Utilisateur
What’s inside bacteria (DNA, ribosomes, cytoskeleton, storage bodies, microcompartments, endospores) and how those structures help survival/function.
DNA (nucleoid + plasmids), ribosomes, cytoskeleton, inclusions/microcompartments, endospores.
Storage + specialized metabolic “zones” that make reactions more efficient or safer.
The bacterial genome + proteins (DNA isn’t floating “naked”; it’s organized with proteins).
They tend to be circular, meaning replication doesn’t “lose the ends” like linear chromosomes can.
No chromosome ends to shorten each cycle → avoids “end-replication” problems.
Small circular DNA (about 1,000–100,000 bp) separate from the main genome.
They have their own origin of replication → replicate independently.
Yes, many cells carry multiple plasmid copies.
Antibiotic resistance, conjugation/transfer genes, virulence genes.
They can spread antibiotic resistance quickly between bacteria.
Plasmids appear as small circular structures compared to the large chromosome mass.
Protein synthesis (translate mRNA into protein).
50S (large) + 30S (small) subunits (together = bacterial 70S).
Many antibiotics target bacterial ribosomes because they differ from eukaryotic ribosomes.
A tubulin homolog for cell division (forms the division ring).
Plasmid segregation (notably in Bacillus spp.).
An actin homolog important for cell shape, especially rod-shaped bacteria
Actin homolog that positions magnetosomes in magnetotactic bacteria.
Intermediate filament-like protein that makes rods curved (Caulobacter crescentus).
Prevents FtsZ polymerization at cell poles, helping division occur mid-cell.
FtsZ forming rings at the poles (ends), so division happens in the right place.
Misplaced septa / division near poles → uneven daughter cells.
MreB is essential for maintaining rod morphology in many bacteria (like E. coli).
Rod cells often become rounder or lose proper elongation.
Crescentin (CreS).
Can affect attachment, swimming behavior, or positioning in flow (conceptual
It shifts from its normal shape toward a rod-like shape (loss of characteristic morphology)
They strongly control bacterial shape, which can affect motility/colonization.
Inclusions and then microcompartments and endospores.
Intracellular bodies/granules of organic or inorganic material, often with enzymes, used for storage.
Glycogen (glucose), poly-β-hydroxybutyrate (carbon), polyphosphate (volutin), cyanophycin (amino acids).
Helps survive fluctuating environments—store during abundance, use during scarcity.
Carbon storage.
No membrane (precipitated/storage material).
Phosphate reserves.
Sulfur reserves (often from sulfur metabolism).
They’re basically precipitated material (storage deposits).
Protein-based “mini-organelles” that concentrate enzymes/substrates and/or isolate reactions to improve efficiency and protect the cell. Protein-based “mini-organelles” that concentrate enzymes/substrates and/or isolate reactions to improve efficiency and protect the cell.
Protein-shell compartments with carbonic anhydrase + RuBisCo; they trap CO₂ near RuBisCo, boosting carbon fixation efficiency.
Gas-filled structures that provide buoyancy control, letting cells position for optimal light/nutrients in water.
Membrane-enclosed magnetic iron particles that allow alignment with Earth’s magnetic field (magnetotaxis) to find favorable environments (often oxygen gradients).
Made under stress (nutrient lack, heat, chemicals, radiation, drying). They’re dormant survival structures, non-reproductive, extremely resistant.
Sporulation = vegetative cell → endospore. Germination = endospore → active vegetative cell when conditions improve.
They survive harsh cleaning/antibiotics → persist and cause recurring contamination/infection risk.
The position of the spore inside the cell—useful for identification.
Phospholipid bilayer + proteins. Jobs: selective barrier, transport/protein platform, energy conservation (maintains gradients like PMF).
Fatty acid length + saturation: more unsaturated/shorter → more fluid; more saturated/longer → less fluid (cold adaptation often increases fluidity).
They change membrane charge and interactions, affecting protein binding and transport.
A lipid carrier that shuttles cell-envelope building blocks across the membrane for assembly outside.
