Bio Final
3-1 Macromolecules
Carbon Based Life
All living things on Earth made up of molecules based on carbon
Carbon can bond with many elements to form molecules of life
These include hydrogen, oxygen, nitrogen, and phosphorus
Carbon atoms able to form long chains of carbon-carbon bonds
Due to carbon/s ability to bond with other carbon atoms, it has ability to form millions of different large and complex structures
Macromolecules
Macromolecules: Large organic compounds that make up living cells
Forming Macromolecules:
Most macromolecules (ex: carbohydrates, nucleic acids, and proteins) formed through process called polymerization
Polymerization: Process in which large compounds are built by joining smaller compounds together
Monomers: The smaller compounds
Polymers: The large compounds
Carbohydrates
Carbohydrates are the main source of energy used by living things
Carbohydrates: Compounds made from carbon, hydrogen, and oxygen atoms. (Quick short bursts of energy that come from sugar)
Breakdown of sugars by mitochondria serve as main source of energy for cellular activity
Animals store excess sugar in polysaccharide called glycogen. When they need sugar they break the glycogen molecules down
Plants store excess sugar in polysaccharide called starch
Polysaccharides: long chains of carbohydrate molecules
Plants and some other organisms use carbohydrates for structural purposes
EX: Plants using cellulose, a polysaccharide as structural component
EX: Fungi, insects, and crustaceans using another polysaccharide, chitin, as structural component in bodies
Carbohydrate Monomers and Polymers
The monomers of carbohydrates are monosaccharides or single sugars
EX: Glucose
Polysaccharides are large macromolecule carbohydrates
Nucleic Acids
Nucleic acids: Store and transmit genetic information
Two kinds: DNA and RNA
Nucleic acids are macromolecules that contain carbon, hydrogen, oxygen, nitrogen, and phosphorous
Nucleic Acid Monomers and Polymers
The individual monomers of nucleic acids are nucleotides
Each nucleotide has 3 parts: a nitrogenous base, a 5-carbon sugar, and a phosphate group
Nucleic acids (DNA & RNA) are large macromolecules assembled from nucleotides
Proteins
Proteins: macromolecules that contain carbon, hydrogen, oxygen, and nitrogen
Proteins serve diverse array of functions, like forming important cellular or body structures, fighting disease, transport of materials, regulation of cell processes, and acting as enzymes
Protein Monomers and Polymers
Monomers that make up proteins are amino acids
When joined together, amino acids form polypeptides, which intern interact with other polypeptides to form proteins
Enzymes:
Enzymes: Proteins that can speed up the rate of a chemical reaction
Living organisms require enzymes to perform chemical reactions that make life possible
Changes in temperature, pH, and presence of regulatory molecules can affect rate of enzyme activity
Lipids
Lipids: The only macromolecules that are not polymer
Not considered polymers because they are made up of two separate sub-units
Can be used to story energy and act as structural components of organisms where they form biological membranes or act as waterproof body coverings
Steroids are lipids that serve as chemical messengers
Lipids are generally made from mostly carbon and hydrogen atoms
Lipids consist of two main components: a glycerol and fatty acid
3-2 Enzymes
Enzymes are proteins that can speed up the rate of a chemical reaction
Also called catalysts because they catalyze (speed up) a chemical reaction
These chemical reactions used to build and break molecules
Sum of all these chemical reactions in a cell called metabolism
Enzymes are not changed or used up in chemical reaction
Enzyme Function
Enzymes lower a reaction’s activation energy
Activation Energy: The amount of energy needed for a reaction to begin
Steps in a Chemical Reaction
The enzyme will bind to a reactant molecule at the enzyme's active site.
Substrate: Reactant molecule
When the substrate is bound to the enzyme, it forms the enzyme-substrate complex
The chemical reaction occurs, creating the product
The product is released from the enzyme’s active site
Enzyme Specificity
Enzymes are specific for the substance they bind to
EX: Lock and key - an enzyme's active site is structured to match the specific substrate it binds to
Enzyme Changes
Changes in temperature, pH, and presence of regulatory molecules can affect rate of enzyme activity
When favorable conditions change, enzyme can be denatured
When enzyme is denatured, its shape has changed and it can no longer function correctly to catalyze chemical reactions
Enzymes do not die since they are not living, but it can restructure itself and function again
3-3 Energy and Life
Intro
Energy: the ability to do work
Comes in many forms
EX: Light, heat, and electricity
Can be stored in chemical bonds
When bonds are broken, energy stored in the bonds are released and the atoms reform new, lower-energy bonds
Life is dependent on ability to obtain and use energy
Chemical Energy and ATP
ATP: One of the most important compounds that cells use to store and release energy
Stands for adenosine triphosphate
Consists of the nitrogenous base adenine, a 5-carbon sugar called ribose, and three phosphate groups
Chemical Energy and ATP
ATP can easily be release and store energy by breaking and forming bonds between its phosphate groups
Energy is stored in the bonds connecting the phosphate groups
ATP’s ability to store and release energy comes from breaking bond between the 2nd and 3rd phosphate groups
When the third phosphate group is broken off the ATP molecule, energy is release and the ATP molecule becomes ADP (Adenosine diphosphate)
When cell has energy available it can use that energy to reattach a phosphate group to an ADP molecule, changing it back to ATP
When there are three phosphate groups energy is stored (ATP) and when there are two (ADP) energy has been released.
