cultivation of sediment microorganisms · quelle: brock biology of microorganisms . 21.01.2010! 5!...
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Cultivation of sediment microorganisms
Martin Könneke www.icbm.de
Martin Könneke www.icbm.de
Cultivation of microbes
•! What’s so important about cultivation
•! Essentials of cultivation
•! Essentials of isolation
•! How to apply cultivation
•! Cultivation of anaerobes
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Recommended literature
Accessing uncultured Microorganisms (K. Zengler 2008)
Principles of enrichment, isolation, cultivation and preservation of Prokaryotes
(J. Overmann 2006)
Martin Könneke www.icbm.de
Early milestones in microbiology
•! Louis Pasteur - Settled spontaneous generation controversy (1864)
•! Robert Koch - Methods for study bacteria in pure culture (1881)
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Quelle: Brock Biology of Microorganisms
Quelle: Brock Biology of Microorganisms
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Quelle: Brock Biology of Microorganisms
Quelle: Brock Biology of Microorganisms
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Martin Könneke www.icbm.de
Koch’s Postulates
•! The microorganism should be constantly present in animals suffering from disease, but should not be present in healthy individuals
•! Microorganism must be cultivated in pure culture outside the diseased animal
•! Healthy animals infected with these pure cultures must display the characteristic disease symptomes
•! Microorganism should be reisolated from the experimental animals and shown to be the same
Martin Könneke www.icbm.de
Early milestones in microbiology
•! Louis Pasteur - Settled spontaneous generation controversy (1864)
•! Robert Koch - Methods for study bacteria in pure culture (1881)
•! Sergey Winogradsky - Concept of lithoautotrophy (1889)
•! Martinus Beijerinck - Selective cultures (1901)
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Martin Könneke www.icbm.de
Use in old and modern biotechnology
•! Food production
•! Identification of infective agents and diseases
•! Production of pharmaceuticals
•! Precursor for chemical products
Martin Könneke www.icbm.de
Scientific use of cultivation based methods
•! Physiology
•! Biochemistry
•! Identification
•! Quantification
•! Whole genome analysis
To study microorganisms in the lab, it is usually necessary to culture (grow) them.
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Martin Könneke www.icbm.de
Nature Reviews Microbiology Vol. 5, Oct. 2007
Martin Könneke www.icbm.de
•! Pure cultures provides whole genomes essential to evaluate metagenomes
•! Proof of hypothesis constructed from metagenomes
•! Complete reconstruction of whole genomes is still not possible
•! But, metagenomes can provide hints to physiological properties
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Giovannoni and Stingl 2007
Essentials of successful cultivation
•! Scientific question/ hypothesis •! Medium choice •! Carbon and energy source •! Other media components •! Gelling agent •! Inoculum and interaction •! Growth conditions, temperature, pH,
atmosphere •! Incubation time
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What do I need for successful cultivation
•! Organism source •! Media •! Culture vessel •! Incubator •! Detection system
•! Creativity
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Chemical composition of a prokaryotic cell
Molecule Percent of dry weight
Protein 55
Polysaccharide 5
Lipid 9
Lipopolysaccharide 4
DNA 3
RNA 19
Amino acids and precursors 1
Sugars and precursors 2
Nucleotides and precursors 1
Inorganic ions 1
Macro elements of a prokaryotic cell
Macro element Percent of dry weight
Carbon (C) 50
Hydrogen (H) 8
Oxygen (O) 20
Nitrogen (N) 14
Phosphorus (P) 3
Sulfur (S) 1
Potassium (K) 1
Magnesium (Mg) 0.5
Calcium (Ca) 0.5
Iron (Fe) 0.2
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Trace elements of prokaryotic cell
Trace element Cellular function (example)
Cobalt (Co) Vitamin B12
Copper (Cu) respiration, photosynthesis
Molybdenum (Mo) nitrogenase, nitrate reductase
Nickel (Ni) hydrogenase
Selenium (Se) Hydrogenase, formate dehydrogenase
Tungsten (W) Formate dehydrogenase
Vanadium (V) Vanadium nitrogenase
Zinc Alcohol dehydrogenase, RNA and DNA polymerases, DNA-binding protein
Iron (Fe) Cytochromes, catalases, oxygenases
General requirements in microbiological media
•! Energy source •! Source of macro elements (including carbon
and nitrogen) •! Source of trace elements •! Buffer •! Growth factors (including Vitamins or
amino acids •! Salt composition
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Chemically defined versus undefined (complex) media
Defined medium for E. coli Undefined medium for E. coli
K2HPO4 7 g Glucose 15 g
KH2PO4 2 g Yest extract 5 g
(NH4)SO4 1 g Peptone 5 g
MgSO4 0.1 g KH2PO4 2 g
CaCl2 0.002 g Destilled water 1000 ml
Glucose 5-10 g
Trace element solution
Destilled water 1000 ml
Isolation of microorganisms into pure cultures
A culture containing only a single kind of microorganism, originate from a single cell (monoclonal).
Most common is the isolation of microbes by the use of solid media. Alternatives: serial agar dilution, serial liquid dilution
Highest priority: Avoid contaminants!
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Why do we need pure cultures?
•! Precise physiology
•! Biochemistry and structure
•! Taxonomy
•! Genetics
•! Reproducibility of experiments
The majority of microbes present in nature have no
counterpart among previously cultured organism.
