Prelim 3 BioG 1440

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190 Terms

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facultative aerobes
bacteria and yeast
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ROS
superoxide anion, hydrogen peroxide, hydroxyl radical
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detoxification enzymes
superoxide dismutase, catalases, peroxidases
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pathologies of OS
neurodegenerative disease, aging, depression injury
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avoidance
anaerobes, particularly bacteria
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diazotrophs
small subset of bacteria and archaea nitrogen protection:
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nitrogen plant sep.
leghemoglobin- buffer oxygen low enough to allow nitrogenase to function, not so low to stop respiration
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nitrogen space sep.
anabaena with heterocysts
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nitrogen time sep.
crocosphaera watsonii
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rubisco
initial step in co2 assimilation
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phytoplankton
in surface waters of oceans, accounts for 50% of all photosynthetic co2 fixation despite only being about 2% of total plant carbon (more efficient)
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common pH
bicarbonate
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acidic pH
carbonic acid
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basic pH
carbonate
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morphological ccm
???
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biochemical ccm
??? ccms:
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cyanobacteria
carboxysomes (with high levels of rubisco and carbonic anhydrase)
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algae
pyrenoids
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c3
typical plant
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c4
spatial, mesophyll cells bring in co2 and concentrate it in organic acids, which are provided to a second cell called the bundle sheath cell where calvin cycle occurs.
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cam
time, co2 in night, calvin cycle in day, stomata only open at night reducing water lost by transpiration look up oxygen evolutionary steps
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o2 carrier proteins
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hemocyanin
o2 binding proteins that float free in hemolymph, 2 copper ions used (mollusks and some arthropods)
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hemoglobin (Hb)
in many vertebrates and some insects
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chloride bicarbonate anion exchanger
example of antiport, drives transport of carbonate anion across rbc into blood plasma
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principal signal to increase respiration
decrease in blood pH blood pH decreases when co2 increases in tissues, detected my major blood vessels and medulla
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dead space
approx 1/3 of each breath, not efficiently exchanged
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peroxiredoxin
?
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heme cofactor
central iron atom that carries o2 bound by iron on one side and nitrogen histamine on other, creating binding pocket for o2 in carrier protein myoglobin has much higher o2 affinity compared to hemoglobin
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hyperbolic/simple binding curve
Mb
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sigmoidal/s
shape binding curve- Hb, due to cooperative binding
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hemoglobin is a tetramer
4 subunits (2 alpha, 2 beta)
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Hb T state (tense)
binds hemoglobin, then allosteric change in shape to R
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Hb R state (relaxed)
positive cooperatively allows much easier binding bc of higher affinity O2 effectors, increase O2 offloading into tissues by weakening activity of hemoglobin for o2
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bohr effect
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2,3 BPG
negative molecule, binds in center of tetramer between alpha and beta subunits, comes from isomerized 1,3-BPG from glycolysis as an offshoot, positive charged groups hold it in place.
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H
pH, Hb binds to proton acting as a buffer so pH doesn’t drop at drastically as it otherwise would, binding also helps offloading to tissues
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CO2
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fetal Hb
h143 is no longer +, but neutral. this causes weaker 2,3-BPG binding, making the fetal Hb have a higher affinity for O2. O2 from maternal can be transferred to fetal more easily.
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fetal Hb cell types
instead of beta subunit, has a gamma chain, which persists early after birth.