Cells and Energy
Cells use ATP to power several important processes:
Active transport
Movement
Bioluminescence
Protein Synthesis
Drawbacks of ATP
ATP is important and useful for cells, but it’s not a good molecule for storing large amounts of energy long term
Cells use molecules like glucose to store energy in the long term because they are more stable and store more energy
The energy in a molecule of glucose can be converted to ATP
Heterotrophs and Autotrophs
All living things must take in energy to power their life processes
Heterotrophs: Must consume other living things in order to obtain energy
Autotrophs: Organisms that are able to make their own food
Most autotrophs use photosynthesis to convert energy from sun into high-energy carbohydrates
In process of photosynthesis, plants convert energy of sunlight into chemical energy stored in bonds of carbohydrates
3-4 Photosynthesis
Intro
Photosynthesis: Process by which organisms, like plants and other autotrophs, capture light energy and use it to power chemical reactions that convert carbon dioxide and water into oxygen and energy-rich carbohydrate such as sugars and starches
Almost all living things on Earth depend on the process of photosynthesis
Chlorophyll and Carotenoids
Chlorophyll: The primary pigment used by most plants to capture sunlight
Pigment: A light absorbing molecule
Carotenoids: Red, orange, and yellow pigments. The color imparted by carotenoids is usually only visible when chlorophyll breaks down or is absent
Carotenoids CAN absorb sunlight, but chlorophyll mainly does
Chloroplasts and Chlorophyll
Chloroplasts: Organelles found in the cells of photosynthetic eukaryotes that capture energy from the sun and convert it into chemical energy
Parts of the Chloroplast:
Thylakoids: Saclike photosynthetic membranes found inside chloroplasts
Granum: A stack of thylakoids
Stroma: The fluid portion of the chloroplast outside the thylakoids
Energy Collection
Chlorophyll absorbs visible light and transfer the energy in the light to electrons in the chlorophyll molecule (what exists in the chloroplasts to take in light energy)
The rest of the process of photosynthesis relies on making use of these high-energy electrons to make carbohydrates
Energy Collections
High energy electrons: High energy electrons that are very reactive and require carrier molecules to transfer them and their energy to another molecule
Electron
carrier: Compound that can accept a pair of high-energy electrons and transfer them and most of their energy to another moleculeNADP+: A carrier molecule able to hold two high-energy electrons along with a hydrogen atom
When NADP+ does this,, it is converted to NADPH
When you see the +, that means the carrier is empty. When it is full (holding onto two electrons), it is converted to NADPH
An Overview of Photosynthesis
The process of Photosynthesis
Light dependent reactions: The first set of reactions in the process of photosynthesis
These reactions require direct involvement of light and light-absorbing pigments
Take place in thylakoid membranes of chloroplasts
Thylakoids contain clusters of chlorophyll and proteins known as photosystems
Photosystems: Absorb sunlight and transfer high-energy electrons to an electron transport chain
Electron transport chain: Series of carrier proteins that move high energy electron during the process of making ATP
The electrons sent through the electron transport chain come from breaking apart water molecules
Light-dependent reactions use energy from sunlight to break up water molecules
They produce oxygen and convert ADP and NADP+ into the energy carriers ATP and NADPH
The light-independent reactions (The Calvin cycle)
Cycle that makes use of several different molecules that are regenerated o that the cycle can continue
Light-independent reactions: Complete the process of photosynthesis and produce the carbohydrates
These reactions use the energy in ATP and NADPH as well as carbon dioxide to build carbohydrates
During light-independent reactions, the ATP and NADPH produced in the light-dependent reactions are used to produce high-energy sugars from carbon dioxide
Carbon dioxide used in Calvin cycle comes from atmosphere
The light-independent reactions take place in the stroma
3-5 Cellular Respiration
Cellular Respiration
Cellular respiration: Process that releases energy from food in presence of oxygen
Can be sumymarized by the following equation
Oxygen
Aerobic: The pathways (or steps) in cellular respiration that require oxygen
Anaerobic: The pathways (or steps) in cellular respiration that do not require oxygen
Comparing Cellular Respiration & Photosynthesis
Photosynthesis and cellular respiration can be seen as opposite processes
Cellular respiration removes oxygen from atmosphere and photosynthesis puts it back
Photosynthesis removes carbon dioxide from atmosphere and cellular respiration puts it back
Stages of Cellular Respiration
Occurs in three stages
Glycolysis
The Krebs cycle
The electron transport chain
Glycolysis
Glycolysis: The first stage in cellular respiration, takes place in the cytoplasm
During glycolysis, 1 molecule of glucose (a 6-carbon compound) is broken into 2 molecules of pyruvic acid ( a 3-carbon compound)
Glycolysis also produces 2 NADH molecules that are sent to the electron transport chain
NADH: Full electron carrier, anytime there is an H it’s full, and you can differentiate between NADPH because there is no P meaning it's not photosynthesis
The goals of glycolysis are the electron carriers NADH and pyruvic acid
The ATP of Glycolysis
In order to break apart the glucose molecule, th cell must spend 2 ATP molecules
The process of glycolysis produces 4 ATP molecules
The cell realizes a net gain of 2 ATP molecules
The Krebs Cycle
Krebs cycle: The second stage of cellular respiration, takes place in the mitochondria
During Krebs cycle, pyruvic acid is broken down into carbon dioxide in a series of energy releasing steps
Krebs cycle also produces 8 molecules of NADH and 2 molecules of FADH2 (both are full) that are sent to the electron transport chain
The ATP Math of the Krebs Cycle
Krebs cycle produces one molecule of ATP for each molecule of pyruvic acid that enters the cycle
One molecule of glucose produces 2 molecules of pyruvic acid, thus 2 ATP molecules are produced
The Electron Transport Chain
Electron transport chain: Uses high energy electrons from glycolysis and the Krebs cycle to convert ADP to ATP
High-energy electrons are transferred to the electron transport chain by the carrier molecules NADH and FADH
Electron transport chain is located in the inner membrane of the mitochondria
The electron transport chain produces 32 molecules of ATP
Purpose of ATP synthase is to catalyze the reaction of making ATP
Summary
The process of cellular respiration (glycolysis, the Krebs cycle, and the electron transport chain) produce 36 ATP molecules from one molecule of glucose
This represents 36% of the total energy available in the glucose molecule, the remaining 64% is lost as heat
3-6 Cell Structure
Cell Structure
Two types of organisms: Prokaryotes and Eukaryotes
Prokaryotes: Organisms made up of cells that do not have membrane-bound organelles
Two groups of prokaryotes, bacteria and archaea
Bacteria can be classified as harmful or helpful
Bacteria if it causes disease
Archaea are unique life form found to live in extreme environments
Archaea have been found in hydrothermal vents in ocean, and arctic ice
Eukaryotes: Organisms made up of cells that have membrane-bound organelles
Three groups of eukaryotes are plants, animals, and fungi
Prokaryotic cells are simple in comparison to eukaryotic cells
Typically, they are single celled organisms
Eukaryotes are much more complex than prokaryotes, and are multi-celled organisms
Cell Organization
Eukaryotes and prokaryotes have distinct cell organization
Cells can be divided into two main sections: Nucleus/nucleoid and cytoplasm
Nucleus and nucleoid
In prokaryotic cells, there is no membrane bound nucleus. Instead DNA is stored in region called the nucleoid
