L24: Flashcards
Methanogens
extreme anaeorbes
*only in archaea across many phylas
*via complex metabolism, based on e- transfer reactions on membrane bound enzymes and co enzymes which allow CO2 as electron acceptor (dumps e- to CO2)
*key in C cycle, many combination of e-acceptors and donors
List all the unique co enzymes for methonogens
MM C FF
MP, MF, CoM, F430 F420
methanogenesis equation, break it down
H2 (energy source) + CO2 (C source) = CH4
*H2 is oxidised as energy source and e- donor
*CO2 is e- acceptor and C source=autotroph
*CH4 is waste product
methongesis e- accors and donors other options
fermentation waste products
different e-donors and acceptors can be used: acetate, formate, methanol, methylmine and diemythlsuflphate
List methanogenic habitats
widespread, aneorbic zomes below fermenation layers, swamps, sediments, garbage, ruminants, stomach
How will the cycle for methanogensis look like
side chains dumping e- (Falling down) to be productive, a version of ETC and methane is the result product
Net emission formula
production - oxidation
6*10^14
top methan emmisions
natural wetlands
rice fields
ruminants
ocean/freshwater
gas leakage
Relationship between fermentation and methanogensis
in aneorbix zones, fermentation products feed methanogensis
*fermentation product like cellulose, polysaccharides and proteins are substrates that feed methanogens
*hydrolisis, fermentation to H2 + CO2, acetate or other organic compounds
*intermediate products acetogensis and secondary fermentation of organic acids/alcohols yield the substractes
draw methane production from fermentation
check slide 141
what is the role of ANME archea in methanogensis, draw this
They drive methane accumulation/removal in estuarine sediments
*fermenters produce hydrogen from organic matter
*in anaerobic oxidation of methane, sulfate reducers bring H concentration so low that methane oxidation is exergenonic
*then during methanogenesis, the SRB have run out of sulphate so hydrogen concentration building up that make ANME switch to forward methanogensis
What were the two approaches to molecular microbial ecology
- quantitative hybridisation
- phylogenetic characterisation
In depth go into quantitative hybridisation
To determine the relative proportions of organisms from different phylogenetic groups in a sample
– quantify the RNA or DNA extracted from the environmental samples blotted onto membranes
– today we might opt for quantitative PCR, microarray or metagenomic sequencing, but the goal is the same
Explain Phylogenetic characterization
To identify organisms via molecular analysis of nucleic acids extracted from a sample
– PCR-amplification of 16S rRNA genes, followed by cloning of the amplified DNA and analysis of the DNA sequences
What level of methodological detail
- reproducible
- allow research to extrapolate new methods
- helps others learn new techniques