- Introduction to the Archaea
- The archaea are quite
diverse, both in morphology and physiology
- They may stain gram
positive or gram negative
- They may be
spherical, rod-shaped, spiral, lobed, plate-shaped, irregularly shaped
or pleomorphic
- They may exist as
single cells, aggregates or filaments
- They may multiply by
binary fission, budding, fragmentation, or other mechanisms
- They may be aerobic,
facultatively anaerobic, or strictly anaerobic
- Nutritionally, they
range from chemilithoautotrophs to organotrophs
- Some are mesophiles,
while others are hyperthermophiles that can grow above 100°C
- They are often found
in extreme aquatic and terrestrial habitats; recently, archaea have been
found in cold environments and may constitute up to 34% of the
procaryotic biomass in Antarctic surface waters; a few are symbionts in
animal digestive systems
- Archaeal cell walls
- Archaea can stain
either gram positive or gram negative, but their cell wall structure
differs significantly from that of bacteria
- Many archaea that
stain gram positive have a cell wall made of a single homogeneous layer
- The archaea that
stain gram negative lack the outer membrane and complex peptidoglycan
network associated with gram-negative bacteria
- Archaeal cell wall
chemistry is different from that of bacteria
- Lacks muramic acid
and D-amino acids and therefore is resistant to lysozyme and b-lactam
antibiotics
- Some have
pseudomurein, a peptidoglycan-like polymer that has L-amino acids in
its cross-links and different monosaccharide subunits and linkage
- Others have
different polysaccharides
- The archaea that
stain gram negative have a layer of protein or glycoprotein outside
their plasma membrane
- Archaeal lipids and
membranes
- Lipids have branched
hydrocarbons attached to glycerol by ether links rather than
straight-chain fatty acids attached to glycerol by ester links as seen
in Bacteria and Eucarya
- Other, more complex
tetraether structures are also found
- Membranes contain
polar lipids such as phospholipids, sulfolipids, and glycolipids and
also contain nonpolar lipids (7-30%), which are usually derivatives of
squalene
- Membranes of extreme
thermophiles are almost completely tetraether monolayers
- Genetics and molecular
biology
- The archaeal
chromosomes that have been studied consist of a single, closed DNA
circle like those of bacteria, except that some are considerably smaller;
Archaea have few plasmids; genomic analysis suggests are as distinctive
genotypically as they are in other respects
- Archaeal mRNA is like
that of bacteria (i.e., it may be polygenic, there is no evidence of
intron-containing precursors, and its promoters are similar to those of
bacteria)
- There are many other
differences between archaea and other organisms, including:
- The observation of
modified bases in archaeal tRNA molecules that are not found in
bacterial tRNA molecules
- Ribosomes with
different morphological and physiological properties than bacterial and
eucaryotic ribosomes
- Archaeal RNA
polymerase enzymes that are more similar to eucaryotic enzymes than to
bacterial enzymes
- Metabolism
- Carbohydrate
metabolism is best understood
- Archaea do not use
the Embden-Meyerhof pathway for glucose catabolism; however they
frequently use a reversal of that pathway for gluconeogenesis
- Some (halophiles and
extreme thermophiles) have a complete TCA cycle while others
(methanogens) do not
- Archaeal biosynthetic
pathways appear to be similar to those of other organisms
- Autotrophy is
widespread; reductive TCA cycle and reductive Acetyl-CoA cycle are used
for carbon fixation
- Archaeal Taxonomy-the
new edition of Bergey’s Manual will divide the archaea into two phyla:
Euryarchaeota and Crenarchaeota
- Phylum Crenarchaeota
- Many are extremely
thermophilic, acidophilic, and sulfur-dependent
- Sulfur may be used as
an electron acceptor in anaerobic respiration, or as an electron source
by lithotrophs
- Almost all are strict
anaerobes
- They grow in
geothermally heated water or soils (solfatara) that contain elemental
sulfur (sulfur-rich hot springs, waters surrounding submarine volcanic
activity); some (e.g., Pyrodictum spp.) can grow quite well above the
boiling point of water (optimum @ 105oC)
- Some are
organotrophic; others are lithotrophic
- There are 69 genera;
two of the better-studied genera are Sulfolobus and Thermoproteus
- Sulfolobus
- Stain gram negative;
are aerobic, irregularly lobed, spherical bacteria
- Thermoacidophiles
- Cell walls lack
