Macromolecules Flashcards

1
Q

Molecule

A

This is made up of elements.

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2
Q

Element

A

A substance that cannot be broken down or converted into another substance by chemical means. These are made up of 1 type of atom.

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3
Q

Atom

A

The smallest particle of an element that still retains the elements distinctive chemical properties.

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4
Q

Neutrons

A

A non-charged or neutral subatomic particle found in the nucleus of an atom.

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5
Q

Protons

A

Positively charged subatomic particles found in the nucleus of an atom. The number of protons is what determines the atomic number and therefore the element.

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6
Q

Electrons

A

Negatively charged subatomic particles found in shells that orbit the nucleus of an atom.

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7
Q

Electron Shells

A

These orbit the nucleus of an atom and are arranged in different energy levels. These energy levels have a maximum number of electrons they can contain. Most elements have an incomplete outer energy level which can undergo chemical reactions in order to fill up or empty the outer energy level by donating or accepting electrons in order to achieve stability.

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8
Q

Covalent Bonds

A

A type of chemical bond in which the electrons are shared between both molecules which results in a neutral or non-charged product as the number of electrons and protons (charges) are the same. There are a few types of these with 2 examples being singular and others being double.

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9
Q

Single Covalent Bonds

A

This is when there is an equal sharing of 2 electrons by both atoms. This allows for rotation which can change the orientation to other molecules attached to the bonded molecules.

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10
Q

Double Covalent Bonds

A

This is when 4 electrons are equally shared by both atoms. The presence of 2 bonds means the structure is rigid and doesn’t allow for any rotation.

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11
Q

Macromolecules

A

Aside from water these are the most abundant compounds inside cells e.g. DNA, RNA, proteins etc. These are constructed by linking smaller molecules together via covalent bonds. Carbon is a part of nearly all of these which can form into small organic molecules or into highly stable chains and rings. Carbon molecules are the building blocks for these and are used for structural support, work, information and energy storage etc.

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12
Q

Carbohydrates

A

A macromolecule formed by simple sugars. These are a hydrate of carbon (water + carbon) (CH2O)*n where n is typically 3,4,5 or 6.

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13
Q

Monosaccharide

A

A singular sugar molecule e.g. glucose.

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14
Q

Disaccharide

A

A sugar molecule composed of 2 monosaccharides e.g. sucrose from glucose and fructose.

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15
Q

Oligosaccharide

A

A sugar molecule composed of 3-50 monosaccharides.

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16
Q

Polysaccharide

A

A sugar molecule composed of 100s - 1000s of monosaccharides. These can be branched or linear in structure.

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17
Q

Aldose Sugar

A

When these cyclise the hydroxyl group on the second to last carbon undergoes an intramolecular reaction with the aldehyde carbonyl group.

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18
Q

Ketose Sugar

A

When these cyclise the hydroxyl group on the second to last carbon undergoes an intramolecular reaction with the ketone carbonyl group.

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19
Q

Condensation Reaction

A

These reactions lead to water being released as a product. This is the reaction that occurs when a covalent bond between the subunits of macromolecules is formed. This reaction leads to 2 subunits with one containing a hydroxyl group and the other without one and water as the other product.

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20
Q

Hydrolysis Reaction

A

These reactions require the addition of water as a reactant. These occur when a covalent bond between subunits of a macromolecule is broken. This reaction requires water and 2 subunits with the result being a combination of the subunits which will contain 2 hydroxyl groups which are gained from the water and 1 hydrogen already present on the subunit.

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21
Q

Alpha Glucose

A

This makes up 36% of the glucose in the body. This variation exists when the hydroxyl group on carbon 1 of the ring is positioned below the ring.

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22
Q

Beta Glucose

A

This makes up 64% of the glucose in the body. This variation exists when the hydroxyl group on carbon 1 of the ring is position above the ring.

23
Q

Structural Role of Carbohydrates

A

The linking of 1-4 (the hydroxyl group attached to carbon 1 loses the hydrogen and bonds to carbon 4 on the next glucose ring) beta glucose forms the molecule cellulose. This is the most abundant organic molecule on Earth. It makes up the walls of plant cells and provides structure and can be made up of 100s - 10000s of units of glucose.

24
Q

Energy Source Role of Carbohydrates

A

This is gained from glycogen in animal cells which has alpha 1-4 (linear) and alpha 1-6 (branched) bonds. In plant cells starch is used for this purpose which has the same bonding types. The difference between glycogen and starch however is that glycogen has more branches and starch is made up of more than 1 polysaccharide.