4700 validly described species versus
about 20000 species in 1L sea water about 40000 species in 1g soil
total of 10 millions (estimations)
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How to apply cultivation?
•! Estimation of bacterial numbers using MPN
•! Selective enrichment and isolation of members belonging to one physiological group
•! Culturing an abundant phylotype
•! Cultivation of all microorganisms from a marine environment
Estimation of bacteria numbers by tenfold dilution series
“MPN - most probable number”
•! Estimation of viable microorganisms
•! Obtained by the statistical method of maximum likelihood
•! Many variations in cultivation conditions possible (complex - defined medium)
•! Detection of growth essential
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Quelle: Brock Biology of Microorganisms
Continuous culture- culture in steady state
Quelle: Brock Biology of Microorganisms
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Selective enrichment and isolation of
an relevant physiological group
Example: Cultivation of sulfate-reducing bacteria from the German Wadden Sea
(Antje Gittel)
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pSRR /nmol*cm-3
*d-1
0 10 20 30 40 50
Se
dim
en
t de
pth
/cm
0
100
200
300
400
500
SO4
2- concentration /mM
0 5 10 15 20 25 30
pSRR
sulfate
SRR at the study site Janssand, September 2005
A. Gittel, Paleomicrobiology, ICBM
Selective enrichment and isolation of sulfate-reducing bacteria from the German
Wadden Sea (Antje Gittel)
Chemically defined medium (Widdel& Bak, modified)
Basic medium (salt concentration adapted to sea water) Reducing agent: Sodium sulfide Buffer: Carbonate/Carbon dioxide Redox indicator: Resazurin Carbon source: Lactate, acetate, or carbon dioxide Electron donor: Lactate, acetate, or hydrogen Electron acceptor: Sulfate
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Cultivation
Liquid dilution series in anoxic media
Repeated application of the liquid and
deep agar dilution method (in progress)
SO42- Lactate
Acetate
H2/CO2
Growth of sulfate-reducers
Production of sulfide
Identification
Molecular analysis of the highest
sulfide-positive dilutions
Pure cultures
Growth was stimulated in liquid dilution
cultures from each depth and with
each substrate
Variety of partial 16S rRNA genes,
most of them related to known marine
sulfate-reducing bacteria
A. Gittel, Paleomicrobiology, ICBM
A. Gittel, Paleomicrobiology, ICBM
50 cm
100 cm
250 cm
400 cm
Desulfotalea spp.
Desulfosarcina spp.
Desulfobacula spp. H2/CO2
Acetate
Lactate
H2/CO2
Acetate
Lactate
Who is there?
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Selective enrichment and isolation of
an abundant phylotype
Example: The abundant marine, mesophilic Crenarchaeota
The domain Archaea
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Abundance of marine Crenarchaea
What did we know about marine Crenarchaea
•! Discovered in 1992 by Furhman et al. and DeLong
•! Account for nearly 20% of all oceanic bacterioplankton (~1028 cells) [Karner et al., 2001]
•! Detected in marine and terrestrial habitats
•! Isotopic analyses and tracer experiments suggest possible autotrophy [Pearson et al., 2001; Wuchter et al. 2003]
•! No cultivated representatives
•! Physiology has remained uncertain
•! May play important roles in global geochemical cycles
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Starting point
•! Detection in a tropical fish tank > Organism source
•! Molecular techniques (quantitative PCR) > screening tool
•! Some hints to autotrophy and ammonium oxidation
Steps to the pure culture
1)! Enrichment in filtered aquarium water + ammonium > increase of phylotype and nitrite production
2)! Isolation by liquid dilution in chemically defined medium, facilitated by filtration (size) and addition of antibiotics (archaea)
Strain SCM1
a DAPI
b FISH
Scale: 1 !m
c TEM
b SEM
Scale: 0.1 !m
Koenneke et al. Nature 2005)
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Starting point
•! Detection in a tropical fish tank > Organism source
•! Molecular techniques (quantitative PCR) > sreening tool
•! Some hints to autotrophy and ammonium oxidation
Steps to the pure culture
1)! Enrichment in filtered aquarium water + ammonium > increase of phylotype and nitrite production
2)! Isolation by liquid dilution in chemically defined medium, facilitated by filtration (size) and addition of antibiotics (archaea)
3)! Prove of its physiology by monitoring growth, ammonium consumption and nitrite formation
Growth of Strain SCM1 at 28 ˚C
NH3 + 1.5 O2 ! NO2- + H2O + H+ (!G0’ = - 235 kJ mol-1)
The first nitrifyer within the domain Archaea
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Cultivating the uncultured (K. Zengler) How many microbes can we stimulate to grow?
Simulate the environmental condition as good as possible!
Culturing anaerobes
•! Oxygen free media.
!!Remove oxygen
!!Keep it away
•! Low redox potential !!Addition of reducing agents
•! Optional: oxygen (redox) indicator
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Culturing anaerobes
•! Flush headspace (Hungate-technique)
•! Cultivation in sealed anaerobic jars or chambers
•! Cultivation without gaseous headspace
•! Co-culture with oxygen consuming bacteria
The Widdel-flask
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Take home messages!
•! There is no microbiology without cultivation
•! We have no universal media nor technique to culture all microbes with
•! We need more pure cultures
•! Be creative
Giovannoni and Stingl 2007