BCH 201- GENERAL BIOCHEMISTRY I 2019/2020

BCH 201 - General Biochemistry I 2019/2020

PART 1


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BCH 201 - GENERAL BIOCHEMISTRY I 2019/2020
PROF. O. ADEMUYIWA


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OVERVIEW

  • The Nature of Biochemistry
  • Cellular Basis of Life
  • Cell Composition
  • Organelles in the Cell

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NATURE OF BIOCHEMISTRY

  • Definition: Biochemistry is the study of the chemistry of life.
  • Biochemistry can also be defined as the study of the molecular events that correspond to the phenomenon of life.
  • The term "study" indicates that Biochemistry is both a theoretical and a laboratory-based science.
  • Chemistry refers to the chemical processes taking place within cells.
  • Objective: The major objective of Biochemistry is to achieve a complete understanding of all the chemical processes associated with living cells at the molecular level.

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CELLULAR BASIS OF LIFE

  • Organisms are composed of membrane-enclosed objects called cells.
  • Cells are the fundamental units of life (living organisms) and vary in size and shape.
  • Two types of cells:
    • Plant cells
    • Animal cells
  • The cell is enclosed by a delicate, semi-permeable structure called the plasma membrane.
  • Many plant and bacterial cells have a cell wall surrounding the plasma membrane.
  • Contents enclosed by the plasma membrane: cytoplasm.
  • Liquid portion of the cytoplasm is called cytosol.
  • The plasma membrane contains transporters and receptors.

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PLANT AND ANIMAL CELLS

  • Cross-Section of an Animal Cell:

    • Cell Membrane
    • Centrosome
    • Lysosome
    • Nucleus
    • Nucleolus
    • Nuclear Membrane
    • Vacuole
    • Mitochondrion
    • Rough ER
    • Smooth ER
    • Ribosomes
    • Golgi Body
    • Other organelles as shown in the diagram.
  • Cross-Section of a Plant Cell:

    • Similar structure to animal cells; notable differences include:
    • Cell Wall
    • Chloroplasts
    • Vacuoles

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CELL COMPOSITION

  • A cell consists of:
    • Small molecules
    • Macromolecules
    • Organelles
  • Water is the most abundant molecule in cells, accounting for 70% of cell weight, with other components existing in an aqueous environment.
  • Except for water, most molecules in the cell are macromolecules classified into four groups:
    • Lipids
    • Carbohydrates
    • Proteins
    • Nucleic acids
  • Each macromolecule has distinct chemical properties that suit its specific function in the cell.

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CELL COMPOSITION CONTD - STRUCTURES OF SOME LIPIDS

  • Lauric Acid:

    • A fatty acid commonly found in coconut oil.
  • Cholesterol:

  • Triglyceride:

  • Phospholipid:

  • Structures:

    • Lauric Acid:

      HO-C-C-C-C-C-C-C-C-C-C-C-C-H
      HHHHHHHHHHHHHHHHHH

    • Other structures include hydrocarbon chains and functional groups as depicted in diagrams.


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CELL COMPOSITION CONTD

  • Carbohydrates:
    • Composed primarily of hydrocarbon structures with many polar hydroxyl (OH) groups, making them highly soluble in water.
    • Large carbohydrate molecules (Polysaccharides) are formed by many small sugar molecules linked by glycosidic bonds.
    • Function: Storage (e.g., starch, glycogen) and providing carbon skeletons for synthesis of other compounds.
  • Structural Functions:
    • Linear polysaccharides are major components of plant cell walls; bacterial cell walls are composed of cross-linked polysaccharides.

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CELL COMPOSITION CONTD

  • Proteins:
    • Most complex macromolecules; made up of linear polymers called polypeptides.
    • Polypeptides consist of amino acid monomers joined by peptide bonds.
    • Each amino acid has:
    • Central carbon atom
    • Carboxyl group
    • Amino group
    • Hydrogen atom
    • Unique R group
    • Properties of proteins determined by the sequence of amino acids in the polypeptide chain.

