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what happens when O2 present in glycolysis
pyruvate converted to Acetyl-CoA (substrate for redox)
What are lipids?
fats and oils. soluble in non polar solvents. hydrophobic
What is a polysaccharide?
long polymer chain of monosacchraides joined together by glycosidic bonds (sugar)
what are proteins
polymers of amino acids
What is an unsaturated fatty acid?
One with double bonds (kinky)
What is a saturated fatty acid?
One without double bonds (not kinky)
what is TAG
triacylglycerol. made of 1 glycerol and 3 fatty acids
What is a phospholipid?
a lipid containing a phosphate group in its molecule. hydrophilic head and 2 hydrophobic tails. main component of membranes
What is a terpene?
type of lipids with an aromatic ring
example of disaccharide
sucrose, lactose, maltose
What do polysaccharides do?
energy storage and structural support
what are 2 polysaccharides that provide structure
cellulose (in plant cell walls) and chitin (in insect exoskeletons)
What is an amino acid?
organic compound containing both a carboxyl and an amino group.
What are the 4 levels of protein structure?
primary, secondary, tertiary, quaternary
What is the primary structure of a protein?
sequence of amino acids
What is the secondary structure of a protein?
region stabilized by H bonds between polypeptide back bone. alpha helix or beta pleated sheet
What is the tertiary structure of a protein?
3D structure including bending
What is the quarternary structure of a protein?
Overall structure when a protein is made up of two or more polypeptides
What are nucleotides made of?
5 carbon sugar, phosphate group, nitrogenous base
What are pyrimidines?
cytosine, thymine, uracil
what are the purines
Adenine and Guanine
how are nucleotides joined in DNA
phosphodiester bonds
What is transcription?
The process of making RNA from DNA via rna polymerase
What is translation?
Ribosome reads code from mRNA (in cytoplasm). Assembles amino acids into polypeptide chain
What is the central dogma?
DNA -> RNA -> Protein
What is the TATAA box?
A promoter region upstream from a gene. recognized by rna polymerase. rna polymerase 2 binds to TATA binding proteins to start transcription
what does nuclear pore complex do
controls movement of molecules in and out of nucleus. how mrna, proteins and ribosomes leave
how are nucleotides read by a ribosome
3 at a time (codon)
what are the ribosome subunit sizes
60s and 40s
what does the 60s ribosome subunit have
catalytic site where protein is made
what does the 40s ribosome subunit do
finds mrna and checks each codon with anti codon
what is trna and what does it do
Transfer RNA; tRNA brings appropriate amino acid into the ribosome and attaches it onto the growing polypeptide. has anticodon to check
which amino acid is the start codon
Methionine (AUG)
How are introns removed?
splicing carried out by a spliceosome to paste all exons together
What are adipocytes?
specialized fat cells that house triglycerides
What are acyltransferases?
catalyze the transfer of fatty acids from acyl CoAs to the 3 carbon unit. successive transfers give a triacylglycerol. TG is then stored in the lipid droplet
Where is TAG made?
Smooth ER. accumulates in lipid droplets
what are lipid droplets
Storage organelles that help to maintain the lipid and energy homeostasis. single layer membrane
What are perilipins?
coat proteins of lipid droplets
step 1 of lipid droplet formation
tag making enzymes and cholesterol ester making enzymes deposit neutral lipidsin between ER bilayer
step 2 of lipid droplet formation
sepin and other lipid droplet proteins form complex in ER side to grow lipid and push it out of membrane
step 3 of lipid droplet formation
lipid droplets bud toward cytoplasmic side. pushed by seipin. droplets grow by fusion or more tag synthesis
what is phosphatic acid
smallest phospholipid. removing a phosphate makes TAG.
where are enzymes that metabolize phospholipids found
membrane. not cytosol
how can phospholipids move within bilayer
rotate, move laterally (along same layer), transversely (from one layer to another)
what are translocases
proteins that move phospholipids between layers. maintains lipid asymmetry (flippase, floppase, scramblase)
what is frap
fluorescence recovery after photobleaching. method to study molecule mobility in cells by adding dye, bleaching an area, and watching other dyed molecules diffuse into area
integral membrane proteins
firmly embedded in the membrane
peripheral membrane proteins
proteins associated with but not embedded within the plasma membrane. make weak and reversible bonds to membrane by binding to integral proteins
lipid-anchored membrane proteins
sit on the surface of the lipid bilayer but are covalently bound to a lipid molecule
What do membrane proteins do?
detect and transmit signals, has receptors for chem signals, mediate cell-cell communication and adhesion
what are integral monotopic proteins
They are permanently embedded on the cell membrane from just one side.
what is glycosylation
Process of covalently attaching a carbohydrate to a protein or lipid
where can you find glycosylated proteins or lipids
outside membrane
types of passive transport
simple diffusion, facilitated diffusion, osmosis
types of active transport
primary and secondary
What is facilitated diffusion?