In eukaryotic cells, there is a membrane bound nucleus. Nucleus stores nearly all of cell’s DNA and controls most of cell’s activity and hold instructions to make proteins
Cytoplasm
The cytoplasm is the inside of the cell
In prokaryotes, everything inside cell is located in cytoplasm because prokaryotes do not have membrane bound organelles
In eukaryotes, the majority of cells’ organelles are located in the cytoplasm
Organelles: Specialized structures that perform important cellular functions
Storage, Cleanup, and Support
Eukaryotic cells have organelles responsible for storage, cleanup, and support
Vacuoles, lysosomes and cytoskeleton fulfill the roles of storage cleanup, and support in cell
Vacuoles and Vesicles
Vacuoles: Cellular organelles that store materials like water, salts, proteins, and carbohydrates
Vesicles: Smaller membrane enclosed structures that store and move materials between organelles
Lysosomes
Lysosomes: Small organelles that are filled with enzymes
Enzymes contain in lysosomes break down lipids, carbohydrates, and proteins into small molecules that can be used by rest of cell
Cytoskeleton
Cytoskeleton: Network of protein filaments in a eukaryotic cell that gives the cell its shape and internal organization and is involved in movement
Microfilaments: Thread like structures that support the cell
Microfilaments also help cell move
Microtubules: Hollow structures that help to maintain cell shape
Cell Movement
Prokaryotes have flagella and pili are protein-based filaments found on the outer surface of the cell to help prokaryotes move
Building Proteins
Eukaryotes have organelles responsible for building proteins
Cells need to build new molecules all the time, especially proteins, which catalyze chemical reactions and make up important structures in cell
Since proteins carry out many of essential functions in living things, big part of cell is devoted to their production and distribution
Ribosomes
Ribosomes: Small particles of RNA and protein found throughout the cytoplasm in all cells that produce proteins
Endoplasmic Reticulum:
Two types: smooth and rough
Endoplasmic reticulum is where lipid components of cell membrane are assembled, along with proteins and other materials that are exported from cell
Rough endoplasmic reticulum
Portion of the ER involved in synthesis of proteins
Given this name because ribosomes are found in its surface
Newly made proteins leave these ribosomes and are inserted in the rough ER, where they may be chemically modified
Smooth endoplasmic reticulum
Called smooth ER because ribosomes are not found on its surface
In many cells, smooth ER contains collections of enzymes that perform specialized tasks, including synthesis of membrane lipids and detoxification of drugs
Golgi Apparatus
Golgi apparatus: Modifies, sorts, and packages proteins and other materials from the ER for storage in the cell or release outside the cell
Proteins produced in rough ER move next into golgi apparatus, which appears as stack of flattened membranes
The proteins are bundled into tiny vesicles that bud from the ER and carry them to the Golgi apparatus
Capturing and Releasing Energy
Eukaryotes have organelles responsible for capturing energy and releasing energy
All living things require a source of energy. Most cells are powered by food molecules that are built using energy from sun
Chloroplasts and mitochondria both involved in energy conversion process within cell
Chloroplasts
Chloroplasts: Capture energy from sunlight and convert it into food that contains chemical energy in a process called photosynthesis
Mitochondria
Mitochondria: Convert the chemical energy stored in food into compounds that are more convenient for the cell to use
Cell Boundaries
Eukaryotes and prokaryotes are made up of cells with important cell boundaries
Cell Walls
Main function of cell wall is to provide support and protection for cell
Prokaryotes, plants, algae, fungi, and have cell walls
Animal cells do not have cell walls
Cell walls lie outside the cell membrane and most are porous enough to allow water,, oxygen, carbon dioxide, and certain other substances to pass through easily
Cell Membrane
Cell membrane regulates what enters and leaves the cell and also protects and supports the cell
The composition of nearly all cell membranes is a double-layered sheet called a lipid layer, which gives cell membranes a flexible structure and forms a strong barrier between the cell and its surroundings
3-7 Introduction to Homeostasis
The Cell as an Organism
Homeostasis: The existence and maintenance of a relatively constant environment within the body of an organism
To maintain homeostasis, unicellular organisms grow, respond to the environment, transform energy and reproduce
Unicellular organisms are capable of surviving and performing all life processes on their own
Can include both prokaryotes and eukaryotes
In terms of number of individuals, single-celled organisms make up majority of life on Earth
Multicellular Life
Cells in multicellular organisms are not capable of surviving on their own. They require the “services” of other cells in order to survive
Cells of multicellular organisms become specialized for particular tasks and communicate with one another to maintain homeostasis
Different cell types play different roles within the organism
Specialized cells in multicellular organisms are organized into different levels
Cells make up tissues
Tissue: Similar group of cells that perform a particular function
Tissues make up organs
Organ: A group of tissues that work together to carry out complex function
Organs make up systems
Organ System: A group of organs that work together to carry out complex functions
Cells in multicellular organisms must communicate to survive
This communication is accomplished by means of chemical signals passed from one cell to another
These signals can slow down or speed up cellular activity
Cells have receptors onto which signaling molecules can bind
Limits to Cell Size
The larger a cell becomes, the more demands the cell places on its DNA
Additionally, a larger cell is less efficient in moving nutrients and waste materials across its cell membrane
Information Overload
Living cells store satirical information in DNA
As a cell grows, that info is used to build the molecules needed for growth
As cell size increases, the demands on that information grow as well
If a cell were to grow without limit, an “information crisis” would occur
Division of the Cell
Cell division: A cell splitting into two new “daughter cells” before becoming too large
Before cell division the cell copies all of its DNa
It then divides into two “daughter” cells. Each daughter cell receives a complete set of DNA
Cell division reduces cell volume
Homeostasis
Homeostasis: The existence and maintenance of a relatively constant environment within the body of an organism
Each cell in the body is surrounded by a small amount of fluid and the normal functioning of the cell is dependent on the maintenance of its environment within a narrow range of conditions
Like all organisms, animals must maintain homeostasis by:
Gathering and responding to information
Obtaining and distributing oxygen and nutrients
Collection and eliminating carbon dioxide and other wastes
Reproduction
Feedback
Regulating homeostatic control system
Most homeostatic control systems function by negative feedback
In negative feedback, a buildup of the end product of the system shut the off
Some homeostatic control systems function by positive feedback
In positive feedback, a change in some variable that triggers mechanisms that amplify the change (Instead of going back to an end up point, were trying to get to and end goal then shut down the system)
Essential Functions Animals Perform to Survive
One way homeostasis is maintained is by feedback inhibition
Negative Feedback: A system in which the product or result of a process limits the process itself
EX: Your house is getting too cold so your thermostat turns on the heat. As the heat warms the house, the thermostat turns the heater off.
