Biology 231 Human Anatomy and Physiology Chapter 2 Lecture Outline Chemical Level of Organization elements – building block of matter; cannot be split into a simpler substance by ordinary chemical means 92 occur naturally chemical symbol – 1 or 2 letters representing an element (eg. C for carbon) atom – smallest unit of an element nucleus – dense core of atom; protons – positively charged particles neutrons – uncharged particles electrons – negatively charged particles; surround nucleus electron shells – regions where electrons are usually found # of protons = # of electrons (electrically neutral) atomic number – number of protons (different for each element) mass number – number of protons + neutrons isotopes – atoms of an element with different numbers of neutrons; electrical charge is the same (same chemical properties) radioactive isotopes – unstable nuclei; decay and release radiation (eg. C-14) decay at different rates molecule – 2 or more atoms held together by chemical bonds Chemical Bonds – forces that hold atoms of a molecule together; depends on arrangement of electrons valence shell – outer, reactive electron shell octet rule – 8 electrons in the valence shell is most stable; allows prediction of reactivity (in some small atoms the valance shell has only 2 electrons) Ionic Bonds – one atom loses valence electrons to another; held together by electrical attraction of opposite charges ion – charged particle anion – gains electrons (negatively charged) cation – loses electrons (positively charged) ionic compounds break into ions in water Covalent Bonds – atoms share valence electrons; most common bonds in body single bond (share 1 pair of electrons) – hydrogen molecule double bond (share 2 pairs of electrons) – oxygen molecule nonpolar covalent bond – electrons shared equally polar covalent bond – unequal electron sharing; produces partial electrical charges on atoms sharing electrons 1 Hydrogen Bonds – weak bonds between hydrogen atoms (partial positive charge) and neighboring atoms with partial negative charges (eg. O or N) too weak to form molecules; form attractions between molecules or parts of molecules Chemical Reactions – foundation of all life processes metabolism – sum of all chemical reactions occurring in the body reactants – starting substances products – ending substances Types of Reactions: synthesis reactions (anabolism) – 2 or more atoms, ions, or molecules combine to form new, larger molecules decomposition reactions (catabolism) – larger molecules split into smaller atoms, ions, or molecules exchange reactions – concurrent synthesis and decomposition (old bonds break and new ones form) reversible reactions – reaction may proceed in either direction, usually depending on conditions in the environment Energy of Chemical Reactions (energy = ability to do work) kinetic energy - energy of motion activation energy – energy investment needed to start a reaction; makes valence electrons unstable so they can react factors affecting reaction rate: concentration of reactants – more = faster temperature – higher = faster catalysts – lower activation energy so reaction proceeds faster (enzymes – biological catalysts) potential energy – stored energy chemical energy – stored energy in chemical bonds; cannot be created or destroyed, but can be converted into other forms (other chemical bonds, mechanical energy, heat) exergonic reaction – reaction that releases energy; products have less chemical energy that reactants (catabolism) endergonic reaction – reaction that requires energy input; products have more chemical energy than reactants (anabolism) 2 INORGANIC COMPOUNDS – usually lack carbon and are structurally simple (eg. water, oxygen, carbon dioxide) Water – most important inorganic compound in body polar covalent molecule – biological solvent (solvent + solutes = solution) hydrophilic (water-loving) – dissolves easily in water (ions and polar covalent molecules) hydrophobic (water-fearing) – dissolve poorly in water (mainly nonpolar covalent molecules) participates in metabolic reactions hydrolysis reaction – using water to break down larger molecules dehydration synthesis – joining 2 smaller molecules by removing a molecule of water Acids, Bases, and Salts – ionic compounds acids – dissolve to form hydrogen ions (H+); (proton donors) bases – dissolve to form anions that can bind H+ (proton acceptors) salts – do not affect pH of solution pH – measurement of a solution’s acidity or alkalinity(basicity) pH scale (Fig 2-9) pH 7 = neutral lower pH = more acidic = more hydrogen ions higher pH = more basic = fewer hydrogen ions body fluids maintain narrow pH ranges buffers – chemicals that stabilize pH of a solution by accepting or donating H+ when needed ORGANIC COMPOUNDS – contain carbon and hydrogen (+ oxygen, nitrogen, phosphorus, and other elements) joined almost entirely by covalent bonds; may be very large and structurally complex carbon skeleton – chain of carbon atoms; each can form 4 covalent bonds functional groups – other atoms in specific arrangements attached to carbon skeleton; confer characteristic chemical properties CLASSES OF ORGANIC COMPOUNDS Carbohydrates - sugars, starches, glycogen, cellulose primarily an energy source in the body (some structural) general chemical formula – 1 carbon:2 hydrogen:1 oxygen monosaccharides – simple sugars(monomers); 3-7 carbons (eg. glucose) disaccharides – 2 monosaccharides joined by dehydration (eg. sucrose) polysaccharides – 10s to 100s of monosaccharides (eg. glycogen) 3 Lipids – fats and oils, phospholipids, steroids, fatty acids energy storage, insulation, main component of cell membranes contain carbon, hydrogen, less oxygen than carbohydrates mainly hydrophobic fatty acids – carbon/hydrogen chains with carboxyl group saturated fatty acids – only single covalent bonds unsaturated fatty acids – at least 1 double covalent bond triglycerides – energy storage, insulation, protection glycerol – 3-carbon backbone 3 fatty acids phospholipids – main component of cell membranes glycerol + 2 fatty acids – nonpolar tail phosphate linked polar head amphipathic – has polar (charged) and nonpolar (uncharged) regions steroids – cholesterol, sex hormones, cortisol have 4 carbon rings Proteins – major structural and functional molecules of body contain carbon, hydrogen, oxygen, and nitrogen (some sulfur) amino acids – 20 different protein monomers central carbon with one H amino group (-NH2) carboxyl group (-COOH) side chain (R group) peptide bond – covalent dehydration reaction links amino acids peptides – dipeptide (2), tripeptide (3), polypeptide (>10) proteins – 1 or more polypeptide chains, may be very structurally complex; function is related to shape primary structure – sequence of amino acids secondary structure – repeated twisting or folding due to hydrogen bonds – alpha helix, beta pleated sheet tertiary structure – 3-D folding due to hydrogen bonds, hydrophobic interactions, and disulfide bridges quaternary structure – some proteins are composed of more than 1 polypeptide chain held together like tertiary structures enzymes – protein catalysts; most common catalysts in body very specific – only catalyze specific reactions substrate – reactant molecule enzyme acts on active site – recognizes and binds specific substrate very efficient – may increase reaction rate billions of times enzyme is not altered or used up enzyme regulation – cofactors, coenzymes, concentration denatured enzyme – loses its functional structure (eg. change in pH, temperature) 4 Nucleic Acids – DNA, RNA control heredity and cell function through protein synthesis composed of carbon, hydrogen, oxygen, nitrogen, and phosphorus nucleotides – monomers of nucleic acids pentose sugar (5-carbon) DNA – deoxyribose RNA – ribose phosphate group nitrogenous base (5 types) adenine (A) – DNA and RNA guanine (G) – DNA and RNA cytosine (C) – DNA and RNA thymine (T) – DNA only uracil (U) – RNA only nucleic acids are strands of nucleotides joined by dehydration reactions RNA is single-stranded DNA is a double-stranded helix held together by hydrogen bonds between bases of adjacent strands ATP (adenosine triphosphate) – high energy organic compound energy currency of body – temporarily stores energy released by catabolic reactions so it can be released later, where it is needed nucleotide – adenosine monophosphate + phosphate groups phosphorylation (addition of phosphate groups by enzymes) high-energy bonds formed by specific enzymes ADP – 1 high-energy phosphate bond ATP – 2 high-energy phosphate bonds Breaking the high-energy bonds releases the energy for use in endergonic reactions in the body. 5