microbial acetogenesis lindsay rollick, gerrit voordouw
DESCRIPTION
O 2. Fe 3+. CO 2. Microbial Acetogenesis Lindsay Rollick, Gerrit Voordouw. CO 2. SO 4 2-. Mn 4+. NO 3 -. Nitrate Reduction. Methanogenesis. Iron Reduction. Acetogenesis. Sulfate Reduction. Manganese Reduction. Aerobic Respiration. Fe 2+. S 2-. CH 3 COOH. Mn 2+. CH 4. CO 2 . - PowerPoint PPT PresentationTRANSCRIPT
Figure 4. Mean acetic acid and mean methane in millimolar of A) medium with doubled nitrogen, B) doubled nitrogen and with no tracemetals and doubled trace metals. Changes are measured against controls.
1. Drake, H.L., Kusel, K. and Matthies, C. 2002. Ecological consequences of the phylogenetic and physiological diversities of acetogens. Antonie van Leeuwen hoek. 81:203-213.
2. Nathoo, S., Folarin, Y., and Voordouw, G. (2012). Potential of microbial formation of acetic acid from hydrogen and carbon dioxide for permeability modification in carbonate reservoirs. World Heavy Oil Congress. Aberdeen, UK, Paper WHOC-12
3. Müller, V. 2003. Energy conservation in acetogenic bacteria. Applied Environmental Microbiology. 69: 6345–6353.
Early ResultsNo Added CaCO3 or HCO3
-
Current ResultsExperiment Methan
e (mM)%
ChangeAcetic Acid (mM)
% Change
Early Reg. 6.72 N/A 4.01 N/AEarly Low 0.259 N/A 2.19 N/A
CaCO3 Reg. 11.01 +39.0 8.63 +53.5CaCO3 Low 4.62 +94.4 2.49 +12.0Subculture
Reg. 12.34 +10.8 2.19 -74.6
Subculture Low 2.49 -85.5 6.35 +60.8
2XN Reg. 13.47 +18.2 15.67 +44.92XN Low 0.748 -83.8 4.84 +48.6No TM 14.32 +5.9 11.33 -38.32XTM 13.01 -3.5 22.08 +29.01) Nutrient levels other than energy
substrate can influence the balance between acetogenesis and methanogenesis.
2) Low nutrients in subculture and adding CaCO3 promoted acetogenesis and decreased methanogenesis.
3) Acetogenesis is promoted by greater nitrogen and trace metal availability.
4) Microbial growth can occur in the presence of CaCO3 which can act as a pH buffer for acid-intolerant microbes.
Microbial AcetogenesisLindsay Rollick, Gerrit Voordouw
Microbial Metabolism: What’s for Dinner?
Introduction
Aerobic RespirationO2
CO2
Nitrate ReductionNO3
-
N2
Manganese ReductionMn4+
Mn2+
Iron ReductionFe3+
Fe2+
MethanogenesisCO2
CH4
Sulfate ReductionSO4
2-
S2-
AcetogenesisCO2
CH3COOH
Highest energy yield Lowest energy yieldMicrobes tend to be grouped by lifestyle: Energy Metabolism Methanogens make methane Acetogens make acetic acid 4H2 + CO2 → CH4 + 2H2O 4H2 + 2CO2 → CH3COOH + 2H2O Ae
robe
s
Anae
rob
es
Acetogens and methanogens live at the lowest energy levels and compete for H2 and CO2.
Who wins? Thermodynamics: Methanogens
Methanogenesis (Hydrogenotrophic) ΔG`0 = -135 kj/mol1
Acetogenesis ΔG`0 = -104.6 kj/mol1 (free energy)But: Over 200 species of acetogens have been identified 1
- Some grow in anti-methanogenic conditions or have higher substrate diversity
How do they compete under methanogenic conditions?
Objectives1) Observe competition between methanogenic
archea and acetogenic bacteria under controlled conditions.