Body’s thermostat works the same way
If you get too cold you shiver, using muscle activity to generate heat. If you get too hot you sweat, which helps you lose heat
All body systems work together to maintain homeostasis
In most animals, repository and digestive system would be useless without circulatory systems to distribute oxygen and nutrients
The excretory system needs a circulatory system to collect carbon dioxide and nitrogenous wastes from body tissues and deliver them to the lungs and excretory organs
Muscles wouldn't work without a nervous system to direct them and a skeletal system to support them
4-1 Discovering DNA
Intro:
Many discoveries in science come when scientists are looking for something completely different
Discovery of the structure of DNA is an example
In 1928 scientist named Fredrick Grifffth was trying to figure out how bacteria make people sick
Bacterial Transformation
Griffith’s Experiment:
Griffith isolated two different strains of the same bacterial species
He then injected mice with both strains of th bacteria
Mice that got the S strain got pneumonia and died
Mice that got the R strain stayed healthy
Girffith then heat killed the strain of bacteria and mixed it with R strain of bacteria and injected it into mice
The mice died of pneumonia
When he cultured the bacteria in their lung, he found live S strain bacteria
Griffith’s Reasoning
Reasoned that some chemical factor that could change harmless bacteria into disease-causing bacteria was transferred from the heat-killed cells of the S strain into the live cells of the R strain
He called this Transformation
Transformation: Process in which one strain of bacteria is changed by a gene or genes from another strain of bacteria
Concluded that the chemical factor was a gene
Griffith’s work continued by a group of scientists led by Oswald Avery
Avery’s group wanted to determine which molecule was responsible for transformation
Avery’’s Experiment:
In 1944, Avery extracted molecules from the heat killed bacteria and treated them with different chemicals designed to destroy different molecules including proteins, lipids, carbohydrates, and RNA
Even after all of these molecules were destroyed transformation still occurred
Avery then destroyed the DNA and transformation did not occur
Avery’s Conclusion: DNA was the transforming factor
By observing bacterial transformation, Avery and other scientists discovered that the nucleic acid DNA stores and transmits genetic information from one generation of bacteria to the next
The Hershey-Chase experiment
Bacteriophage: A virus that infects bacteria
Bacteriophages work by injecting their genetic material into a bacterium. This DNA then hijacks the cell's machinery and produces more viruses. Eventually the cell bursts open and the new viruses burst out and go on to infect other bacteria
In 1952, Hershey and Chase wanted to determine which part of the virus, the protein cat or DNA core infected the cell
Hershey and Chase grew viruses in cultures containing radioactive isotopes of phosphorus-32 (p-32) sulfur-35 (S-35)
The two scientists mixed the marked viruses with bacterial cells, waited a few minutes for the viruses to inject their genetic material, and then tested the bacteria for radioactivity
Nearly all the radioactivity in the bacteria was from phosphorus P-32, the marker found in DNA
Hershey and Chase concluded that the genetic material of the bacteriophage was DNA, not protein
Heryshey and Chase’s experiment with bacteriophage confirmed Avery’s results, convincing many scientists that DNA was the genetic material found in genes - not just living organisms.
Solving the structure of DNA
Chargaff’s Rule
In 1949, Chargaff discovered that the percentages of adenine [A] and thymine [T] bases are almost equal in any sample of DNA. The same thing is true for the other two nucleotides, guanine [G] and cytosine [C]
The observation that [A]=[T] and [G]=[C] became known as “Chargaff’s rules”
In 1952, Rosalind Franklin used a technique called X-ray diffraction to get information about the structure of the DNA molecule
X-ray diffraction revealed an X-shaped pattern showing that the strands in DNA are twisted around each other like the coils of a spring
The angle of the X-shaped pattern suggested that there are two strands in the structure
Other clues suggest that the nitrogenous bases are near the center of the DNA molecule
Work of Watson and Crick
In 1953, Watson and Crick built 3 dimensional models of DNA
The clues in Franklin's X-ray pattern enabled Watson and Crick to build a model that explained the specific structure and properties of DNA
Watson and Crick’s breakthrough discovery was the double helix model of DNA
In the double helix model two strands of nucleotide sequences are wound around each other - like a spiral staircase
The Double Helix Model
The Double helix model explains Chargaff’s rule of base pairing and how the two strands of DNa are held together
In the double-helix model, the two strand of DNA are “antiparallel”- they run in opposite directions
This arrangement enables the nitrogenous bases on both strands to come into contact at the center of the molecule
Nitrogenous bases are held together by hydrogen bonds
Hydrogen bonds are relatively weak chemical forces that allow the two strands of helix to separate
The ability of the two strands to separate is critical to DNA’s functions
Watson and Crick discovered that bases pair in a specific way.
