which breaks the bond between monosaccharides. (correct)
- By introducing a catalyst that weakens the glycosidic bond.
- By removing a water molecule, stabilizing the bond between monosaccharides.
In what way would the excessive consumption of fructose, compared to sucrose, be more advantageous for individuals managing diabetes?
In what way would the excessive consumption of fructose, compared to sucrose, be more advantageous for individuals managing diabetes?
- Fructose does not require insulin for cellular uptake, unlike glucose from sucrose. (correct)
- Fructose stimulates the production of insulin, helping to regulate blood sugar levels.
- Fructose is more readily converted into glycogen, reducing blood sugar spikes.
- Fructose has a lower caloric content, aiding in overall weight management.
How do 1-6 glycosidic bonds contribute to the unique structural properties of glycogen compared to amylose?
How do 1-6 glycosidic bonds contribute to the unique structural properties of glycogen compared to amylose?
What effect does the presence of cis-double bonds in unsaturated fatty acids have on the physical properties of triglycerides, and how does this relate to their function?
What effect does the presence of cis-double bonds in unsaturated fatty acids have on the physical properties of triglycerides, and how does this relate to their function?
How does the amphipathic nature of phospholipids contribute to the structure and function of cell membranes?
How does the amphipathic nature of phospholipids contribute to the structure and function of cell membranes?
What impact would a mutation that prevents the formation of disulfide bridges in a globular protein have on its overall structure and function?
What impact would a mutation that prevents the formation of disulfide bridges in a globular protein have on its overall structure and function?
A protein's primary structure is determined by the sequence of amino acids. How does this primary structure dictate the protein's final three-dimensional conformation?
A protein's primary structure is determined by the sequence of amino acids. How does this primary structure dictate the protein's final three-dimensional conformation?
What is the fundamental difference between fibrous and globular proteins in terms of their structure and biological roles?
What is the fundamental difference between fibrous and globular proteins in terms of their structure and biological roles?
In the context of protein denaturation, what is the most critical consequence for a globular protein's function, and why?
In the context of protein denaturation, what is the most critical consequence for a globular protein's function, and why?
How do amino acids function as buffers in biological systems, and why is this capability critical for maintaining cellular homeostasis?
How do amino acids function as buffers in biological systems, and why is this capability critical for maintaining cellular homeostasis?
What is the primary role of ATP in cellular metabolism, and how does phosphorylation contribute to this role?
What is the primary role of ATP in cellular metabolism, and how does phosphorylation contribute to this role?
Why is the exergonic breakdown of ATP coupled with endergonic reactions in cells, and what is the direct consequence of this coupling?
Why is the exergonic breakdown of ATP coupled with endergonic reactions in cells, and what is the direct consequence of this coupling?
How does the continuous regeneration of ATP from ADP and inorganic phosphate by respiration maintain cellular function, particularly during intense physical activity?
How does the continuous regeneration of ATP from ADP and inorganic phosphate by respiration maintain cellular function, particularly during intense physical activity?
How would a mutation that prevents the formation of zwitterions in amino acids affect their behavior in solution, and what would be the broader implications for biological systems?
How would a mutation that prevents the formation of zwitterions in amino acids affect their behavior in solution, and what would be the broader implications for biological systems?
Considering the specific roles of ribose and deoxyribose in nucleotides, what would be the most significant consequence of a cell's inability to produce deoxyribose?
Considering the specific roles of ribose and deoxyribose in nucleotides, what would be the most significant consequence of a cell's inability to produce deoxyribose?
How do the structural differences between amylose and amylopectin influence their roles in energy storage within plant cells?
How do the structural differences between amylose and amylopectin influence their roles in energy storage within plant cells?
If a mutation caused a protein's hydrophobic amino acids to be located on the exterior surface instead of the interior, how would this change affect its structure and function in an aqueous cellular environment?
If a mutation caused a protein's hydrophobic amino acids to be located on the exterior surface instead of the interior, how would this change affect its structure and function in an aqueous cellular environment?
What role do conjugated molecules perform, and how does the combination of monosaccharides with other molecule types enable this?
What role do conjugated molecules perform, and how does the combination of monosaccharides with other molecule types enable this?
Flashcards
Carbohydrates
Carbohydrates
Organic compounds containing carbon, hydrogen, and oxygen.
Monosaccharides
Monosaccharides
Simple sugars with the general formula (CH2O)n, where n is 3 to 7.
Glucose
Glucose
The best-known and most abundant hexose sugar; C6H12O6.
Isomerism
Isomerism
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Condensation Reaction
Condensation Reaction
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Disaccharide
Disaccharide
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Maltose
Maltose
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Sucrose
Sucrose
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Lactose
Lactose
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Hydrolysis
Hydrolysis
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Oligosaccharide
Oligosaccharide
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Polysaccharide
Polysaccharide
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Polymerisation
Polymerisation
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Polymers
Polymers
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Monomer
Monomer
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Conjugated molecules
Conjugated molecules
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Starch
Starch
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Amylose
Amylose
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Amylopectin
Amylopectin
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Glycogen
Glycogen
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Study Notes
- All carbohydrates contain carbon, hydrogen, and oxygen with the formula Cₙ(H₂O)ₙ, where n may be the same or different.
