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108 Cards in this Set
- Front
- Back
When did the scientific method start? |
In the late 1600s, scientific thinking emerged, and with it, the scientific method |
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What is the scientific method? |
A method of answering questions and observations about the world in a way that allows us to draw scientific conclusions. Based on the hypothetico-deductive method |
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What is the hypothetico-Deductive method? |
1. Observation 2. Hypothesis 3. Testable prediction, that either passes or fails 4. Reject or accept hypothesis 5. Add to current knowledge, or come up with another experiment |
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What is the difference between a hypothesis, a theory, and a law? |
A hypothesis is an estimated guess. A Theory is a hypothesis that has been proven over and over by multiple people. A Law is a theory that is now accepted as fact. |
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Who makes hypothesis? Who makes laws? |
Scientists make hypotheses, the scientific community makes laws |
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What is evolution and why is it important for a class like microbiology? |
Evolution is the concept of natural selection, and organisms changing over time due to genetic mutations that prove to have a increased benefit to the organisms. Evolution is useful to microbiology because it allows us to understand how cells have changed over time, and concepts such as the endosymbiotic theory. |
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What is Microbiology? |
The study of very small organisms that can not be seen with the naked eye. |
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What are the three main groups of microbes? |
Eukarya, Bacteria, Archaea |
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What are the two main types of cells? What are their distinguishing characteristics? |
Prokaryotes- single celled, smaller, no organelles Eukaryotes- may be single celled or multicellular, larger, have organelles |
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What is the importance of microbes, in regards to human disease? |
Microbes live side by side, and inside of humans. Some microbes are beneficial to humans, such as intestinal flora that help digest food. Other microbes are disease-causing, that infect humans and cause disease. |
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How were microbes discovered? Who discovered them? |
Leeuwenhoek first made a microscope and was the first person to describe bacteria. Hooke looked at cells under a microscope, and named them. Tyndall and later, Cohn, discovered and described endospores. Koch described the idea that a microbe is associated with a disease, and Pasteur came up with Germ Theory. |
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Who create techniques to stop infection? |
Holmes and Semmelweis together described the importance of washing hands to prevent infection. Lister developed aseptic technique and Pasteur invented pasteurization. |
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How was human disease linked to microbes? |
Semmelweis and Holmes described the phenomenon of many more women and babies dying when the baby was delivered by a physician who had been doing autopsies earlier. Pasteur described Germ Theory, by drawing on previous scientists and Koch established proofs that verifed Germ Theory |
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How are Microbes used by humans to benefit us? |
Our intestinal flora aids us in digestion, we use yeast in beer and bread, cheese and yogurt use microbes, fungi producing penicillin |
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What are Koch's postulates? |
1. Microbes are always in sick people 2. Microbes can be isolated and grown 3. Infection with microbe grown in labs can cause disease 4. You can then reisolate the microbe from infected persons |
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What is nomenclature? |
The process of naming a new species according to a set of rules |
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How do you properly write a name? |
Genus species (capitalized genus name, lower case species name, italicized when in print, underlined if written, if you want to shorten it- G. species |
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What are the levels of organizations from Domain to Species? |
1. Domain 2. Kingdom 3. Phylogeny 4. Class 5. Order 6. Family 7. Genus 8. Species |
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What is the 2-kingdom scheme? |
Darwin first hypothesized that there were two kingdoms- Animals and Plants |
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What is the 5- kingdom scheme? |
Robert Whittaker: Monera, Protozoa, Fungi, Plants, and Animals- based on morphological similarities |
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What is the 3-domain scheme? |
Woese and Fox: The current scheme- Eukarya, Bacteria, Archaea, based on genetic similarities |
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How has our perception of living organisms changed since Darwin? |
Darwin first came up with the two kingdom system that encompassed animals and plants. He had no knowledge of microbes. Now, with our current understanding, we know that bacteria and archaea are extremely diverse and genetically dissimilar |
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What is an organic molecule? |
A molecule with carbon |
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What about carbon allows it to bond in unique ways? |
Carbon bonds to four atoms or molecules, which allows it to create complex 3D and 4D structures |
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What are the four biological macromolecules? |
Lipids, proteins, nucleic acids, carbs |
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What are the basic subunits of lipids and the bonds that hold them together? |
Basic subunits are phospholipids, triglycerides, and sterols, held together via ester bonds |
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What are the basic subunits of proteins and what are the bonds that hold them together? |
Amino acids, held together by peptide bonds |
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what are the basic subunits of carbs and what bonds hold them together? |
Monosaccharides, held together by glycosidic bond |
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What are the functions of carbs? |
Structural support (builds cell walls and cellulose), energy and nutrient stores |
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What are the functions of lipids? |
Create cell membranes, which help with selective permeability. |
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what are the functions of proteins? |
Provide structural support by building cytoskeletons, mechanical energy, and enzymes |
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What glycosidic, ester, and peptide bonds? What is the chemistry behind how they bond things? |