The hydrogen bonds needed to hold the nucleotides together only form in specific ways
Adenine will only pair with Thymine
Cytosine will only pair with Guanine
Base pairing is the principle that bonds DNA can form only between adenine and thymine and between cytosine and guanine
Pulse-Chase Primer: The Meselson-Stahl Experiment
In the 1950s, James Watson and Francis Crick suggested a mechanism for the replication of DNA, which they called the “Semiconservative model of Replication”
During replication, each of the two strands of DNA would act as a template for the synthesis of a new strand. The two new DNA molecules would consist of one strand from the original molecule and a newly synthesized strand
At the time, scientists were considering three possible replication models
Conservative replication
Semiconservative replication
Dispersive replication
In 1958, Matthew Meselson and Franklin Sthal conducted their now-famous pulse-chase experiment to determine which of these three models was correct
Their experiment demonstrated that DNA goes through semiconservative replication
4-2 The Structure and Function of DNA
The Components of DNA
DNA: A nucleic acid made up of nucleotides joined into long strands or chains by covalent bonds
Nucleotides are the building blocks of nucleic acids
Nucleotides are made up of three components:
A 5-Carbon sugar
In DNA, the 5-carbon sugar is deoxyribose
A phosphate group
A nitrogenous base
Nitrogenous bases are bases that contain nitrogen
In DNA there are four nitrogenous bases. These bases are referred to y scientists by the first letter of their name
Adenine - A
Guanine - G
Cytosine - C
Thymine - T
Nucleotides in DNA on the same strand are joined together by covalent bonds
Covalent bond: electrons pairs being shared between two atoms
The nucleotides can be joined together in any order, meaning that any sequence of bases is possible
Nucleotides in DNA on opposite strands are joined together by hydrogen bonds
A bonds with T
G bonds with C
The Role of DNA
The DNA that makes up genes must be able to store, copy, and transmit genetic information in a cell
DNA has three functions:
Storing Information
DNA is the molecule of heredity, meaning that its most important job is storing information
Genes control patterns of development, which means that the instructions that cause a single cell to develop into an oak tree or a dog must be written into the DNA of each of these organisms
Copying Information
Before a cell divides, it must make a complete copy of every one of its genes
Transmitting Information
When a cell divides, each daughter cell must receive a complete copy of the genetic information
DNA Molecule:
RNA
RNA (ribonucleic acid) is another nucleic acid that has a different structure and a different function than DNA
Like DNA, RNA is made up of nucleotides joined into long strands of chains by covalent bonds
RNA nucleotides are made up of three components
A 5-Carbon sugar
5-Carbon sugar is Ribose
A phosphate group
A nitrogenous Base
Adenine - A
Cytosine - C
Guanine - G
Uracil - U
4-3 Protein Synthesis
Intro to RNA
Watson & Cricks discovery of the structure of DNA explained how DNA could be copied but not how genes actually work
Discovery of RNA explained how the information in the genetic code is put into action
RNA is a single stranded nucleic acid that contains the sugar ribose
RNA:
Nucleotides in DNA are made of a 5 carbon sugar (deoxyribose), a phosphate group and a nitrogenous base
Three important differences between DNA and RNA
Sugar in RNA is ribose
RNA is single stranded (no double helix)
Rna contain the nitrogenous base uracil in place of thymine
The Role of RNA
DNA is the master plan for the cell and as such is very valuable. If DNA were taken out into the cytoplasm to have it information assessed, it would risk having the information lost or damaged
RNA is produced so that the DNA can remain safely stored in the nucleus
Three types of RNA are involved in taking the information stored in DNA and turning it into proteins
Messenger RNA (mRNA):
Messenger RNA (mRNA) is the type of RNA that carries copies of instructions for the assembly of amino acid into proteins from DNA to the rest of the cell
A set of three bases in mRNA is called a codon, and each codon “codes” for an amino acid
Ribosomal RNA (rRNA):
Ribosomal RNA (rRNA) is the type of RNA that combines with proteins to form ribosomes
Transfer RNA (tRNA):
Transfer RNA (tRNA) is the type of RNA that carries each amino acid to a ribosome during protein synthesis
RNA Synthesis p
Most of the work in making RNA occurs during a process transcription
Transcription: The synthesis of an RNA molecule from a DNA template
In transcription, segments of the transcribed RNA complement the base sequences of the template of DNA
The base sequences of the transcribed RNA compliment the base sequences of the template DNA
The Genetic Code
First step in decoding the genetic messages is to transcribe DNA to RNA
Proteins are made by joining together long chains of amino acids
Polypeptides: Long chains of amino acids
The contents of the polypeptide as well as how it is arranged determines the type of protein
Different proteins have different functions
RNA contains 4 bases: adenine, guanine, cytosine, uracil
These four bases make up the alphabet of RNA
Combination of bases which make up the language of RNA is known as the genetic code
All of the words in this language are made of only three letters
Codon: A three letter word in mRNA
The genetic code is read three letters at a time, so that each word is three bases long and corresponds to a single amino acid
Since there are four different bases in mRNA, 64 codons are possible
RNA has its own punctuation system which signals protein synthesis to start and stop
Methionine is the start of codon
The codon from start mRNA is AUG
Three different stop codons exist
UGA, UAA, and UAG
When a stop codon is reached translation ends
Transcription and Translation
Transcription: The coding of DNA into RNA
In eukaryotes, transcription occurs in the nucleus
In prokaryotes, transcription occurs in the cytoplasm
Translation: The assembling of a protein from mRNA
Ribosomes use the sequence of codons in mRNA to assemble amino acids into polypeptides chains
Translation occurs in the cytoplasm
The process of Translation
After mRNA sequence is transcribed, it enters the cytoplasm and heads for a ribosome to be translate into a protein
Step 1: Initiation
TRanslation begins when a ribosome attaches to an mRNA molecule in the cytoplasm
As the ribosome reads the coded molecules 3 bases at a time searching for the start codon, AUG
When AUG is read, it directs tRNA ti bring the amino acid to methionine into the ribosome
Step 2: Elongation
The ribosome shifts the mRNA molecule to the next codon and reads it
It directs the tRNA to bring the specified amino acid
Each tRNA molecule carries just one kind of amino acid
In addition, each tRNA molecule has three unpaired bases, called the anticodon which are complementary to one mRNA codon
Once the tRNA molecule has dropped off its amino acid, it moves away from the binding site
Step 3: Termination
The polypeptide chain continues to grow until the ribosome reaches a “stop” codon on the mRNA molecule
When the ribosome reaches a stop codon, it releases both the newly formed polypeptide and the mRNA molecule, completing the process of translation
The Molecular Basis of Heredity
Gene expression: The process by which a gene produces its product and the product carries out its function
The central dogma of molecular biology is that information is transferred from DNA to RNA to protein
4-4 Mutations
Intro
Mutation: Any change in the genetic material of a cell
Mutations are heritable changes in genetic information (each new daughter cell will made the mutated cell will have the mutation
Not all mutation are inherited from parent to offspring
Only those taking place in cells that produce gametes (sperm and egg) will be inherited
Types of Mutations
Gene mutations: Mutations that produce a change in a single gene
Chromosomal mutations: Mutations that produce changes in whole chromosomes.