25
Q

Lipids

A

These are amphipathic meaning they have both a hydrophilic (water loving) and hydrophobic (water hating) part. This means that the base units fatty acids are insoluble in water but are soluble in fat and organic solvents.

26
Q

Unsaturated Fatty Acid

A

These contain double bonds linking carbon atoms in the hydrophobic tail. The double bond repels the molecules around it meaning kinks in the chain which don’t allow for the close packing of molecules. These fats are liquid at room temperature e.g. plant oils (canola, corn, olive).

27
Q

Saturated Fatty Acid

A

These don’t contain double bonds in the hydrophobic tail. This means there is no repulsion forces meaning that molecules can be tightly packed together. These are typically solid at room temperature e.g. animal fats (butter, lard).

28
Q

Fatty Acid

A

These are the subunits of fat and is mostly used as energy reserves in cells and can store 6x as much energy as glucose per weight. This general fat is solid whereas oil is liquid at room temperature (25C). These are typically stored as triglyceride molecules which contains 3 fatty acids attached to 1 glycerol. This is through an ester linkage between the glycerol and the carboxylic head on the fatty acid.

29
Q

Phospholipids

A

These molecules are made up of 2 fatty acids linked to glycerol meaning there are 2 hydrocarbon tails. The 3rd site on the glycerol is linked to a phosphate group which also has a small hydrophilic group attached covalently to the phosphate group. These molecules are highly amphipathic. These molecules are the main component of cell membranes which makes a bilayer with the hydrophilic sections of both layers facing outward and the hydrophobic sections facing each other inwards.

30
Q

Glycolipids

A

These are similar to phospholipids but the sugar groups replace the phosphate and the hydrophilic part of the molecule. These are amphipathic. They are mainly on the cytosolic surface of the plasma membrane which is useful for cell-to-cell recognition for intercellular connections.

31
Q

Steroids

A

These are hormones such as testosterone and estradiol. These are signaling molecules and can pass through cell membranes.

32
Q

Nucleic Acid

A

DNA is transcribed into RNA which is then translated into proteins. DNA is deoxyribonucleic acid which is used a long-term storage of hereditary material. RNA is ribonucleic acid which is used as a transient carrier of information. Both of these molecules consist of nucleotides.

33
Q

Nucleotides

A

These organic molecules typically contain nitrogen, carbon and hydrogen with some also containing oxygen. This structure typically has a phosphate backbone, a pentose sugar group and a nitrogenous base. These are classified into 2 types which are pyrimidines (single ring structures e.g. cytosine (C), thymine (T) and uracil (U)). The second type are purines (double ring structures e.g. adenine (A) and guanine (G)).

34
Q

Nucleoside

A

The structural unit considered when ignoring the phosphate backbone on a nucleotide. This means it consists only of the pentose sugar (deoxyribose or ribose) and the nitrogenous base (A, T, U, C or G).

35
Q

Phosphoanhydride Bond

A

These bonds connect phosphate groups together in a condensation reaction.

36
Q

Nucleotide Structure

A

In DNA and RNA the phosphates are normally joined the the C5 hydroxyl group of the pentose sugar. This means that mono, di and triphosphate molecules are common. The difference in sugars also means that there are different nucleotides for DNA and RNA. DNA has dATP, dTTP, dCTP and dGTP while RNA has ATP, UTP, CTP and GTP.

37
Q

Nucleic Acid Sequence & Direction

A

The hydroxyl group on the 3rd carbon of the pentose sugar is covalently linked to the phosphate group attached to the 5th carbon of the adjacent pentose (this creates the sugar phosphate backbone for DNA and RNA). These polymers (strands) have directionality a 5’ end and a 3’ end. By convention the sequences of bases (genetic information) in a nucleic acid strand is read from 5’ - 3’ using the single letter code e.g. 5’-G-A-C-T-T-3’. The DNA molecules are double stranded whereas the RNA molecules are single stranded.

38
Q

Chemical Energy

A

A function of nucleotides in which phosphoanhydride bonds are hydrolysed. When this occurs the energy conserved in that bond is released and can be used by cells e.g. ATP energy.

39
Q

Signaling Molecule

A

A function of nucleotides in which starved bacterial cells begin to produce cyclic AMP (cAMP) which is a ring shaped molecule formed by the phosphate group with multiple carbons on the same sugar. The cAMP activates enzymes and turns on genes to find or create more ATP.

