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Lots of ATP produced
proton gradient drives ATP synthase, ADP + Pi --> ATP
O2 combines with e- and protons to form water
H+ pumped into intermembrane space, creates proton gradient
e- go through protein complexes
NADH and FADH2 made from glycolysis and citirc acid cycle, give e- to ETC
ATP generation: 2 ATP made through substrate level phosphorylation
ATP usage: 2 ATP consumed in first 5 steps of glycolysis
ATP generation: 2 ATP made thourgh substrate level phosphorylation
cAMP activates first kinase
Adynylyl cyclase converts ATP --> cAMP
Activated G protein activates adenylyl cyclase
GPT --> GTP and activates G protein
Ligand binds to GCPR receptor
Cell recognition, stability & protection
Cell-cell recognition & signal reception
Maintains Flexibility
Phospholipids
Hydrophobic Tails (fatty acids)
Isomers
Trans Isomers
Cis Isomer
Charges (+/-)
OH-
pOH
Hydroxide Ions
H+
pH
> 7
= 7
< 7
Basic
Neutral
Acidic
Hydrogen Ions
Peptide Bonds
Glycosidic Bonds
Nonpolar
Polar
Cytoplasm
Cell Wall (plants, fungi, and bacteria)
Ribosomes
Cell wall: Bacteria (peptidoglycan), Archaea (branched lipids)
No membrane-bound organelles
No nucleus, DNA in nucleoid region
Unicellular or multicellular
Larger in size (10-100 µm)
Contain membrane-bound organelles
Have nucleus (DNA enclosed in membrane)
ATP used in:
Chemical Work (Biosynthesis)
Transport Work (Active Transport)
Mechanical Work (Motor Proteins)
ATP Synthesis: ADP + Pᵢ → ATP (Requires energy)
ATP Hydrolysis: ATP → ADP + Pᵢ (Releases energy)
Comparison to Cellular Respiration
ATP is generated using a proton gradient in both mitochondria and chloroplasts.
Both processes use electron transport chains.
Calvin Cycle (Stroma)
ATP & NADPH used to fix CO₂ into glucose.
Light-Dependent Reactions (Thylakoid Membrane)
Electron transport & proton pumping to create ATP and NADPH.
ATP is generated by oxidative phosphorylation.
Proton (H⁺) gradient in the intermembrane space drives ATP Synthase.
Oxidative Phosphorylation (ETC + Chemiosmosis) (Inner Mitochondrial Membrane)
Outputs: ATP (32-34), H₂O
Inputs: NADH, FADH₂, O₂
Citric Acid Cycle (Krebs Cycle) (Mitochondrial Matrix)
Outputs: ATP, NADH, FADH₂, CO₂
Inputs: Acetyl-CoA, NAD+, FAD
Pyruvate Oxidation (Mitochondrial Matrix)
Inputs: Pyruvate, NAD+
Outputs: Acetyl-CoA, NADH, CO₂
Glycolysis (Cytoplasm)
Inputs: Glucose, ATP, NAD+
Outputs: Pyruvate, ATP (net 2), NADH
Anabolic Pathways ( Photosynthesis: synthesis of glucose using light energy)
Catabolic Pathways (Cellular Respiration: breakdown of glucose for ATP)
2nd Law: Energy transfer increases entropy.
1st Law: Energy is transferred and transformed, not created or destroyed.
Frameshift Mutations
Reading frame shift
Deletion
Insertion
Point Mutations
Nonsense
Creates premature stop codon
Missense
Changes one amino acid
Silent
No change in amino acid
Cel Membrane
Lysosome
Plasma Membrane
Ribosomal subunits separate.
Release factor binds
Ribosome reaches a stop codon (UAA, UAG, UGA).
Amino acids are joined by peptide bonds
Matching tRNAs bring amino acids.
Ribosome moves along mRNA, reading codons.
Large ribosomal subunit joins to form complete ribosome.
tRNA carries methionine to start codon
Small ribosomal subunits bind to mRNA at start codon (AUG)
No mRNA processing
smaller ribosomes
larger ribosomes
mRNA Processing: Capped, spliced, poly-A-Tail
Polymerases need a primer to begin synthesis
Requires dNTPs as substrates
High fidelity (1 error per 10⁶ bases, proofreading)
High speed (E. coli: 2000 nt/sec)
Directionality matters: DNA pol adds only to 3′ end
Okazaki fragments
Lagging strand synthesized discontinuously
Leading strand synthesized continuously
Replication bubble
Bidirectional replication
Replication fork
Replication origin (ORI)
Meselson-Stahl experiment (14N vs. 15N labeling)
Semiconservative replication model
Ligase – seals nicks between Okazaki fragments
DNA Polymerase I – removes RNA primers & fills gaps
Sliding clamp – increases DNA pol processivity
DNA Polymerase III – synthesizes new strand (5′→3′)
Primase – adds RNA primers
Single-Stranded Binding Proteins (SSBPs) – stabilize separated strands
Topoisomerase – relieves tension ahead of fork
Helicase – unwinds DNA
RNA polymerase detaches
Cleavage factors cut RNA transcript
RNA polymerase reads termination factor
U --> T in RNA
RNA polymerase reads 5' --> 3'
synthesizes complementary RNA 3' --> 5'
Initiation
forms transcription bubble
Transcription factors bind to promotor sequnce
recruits RNA Polymerase II to bind to promotor
Promotor region
Enhancer sequences
Promotor = TATA box
Location
goes to cytoplasm for translation
Nucleus
Termination
Newly synthesized mRNA released
Termination factor reached
Elongation
RNA synthesis in the 5' --> 3' direction
RNA polymerase adds complementary nucleotides
C-G
A-U
Initiaton
Topoisomerase keeps it from rewinding and relieves stress
Helicase unwinds DNA at promotor
Unwinds DNA
Forms transcription bubble
RNA polymerase binds to promotor
promotor = specific sequece on DNA
Location
Cytoplasm
Transcription and Translation coupled here
Alternative splicing
makes many proteins from one gene
Splicesome
snRNA + proteins
Joins exons
Removes introns
Poly-A Polymerase adds A LOT of A's to 3' end
~100-300
Cut RNA downstream
Cleavage factor binds
Protects mRNA
Happens as RNA is synthesized