2) Find factors to optimize growth of acetogens over methanogens.
MethodsMicrobes: complex sample from Medicine Hat oil field subsurface watersAnaerobic Minimal salts medium:No O2, or other electron acceptors: only acetogens and methanogens can grow = methanogenic conditionsCompare with regular version with a low nutrient version:No added nitrogen, phosphate, trace metals or tungstate-seleniteExcess 80%H2/20%CO2 Headspace Consumed gas replenished
Subculture - account for inoculum nutrients and transport shockAnalysis - Methane production was tracked with gas chromatography (GC-FID), acetic acid production was tracked with liquid chromatography (HPLC), pH with a pH meter
Why do we care?1) Acetogenesis consumes 2 CO2 = carbon
storage2) Acetogenesis could be a useful biotechnology in
unconventional oil fields3) To understand how to control methanogenesis.
Methane is a worse greenhouse gas than CO2!
Figure 1. A serum bottle experiment containing added solid CaCO3. All experiments are done in triplicate. Incubation is done at 300C.
0
5
10
15
Methane
Medium Nutrient Type
Mea
n C
once
ntra
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Low Regular BESA5
6
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8 Start pH Final pH
Nutrient Type
Mae
n pH
Figure 2. A) Mean acetic acid and mean methane in millimolar for low and regular nutrient medium. B) Mean start and final pH for low and regular nutrient medium. All bottles were performed in triplicate. No bicarbonate or carbonate mineral was added.
A
B
No added bicarbonate led to poor pH buffering of the solution which inhibited microbial growth. Acetogens and methanogens are acid-intolerant below pH 62.
Added Solid CaCO3
Low Regular BESA
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MethaneAcetic Acid
Medium Nutrient Type
Mea
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(mM
)
Low Regular BESA
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MethaneAcetic Acid
Medium Nutrient Type
Mea
n C
once
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(mM
)
A
B
6
6.5
7
7.5
8 Start pHFinal pH
Nutrient Type
Mea
n pH
C
Figure 3. Mean acetic acid and mean methane in millimolar of A) primary culture and B) of subculture. C) Mean start and final pH for low and regular nutrient medium. All bottles were performed in triplicate. Change is measured against controls.
Adding CaCO3 - buffered pH- ↑ biofilm growthRegular Nutrients↑ Methane (+39%) ↑ Acetic acid (+53.5%)Subculture Low Nutrients↓ Methane (-85.5%)↑ Acetic acid (+60.8%)
Nutrient Optimization
Low Regular
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20
MethaneAcetic Acid
2X Nitrogen
Medium Nutrient Type
Mea
n C
once
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(mM
)
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No TM 2XTM
05
10152025
MethaneAcetic Acid
Variations in Trace Metals
Medium Nutrient Type
Mea
n C
once
ntra
tion
(mM
)
B
Doubling Nitrogen Regular Nutrients: ↑ Acetic acid (+39%) ↑ Methane (+18.2%)Low Nutrients: ↓ Acetic acid (+49%) ↓ Methane (-83.8%)(relative to low nutrients)
Trace MetalsRemoving:↓ Acetic acid (-38%) ≈ Methane (+5.9%)Doubling: ↑ Acetic acid (+29%) ≈ Methane (-3.5%)
Varying phosphate and salts had no discerning difference (not shown).
Conclusions
Table 1. Summary of results for experiments. Methane and acetic acid are averages of 3 replicates and % change is calculated based on comparable control. Promising cultures shown are high-lighted in yellow.
References AcknowledgementsI’d like to thank my supervisor Dr. Gerrit Voordouw for giving me this project and all of the lab members of the Voordouw and Gieg lab for their help and support. I thank the University of Calgary, the Natural Science Research Council of Canada and Suncor Ltd. for financial support and Baker Hughes for providing the water samples used for source microbes in this research.
Oil field microbesConventional
Unconventional
Model for Potential
Acetogenesis
Biotechnology