They are bonds formed between the same macromolecules, that are formed through dehydration synthesis- removing H20 to bond the two molecules together |
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What are the six characteristics of all cells? |
1. Spherical, cylindrical, cubical, or polygonal shaped 2. Cell membrane 3. Chromosomes 4. Able to produce energy from the environment 5. Able to reproduce 6. Ribosomes that produce proteins |
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Why do viruses not qualify as cells, according to the 6 characteristics of all cells? |
Viruses rely on other organisms to produce energy, reproduce, come in different shapes, and do not have cytoplasmic membranes |
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What is the endosymbiotic theory? |
The endosymbiotic theory is the theory that Eukaryotes took up Prokaryotes into their cell, and used the prokaryotes for a certain function, and the prokaryotes stayed in the cell because they became specialized to perform that specific function and were unable to live without the eukaryote |
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What are 5 pieces of evidence for the endosymbiotic theory? |
1. Mitochondrial DNA is circular 2. Mitochondria reproduce via binary fission 3. Ribosomes on mitochondria look like bacteria ribosomes 4. Mitochondrial genes look like bacterial genes 5. Have both an inner and outer membrane |
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What are differences between flagella and cilia? |
Cilia- small, lots of them, used for adhesion and digestion Flagella- not as many as cilia, much larger, used only for movement |
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Describe the glycocalyx |
The glycocalyx is the very outer membrane around a cell. AKA the extracellular matrix, composed of polysaccharides. The three layers are an acellular network of fibers, a slime layer, and a capsule.
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What is the Eukaryotic cell wall, and how is it different than bacterial cell walls? |
Eukaryotic cell walls are found in plants, fungi, and algae. They provide structural support and shape, and are composed of chitin, glycoprotein, and mixed glycans. Bacterial cell walls are made of peptidoglycan |
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Describe the nucleus |
The nucleus is a membrane bound organ that houses DNA. It has nuclear pores that the mRNA leaves through. It is covered by two cell membranes, which are called the nuclear envelope |
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Describe the Rough ER |
Called the rough ER because it is studded with ribosomes. The rough ER creates proteins and holds the proteins for packaging |
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Describe the smooth ER |
synthesizes and stores non-protein molecules |
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Describe the Golgi Apparatus |
Made of stacked, flattened sacs of membranes, this puts proteins into transitional or condensing vesicles, and sends them out to become lysosomes or secretory vesicles |
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Describe lysosomes |
originate in the golgi apparatus, and contain a variety of enzymes. When the cell brings in a vesicle with food in it, the lysosome attached to the vesicle, and secretes enzymes, digesting the food |
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What are vacuoles? |
A membrane bound sac that brings in food to the cell to be digested by the lysosome |
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Describe the mitochondria |
"energy powerhouse"- a series of folded, flattened membranes called christae, surrounded by an outer membrane. The christae are studded with ribosomes. Mitochondria produces ATP via the electron transport chain. The matrix holds ribosomes, DNA, and enzymes used in metabolism |
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Ribosomes |
Make proteins, are scattered throughout the cell- in the cytoplasm, mitochondria, rough ER |
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Describe the cytoplasm |
a gelatinous solution that provides a spot for biochemical and enzymatic activities. Composed of water, sugars, amino acids, salts, chromatin, ribosomes, granules, and cytoskeleton |
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What is a sporangium? |
A vegetative cell that has turned into a sporulating cell- takes 6-8 hours |
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Describe the germination of an endospore |
Must have favorable conditions, which includes exposure to H20 and a germination agent. The core rehydrates and takes up nutrients, causing the bacterium to begin to grow |
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What are some examples of endospores? |
Anthrax, Tetanus, and Botulism |
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What is the definition of metabolism |
All chemical reactions that work inside a cell |
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Anabolism |
Synthesizing and making the building blocks of macromolecules, using ATP |
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Catabolism |
Breaking down macromolecules into their building blocks, releasing ATP |
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What are enzymes used for? |
They are critical in regulating metabolism, because they speed up chemical reactions to the speed of life. If we did not have enzymes, reactions would occur too slowly. |
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What are examples of catabolism? |
Glycolysis, Kreb's Cycle, Fermentation |
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Are enzymes used up throughout a reaction? |
No, they can be reused over and over |
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Describe how enzymes work |
Enzymes bind to a substrate, and change the structure of the substrate. They bind to the active site |
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What are two kinds of enzymes? |
Simple (just folded protein), and conjugated (haloenzymes) |
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What is the structure of conjugated enzymes? |
They are made of the apoenzyme, which is just the protein, and a cofactor, which is non-protein, that supports the apoenzyme. |
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What happens when an enzyme denatures? |
The bonds are broken, changing the shape of the substrate. This causes a change in the active site, blocking the enzyme from binding to the substrate. Can lead to cell death |
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Why would a bacterium create and secrete enzymes? |
To digest large cells or food molecules so the bacteria can digest them |
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Endoenzymes vs. Exoenzymes |
Exo: created then released outside the cell Endo: retained intracellularly |
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What are constitutive enzymes? |