- Carbohydrates include sugars, starch, glycogen, and cellulose.
Monosaccharides
- Monosaccharides are simple sugars with the general formula (CH₂O)ₙ, where n ranges from 3 to 7.
- Monosaccharides are grouped by the number of carbon atoms: trioses (n=3), tetroses (n=4), pentoses (n=5), hexoses (n=6), and heptoses (n=7).
- Glucose is the most abundant hexose, with the chemical formula C₆H₁₂O₆.
- Isomerism is when a molecule can take up a number of different shapes, but has the same chemical formula.
- Important pentoses include ribose and deoxyribose and Important hexoses include fructose and galactose
Glucose Isomers
- Alpha and beta glucose are two common isomers that differ only in the arrangement of hydrogen and hydroxyl groups on carbon atom 1.
- In alpha glucose, the OH group is below carbon atom 1, while in beta glucose, it is above.
- Alpha glucose molecules combine to form starch, while beta glucose molecules form cellulose.
- The detailed positions of atoms in a biological molecule determine both the shape of the molecule and its function.
Disaccharides
- Disaccharides form when two monosaccharides combine through a condensation reaction, releasing a water molecule.
- Maltose consists of two glucose molecules.
- Sucrose consists of glucose and fructose.
- Lactose consists of glucose and galactose.
- Disaccharides can be broken down into monosaccharides by hydrolysis, which involves adding water.
Polysaccharides
- A molecule with between three and ten monosaccharide units is called an oligosaccharide.
- Polysaccharides are formed when many monosaccharide units are added via polymerisation.
- Polymers are large molecules made up of repeating units (monomers).
- Polysaccharides are polymers made up of monosaccharide monomers.
- Monosaccharide monomers may also combine with other types of molecule to form conjugated molecules.
Functions of Simple Sugars
- Glucose is a major energy source for most animals.
- Lactose is the main sugar in milk.
- Maltose is produced by the breakdown of amylose in germinating seeds.
- In plants, carbohydrate is moved as sucrose.
Polysaccharides
- Polysaccharides are polymers of monosaccharide units linked by condensation reactions.
- They have the general formula (C₆H₁₀O₅)ₙ, are relatively insoluble in water, not sweet, and cannot crystallise.
- Monosaccharides can join as straight, helical, coiled, or branched chains.
- Polymer properties depend on the number and type of monomers and how they are joined.
- Each carbon atom in a monosaccharide unit is identified by a number.
- A 1-4 glycosidic bond forms between the hydroxyl groups at carbon 1 of one monosaccharide and carbon 4 of another.
- A 1-6 glycosidic bond forms similarly between carbon 1 and carbon 6.
- Straight chains are formed by monomers linked by 1-4 glycosidic bonds, while branched chains have 1-6 glycosidic bonds.
Starch
- Starch is a polysaccharide of alpha glucose units, consisting of amylose and amylopectin.
- It is formed by the condensation of alpha glucose units.
- In amylose, units are linked by 1-4 glycosidic bonds forming unbranched chains.
- Amylopectin has more 1-6 glycosidic bonds, producing highly branched chains.
- Starch is compact, and ideal for storage.
- In flowering plants, starch granules are inside plastids, which may be amyloplasts in storage structures like potato tubers.
Glycogen
- Glycogen is a storage polysaccharide abundant in liver and muscle cells.
- It has a similar role and structure to starch, and is sometimes called 'animal starch'.
- Glycogen is more branched due to more 1–6 glycosidic bonds.
- Glycogen breaks down more rapidly than starch due to its structure.
Lipids
- Lipids are compounds insoluble in water but soluble in other lipids and organic solvents.
- Triglycerides are lipids made from glycerol and fatty acids (also called triacylglycerols or neutral fats).
- Glycerol is an alcohol with three carbon atoms each linked to a hydroxyl group.
- A fatty acid has a long hydrocarbon chain ending in an acidic carboxyl (-COOH) group.
- The carboxyl group ionizes in water, releasing a hydrogen ion (proton).
- A triglyceride forms when each hydroxyl group on glycerol combines with a carboxyl group on a fatty acid during condensation, forming an ester bond.
- Lipids are grouped as oils (liquid at room temperature) and fats (solid).
- Fatty acids can be saturated or unsaturated.
- A saturated fatty acid has each carbon atom in the hydrocarbon chain linked to a carbon atom on either side and also to two hydrogen atoms (bonded to the maximum number of other atoms).
- Saturated fatty acids have only single bonds, making the chain straight and allowing triglycerides to pack closely (tend to be solid at room temperature).