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deoxyhemoglobin
Hb form that releases o2 (low affinity)
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allosteric regulation
binding process alters shape and this o2 affinity, leading to sigmoidal curve
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In was one of the earliest examples of
genetic disease (sickle cell anemia)
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Hb was one of first proteins to
have a known sequence (molecular clocks)
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parabronchus
in birds, have extensive air capillaries to increase the exchange of air with the bloodstream
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cross
current- beds of capillaries run across the exchange surface to efficiently exchange (contrast to mixing in mammals in this chamber)
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bar
headed goose- provided example of bird at high altitude, has an ADAPTATION that is a mutation of their Hb. Hb has a higher affinity for O2, as graph shifts to LEFT compared to related species. - o2 partial pressure is much lower at high altitudes, needs high affinity to be able to bind enough
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living pathogens
bacteria, fungi, helminthes: PROLIFERATE
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non living pathogens
viruses, prions: REPLICATE
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resistance mechanisms
eliminate the parasite
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tolerance mechanisms
endure damage of pathogen
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susceptibility
determined by resistance and tolerance (hosts die when one is lacking)
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mucosal and epithelial immunity
cells like body, exposed to outside, prevent initiation of infection
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cellular and humoral immunity
block growth of pathogen / clear infection
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cellular
eat or kill microbes or infected cells
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humoral
diffusible molecules in ECF that interact with microbes to block them or kill them
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epithelial and innate are encoded in
germline
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adaptive immunity requires
somatic DNA recombination (multiple steps to generate, select, and amplify cells and effectors) mucosal physical: epithelial barrier, gelatinous mucus chemical: pH enzymatic: lysozymes, digestive enzymes innate cellular: phagocytosis humoral: antimicrobial peptides adaptive cellular: T cells and B cells (lymphocytes) humoral: antibodies
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only rely on innate
invertebrates and protochordates
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adaptive immunity organisms
cartilaginous fish, bony fish, amphibians, birds, tetrapods, mammals
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agnathans
peculiar case, subcategory of vertebrates called JAWLESS vertebrates. do not have canonical adaptive immunity, but have a kind of adaptive response (adaptive-like immunity)
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jawless and jawed
case of convergent evolution, two independent appearance of adaptive immunity
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why is adaptive immunity not as broadly distributed
fairly recent innovation
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NF
kB- transcription factor that is activated when a host detects an infection, this factor activate immune cells and transcribe immune effectors
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DAMPs
damage associated molecular patterns, part of innate, recognize tissue damage, indirect
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PAMPs
pathogen associated molecular patterns (non-self), innate, recognize FEW microbial patterns,
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if you have PAMPs and DAMPs
innate response is activated
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PRRs
pattern recognition receptors, receptor for innate immunity, activate innate response
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antigens
recognize ALL domains (epitomes) that are non-self, trigger adaptive immunity
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adaptive recognition of ANY NON
SELF- specific receptors like B-cell or T-cell (antibodies also interact)
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phagocytosis
innate immune cells (phagocytes) 1. recognize pathogens 2. internalize microbe into a vacuole called a phagosome 3. phagosome acidifies the vesicle (low pH) 4. fuses with lysosomes (degrading enzymes) 5. generates oxygen species
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mature form of phagosome
phagolysosome
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antimicrobial peptides
example of a humoral effector molecule (innate), small, POSITIVELY CHARGED (catonic), bind to membrane of bacteria, amphipathic
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bacterial membrane charge
negative
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amphipathic
hydrophilic and hydrophobic part
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when antimicrobial peptides insert in membrane
pore is formed, leading to bacterial lysis (bacterial cell destruction by membrane breakdown)
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inflammation
activation of innate immunity leads to release of mediator molecules (cytokines, chemokines, histamine) that effect local circulatory system
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4 cardinal signs of inflammation
tumor, rubor, calor, dolor (signs of an infection response is ongoing)
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tumor
swelling (edema bc of vasodilation and leakage)
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rubor
redness (more blood coming)
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calor
heat (blood to skin surface)
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dolor
pain (synthesized nerve cells)
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why inflammation
so innate cells can use circulatory system to leave and do their job
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Somatic dna recombination in jawless (agnathans)
gene conversion
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Immune repretoire
huge diversity of effector molecules and recognition receptors to be able to bind any pathogen
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Negative selection
subtract cells with receptors that recognize SELF
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T lymphocyte cytotoxicity
in case of viral infection, cytotoxic T cell can bind to infected cell by a self non-self complex, and kill that infected cell
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Self
nonself complex- MHC molecule that presents little bit of the foreign antigen (non self), exposing T cell to antigen
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MHC
presents antigen
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Perforin
???
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Antibodies do…
neutralization, recruitment to complement, and opsonization
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What generates antibodies
B lymphocytes, which generate SPECIFIC antibodies
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Neutralization
antibodies bind inactive viruses and toxins, preventing them from reaching or entering cell
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Recruitment to Complement
complex makes a pore formation (like antimicrobial peptides), where complements (proteins) can lysis bacteria
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Opsonization
tagging microbes fro phagocytosis (boosting innate efficiency)
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Ancestral antiviral immune processes
RNA interference and CRISPR
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RNA interference (RNAi)
in all eukaryotes 1. virus replicates and generates dsRNA (likelihood of virus bc only usually found in viruses) 2. DICER is an enzyme that that immediately destroys the dsRNA into siRNA 3. siRNA are bound to RISC to be guides to find and degrade any RNA homologous
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CRISPR
in bacteria, aims at eliminating DNA 1. bacteria captures fragments of DNA of invading bacteriophage into CRISPR locus 2. CRISPR locus is transcribed into RNA, where it can be integrated to Cas9 protein 3. RNA Cas9 complex can receive invader if has homologous to pieces of foreign DNA, binding and cleaving it
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SIMPLE cell cell communication requires
contact, so info can be exchanged directly. molecules can be exchanged or signals, that alter cel activity with protein or gene expression changes
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simple junction types
gap junctions (animals), plasmodesmata (plants)