The diffusion of molecules across a membrane through transport proteins. glucose
how do solute carriers and ion channels differ
solute carriers have conformational change and are slower
what is a uniporter
carrier protein that transports a single solute at a time
what is a symporter
a carrier protein that transports multiple solutes in the same direction
what is an antiporter
two or more ions or molecules transported in opposite directions
what are porins
non specific channel proteins allow other molecules to move through the outer membrane. in mitochondria, chloroplasts, bacteria
why do k+ channels not let smaller na+ molecules through
na+ cant interact w oxygen due to size
why cant atp diffuse through membranes
negative charge
ways to move solutes against conc gradient
via ATP or electrochem gradient
What are the 4 ATPases for active transport
P-ATPase, Vacuolar-ATPase, F-type ATPases, ABC-type ATPases
P-ATPase
4 types. regulated by phosphorylation. maintains electrochem gradient
Ca2+/H+ ATPase
in SR or PM. In muscle cells. keeps Ca2+ conc in cytoplasm low
Na+/K+ ATPase
3 Na+ out per 2 K+ in per ATP. maintains Vm and Electrochem gradient
H+/K+ ATPase
enzyme responsible for pumping acid onto the mucosal surface of the stomach
what is a Vacuolar ATPase
2 rotary motors which turn axle and pump protons across the membrane to increase acidity. atp powered
What are F-type ATPases?
ATP synthases
H+ F-type ATPase
in inner mitochondrial membrane. uses H+ gradient to drive ATP synthesis. F0 is electric motor. F1 motor chem motor. both connected by stator
ABC-type ATPases
ATP binding cassette. mediates ATP powered movement of substrates across membrane. has 2 importers and 2 exporters to move big molecules. have hetero dimer
what is a heterodimer
2 different proteins that come together
where is ATP made in the mitochondria
matrix
What is an anabolic pathway?
make large molecules. endergonic (needs energy)
what is a catabolic pathway
breaks large molecules (exeergonic)
what is oxidation
loss of electrons
what is reduction
gain of electrons
What are NAD and FAD?
coenzymes of redox reactions. electron carriers. accept e-
What are coenzymes?
organic molecules that bind to active site of certain enzymes
what is a substrate of glycolysis
glucose and pretty much anything that ends in "-ose"
What kind of pathway is glycolysis?
catabolic - releases energy
What does glycolysis produce?
2 ATP, 2 NADH, 2 pyruvate
what happens in phase 1 of glycolysis
glucose phosphorylated twice and cleaved (needs ATP)
what happens in phase 2 of glycolysis
the 2 cleaved molecules are oxidized (2 ATP and 2 NADH made)
what happens in phase 3 of glycolysis
2 oxidized molecules converted into pyruvate (2 more ATP made)
What are disaccharides broken into?
monosaccharides (glucose, galactose, fructose)
What are monosaccharides turned into?
glycolysis intermediates
what happens when O2 present after glycolysis
pyruvate converted into Acetyl-CoA (substrate for redox)
what happens when O2 not present after glycolysis
pyruvate reduced to NAD+
where does glycolysis happen
cytoplasm
what does the mitochondrial pyruvate carrier do
transports pyruvate into mitochondria
Where does the TCA cycle occur?
mitochondrial matrix
What is the TCA cycle?
Krebs cycle (Citric Acid Cycle)
what happens in the krebs cycle
pyruvic acid is broken down into carbon dioxide in a series of energy-extracting reactions
what is a dehydrogenase
an enzyme that removes a pair of hydrogen atoms from a substrate (oxidizes it)
What is the pyruvate dehydrogenase complex?
mitochondrial enzyme complex linking glycolysis and Citric Acid cycle
What does pyruvate dehydrogenase do?
converts pyruvate to acetyl-CoA. releases lots of energy. needs vitamin B1 as co-factor