Gene Mutations
Two types of gene mutations
Point mutations
Frameshift mutations
These types of mutations generally occur during DNA replication.
If mistake is not caught, mutation will be passed onto every cell that develops from the original one
Point mutations
Mutations in which a single base pair of DNA has been changed
Substitutions: The only point mutation and occur when on base pair is substituted for another
Substitutions often affect only one amino acid and sometimes have no effect at all
Frameshift Mutations
Frameshift mutations: Mutations that shift the reading frame of the genetic message by inserting or deleting nucleotides
Frameshift mutations can change every amino acid that follows the point of the mutation and can alter protein so much that it is unable to perform its normal functions
Two types of frameshift mutations
Insertions
EX: ACG but insert a T in between two letters and now its ACTG, which is read as ACT. This could change an amino acid
Deletions
EX: ACGATT but delete the G, turning the letters into ACATT, possibly changing the amino acid
If a nucleotide is added or deleted, the bases are still read in groups of three, but now those groupings shift every codon that follows the mutation
Effects of Mutations
Genetic material can be altered by natural events or by artificial means
Many mutations are produced by eros in genetic processes including mistakes during DNA replication, mitosis or meiosis
Some mutations come from mutagens
Mutagen: A chemical or physical agent in the environment which causes mutations
Chemical mutagens include pesticides, tobacco smoke, environmental pollutants, and certain plant alkaloids
Physical mutagens include some forms of electromagnetic radiation, X-rays, gamma rays, UVA & UVB rays are all known mutagens
Effects of mutations can vary widely. They can be:
Silent (or Neutral)
The redundancy of genetic code allows for some mutations to not change the final outcome of a protein
Beneficial
Beneficial mutations are responsible for evolution and contribute to genetic variability within a species
Harmful:
Some of most harmful mutations are those that dramatically change protein structure or gene activity
Defective proteins produced by these mutations can disrupt normal biological activities, and result in genetic disorders
EX: Some cancers are product of mutations that cause the uncontrolled growth of cells
4-5 Reproductive Strategies
Asexual vs. Sexual Reproduction
Prokaryotes and eukaryotes differ in reproduction strategies
Prokaryotes (and some eukaryotes) go through the process of asexual reproduction
In asexual reproduction, a single parent produces offspring that are genetically identical
There are three asexual reproduction strategies: binary fission, budding, and fragmentation
Binary fission: The parent splits in half to create two new organisms
EX: amoeba, paramecium
Budding: The parent will create a small cell known as a bud. The bud will grow and develop, and when it’s mature, it will be released as a new organism
EX: Yeast, coral
Fragmentation: The parent splits into fragments. These fragments will then form into a new organism
EX: Sea Star, lichen
Asexual reproduction is a very fast process, and can be an advantage to many organisms
Most eukaryotes go through process of sexual reproduction
In sexual reproduction, two parents create genetically unique offspring
Parents produce unique cells called gametes that will combine through the process of fertilization to create a new organism called a zygote
Each zygote receives half of their mother’s chromosomes and half of their father’s chromosomes
The gametes that are needed for sexual reproduction are created through a process called meiosis
Meiosis
Meiosis: Cell division that creates gametes: sperm and egg cells
Sexual reproduction combines gametes from two parents to produce a living organism
When gametes are produced, the number of chromosomes just be half
The zygote created from sexual reproduction must contain genetic information from the mother and the father, so the gametes must have half of the chromosomes found in normal body cells
When two gametes come together at fertilization, the normal amount of chromosomes are found (23+23=46)
4-6 Meiosis
Meiosis
Meiosis: Cell division that creates gametes: sperm and egg cells
Sexual reproduction combines gametes from two parents to produce a living organism
When two gametes come together at fertilization, the normal amount of chromosomes are result
Homologous Chromosomes
Human cells have 23 pairs of chromosomes; each chromosome within a pair is a called homologous chromosome
For each of the 23 chromosome pairs, you received one chromosome from your father and one chromosome from your mother. Together they are a homologous pair
Alleles: alternate forms of genes found on chromosomes
Homologous chromosomes have the same genes, but they may have different alleles
Therefore, homologous chromosomes are very similar, but they are not identical
The homologous chromosomes are separated when gametes are formed.
Gametes only have 23 chromosomes, not 23 pairs.