peptidoglycan but contain lipoproteins and carbohydrates
- Oxidize sulfur to
sulfuric acid; oxygen is the normal electron acceptor, but ferric iron
can also be used
- Sugars and amino
acids may serve as carbon and energy sources
- Thermoproteus
- Long, thin, bent or
branched rods
- Cell wall is composed
of glycoprotein
- Strict anaerobes
- They have temperature
optima from 70-97°C and pH optima from 2.5 to 6.5
- They grow in hot
springs and other hot aquatic habitats that contain elemental sulfur
- They carry out
anaerobic respiration using organic molecules as electron donors and
elemental sulfur as the electron acceptor; they can also grow
lithotrophically using H2 and S0as electron donors and CO or
CO2 as the sole carbon source
- Phylum Euryarchaeota
- The Methanogens
- Strict anaerobes that
obtain energy by converting CO2, H2, formate,
methanol, acetate, and other compounds to either methane or to methane
and CO2; there are at least five orders, which differ greatly
in shape, 16S rRNA sequence, cell wall chemistry and structure, membrane
lipids, and other features
- Methanogens belonging
to the order Methanopyrales have been suggested to be among the earliest
organisms to evolve on Earth
- Methanogenesis is an
unusual metabolic process and methanogens contain several unique
cofactors
- They thrive in
anaerobic environments rich in organic matter, such as animal rumens and
intestinal tracts, freshwater and marine sediments, swamps, marshes, hot
springs, anaerobic sludge digesters, and even within anaerobic protozoa
- They are of great
potential importance because methane is a clean-burning fuel and an
excellent energy source
- They may be an
ecological problem, however, because methane is a greenhouse gas that
could contribute to global warming and also because methanogens can
oxidize iron, which contributes significantly to the corrosion of iron
pipes
- The Halobacteria
- A group of extremely
halophilic organisms divided into 15 genera
- They are aerobic
chemoheterotrophs with respiratory metabolism; they require complex
nutrients
- Motile or nonmotile
by lophotrichous flagella
- They require at least
1.5 M NaCl and have growth optima near 3-4 M NaCl (if the NaCl
concentration drops below 1.5 M the cell walls disintegrate; because of
this they are found in high-salinity habitats and can cause spoilage of
salted foods
- Halobacterium
salinarum uses four different light-utilizing rhodopsin molecules
- Bacteriorhodopsin
uses light energy to drive outward proton transport for ATP synthesis;
thus they carry out a type of photosynthesis that does not involve
chlorophyll
- Halorhodopsin uses
light energy to transport chloride ions into the cell to maintain a 4-5
M intracellular KCl concentration
- Two other rhodopsins
act as photoreceptors that control flagellar activity to position the
bacterium in the water column at a location of high light intensity,
but one in which the UV light is not sufficiently intense to be lethal
- The Thermoplasms
0. Thermoacidic
organisms that lack cell walls; only two genera are know: Thermoplasma and
Picrophilus
1. Thermoplasma
- Frequently found in
coal mine refuse, in which chemolithotrophic bacteria oxidize iron
pyrite to sulfuric acid and thereby produce a hot acidic environment
- Optimum temperature
for growth of 55-59°C and an optimal PH of 1 to 2
- Cell membrane is
strengthened by large quantities ofdiglycerol tetraethers,
lipopolysaccharides, and glycoproteins
- Histonelike proteins
stabilize their DNA; DNA-protein complex forms particles resembling
eucaryotic nucleosomes
- At 59oC
Thermoplasma takes the form of an irregular filament; the cells may be
flagellated and motile
2. Picrophilus
- Isolated from hot
solfateric fields
- Has an S-layer
outside the plasma membrane
- Irregularly shaped
cocci with large cytoplasmic cavities that are not membrane bounded
- Aerobic and grows
between 47°C and 65°C with an optimum of 60°C
- It grows only below
pH 3.5, has an optimum of pH 0.7 and will even grow at or near pH 0
- Extremely thermophilic
S0 metabolizers
0. Strictly
anaerobic, reduce sulfur to sulfide
1. Are
motile by means of flagella
2. Have
optimum growth temperatures around 88-100°C
- Sulfate-reducing
archaea
0. Gram-negative,
irregular coccoid cells with walls of glycoprotein subunits
1. Use
a variety of electron donors (hydrogen, lactate, glucose) and reduce sulfite,
sulfate, or thiosulfate to sulfide
2. Are
extremely thermophilic (optimum around 83°C); they are usually found near
marine hydrothermal vents
3. Contain
two methanogen coenzymes