Transcript Document

Summaries - 4
Proteobacteria:
1.- Phototrophes anoxygenic:
a – Purple sulfur: Chromatium, Ectothiorhodospira, Thiocapsa
b – Purple non-sulfur: Rhodospirillum, Rhodomicrobium
2.- Chemolithotrophs:
a - Nitrosifyers & nitrifyers: Nitrosococcus, Nitrobacter
b - Sulfur oxidizers: Thiobacillus, Beggiatoa, Thioploca
c - Iron oxidizers: Leptothrix, Gallionella
d - Hydrogen oxidizers
e - Methane oxidizer
3.- Chemoorganotrophs:
a - Aerobic respirers: Pseudomonads, Acetic A., N-fixers:
Azotobacter, Photobacteria
b - Anaerobic respirers: S - reducers, Desulfovibrio
c - Facultative aerobes: Enteric bacteria, E. coli
d - Fermenters: Zymomonas
e - Pathogens: Neisseria, Campylobacter, Salmonella
Vibrios, Spirilla, Prostecate bacteria, Myxobacteria
Ammonia and nitrite can be used as electron
donors by the nitrifying bacteria. The
ammonia-oxidizing bacteria produce nitrite,
which is then oxidized by the nitrite-oxidizing
bacteria to nitrate. Anoxic NH3 oxidation is
coupled to both N2 and NO3– production in the
anammoxosome.
Thiocapsa roseopersicina
- a sulfide oxidizing,
non-oxygenic phototroph
containing intracellular
sulfur grains and bundled
tubular pigment vesicles
So
Purple bacteria are anoxygenic phototrophs
that grow phototrophically, obtaining carbon
from CO2 + H2S (purple sulfur bacteria) or
organic compounds (purple nonsulfur
bacteria). Purple nonsulfur bacteria are
physiologically diverse and most can grow
as chemoorganotrophs in darkness. The
purple bacteria reside in the alpha, beta, and
gamma subdivisions of the
Proteobacteria.
3 – Cyanobacteria
• Gram-negative bacteria (formerly blue-green ‘algae’)
• Evolutionary origins and paleoecology of:
Oxygenic phototrophy (unique event in evolution)
All chloroplasts in eukaryotes through endosymbiosis
Atmospheric oxygen provided by Cyanobacteria
Most of the global primary production
Stromatolites, organo-sedimentery structures
• Ecological significance today:
Dinitrogen fixation, respond to P-load as ‘algal blooms’
in coastal and interior waters and enrichment of tropical
ocean (Trichodesmium)
Picoplankton contribution to open ocean (Synechococcus,
Prochlorococcus).
Sediment and soil stabilization
Microbial endoliths and bioerosion
Microcystis flos aquae – a bloomForming, gas-vesicle loaded,
Toxic coccoid cyanobacterium
Petalonema alatum – a
Heterocystous, N2-fixing,
Filamentous cyanobacterium
hν
Phycoerythrin
Phycocyanin
Allophycocyanin
Thylakoid membrane
Chlorophyll a
Phycobilisome
Microbial Bioerosion
Microbial bioerosion is carried by phototrophic
cyanobacteria, green and red algae and
organotrophic fungi. They may remove up to 50% of
carbonate along the surfaces of substrates, such as
shells, corals and limestone rocks.
Solentia achromatica
Endolithic cyanobacterium
responsible for destruction
of limestone coasts at the
intertidal zone.
Hyella racemus – a modern
endolithic cyanobacterium
and its
Neoproterozoic counterpart
Eohyella dichotoma
After microbial endoliths
have Successfully
colonized the rock……
Microbial euendoliths are integrated in the
community of prokaryotes and eukaryotes.
Consequently, the combined bioerosion of
microbial endoliths (bio-corrosion) and their
grazers becomes a progressive force that
undercuts limestone coasts, and creates sharp
and bizarre shapes called ‘biokarst’.
Biokarst & bioerosional notch are geologically significant
Modifications of limestones caused by combined biocorrosion
by microbial endoliths and bioabrasion
by heir grazers
detail
Ammonia and nitrite can be used as electron
donors by the nitrifying bacteria. The
ammonia-oxidizing bacteria produce nitrite,
which is then oxidized by the nitrite-oxidizing
bacteria to nitrate. Anoxic NH3 oxidation is
coupled to both N2 and NO3– production in the
anammoxosome.
Iron Bacteria
They are chemolithotrophs able to use ferrous
iron (Fe2+) as sole energy source. Most iron
bacteria grow only at acid pH and are often
associated with acid pollution from mineral and
coal mining. Some phototrophic purple bacteria
can oxidize Fe2+ to Fe3+ anaerobically.
Methanotrophy & Methylotrophy
Methane is oxidized by methanotrophic bacteria.
Methane (CH4 ) is converted to methanol (CH3OH)
by the enzyme methane monooxygenase (MMO).
The electrons needed to drive this first step come
from cytochrome c, and no energy is conserved in
this reaction. A proton motive force is established
from electron flow in the membrane, and this fuels
ATPase. Carbon for biosynthesis comes primarily
from formaldehyde (CH2O), MMO is a membraneassociated enzyme.