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CELL COMPOSITION CONTD - AMINO ACID, PEPTIDE BOND AND POLYPEPTIDE

  • Peptide Bond:
    • Formed by the removal of a molecule of water from two amino acids.
  • Structure of a peptide chain:
Example: Glycine Amino Acids
N-C-C  
O R
H—N—C-C  
HAA  
H-C  
  • Important Terms:
    • N-terminus: Beginning of a polypeptide chain
    • C-terminus: End of a polypeptide chain

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CELL COMPOSITION CONTD

  • Nucleic Acids:
    • Largest macromolecules composed of long linear polymers called polynucleotides.
    • Made of nucleotide monomers, comprising a five-carbon sugar, phosphate groups, and nitrogenous bases.
    • Two types:
    • Deoxyribonucleic acid (DNA): Contains genetic information inherited during cell division.
    • Ribonucleic acid (RNA): Involved in protein synthesis.
  • Chromosomes contain specific genetic information required for synthesis of cell compounds and replication processes.

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CELL COMPOSITION CONTD - NUCLEOTIDE AND POLYNUCLEOTIDE

  • Structure of a Nucleotide:
    • Composed of:
    • Nitrogenous base (purines and pyrimidines)
    • Pentose sugar (ribose or deoxyribose)
    • Phosphate group
    • Purines: Adenine (A), Guanine (G)
    • Pyrimidines: Cytosine (C), Thymine (T), Uracil (U)

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CELL COMPOSITION CONTD

  • Each chromosome carries a single DNA molecule with approx. 10^6 or more nucleotides in a specific arrangement.
  • The sequence of bases in chromosomal DNA determines amino acid sequences in proteins.
  • RNA Types:
    • Messenger RNA (mRNA): Transmits genetic information from DNA to the cytoplasm for protein synthesis.
    • Ribosomal RNA (rRNA): Found in ribosomes, facilitates protein synthesis.
    • Transfer RNA (tRNA): Transports amino acids to ribosomes.

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CELL COMPOSITION CONTD

  • Additional Cell Components:
    • Inorganic components:
    • Metal ions (Na+, K+, Mg2+, Ca2+, Zn2+, Fe2+/Fe3+)
    • Other trace elements (molybdenum, selenium, copper, etc.)
    • Organic/inorganic molecules involved in normal cellular functions.
    • Bioinorganic molecules and coenzymes work with enzymes to maintain homeostasis.

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CELL COMPOSITION CONTD - ORGANELLES IN CELLS

  • Organelles: Subcellular membranous structures.
    • Nucleus: Repository of genetic information.
    • Endoplasmic Reticulum (ER): Site of protein and lipid synthesis (Rough ER and Smooth ER).
    • Golgi Complex: Processing and sorting of proteins.
    • Lysosomes: Sites of degradative reactions (animal cells only).

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CELL COMPOSITION CONTD - ORGANELLES IN CELLS

  • Plant Cells: Do not contain lysosomes; vacuoles serve similar functions.
  • Peroxisomes: Break down hydrogen peroxide.
  • Mitochondria: Power plants of eukaryotic cells, responsible for ATP production and have their own DNA.
    • Chloroplasts: Convert solar energy to chemical energy in plants.
    • Cytoskeleton: Interlocking filaments that stabilize cell shape and organize the cytoplasm.

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BCH 201 - pH and BUFFERS

  • pH: Defined as –log aH+.
  • The activity of ions in a solution can be expressed as:
    • $a = c imes ext{γ} $
    • where $a$ is activity, $c$ is concentration, $ ext{γ}$ is activity coefficient.
  • In dilute solutions, $ ext{γ} ightarrow 1$, and at infinite dilution, $a = c$.
    • For hydrogen ions:
    • $aH+ = [H+]$
    • pH = –log10$[H+]$

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DISSOCIATION OF H2O AND ITS ION PRODUCT

  • Water is a weak electrolyte:
    • $H2O
      ightleftharpoons H^+ + OH^-$
    • Equilibrium constant $K_{eq} = [H^+] imes [OH^-] = 1.8 imes 10^{-16}$ mole/Litre at 25° C.

