1.0 MOLECULES OF LIFE BY : MDM. NURFAZLINI ISMAIL (MDM FAZ)

Slides:



Advertisements
Similar presentations
The Structure and Function of Macromolecules: Carbohydrates, Lipids & Phospholipids.
Advertisements

1 Molecular basis of life (1). 2 Chemical basis of molecular interactions Polar and nonpolar molecules Water Universal solvent O-H bonds are polarized.
Lipids are a diverse group of hydrophobic molecules Lipids are the one class of large biological molecules that do not form polymers Lipids are hydrophobic.
Biochemistry A living things are composed of compound which contain these four elements: Carbon Hydrogen Oxygen Nitrogen.
Structure & Function of Large Biological Molecules (Macromolecules)
Carbohydrates & Lipids
Review Questions 1. How are polymers formed (what type of reaction)? 2. What occurs in this reaction? 3. How are polymers broken down (what type of reaction)?
Chapter 5.
Chapter 5 The Structure and Function of Large Biological Molecules
Focus on: u Elements in each molecule u How molecules are linked and unlinked u Examples and functions of each type of molecule.
Chapter 5: The Structure and Function of Large Biological Molecules
The Nature of Molecules
Biomolecules The Molecules of Life
UNIT 1 – UNDERSTANDING LIFE ON EARTH BIOMOLECULES.
Properties of Water Water molecules are polar so hydrogen bonds form between them. An average of 3.4 hydrogen bonds are formed between each molecule in.
Chapter 5: Macromolecules Macromolecules A large molecule in a living organism –Proteins, Carbohydrates, Nucleic Acids Polymer- long molecules built.
1 Biomolecules. 2 Carbon-based Molecules Although a cell is mostly water, the rest of the cell consists mostly of carbon-based molecules Organic chemistry.
Macromolecules. Composed of long chains of smaller molecules Macromolecules are formed through the process of _____________. Polymerization= large compounds.
The Chemistry of Life: Organic Compounds The Chemistry of Life: Organic Compounds Chapter 3.
Chapter 5: The Structure and Function of Macromolecules.
6.3 a – Introduction to Biomolecules. What is an organic compound? What is so special about Carbon? Compounds containing C, H, O and often N, P, & S.
Organic Compounds “Macromolecules”.
Macromolecules Carbon based molecules
Chapter 3 Carbohydrates and Lipids. You Must Know The cellular functions of carbohydrates and lipids. How the sequence and subcomponents of carbohydrates.
Macromolecules Chapter 5 All are polymers Monomer – subunit of polymer Macromolecule – large organic polymer Those found in living systems: Carbohydrates.
Copyright © 2005 Pearson Education, Inc. publishing as Benjamin Cummings Overview: The Molecules of Life Within cells, small organic molecules are joined.
Biochemistry. I. Water A. Uneven charge on molecule makes it polar. 1. Good solvent- Breaks up ionic compounds. 2. Dissolves other polar molecules. B.
The Chemical Building Blocks of Life Chapter 3. 2 Biological Molecules Biological molecules consist primarily of -carbon bonded to carbon, or -carbon.
The Chemistry of Life Chapter 2-3 What macromolecules are important to living things? What are the functions of each group of macromolecules?
Large Molecules are the Hallmark of Life
What are macromolecules?
Chapter 3: Biochemistry
The Structure and Function of Large Biological Molecules
The Chemical Building Blocks of Life
Immagini e concetti della biologia Sylvia S. Mader
Chapter 5 The Molecules of Life.
Part 2: Organic Chemistry (Carbon and Macromolecules)
Chapter 5 The Structure and Functions of Large Biological Molecules
Polymers Most macromolecules are polymers build from monomers.
AP Review Chapters 2-5.
Warm up! Grab your composition book
ORGANIC COMPOUNDS Bio CP.
Carbohydrates and Lipids
The Molecules of Cells Chapter Three.
copyright cmassengale
Carbon-based molecules are the foundation of life
The Exciting World of Organic Compounds.
Lipids Lipids are hydrophobic molecules Mostly C-H (non-polar)
BIOCHEMISTRY The chemistry of Life
Structure and Function of Macromolecules
AP Review Chapters 2-5.
The Molecules of Cells Chapter Three.
The Molecules of Cells Chapter Three.
Chapter 2 The Chemistry of Life Part 2
Immagini e concetti della biologia Sylvia S. Mader
Nucleic acids.
copyright cmassengale
copyright cmassengale
The Molecules of Cells Chapter Three.
Macromolecules.
The building blocks of LIFE
copyright cmassengale
Macromolecules Introduction
Bio-Macromolecules.
Structure and Function of Macromolecules
Chapter 3 Biological Molecules
Structure and Function of Macromolecules
The Structure and Function of Macromolecules
TOPIC 3.2 Carbohydrates, Lipids and Proteins
The Molecules of Cells Chapter Three.
Presentation transcript:

1.0 MOLECULES OF LIFE BY : MDM. NURFAZLINI ISMAIL (MDM FAZ) 1.1 Water 1.2 Carbohydrates 1.3 Lipids 1.4 Proteins 1.5 DNA and RNA molecules faz/molecules of life/2018

faz/molecules of life/2018 1.1 WATER At the end of this topic, students should be able to : Explain the structure of water and properties of water molecule. faz/molecules of life/2018

faz/molecules of life/2018

Molecular Structure Of Water Water is composed of : 2 hydrogen atoms and 1 oxygen atom. The chemical formula is H2O. Each H is linked to O by a single covalent bond. faz/molecules of life/2018

faz/molecules of life/2018 Covalent bond Hydrogen atoms Oxygen atom faz/molecules of life/2018

faz/molecules of life/2018

faz/molecules of life/2018

faz/molecules of life/2018 Water is a polar molecule. One end (oxygen) is slightly negative One end (hydrogen) is slightly positive Oxygen is more electronegative than hydrogen. Tends to attract more electrons. faz/molecules of life/2018

faz/molecules of life/2018 The bond angle between the hydrogen and the oxygen is 104.5o Producing an electric dipole. faz/molecules of life/2018

faz/molecules of life/2018 Polarity allows water molecules to form hydrogen bonds with each other The slightly negative regions of one water molecule are attracted to the slightly positive regions of nearby water molecules, forming hydrogen bonds. Each water molecule can form hydrogen bonds with up to four neighbors. faz/molecules of life/2018

faz/molecules of life/2018 Covalent bond Hydrogen bond faz/molecules of life/2018

H O H  – Hydrogen bond  +  –  +  –  +  –  + —— —— Fig. 3-2 Figure 3.2 Hydrogen bonds between water molecules  +

Properties Of Water Molecule Universal Solvent ( Polar Molecule) Low Viscosity High Specific Heat Capacity High Latent Heat of Vaporization High Surface Tension Maximum Density at 4⁰C Due hydrogen bonding between polar water molecules faz/molecules of life/2018

faz/molecules of life/2018 1.2 CARBOHYDRATES At the end of this topic, students should be able to : State the classes of carbohydrates such as monosaccharides, disaccharides and polysaccharides. faz/molecules of life/2018

faz/molecules of life/2018 An organic compound containing the elements carbon, hydrogen, and oxygen. (CH2O)n ; n = no. of carbon atom. Most abundance class of organic compound. Three main classes of carbohydrates: Monosaccharides Disaccharides Polysaccharides faz/molecules of life/2018

faz/molecules of life/2018 Monosaccharides Monosaccharide composed of one sugar unit. Glucose (C6H12O6) is the most common monosaccharide. Monosaccharides serve as : major energy source for cells. Component in the synthesis of other compound. Major nutrients for cell. faz/molecules of life/2018

faz/molecules of life/2018 Monosaccharides molecule contain carbonyl group (-C=O) at only one of C atom and hydroxyl groups (-OH) at all another C atom. Monosaccharides are classified by The location of the carbonyl group (as aldose or ketose) The number of carbons in the carbon skeleton faz/molecules of life/2018

faz/molecules of life/2018

(a) α and β glucose ring structures Figure 5.7 Starch and cellulose structures (a) α and β glucose ring structures

faz/molecules of life/2018 Disaccharides A disaccharide is formed when two monosaccharides joined by a glycosidic linkage. Glycodisic linkage is a covalent bond formed by a condensation reaction between two MS. Condensation reaction involves the removal of H atom from one sugar and –OH group from another (removal of a water molecule) faz/molecules of life/2018

faz/molecules of life/2018 Main disaccharides: Maltose (glucose + glucose) Sucrose (glucose + fructose) Lactose (glucose + galactose) faz/molecules of life/2018

(a) Dehydration reaction in the synthesis of maltose 1–4 glycosidic linkage Glucose Glucose Maltose (a) Dehydration reaction in the synthesis of maltose 1–2 glycosidic linkage Figure 5.5 Examples of disaccharide synthesis Glucose Fructose Sucrose (b) Dehydration reaction in the synthesis of sucrose

faz/molecules of life/2018 Polysaccharides Polysaccharides, the polymers of sugars, have storage and structural roles The structure and function of a polysaccharide are determined by its sugar monomers and the positions of glycosidic linkages faz/molecules of life/2018

faz/molecules of life/2018 POLYSACCHARIDES faz/molecules of life/2018

Storage polysaccharides Both made up of α glucose monomers. Starch A storage polysaccharide of plants Plants store surplus starch as granules within chloroplasts and other plastids Glycogen Is a storage polysaccharide in animals Humans and other vertebrates store glycogen mainly in liver and muscle cells faz/molecules of life/2018

(a) Starch: a plant polysaccharide Chloroplast Starch Mitochondria Glycogen granules 0.5 µm 1 µm Figure 5.6 Storage polysaccharides of plants and animals Amylose Glycogen Amylopectin (a) Starch: a plant polysaccharide (b) Glycogen: an animal polysaccharide

