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Prokaryotes
Organisms lacking a membrane-bound nucleus, divided into bacteria and archaea based on this characteristic.
Archaea
Morphologically similar to bacteria but more closely related to Eukaryota, with unique membrane structures and flagella.
Archaeal membranes
Chemically and structurally diverse. Semi-rigid lattice of pseudomurein, sugars, proteins or glycoproteins. S layer is a very common arrangement
1,2-sn-glycerol aka D-glycerol
found in bacterial and eukaryotic membranes
2,3-sn glycerol aka L-glycerol
archaeal membranes
difference between bacterial and archaeal phospholipids
Bacterial phospholipids contain ester linkages and unbranched fatty acids whereas archaeal phospholipids contain ether linkages and branched isoprene lipids
bacterial flagella
Thicker, helical, hollow filaments which rotate. Produced by adding flagellin to the tip
archaeal flagella
Similar in appearance but non-homologous to bacterial flagella. Grow by addition to the base
similarities between bacteria and archaea
contain plasmids, are unicellular and arrange their genes in operons
similarities between archaea and eukaryotes
insensitive to antibiotics, sensitive to diphtheria toxin, arrange DNA by histones and have complex DNA and RNA polymerases
5 major groups of archaea
Euryarchaeota, Crenarchaeota, Thaumarchaeota, Korarchaeota and Nanoarchaeota
Key Euryarchaeota genera
Halobacterium, Haloferax and Natronobacterium
Euryarchaeota habitat
high temperature, high salt or high acid content eg artificial saline habitats, solar salt evaporation ponds and salt lakes
properties of Euryarchaeota
binary fission
non motile, obligate aerobes
very thick glycoprotein cell wall stabilised by sodium ions
coloured due to bacteriorhodopsin
Halobacterium osmotic balance
Pump potassium ions into cell so intracellular [K+] exceeds extracellular [Na+] to maintain positive water balance
How do halophiles typically maintain osmotic balance?
Accumulation or synthesis of compatible solutes such as glycerol. Highly acidic, contain fewer hydrophobic amino acids and lysine residues.
Key genera of Methanogenic archaea
Methanobacterium, Methanocaldococcus and Methanosarcine
properties of methanogens
obligate anaerobes
very diverse cell wall chemistries eg pseudomurein or methanocondroitin
11 substrates of 3 different classes converted to methane by pure cultures
can convert glucose to methane in cooperative reactions with anaerobic bacteria
Thermoplasmatales (taxonomic order within Euryarchaeota)
Includes thermophilic and acidophilic genera like Thermoplasma and Ferroplasma
key genera of thermopasmatales (taxonomic order within Euryarchaeota)
Thermoplasma, Picrophilus and Ferroplasma
Thermoplasma
thermophilic, acidophilic chemoorganotrophs. Facultative aerobes via sulphur respiration. Found in self-heating coal piles.
Thermoplasma unique membrane structure
contains glycoproteins, no sterols and lipoglycan. Tetraether lipid monolayer membrane with mannose and glucose
Ferroplasma
Chemolithotrophic, acidophilic. Oxidise Fe(II) to Fe(III) generating acid. Grow in mine tailings containing pyrite
Picophilus
Extreme acidophiles, grow optimally at pH 0.7
key Thermococcales and Methanopyrus genera (hyperthermophilic Euryarchaeota)
Thermococcus, Pyrococcus and Methanopyrus
Thermococcus and Pyrococcus
highly motile and indigenous to anoxic thermal waters. Uses in biotechnology include PCR.
Key crenarchaeota genera
Sulfolobus, Acidianus, Thermoproteus and Pyrobaculum
Sulfolobales
aerobic chemolithotrophs which oxidise reduced sulphur or iron. Grow in sulphur-rich acidic hot springs
Acidianus
live in acidic sulphur hot springs, use elemental sulphur aerobically and anaerobically
How do thermophilic species increase thermostability?
high cytoplasmic solute concentration for protein monomer stability
heat stable molecules eg non heme iron proteins
DNA gyrase to introduce +ve supercoils (hyperthermophiles)
high polyamine levels
dibiphytanul tetraether type lipids which form monolayer
higher GC content
Hyperthermophiles
Organisms with high temperature tolerance, using heat-stable molecules and unique adaptations for survival in extreme environments.
H₂ oxidation
common to many hyperthermophiles, may have been first energy yielding metabolism