- An unsaturated fatty acid, has carbon atoms not bonded to the maximum number of other atoms (two or more carbon atoms have double bonds between them)
- Fatty acids with one double bond are called monounsaturated. Fatty acids with two or more double bonds are called polyunsaturated.
- The atoms around a double bond are in either the cis-form or the trans-form.
- Triglycerides with a high proportion of unsaturated cis-fatty acids tend to be oils, because the cis-double bonds twist the hydrocarbon chain, which prevents packing closely.
- Triglycerides with more unsaturated trans-fatty acids tend to be solids.
Functions of Fats and Oils
- Triglycerides have a higher proportion of hydrogen atoms than proteins or carbohydrates.
- Fats and oils have functions including; energy storage, heat insulation, shock absorption, buoyancy.
Phospholipids
- Form a part of cells membranes
- Consist of glycerol attached to two fatty acid chains.
- The third hydroxyl group of glycerol combines with phosphoric acid to form a polar phosphate group.
- Amphipathic, one end hydrophilic and the other end is hydrophobic.
Steroids
- Steroids contain four rings of carbon and hydrogen with various side chains.
- Many animal hormones are steroids, including oestrogen and testosterone, which are made from cholesterol.
- Cholesterol is a raw material for vitamin D and strengthens mammalian cell membranes.
Proteins
- Proteins are large complex biological molecules that play many roles in organisms.
- Proteins make up a large percentage of the structure, and their specific folding enable specific functions.
Types of Protein
- Proteins are grouped into seven major classes based on their functions:
- Enzymes such as amylase.
- Structural proteins.
- Signal proteins.
- Contractile proteins, myosin.
- Storage protein, ovalbumin.
- Defensive proteins.
- Transport proteins, hemoglobin.
- Although there are many millions of proteins, all are made from the same basic building blocks, namely ~20 kinds of amino acid.
Amino Acids
- All amino acids have an amino group (-NH₂) and a carboxyl group (-COOH).
- The amino group is attached by a covalent bond to the alpha carbon.
- A hydrogen atom, another carbon atom, and a side chain (R group) are also linked to the alpha carbon.
- The R group is different for each of the 20 amino acids.
Amino Acids as buffers
- Amino acids are amphoteric (having both acidic and basic properties).
- Acidic properties are derived from the carboxyl group (can donate a proton).
- Basic properties are derived from the amino group (can take up a proton).
- Zwitterions have positively and negatively charged groups simultaneously.
- The ability to donate or receive protons causes amino acid solutions to behave as buffers.
- Buffer systems play a major role in the human body.
Peptide Bonds
- Two amino acids can combine to form a dipeptide by a condensation reaction, the resulting bond is called a peptide bond.
- Further amino acids connect to form a polypeptide chain.
- Proteins consist of one or more polypeptide chains, and are polymers of amino acid monomers.
Protein Primary Structure
- A protein's primary structure is the sequence of amino acids that make up its polypeptide chain or chains.
Secondary Structure
- When amino acids join up in the polypeptide chain, forces between molecule parts and hydrogen bonding cause coiling into an alpha-helix or folding into a beta-pleated sheet.
- This coiling or folding is the protein's secondary structure.
- The shape is maintained by hydrogen bonds between the -N-H group of one amino acid and -C=O group of another.
- A single polypeptide chain may have some regions coiled into an alpha-helix and others folded into beta-pleated sheets.
Tertiary Structure
- The tertiary structure refers to the overall three-dimensional shape of a polypeptide chain.
- Proteins are either fibrous or globular.
- Fibrous proteins are crossed linked parallel chains.
- Globular proteins have tightly folded polypeptide chains forming a spherical shape.
Quaternary Structure
- Many proteins consist of more than one polypeptide chain chemically bonded to each other
- Proteins are denatured if bonds holding structure are broken.
Nucleotides and Nucleic Acids
- Nucleotides are nitrogen-containing organic substances which play a vital part in every aspect of an organism’s life.
- Nucleotide molecules can be mononucleotides or polynucleotides that consist of three parts; a nitrogen-containing base, a five-carbon sugar and one or more phosphate groups.
ATP
- Adenosine triphosphate (ATP) is a mononucleotide which contains the base adenine, the sugar ribose and three phosphate groups.
- The covalent bond linking the second and third phosphate groups is unstable and easily broken by hydrolysis.
- When the bond is broken a phosphate group is removed and ATP becomes ADP (adenosine diphosphate) and at least 30kJ of energy is released.
- Energy is released in a process called an exergonic reaction.
- ATP can be resynthesised from ADP and inorganic phosphates by a condensation reaction
- This reaction gets the energy needed from respiration.
- The energy of the exergonic breakdown of ATP is coupled to energy-consuming (endergonic) reactions.
- Phosphate groups liberated from ATP attach to other molecules (phosphorylation), which energises them to work.
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