Diploid vs. Haploid
A cell with two sets of chromosomes is diploid
Most of the cells in a human body are diploid
A cell with one set of chromosomes, like a gamete, is haploid
Sex cells are haploid
When a haploid sperm and a haploid egg combine, a diploid zygote will be formed
The process of Meiosis
Before meiosis begins, DNA replication occurs, so each chromosome contains two sister chromatids that are identical to the original chromosome
Meiosis is divided into two divisions: Meiosis I and Meiosis II
Each division can be divided into the same phases as mitosis: Prophase, metaphase, anaphase, and telophase. Cytokinesis follows telophase each time
Between the two cell divisions, DNA replication does not occur
By the end of Meiosis II, one diploid cell will divided into four haploid cells
Meiosis I
During meiosis 1, the pairs of homologous chromosomes are separated from each other
Prophase 1: The homologous chromosomes line up together and exchange genetic information in a process called crossing over. Crossing over forms new combinations of alleles on the resulting chromosome
Without crossing over, the offspring would always inherit all of the alleles on one of the homologous chromosomes. The spindle forms, the chromosomes condense as they coil rightly, and the nuclear envelope disappears
Metaphase 1: The homologous chromosomes line up in their pairs in the middle of the cell
Anaphase 1: The homologous chromosomes are separated, and begin to move to opposite sides of the cell
Telophase 1: The spindle fibers dissolve, but a new nuclear envelope does not need to form. This is because after cytokinesis, the nucleus will immediately begin to divide again
Meiosis II
During meiosis 2, sister chromatids are separated and the gametes are generated.This cell division is similar to mitosis, but results in four genetically unique haploid cells
Prophase 2: The chromosomes condense
Metaphase 2: The chromosomes line up one on top of each other along the middle of the cell (like in mitosis). The spindle is attached to the centromere of each chromosome
Anaphase 2: The sister chromatids separate and move to opposite ends of the cell
Telophase 2: The nuclear envelope forms around the chromosomes in all four cells This is followed by cytokinesis
Meiosis results in four haploid, genetically unique daughter cells. Each cell has half the DNA of the parent cell.
In human cells, the parent cell has 46 chromosomes, so the cells produced by meiosis have 23 chromosomes
Chromosomal Mutations
Chromosomal mutations: Involve changes in the number or structure of chromosomes.
These mutations can change the location of genes on chromosomes and can change the number of copies of some genes
Four types of chromosomal mutations:
Deletion: The loss of all or part of a chromosome
Duplication: Produces an extra copy of all or part of a chromosome
EX: Down syndrome
Inversion: Reverses the directions of parts of a chromosome
Translocation: Occurs when part of one chromosome breaks off and attaches to another
4-7 Mendelian Inheritance
Gregor Mendel
All living things have a set of characteristics that they have inherited from their parents
Genetics: The scientific study of heredity
Heredity is the delivery of a set of characteristics from parent to offspring
The modern science of genetics was discovered by Gregor Mendel
Mendel conducted his experiments using pea plants
Pea plants as “model systems”
Scientists use model system because they are convenient to study and may tell us how other organisms, including humans, actually function
By using peas, Mendel was able to carry out, in just one or two growing seasons, experiments that would have been impossible to do with humans and that would have taken decades
Mendel’s Conclusions
Mendel's first conclusion: The Theory of Particulate inheritance
An individual’s characteristics are determined by factors that are passed from one parental generation to the next
Today scientists call these factors genes
Gene: A sequence of DNA that codes for a protein and thus determines a trait
Different forms of a gene are called alleles
EX: The gene that codes for plant height came in two forms; tall and short
Mendel’s Second Conclusion: The Principle of Dominance
The principle of dominance states that some alleles are dominant and other recessive
If an offspring contains one dominant and one recessive allele it will display the trait of the dominant gene
The only way that the recessive trait will be shown is if no dominant allele is present
Mendel’s Third Conclusion: The Principle of Independent Assortment
The principle of independent assortment states that genes for different traits can segregate independently during the formation of gametes
Probability and Punnett Squares
Probability: The likelihood that a particular event will occur
EX: Coin Flip
Gene segregation during meiosis is random. This random segregation allows for the principles of probability to be used to predict the outcomes of genetic cross
Probabilities predict the outcome of a large number of events. The greater the number of events, the closer the results will be to the predicted values
Homozygous and Heterozygous
Not all organisms with the same characteristics have the same set of alleles
Both TT and Tt allele combinations will produce tall plants
Organisms that have two identical alleles for a particular gene are said to be homozygous
Organisms that have two different allele for a particular gene are said to be heterozygous
Mendel noticed that the F1 generation of plants had the same phenotype as the P generation but had a different genotype
Genotype is the genetic makeup an organism
Phenotype is the makeup of an organism
Punnett Squares
The punnett square is a tool that can be used to predict the outcome of genetic cross
Punnett squares use mathematical probabilities to help predict the genotype and phenotype combinations in a genetic cross
Summarizing Mendel’s Principles
Mendel’s principles of heredity, observed through patterns of inheritance, form the basis of modern genetics
The inheritance of biological characteristics is determined by individual units called genes, which are passed from parent to offspring
In most sexually reproducing organisms, each adult has two copies of each gene, one from each parent
Where two or more alleles of the gene for a single trait exist some may be dominant and other recessive
Alleles for different genes usually segregate independently of one another
4-8 Beyond Mendelian Inheritance
Beyond Dominant and Recessive Alleles
There are some exceptions to Mendel’s principles: incomplete dominance and codominance
Incomplete Dominance
Some alleles are neither dominant nor recessive
Incomplete dominance: A situation in which one allele is not completely dominant over the other allele
In incomplete dominance, the heterozygous phenotype is somewhere between the two homozygous phenotypes
Codominance: A situation in which the phenotype produced by both alleles are completely expressed
In certain varieties of chicken, the allele for black feathers is codominant with the allele for white feathers. Heterozygous chickens have a color described as “erminette,” speckled with black and white feathers
4-9 Cell Membrane Structure
Cell Membranes
All cells (whether prokaryotic or eukaryotic) have cell membranes to protect and organize the content of the cell
Cell membranes regulate what can enter and what can exit a cell
Cell Membrane Composition
Cell membranes are made up of a double-layered sheet. This is called a lipid bilayer.
The lipid bilayer is important because it gives the cell membrane flexibility and strength
Cell Membrane Composition
The lipid bilayer is made up of phospholipids
These molecules are composed of a phosphate group and two fatty acid chains
The fatty acid chains are considered hydrophobic, or “water-hating”. They do not come into contact with water and are instead buried in the middle of the membrane. This keeps water from entering or exiting the cell
The phosphate groups are considered hydrophilic, or “water-loving”. They are at the ends of the fatty acid chains, and face the inside and outside of the cell
The Lipid bilayer is made up of phospholipids
The tendency of the fatty acid chains to oppose water, and the phosphate groups to attract water, gives the cell membrane its lipid bilayer arrangement
Another lipid found in cell membranes is cholesterol. Cholesterol helps to maintain the flexibility of the membrane.