Enzymes that are always present in constant amounts, regardless of external conditions |
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What are regulated enzymes? |
Enzymes whos levels in the cell are determined by outside conditions. They are repressed or induced depending on those conditions |
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Competative Inhibition |
A molecule that resembles the substrate, and binds to the active site, blocking the enzyme from binding and acting on it |
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What is an example of competative inhibition? |
Cyanide- a competative inhibitor for cytochrome C oxidase- stops the electron transport chain |
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Non-competition Inhibition |
When the binding of enzymes to an active site is regulated by regulatory molecules, who are often the product of an enzymatic reaction |
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What is an example of non-competition inhibition? |
Penicillin- binds to a bacterial enzyme that catalyzes the formation of peptinoglycan |
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Enzyme repression |
Stops further synthesis and enzymatic reactions when the end product reaches excess |
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Enzyme induction |
Induced when a suitable substrate is present |
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Exoergonic- |
To release energy, used for cellular work |
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Endergonic- |
driven by the addition of energy |
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Glucose breaking down is what kind of reaction? |
Exergonic |
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What is the point to all of the steps in breaking down glucose? |
You are able to capture and use more of the energy when it is released slowly, over many steps. |
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How is energy released from ATP? |
You break the bond of the terminal phosphate |
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What is the purpose of electron carriers? |
They slow the energy release from glucose |
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Oxidation vs. REduction |
Oxidation: removal of an electron Reduction: addition of an electron |
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What are two common electron carriers? |
NAD and FAD |
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What are the ways glucose is catabolized? |
An/Aerobic cellular respiration and fermentation |
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What are the three steps in aerobic cellular respiration? |
Glycolysis, Kreb's Cycle, and electron transport chain |
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What is the final electron receptor in aerobic respiration? |
Free oxygen |
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What is the first step in aerobic, anaerobic cellular respiration and fermentation? |
Glycolysis |
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How many ATP does glycolysis create? |
2 (but multiple electron carriers) |
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Where does the Kreb's Cycle take place in Eukaryotes? In bacteria? |
Euks: in the mitochondrial matrix Bacteria: in the cytoplasm |
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Describe the Kreb's Cycle: |
A cyclical pathway of 8 reactions that starts and ends with acetyl CoA |
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What is the point of the Kreb's Cycle? |
Adds electrons to electron carriers |
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What is the point of the electron transport chain? |
A chain of special electron carriers that passes electrons to transport H+ outside the membrane, setting up an energy gradient. This energy gradient is used to turn ADP into ATP |
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Where does the ETC take place in Euks? in Proks? |
Euk: in the inner membrane of the mitochondria Proks: within the cell membrane |
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What is oxidative phosphorylation? |
The coupling of ATP synthase to electron transport |
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How many ATPs does the ETC create? |
34 |
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What must be present for the electron transport chain? |
Oxygen |
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What is the final acceptor in anaerobic respiration? |
oxygen-containing ions, N03, S04 |
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What is the point of nitrate and nitrite reduction systems? |
The organisms that have these systems metabolize nitrate into nitrite, which allows other organisms to metabolize it. An important step in recycling nitrogen in the biosphere |
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Denitrification |
enzymes that further reduce nitrite to nitric oxide, nitrous oxide, and nitrogen gas |
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Fermentation
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Oxygen is not required, and organic compounds are the final electron acceptors |
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What are the steps of fermentation? |
Glycolysis, then either acid fermentation or alcohol fermentation |
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What are the steps in ETOH fermentation? |
Glucose---- pyruvic acid----- ETOH and CO2 |
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What are the two kinds of acidic fermentation? |
Homolactic fermentation- produces lactic acid Heterolactic fermentation- lactic acid, acetic acid, and C02 |
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Who uses mixed acid fermentation? |
Bacteria and some insects, who use the formic acid for protection |
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What is catabolism of proteins due to? |
-excess protein intake -extreme starvation -DKA |
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What are the steps of protein catabolism? |
1. Proteases break down proteins 2. Amino acids get broken down and their amino groups removed 3. The remaining carbon group enters the Kreb's cycle and electron transport chain |
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How many ATP does lipid catabolism yield? |
50 ATP |
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What are lipids best for? |
Long term energy storage |
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Amphibolism |
ability of a cell to integrate anabolic and catabolic pathways to improve cell efficiency, often done using precursors |
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What are two common precursors? |
Pyruvate: provides intermediates for amino acids,used in gluconeogenesis Acetyl CoA: can be converted into amino avids, which can then be condensed into lipids and fatty acids |
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How many amino acids are there? |
20 |
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Describe lipid biosynthesis |
excess carbs turned to lipids |