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Micro-b Unit 3

QuestionAnswer
Catabolic reaction energy producing, breakdown complex molecules
Anabolic reaction energy consuming, synthesize complex molecules
Metabolism The sum of all chemical reactions and processes carried out by living organisms.
Autotroph Fix carbon dioxide to synthesize organic molecules.
Photoautotroph Autotrophs that obtain energy from light.
Chemoautotrophs Obtain energy from oxidizing simple inorganic substances.
Heterotroph Get carbon from ready-made organic molecules.
Photoheterotroph Heterotrophs obtain chemical energy from light
Chemoheterotrophs Heterotrophs that obtain energy from breaking down ready-made organic compounds.
Metabolic pathways Sequence of reactions where the product of the first reaction becomes the reactant of subsequent reaction. Ex: linear, branched and cyclic.
Function of enzymes Increase the rate at which chemical reactions take place within living organisms by lowering the activation energy for the reaction.
Amino acid backbone structure. Amino group+carboxyl group+alpha carbon+residual group. Each amino acid is distinguised by it's R group.
Peptide bonds Carboxyl group of 1 amino acid is bound by a dehydration reaction to the amino group of another amino acid.
Primary protein structure. The types and order of amino acids linked in the chain.
Secondary protein structure. Segments of the chain that coil or fold
Tertiary protein structure. the three-dimensional folding of the chain into a globular mass.
Quaternary protein structure Two or more monomers bound together into a functioning unit.
Enzyme active site Locations on the surface of the enzyme where substrates can bind.
Holoenzyme Certain type of enzyme that functions only when the protein portion binds with a coenzyme (NAD and FAD) and a cofactor (inorganic ion improves the fit)
3 factors affecting enzymes Temperature - higher temps = denatured enzymes,, lower temps - exponentially slower reaction rates. pH - changes the charged features affecting substrate binding capabilities Substrate concentration - increased substrate = more reactions.
Competitive enzyme inhibition Substrate look alikes take up the space on the enzyme reserved for actual substrates.
Non-competitive enzyme inhibition Molecules bind to allosteric sites on the enzyme morphologically changing the shape and preventing substrates from binding.
Feedback enzyme inhibition. The product of the end reaction signals the initial enzyme to slow or stop reactions.
Oxidation and Reduction reactions OIL - Oxidation is Loss (of electrons) RIG - Reduction is Gain (of electrons)
Co enzymes Electron taxis NAD and FAD
Homolactic fermentations Pyruvic acid is reduced to lactic acid
Aerobic respiration and anaerobic respiration both involve: Electron transport chain.
Fermentation A means for recycling NADH to NAD to ensure survival of the cell.
Players of the electron transport chain NADH dehydrogenase, Flavoproteins, Iron-sulful proteins, cytochromes, quinones.
Chemiosmosis Harnessing energy associated with relieving ion gradients across membranes.
Oxidative Phosphorilization ATP is synthesized using energy from proton motive force to bind ADP with an inorganic free Phosphate by a dehydration reaction.
Substrate level phosphorilization moving of inorganic phosphates to or from ADP/ATP at the substrate level (ex: glucose molecule is phosphorilized in glycoloysis)
Proton Motive Force The chemical and electrical gradient across a membrane resulting as a cumulative effect of pumping hydrogen ions to outside the surface of the membrane.
4 phases of bacterial growth in a closed system: Lag phase, exponential growth phase, Stationary phase, Death phase.
Lag phase Cell becomes acclimated to new conditions, no significant increase in cell numbers.
Exponential growth phase Cell metabolism is occuring at maximum efficency, population doubling at a genetically programed "Generation Time"
Stationary Phase Nutrient level begins to decline, waste byproducts accumulate, cell growth rates slow to a level that is balanced by die-off rates.
Death phase Die-off of cells occurs exponentially.
Chemostat Maintains the log phase by providing nutrients and flushing out waste indefinitely.
Standard plate count (# of colonies x Dillution rate)/amount used = ? CFU's
Most probable number method Used to enumerate bacteria in very dilute samples.
Turbidity measures Spectrophotometry - measures light transmittance through a sample. Less light = greater turbidity and more culture growth.
Factors effecting bacterial growth: Carbon - necessary for energy. Nitrogen - Amino Acids and Nucleotides Sulful - Amino Acids Phosphorus - nucleotides Tracemetals - Enzyme cofactors
Aerobes Require oxygen to grow
Anaerobes Do no require oxygen to grow
Obligate aerobes Will not survive without free oxygen.
Obligate anaerobes Will not survive in the presence of free oxygen.
Facultative anaerobes Can complete aerobic metabolism when oxygen is present but shift to anaerobic metabolism when oxygen is absent.
Aerotolerant anaerobes Can survive in the presence of oxygen but do not use it in their metabolism.
Psychrophiles Bacteria that grow best at low temperatures
Mesophiles Bacteria that grow best at middle temperatures
Thermophiles Bacteria that grow best at high temperatures
Acidophiles Bacteria that grow best in highly acidic environments.
Neutrophiles Bacteria that grow best in neutral environments.
Alkaliphiles Bacteria that grow best in highly basic environments.
Hyperosmotic environments Cells loose water and shink (plasmolysis)
Hypoosmotic environment Cells gain water and swell/burst.
Halophiles Salt-loving organisms which require moderate to large quantities of slat.
Hydrostatic pressure Pressure doubles with every 10 meter increase in depth
Barophiles Prokaryotes that live at high pressures.