Permeability if Cell Membranes
Many substances are able to cross the cell membrane
However, substances that are too large or too charged (positive or negative) cannot
Permeable: If a substance is able to cross the cell membrane, then it is considered permeable to that substance
Impermeable: If a substance is unable to cross the cell membrane, the cell membrane is considered impermeable to that substance
The term scientists give to cell membranes is selectively permeable
Selectively Permeable: Some substances can cross the membrane barrier and others cannot
Fluid Mosaic Model
Within the cell membrane, there are many different types of molecules that move throughout the phospholipids
Protein molecules have a variety of functions. Some are channels or pumps, allowing substances to move across the membrane. Other are involved in a cell’s ability to responds to its environment
Carbohydrates molecules are attached to some of these proteins. They are involved in chemical identification, allowing cells to recognize one another.
When a carbohydrate is attached to a protein, it is called a glycoprotein
Due to the variety of different molecules, and the molecules ability to move throughout the phospholipid, cell membranes are also referred to as a fluid mosaic model
“Fluid” because of the movement, and mosaic because of the variety of molecules
4-10 Passive Cell Transport
Cell Membranes
Cell membranes control what enters and exits a cell
Cell membranes are therefore said to be selectively permeable
Some cells require larger amounts of specific substances than other cells and they must have a way of obtaining these materials from extracellular fluids. They do this through the process of membrane transport
Passive Transport
Passive transport: A naturally-occurring phenomenon and does not require the cell to use any energy to accomplish the movement of molecules across the cell membrane
These molecules must be small enough to move through the phospholipids, and are typically uncharged
In passive transport, small molecules move from an area of higher concentration to an area of lower concentration
A physical space in which there is a range of concentrations of a single molecule has what is called a concentration gradient.
Concentration Gradient: The force that allows molecules to move across the cell membrane
Equilibrium: Movement across the cell membrane stopping when the molecules are evenly distributed
Two main types of passive transport: diffusion and osmosis
Diffusion
Diffusion is the movement of molecules across the cell membrane. These molecules will move from an area of high concentration to an area of low concentration
This is called moving down their concentration gradient
Two types: simple diffusion and facilitated diffusion
Simple diffusion: molecules move through the phospholipids
These molecules are small and uncharged so they are easily able to move across the cell membrane
Facilitated diffusion: Molecules move through protein channels
These molecules are too large or are charged (positive or negative) and therefore cannot move through the phospholipids
Many factors can affect the rate of diffusion, including concentration gradient, size of the particles that are diffusing, and temperature.
Osmosis
The cell membrane contains phospholipids made up of hydrophilic phosphate heads and hydrophobic fatty acid chains
This composition keeps water from entering or exiting the cell easily
In order for water molecules to move across the cell membrane, they must travel through special channels called aquaporins
The movement of water across the cell membrane is a type of facilitated diffusion known as osmosis
Because it is a type of diffusion, water will move from an area of high concentration of low concentration
Tonicity
Many molecules are too large to move across cell membranes through diffusion so they do not reach equilibrium. However, water can easily move through aquaporins until equilibrium is reached
The concentration of molecules (called solutes) and the concentration of water (called solvent) are inversely proportional
When the concentration of water is 60%, the concentration of solutes is 40%
When the concentration of water is 40%, the concentration of solutes is 60%
While these solute particles are trapped on one side of the cell, water can easily move
Osmotic pressure: The differences in solute concentration between the two sides of the cell membrane drives the movement of water into and out of the cell.
Osmotic pressure leads to three effects of osmosis on cells:
Hypertonic: the outside of the cell has more solutes/less water compared to the inside of the cell
Water will move down its concentration gradient from inside the cell to outside the cell
This causes the cell to shrink
Hypotonic: the outside of the cell has less solute/more water compared to the inside of the cell
Water will move down its concentration gradient from outside the cell to inside the cell
This causes the cell to swell and eventually burst
Isotonic: The outside of the cell and the inside of the cell have the same concentration of solute and water (ideal condition of a cell)
Water will not move because equilibrium is reached
The cell will not change shape
4-11 Active Cell Transport
Concentration Gradient
Diffusion moves molecules across the cell membrane down their concentration gradient. This means movement occurs from an area of high concentration to an area of low concentration
Sometimes, the cell needs to move molecules in the opposite direction: from an area of low concentration to an area of high concentration. In this case, movement is against the concentration gradient
This is called active transport, and it requires ATP to be accomplished
Active Transport
Active Transport: A process that moves molecules across the cell membrane using energy.
This movement is from an area of low concentration to an area of high concentration.
There are two types of active transport: molecular transport and bulk transport
Molecular Transport
Small molecules and charged ions can move across the cell membrane using protein pumps. These pumps push the molecules or charged ions across the cell membrane against their concentration gradient
The energy stored in ATP is the force that allows these molecules to move across the cell membrane
ATP will bind to the protein pump in the cell membrane, causing the protein to change shape This allows the molecule being transported to bind to the protein pump. It is then released on the other side of the membrane
Bulk Transport
Unlike molecular transport, bulk transport utilizes vesicles and vacuoles to move molecules across the cell membrane against their concentration gradient.
These molecules are too large to be transported through protein pumps
There are two types of bulk transport: endocytosis and exocytosis
Endocytosis: The process of moving molecules from outside the cell to inside the cell. This is done by creating pockets in the cell membrane that will break off inside of the cell
Two types of endocytosis: pinocytosis and phagocytosis
Pinocytosis: Liquid is moved from outside the cell to inside the cell. The membrane will create a pocket filled with fluid that will break off into a vacuole
Phagocytosis: Solid particles are moved from outside the cell to inside the cell. The cell membrane will create a pocket filled with solid particles that will break off into a vesicle
The vesicles and vacuoles created through endocytosis travel through the cytoplasm to their final destination to be used by the cell
Exocytosis: The process of moving molecules from inside the cell to outside the cell. The vacuoles or vesicles inside the cytoplasm will travel to the cell membrane and fuse with it
When this fusion occurs, the contents (either liquid or solid) will be transported out of the cell.