Integral = embedded/spanning (α-helices or β-barrels). Peripheral = surface-associated (ionic/lipid anchors/loops), can detach more easily.
diffusion: passive, no protein, small non polar + some small molecules (O2/co2, water)
facilitated diffusion: passive but needs protein (channels/carriers), selective
active transport: moves agaisnt gradient, requires energy (ATP or PMF)
can: small hydrophobic, O₂/CO₂, some water.
Cannot: ions, large polar molecules (sugars, amino acids) without transport proteins.
Water movement down its gradient; bacteria avoid bursting mainly due to cell wall peptidoglycan (and sometimes S-layers) resisting internal pressure.
Uniport moves one solute. Symport moves two in same direction; antiport opposite directions. Sym/anti commonly use PMF (one downhill drives another uphill).
An H⁺ electrochemical gradient across the membrane. Powers transport (sym/antiport), motility in some bacteria, and supports ATP generation concepts.
To show channels are highly selective—structure can prefer K⁺ over similar ions (like Na⁺).
They phosphorylate glucose immediately → traps it inside and maintains a gradient for continued uptake.
ATP-powered pumps that move substances (often nutrients) against gradients, especially when resources are scarce.
Everything outside cytoplasm: plasma membrane + cell wall (peptidoglycan); Gram− also has an outer membrane with periplasm.
Alternating sugars MurNAc + GlcNAc with peptide cross-links → strong mesh that prevents osmotic lysis and maintains shape.
Humans don’t have it; disrupting synthesis weakens the wall → bacteria can lyse.
gram+: thick PG (many layers, ~20–35 nm).
Gram−: thin PG (~2–7 nm) located between inner and outer membranes.
Space between membranes containing enzymes/transport proteins; important for nutrient processing and defense.
In Gram+ walls, contribute to structure and surface properties (often negatively charged polymers).
It’s asymmetric: inner leaflet phospholipids, outer leaflet LPS → strong barrier.
LPS contributes negative charge, barrier strength, attachment/biofilms; lipid A = endotoxin; O-antigen helps with immune interactions.
Outer membrane is very impermeable; porins (often trimeric β-barrels) allow passive entry of certain small molecules.
The outer membrane + LPS barrier limits entry; access may depend on porins and transport.
It won’t cross without a transporter (channel/carrier/active system).
Active transport (ATP or coupled transport like PMF-driven symport/antiport).
Endospores.
LPS, specifically lipid A.
Crystal violet → iodine → alcohol (decolorizer) → safranin (counterstain).
Pink curved cells (because E. coli is Gram-negative = pink; CreS makes it curved).
Inclusions = precipitated storage materials; microcompartments = protein shell “organelle-like” structures with enzymes inside.
Carboxysome = large, hexagonal; gas vesicle = smaller-looking (endospore would fill the cell more); note: some granules are darker than gas vesicles/endospores.
Endospores
MamK.
Polytopic integral membrane protein (multiple transmembrane segments can form a channel/pore).
Porins are classically associated with the Gram-negative outer membrane; an inner membrane pore is an integral membrane transporter/channel.
diffusion: O₂/CO₂ + water; Facilitated diffusion: K⁺; Active transport: lactose via sym/antiport, glucose via group translocation, maltose via ABC transporter.
It would burst if it weren’t for peptidoglycan holding the cell together.
A symporter (PMF-driven coupled transport).
Gram+ = purple = thick peptidoglycan; Gram− = pink = thin peptidoglycan + outer membrane + periplasm.
Two phosphates linked together (phosphoanhydride).
NDP, undecaprenyl pyrophosphate, and ATP.
Undecaprenyl pyrophosphate (it’s a carrier lipid used in biosynthesis, not a structural OM component).
It’s the outer polysaccharide part of LPS that’s highly variable between strains, which affects immune recognition/strain differences.
Bacteria use both forms (D-Ala and L-Ala) in the tetrapeptide; D-amino acids are uncommon in human proteins, which helps make peptidoglycan distinct.
The major membrane phospholipid is usually phosphatidylethanolamine (PE) (high-yield to remember for Gram-negative inner membranes).
Hypotonic (water moves into the cell).
Lysozyme cleaves the glycan backbone (the sugar-sugar linkages), weakening the wall.
Plasmids (common site for transferable resistance genes).
