SHS General Biology: Macromolecules, Bioenergetics, and Photosynthesis

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Comprehensive vocabulary flashcards covering functional groups, macromolecule structures, protein folding levels, enzymatic digestion, redox bioenergetics, and photosynthetic pathways based on the General Biology review reviewer.

37 Terms

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Hydroxyl Group

A polar functional group (−OH-\text{OH}) that forms hydrogen bonds with water; it occurs biologically in carbohydrates, proteins, nucleic acids, and lipids.

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Carbonyl Group

A polar functional group (−C=O-\text{C=O}) with oxygen double-bonded to carbon; found in nucleic acids and carbohydrates, classifying monosaccharides into aldoses or ketoses.

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Carboxyl Group

An acidic functional group (−COOH-\text{COOH}) that donates a proton (H+\text{H}^+) in solution to become ionized as −COO−-\text{COO}^-; found in amino acids and fatty acids.

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Amino Group

A basic functional group (−NH2-\text{NH}_2) that accepts a proton (H+\text{H}^+) in aqueous solution to become −NH3+-\text{NH}_3^+; found in amino acids and nucleic acids.

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Sulfhydryl Group

A functional group (−SH-\text{SH}) present in cysteine amino acid residues that forms covalent disulfide bridges (−S−S−-\text{S}-\text{S}-).

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Phosphate Group

A negatively charged, highly reactive functional group (−PO42−-\text{PO}_4^{2-}) found in the DNA/RNA backbone, ATP, and phospholipids.

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Methyl Group

A nonpolar, hydrophobic hydrocarbon functional group (−CH3-\text{CH}_3) found in proteins and chemically modified DNA bases.

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Dehydration Synthesis

An energy-requiring condensation reaction that links monomers into polymers by removing an −OH-\text{OH} group from one monomer and an −H-\text{H} from another, releasing a water molecule (H2O\text{H}_2\text{O}).

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Hydrolysis Reaction

An energy-releasing cleavage reaction that breaks down polymers into monomers through the addition of a water molecule (H2O\text{H}_2\text{O}).

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Structural Isomers

Molecules that share an identical chemical formula (such as C6H12O6\text{C}_6\text{H}_{12}\text{O}_6 for glucose and fructose) but differ in the placement of atoms, such as the position of the carbonyl group.

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Stereoisomers

Molecules sharing the same chemical formula and functional group positions but differing in the three-dimensional spatial orientation of groups, such as the −OH-\text{OH} and −H-\text{H} orientation around C-4 in glucose versus galactose.

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Amylose

An unbranched, plant energy storage polysaccharide consisting of α\alpha-glucose linked by α-1,4\alpha\text{-}1,4 glycosidic bonds that coils helically in water.

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Amylopectin

A branched plant energy storage polysaccharide composed of α\alpha-glucose units linked by α-1,4\alpha\text{-}1,4 bonds with α-1,6\alpha\text{-}1,6 branches occurring every 24–3024\text{--}30 glucose units.

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Glycogen

A highly branched animal energy storage carbohydrate stored in liver and muscle cells, formed from α\alpha-glucose with α-1,4\alpha\text{-}1,4 linkages and frequent α-1,6\alpha\text{-}1,6 branch points.

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Cellulose

A structural polysaccharide made of straight, unbranched chains of β\beta-glucose joined by β-1,4\beta\text{-}1,4 linkages that form microfibril fibers within plant cell walls.

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Chitin

A structural polysaccharide consisting of modified β\beta-glucose units (N-acetylglucosamine) linked by β-1,4\beta\text{-}1,4 bonds that cross-link with proteins to form fungal cell walls and arthropod exoskeletons.

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Purines

Double-ring nitrogenous bases found in both DNA and RNA, specifically Adenine (A) and Guanine (G).

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Pyrimidines

Single-ring nitrogenous bases, including Cytosine (C), Thymine (T, specific to DNA), and Uracil (U, specific to RNA and lacking a methyl group).

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Phosphodiester Bond

A covalent linkage connecting the phosphate group on the 5′5' carbon of one nucleotide to the hydroxyl group on the 3′3' carbon of the adjacent pentose sugar.

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Saturated Fatty Acids

Fatty acids containing no C=C\text{C=C} double bonds that are fully saturated with hydrogen, packing tightly together as solids at room temperature.

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Unsaturated (Cis) Fatty Acids

Fatty acids with one or more C=C\text{C=C} double bonds in cis configuration (hydrogens on the same side), causing kinks that prevent tight packing and maintain a liquid oil state at room temperature.

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Trans Fatty Acids

Artificially hydrogenated fatty acids with C=C\text{C=C} double bonds in trans configuration (hydrogens on opposite sides) that adopt straight-chain behavior and raise LDL cholesterol.

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Amphipathic

A structural characteristic of molecules, like phospholipids, that possess both hydrophilic (water-loving) and hydrophobic (water-fearing) regions.

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Primary Structure

The linear sequence of amino acids in a polypeptide chain joined by covalent peptide bonds, which is resistant to mild changes in heat and pH.

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Secondary Structure

Localized regular folding patterns (such as α\alpha-helices and β\beta-pleated sheets) maintained by hydrogen bonds between the polypeptide backbone's C=O\text{C=O} and N-H\text{N-H} groups.

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Tertiary Structure

The overall three-dimensional globular shape of a single polypeptide chain stabilized by R-group interactions, including hydrophobic exclusion, ionic salt bridges, hydrogen bonds, and disulfide bridges.

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Quaternary Structure

The multi-subunit spatial arrangement formed by the aggregation of two or more polypeptide chains joined through hydrophobic interactions and nonpolar interfaces.

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Denaturation

The unfolding of a protein and complete loss of its biological function resulting from environmental disruptions (heat, pH, ionic shifts) that break weak stabilizing bonds.

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Catabolic Pathways

Exergonic metabolic processes (−ΔG-\Delta G) that break down complex molecules into simpler units via hydrolysis, releasing stored free energy.

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Anabolic Pathways

Endergonic metabolic processes (+ΔG+\Delta G) that consume ATP to assemble complex macromolecules from simpler precursor molecules via dehydration synthesis.

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Oxidation

A bioenergetic chemical process defined as the loss of electrons, loss of hydrogen, or gain of oxygen, resulting in a loss of stored chemical energy.

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Reduction

A bioenergetic chemical process defined as the gain of electrons, gain of hydrogen, or loss of oxygen, resulting in a net gain of stored chemical energy.

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Chylomicrons

Lipoprotein aggregates formed inside enterocytes from triglycerides, cholesterol, proteins, and phospholipids that enter lymphatic capillaries (lacteals) for bodily transport.

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Photolysis of Water

The light-driven enzymatic cleavage of water (2H2O→O2+4H++4e−2\text{H}_2\text{O} \rightarrow \text{O}_2 + 4\text{H}^+ + 4e^-) in Photosystem II that replaces oxidized reaction center electrons and releases oxygen.

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Rubisco

The primary carbon-fixing enzyme in the Calvin Cycle that catalyzes the attachment of inorganic CO2\text{CO}_2 to ribulose 1,5-bisphosphate (RuBP).

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C4 Pathway

A photosynthetic adaptation achieving spatial separation of carbon fixation in mesophyll cells (via PEP Carboxylase) and the Calvin cycle in bundle-sheath cells to avoid photorespiration.

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CAM Pathway

A photosynthetic adaptation in arid-zone plants providing temporal separation by capturing CO2\text{CO}_2 with PEP Carboxylase at night and executing the Calvin cycle during daylight.