Purines Double ringed nitrogenous bases (A & G)
Pyrimidines Single ringed nitrogenous bases (C, T & U)
Pentose sugars Ribose and deoxyribose 5 carbon sugars
Base pairing rules A purine always binds with a pyrimidine, specifically A with T (or U in RNA)resulting in 2 hydrogen bonds and C with G resulting in 3 hydrogen bonds.
Transcription mRNA is made by RNA Polymerase according to the DNA template to be used in Translation.
Translation At the ribosome mRNA is "read" and tRNA brings amino acids according to the template.
Replication DNA is semi-conservatively copied to pass genetic information from parent to progeny.
Replication - Step 1 - Initiation Gyrase and Helicase glom on to the DNA strand at the OriC (AT rich section of the strand). The strand is unwound and pulled apart. SSBP's hold the strands apart.
Replication - Step 2 - Copying (leading strand) Primase adds RNA primers. DNA Polymerase 3 reads and copies nucleotide sequences. The leading strand this is continuous proceeding in the 5' to 3' direction.
Replication - Step 2 - Copying (lagging strand) Primase adds RNA primers DNA polymerase 3 reads and copies nucleotide sequence discontinuously in Okazaki fragments.
Replication - Step 3 - Finishing DNA Polymerase 1 replaces RNA primers with DNA. Ligase completes phosphodiester bonds between Okazaki fragments.
OriC Point of origin for replication. An A/T rich section of the strand.
Replication forks Point at which the strand is separated for replication.
Anti parallel replication Replication always occurs in the 5' to 3' direction and is therefore occurring in opposite directions with each half of the strand.
6 components of replisome Gyrase, Helicase, RNA primase, DNA polymerase 3, DNA polymerase 1, ligase.
Mutations Mistakes in replication process, can be harmful or not.
Genes Information for the synthesis of proteins (structural or enzymatic)
Codon Sequence of 3 bases code for a specific amino acid.
Anticodon Base triplicate to the mRNA codon on the tRNA molecule that will bring in the amino acid that mRNA codes for.
Polyribosomes Chain of ribosomes allowing the same strand of mRNA to be translated multiple times simultaneously resulting in mass production of proteins.
Gene regulation Involves both constitutive enzymes (produced continuously) and Inducible enzymes (produced only in response to certain metabolic or environmental conditions).
Repression Stopping protein synthesis due to a certain environmental or metabolic condition.
Vertical Gene Transfer Passing of genetric material from parent to progeny (replication)
Horizontal (Lateral) gene transfer. Passing of genes to microbes of the same generation.
3 basic mechanisms of Lateral Gene Transfer Transformation Transduction Conjugation
Transformation "Naked DNA" from a donor cell is taken up to a host cell in a state of competence. Fragments of the naked DNA is incorporated into the host DNA.
Transduction The transfer of genetic material by bacteriophage.
Bacteriophage A virus that infects bacterial cells.
Virulent phage Capable of cuasing infection and the destruction and death of a bacterial cell
Temperate phage Ordinarily does not cause a disruptive infection
Prophage Phage DNA that is incorporated into the host bacteriums DNA
Lysogeny Persistence of a prophage without phage replication and destruction of the bacterial cell.
Conjugation Delivery of chromosomal material from one cell to another by way of a conjugation pili. Requires direct contact between donor and recipient cells and can transfer larger quantities of DNA than Transformation or Transduction.
Nutritional factors for bacterial growth Carbon (CO2 for autotrophs, glucose for heterotrophs), Nitrogen, Sulfur, Phosphorus, Metals, Vitamins, Water, Energy (phototrophs - radiant, chemotrophs - chemical energy)
Components of stains Benzine ring, chromophore and auxochrome.
Differential media Will display a color change based on what it is differentiating (fermentation or secretion).
Selective media Only certain types of organisms will grow.
Diagnositc results of gram stain Gram positive = purple Gram negative = red/pink
Acidic and Basic stain differences Acidic stains - negative and have a strong affinity for positive constituents of the cells (proteins). Basic stains - Positive charged have a strong affinity for the negative constituents of the cell (nucleic acids)
Benzine ring Organic colorless solvent
Chromophore Chemical group that imparts color to benzene
Auxochrome Chemical group that conveys ionization to the chromogen.
Chromogen Benzene+Chromophore= Colored compound, not a stain.
Most important step of gram stain Decolorization
Growth media selective for Gram - Mac Agar
Mannitol salt agar (MSA) Selective for growth of staphyl-cocci Differential for fermenters of mennitol
Blood Agar Selective for streptococcus Differential based on hemolytic properties.
Gamma hemolysis No lysis of red blood cells (no color change in blood agar)
Alpha hemolysis Partial lysis of red blood cell (greenish halo in blood agar)
Beta hemolysis Complete lysis of red blood cells (clear zone surrounding colonies in blood agar)
MacConkey agar (Mac Agar) Selective for Gram negative. Differential for lactose fermenters (appear red).
Eosin-methylene blue agar (EMB) Differential for lactose fermenters and E. coli. Partially inhibitory to gram positive.
Phenylethyl alcohol agar (PeA) Partially inhibitory to gram-negative.
4 ways to grow organisms anaerobically Brewer jar, GasPak system, Shake-culture technique, paraffin plug technique.
Function of counterstain. To recolorize cells or components that were decolorized previously and allow gram negative components to be viewed.
Purpose of heat fixation To fix cells in place on the slide so they don't slide off during the staining, rinsing process.
Grams iodine Mordant that increases a cells affinity for a stain.
Created by: npeters519
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