40
Q

Coenzyme

A

A function of nucleotides in which nucleotides combine with other groups. When they are activated they transfer groups between these molecules and the combinations will act as enzymes.

41
Q

Proteins

A

These molecules are made up of amino acids. These form into linear polymers with directionality. They begin with an amine group known as the N terminus and ends with a carboxylic acid group known as the C terminus.

42
Q

Amino Acids

A

These are the subunits of proteins which have an alpha (central) carbon, a carboxylic acid group, an amino group and a side chain. The side chain differences is what distinguishes the properties of different amino acids. These can be charged or neutral depending on whether there is an extra hydrogen on the amine group (positive charge) or if a hydrogen is removed from the carboxylic acid group (negative charge). The same group of of these are found in the proteins of bacteria, animals and plants. These will use peptide bonds to combine and form proteins.

43
Q

Peptide Bonds

A

These bonds link amino acids together to form proteins. The carboxylic acid group of 1 amino acid reacts with the amine group of another amino acid. This reaction is a condensation reaction (produces water) whereas breaking the bond is a hydrolysis reaction (requires water). Despite requiring the amine and carboxylic acid groups to form bonds chains of amino acids each individual amino acid still has both groups.

44
Q

Macromolecules

A

These are made up of smaller subunits such as simple sugars, amino acids and nucleotides. These are formed with covalent bonds through condensation reactions. These formed particles can then undergo non-covalent interaction to bond with one another to form larger assemblies e.g. proteins forming into an enzyme.

45
Q

Ionic Interactions

A

When atoms lose or gain electrons which results in electrically charged particles (ions). These come in 2 forms which are cations which are positively charged from the loss of electrons (Na+). The other form in anions which are negatively charged from gaining electrons (Cl-).

46
Q

Attraction

A

Opposite charges attract each other and hold together through ionic bonds. In the presence of water these bonds aren’t as strong as the water molecules shield the charges of the 2 particles. In the absence of water these bonds are much stronger as the charges aren’t shielded from one another.

47
Q

Polar Covalent Bonds

A

The unequal sharing of electrons belonging to a bond between 2 atoms. This is caused if one atom in a bond has a higher electronegativity than other atoms e.g. oxygen in water attracts electrons more strongly that hydrogen.

48
Q

Electronegativity

A

An atoms affinity to gaining electrons.

49
Q

Hydrogen Bonds

A

Bonds which form if the polarised molecule contains a hydrogen atom and is between 2 electron attracting atoms e.g. oxygen in water. This can also be nitrogen in other molecules. These bonds are based on electrostatic interactions and not from electron sharing like covalent bonds. They are weak compared to covalent bonds 1/20th the strength and are strongest when the 3 atoms in it are arranged in a straight line. Despite 1 of these bonds being weak the sum of the bonds allows for a stronger structure but also allows for flexibility and reactivity.

50
Q

Dipole

A

A polarised molecule. This means there is positively charged and negatively charged parts of the molecule. This is created by polar covalent bonds meaning it can attract other polarised molecules.

51
Q

Water

A

This molecule has hydrogen bonds. During extremely cold extended period only the top layer freezes as it forms a liquid crystalised structure which forms tight interactions with some space between. This allows for it to remain fluid beneath and for interaction between different molecules to occur. This means that its solid form is less dense than its liquid form which is why the solid portion floats above the liquid.

52
Q

Hydrophobic Forces

A

Also known as water-hating. These molecules cluster together to exclude water molecules. This detraction to water causes these molecules to squeeze together to form a larger molecule. This creates a new type of bond caused not by the attraction to the same molecules but their shared detraction to water molecules.

53
Q

Van Der Waals Attractions

A

These forces include attraction and repulsions between atoms, molecules and surfaces as well as other intermolecular forces. These result from a transient shift in electron density around a nucleus that creates a transient charge to which a nearby atom is attracted to or repelled by. These are the weakest interaction type and are only effective when atoms have a specific distance from one another.

54
Q

Non-Covalent Interactions

A

These are intermolecular forces which are weaker than the intramolecular forces which involve electron sharing. Although singularly these forces aren’t as strong there are typically many of these interaction together which help to form stronger interactions. This is what helps to maintain the structures of macromolecules such as proteins and DNA but also allows for the flexibility in order to be altered or changed when necessary e.g. DNA split for transcription. There are 4 major types of ionic interactions, hydrogen bonds, hydrophobic forces and Van der Waals attractions.