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DISSOCIATION OF H2O AND ITS ION PRODUCT

  • Given that water is slightly dissociated, we consider

Keq[H2O]=[H+][OH]K_{eq} [H2O] = [H^+] [OH^-]

  • Substituting [H2O]=55.5[H2O] = 55.5 moles/Litre results in:
    Keqimes55.5=[H+][OH]=1.01imes1014K_{eq} imes 55.5 = [H^+] [OH^-] = 1.01 imes 10^{-14}
  • Relationship between [H+] and [OH-] holds true with: [H+][OH]=1.01imes1014[H^+][OH^-] = 1.01 imes 10^{-14}

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DISSOCIATION OF H2O AND ITS ION PRODUCT

  • Taking logarithm gives:
    extLog[H+]+extLog[OH]=14ext{Log}[H^+] + ext{Log}[OH^-] = -14
  • The equations result in the definitions of pH and pOH, leading to the relationship of their sum equaling 14.

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ACIDS AND BASES IN CHEMISTRY

  • Bronsted theory: - Acid: Donates a proton. - Base: Accepts a proton. - Example: HA<br/>ightleftharpoonsH++AHA <br /> ightleftharpoons H^+ + A^-

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HENDERSON-HASSELBALCH EQUATION

  • pH = pKa + ext{Log} rac{[A^-]}{[HA]}

- This equation is used to describe the relationship between pH, pKa, and the concentrations of acid and its conjugate base. Buffers contain weak acids and their conjugate bases.

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BUFFER

  • A buffer is defined as a compound that in solution resists a change in pH upon the addition of an acid ($H^+$) or base ($OH^-$). Example: Acetic acid and its salt sodium acetate.

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PREPARATION OF BUFFERS

  • Example: Preparing a buffer with a pH of 5 using acetic acid and sodium acetate by applying the Henderson-Hasselbalch equation.

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AN EXAMPLE OF BUFFER SYSTEM IN TISSUES

  • Lymph, cerebrospinal fluid, and tissue fluids utilize similar buffering systems (HCO3- and H2CO3).

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ACIDOSIS AND ALKALOSIS

  • Definitions and implications of changes in pH due to metabolic processes.
    • Metabolic and respiratory acidosis and alkalosis described with examples.

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ACIDOSIS AND ALKALOSIS

  • Conditions leading to acid or base accumulation and their physiological effects noted.

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CHEMISTRY OF CARBOHYDRATES

  • Overview of carbohydrates as organic molecules and their roles in energy production, structure, and cellular components.

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FUNCTIONS OF CARBOHYDRATES

  • Breakdown of carbohydrates provide energy and are key in cell structure (e.g., ribose in RNA).

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STRUCTURE AND CLASSIFICATION OF CARBOHYDRATES

  • Definition and classification into monosaccharides, disaccharides, and polysaccharides.

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MONOSACCHARIDES

  • Simplest carbohydrates and their roles as building blocks of more complex carbohydrates.

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MONOSACCHARIDE CLASSIFICATION

  • Types based on carbon count and functional groups (aldoses and ketoses).

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STEREOCHEMISTRY IN CARBOHYDRATES

  • Identification of isomers, chirality, and reference carbons, discussions of stereoisomers and their significance.

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ENANTIOMERS

  • Definition and examples including chiral centers, optical activity and its implications.

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PROJECTION FORMULAS

  • Fischer and Haworth projection formulas for depicting carbohydrate structures clearly.

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CYCLIZATION OF SUGARS

  • Formation of cyclic structures and their biological relevance in aqueous solutions.

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REDUCING SUGARS

  • Characteristics of reducing sugars, distinctions in reactivity among aldoses and ketoses.

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EPIMERS AND DIASTEREOMERS

  • Definitions with examples highlighting structural differences.

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L AND D ISOMERS

  • Designation of isomer forms based on hydroxyl group position relative to chiral center.

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OPTICAL ISOMERISM AND ACTIVITY

  • Interactions of chiral compounds with polarized light, importance of racemic mixtures.

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FISCHER AND HAWORTH FORMULAS

  • Distinctions in representation of carbohydrate structures, their relevance in biochemical contexts.

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SUGARS IN ACYCLIC AND CYCLIC FORM

  • The formation of ring structures from open-chain forms and their implications.

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COMMON BIOLOGICAL FATTY ACIDS

  • Overview of biological roles and structures of essential fatty acids.

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FAT AND ENERGY STORAGE

  • Roles of triglycerides, chemical structures, and saturated vs. unsaturated differences.

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FATTY ACIDS CLASSIFICATION

  • Classification based on saturation levels and implications for metabolism.