Structural polysaccharides The polysaccharide cellulose is a major component of the tough wall of plant cells Like starch, cellulose is a polymer of glucose, but made up of β glucose faz/molecules of life/2018

Cell walls Cellulose microfibrils in a plant cell wall Microfibril Fig. 5-8 Cell walls Cellulose microfibrils in a plant cell wall Microfibril 10 µm 0.5 µm Cellulose molecules Figure 5.8 The arrangement of cellulose in plant cell walls Glucose monomer

faz/molecules of life/2018

faz/molecules of life/2018 1.3 LIPIDS At the end of this topic, students should be able to : State the types of lipids: triglycerides (fat & oil), phospholipids and steroids. faz/molecules of life/2018

General Features of Lipids Lipids contain C, H and O but have a much smaller proportion of oxygen compared to a molecule of carbohydrate The ratio of 0 : H is lower than carbohydrates. The C-H bond is stronger than those in carbohydrates. Stores large amount of energy. Release higher energy when broken down faz/molecules of life/2018

faz/molecules of life/2018 Types of lipids Triglyceride (fats and oil) Triglycerides are constructed from two types of smaller molecules: glycerol and fatty acids Glycerol is a three-carbon alcohol with a hydroxyl group attached to each carbon A fatty acid consists of a carboxyl group attached to a long carbon skeleton In a fat, three fatty acids are joined to glycerol by an ester linkage, creating a triglyceride faz/molecules of life/2018

Fatty acid (palmitic acid) Glycerol (a) Dehydration reaction in the synthesis of a fat Ester linkage Figure 5.11 The synthesis and structure of a fat, or triacylglycerol (b) Fat molecule (triacylglycerol)

faz/molecules of life/2018 Phospholipid In a phospholipid, two fatty acids and a phosphate group are attached to glycerol The two fatty acid tails are hydrophobic, but the phosphate group and its attachments form a hydrophilic head Phospholipids are the major component of all cell membranes faz/molecules of life/2018

Choline Phosphate Hydrophilic head Glycerol Fatty acids Hydrophobic tails Figure 5.13 The structure of a phospholipid (a) Structural formula (b) Space-filling model

faz/molecules of life/2018 Steroids Steroids are lipids characterized by a carbon skeleton consisting of four fused rings Cholesterol, an important steroid, is a component in animal cell membranes Although cholesterol is essential in animals, high levels in the blood may contribute to cardiovascular disease faz/molecules of life/2018

Figure 5.15 Cholesterol, a steroid

faz/molecules of life/2018 1.4 PROTEINS At the end of this topic, students should be able to : Describe the basic structure of amino acids State how amino acids are grouped faz/molecules of life/2018

General features of Protein The monomer is amino acids. Amino acids are organic molecules with carboxyl and amino groups, a hydrogen atom and R group side chain. All are covalently linked to the same carbon atom Amino acids are amphoteric molecules. have both acidic (-COOH) and basic (-NH2 ) faz/molecules of life/2018

faz/molecules of life/2018

faz/molecules of life/2018 Amino acids differ in their properties due to differing side chains, called R groups R groups: Non-polar hydrophobic Polar hydrophilic Electrically charged Basic Acidic faz/molecules of life/2018

faz/molecules of life/2018 NON-POLAR AMINO ACID faz/molecules of life/2018

faz/molecules of life/2018 POLAR AMINO ACID faz/molecules of life/2018

faz/molecules of life/2018 ELECTRICALLY CHARGED faz/molecules of life/2018

faz/molecules of life/2018 1.5 DNA AND RNA MOLECULE At the end of this topic, students should be able to : State the structures of nucleotide as the basic composition of nucleic acids (deoxyribonucleic acid, DNA and ribonucleic acid, RNA) State the types of RNA faz/molecules of life/2018

Structure of nucleotide Nucleotide is the basic unit for nucleic acids. Polynucleotide is made of nucleotides There are two types of nucleic acids: Deoxyribonucleic acid (DNA) Ribonucleic acid (RNA) mRNA tRNA rRNA faz/molecules of life/2018

faz/molecules of life/2018 Nitrogenous bases Pentose sugar faz/molecules of life/2018

(c) Nucleoside components: sugars Deoxyribose (in DNA) Ribose (in RNA) Figure 5.27 Components of nucleic acids (c) Nucleoside components: sugars

faz/molecules of life/2018 There are two types of nitrogenous bases: Pyrimidines (cytosine, thymine, and uracil) have a single six-membered ring Purines (adenine and guanine) have a six-membered ring fused to a five-membered ring In DNA, the sugar is deoxyribose; in RNA, the sugar is ribose faz/molecules of life/2018

(c) Nucleoside components: nitrogenous bases Pyrimidines Cytosine (C) Thymine (T, in DNA) Uracil (U, in RNA) Purines Figure 5.27 Components of nucleic acids Adenine (A) Guanine (G) (c) Nucleoside components: nitrogenous bases