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FATTY ACIDS AND OXIDATION

  • Biological and physiological aspects of fatty acids in energy metabolism.

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SUGAR DERIVATIVES AND BIOSYNTHESIS

  • Overview of sugar derivatives, implications in biological processes and metabolism.

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DISACCHARIDES

  • Formation of disaccharides, linkage types and examples including lactose and sucrose.

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IMPORTANT DISACCHARIDES IN NUTRITION

  • Lactose, maltose, and sucrose characteristics and nutritional importance outlined.

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STRUCTURE AND FUNCTION OF POLYSACCHARIDES

  • Overview of polysaccharides as structural and energy storage molecules.

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IMPORTANCE OF STARCH

  • Starch and its role in plants as a polysaccharide; structure and types.

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FUNCTIONS OF CELLULOSE AND CHITIN

  • Overview of structural polysaccharides in plants and their significance.

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ANIMALS AND POLYSACCHARIDES

  • Glycogen functions in mammals, storage properties, and metabolic implications.

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BIOSYNTHESIS, STRUCTURE AND FUNCTION

  • Overview of polysaccharide biosynthesis, structural roles, and metabolic importance.

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OVERVIEW OF PROTEINS AND AMINO ACIDS

  • Proteins as polymers, their functions, and the role of amino acids in structure and function.

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AMINO ACIDS AND THEIR CHARACTERISTICS

  • Overview of amino acids, their structure, classification, and biological importance.

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DESCRIPTIVE EXAMPLES OF AMINO ACIDS

  • Discussion of polar, charged, and nonpolar amino acids, their properties, and use in proteins.

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AMINO ACID SYNTHESES AND REACTIONS

  • Overview of the synthetic pathways of amino acids and their metabolic implications.

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PEPTIDES AND PROTEINS

  • Detailed discussion of peptide bond formation, sequences in proteins, and terminology.

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PRIMARY, SECONDARY, TERTIARY, AND QUATERNARY STRUCTURES IN PROTEINS

  • Differences between structures in proteins and their biological implications.

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CHEMISTRY OF LIPIDS

  • Overview of lipids, their biochemical functions, and structural differences.

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FUNCTIONS OF LIPIDS

  • Membrane components, energy storage, and signaling roles of lipids outlined.

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FATTY ACIDS DEFINED

  • Structure, classification, and roles of fatty acids in larger biological contexts.

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STEROIDS

  • Structure and biological roles of steroid lipids discussed.

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TRIACYLGLYCEROLS, WAXES, AND PHOSPHOLIPIDS

  • Overview of their structure, roles, structural elements in membranes, and biological significance.

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SPHINGOLIPIDS AND GLYCOSPHINGOLIPIDS

  • Description of sphingolipids structures and functions.

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BIOSYNTHESIS OF LIPIDS

  • Pathways involved in lipid biosynthesis and their physiological implications.

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NUCLEOTIDES AND NUCLEIC ACIDS

  • Journey through the structure, function, and examples of nucleotides and nucleic acids.

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FUNCTIONS OF NUCLEOTIDES

  • Overview of diversity and roles of nucleotides within biological systems.

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STRUCTURES OF NUCLEOTIDES AND NUCLEOSIDES

  • Detailed diagrams and types of nucleotides related to DNA and RNA.

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DNA AND RNA STRUCTURAL COMPONENTS

  • Key differences and similarities between DNA and RNA related to nucleotides.

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DNA SEQUENCE AND STRUCTURE

  • Explanation of how nucleotides link to form structures and chains in DNA.

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BIOCHEMISTRY OF VITAMINS

  • Overview of vitamins, their classifications, structures, and significance in metabolic processes.

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FUNCTIONS OF VITAMINS IN METABOLISM

  • How vitamins support and catalyze metabolic reactions, energy production, and health.

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VITAMINS AND DISEASES

  • Discussing conditions resulting from vitamin deficiencies and their physiological effects.

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VITAMINS AS CO-ENZYMES

  • Roles vitamins play as coenzymes in conjunction with enzymes in metabolic processes.

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MECHANISMS OF VITAMINS IN BIOLOGICAL CONTEXTS

  • Overview of specific examples of vitamins in metabolic pathways and molecular responses.

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COFACTORS

  • Relationship between enzymes and metal ions or organic molecules in catalysis.