Download - S ynthetic M ulticellular B acterium
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Synthetic Multicellular Bacterium
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SMB: Synthetic Multicellular Bacterium
Introduction
Design & models
Experimental validation of the design
Applications & Perspectives: E. colight
Conclusions
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Why a Synthetic Multicellular Bacterium
Multicellularity as a backbone for complex synthetic biology
Tool for metabolic engineering:decoupling growth and transgene expression
Studying fundamental aspects of multicellularity
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Decoupling functions in complex systemsThe germline & soma solution
Differentiation
Tradeoff between growth & transgene expression
Partial dissociation between growth& transgene expression
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Towards a Synthetic Multicellular Bacterium
Feeding
DifferentiationE coli
Differentiation
Feeding
Germline
Soma
Reproduction Reproduction
Tu
rns
ON
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Basin of attraction Exponential growth
Proof of Feasibility
growth
Stability and fixed point analysisPopulation collapsesPopulation size remains constantPopulation growth is exponential
There are sets of parameters for which exponential growth exist
differentiation deathG = GermlineS = Soma
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Design of DevicesDifferentiation device
T
Irreversible recombination
loxscar Y
Feeding deviceDifferentiation In a dapA strain
(+)
lox71 lox66ftsK dapATT
Combining both devices
cre
Differentiation control
chromosomelox66 Ylox71 X
dapA
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Choices
No simple bypass or reversion Overproduction and excretionSurvival in DAP starvationNo growth in LBDAP sensitive expression mechanism
dapA Subtilis
Peptidoglycan and lysine pathways Feedback insensitive
Auxotrophy Metabolite: Essential gene:
Different Soma / Germline phenotypesLongevityLittle impact on metabolismGenetic isolation
ftsK Cellular division
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Concept & Implementation
DAP feeding
Differentiation
loxSc
ftsK
loxScar
gfp T
No replication origin
Somatic cell
dapAftsKlox71 gfp T T lox66
Germline cell
cre
Differentiation control
DAP starvation >> RECOMBINATION >> Differentiation
dapA
cre
T
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Models overviewFour approaches to answer four questions
Qualitative models
Quantitative models
How does differentiation induces feeding? How do spatial organization and distribution evolve?
How sensitive is the system to noise?
How robust and tunable is the system?
Cellular automaton
Multi-agents based system
Gillespie based simulationKinetic model
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Spatial Simulation
An Agent Based Model Mechanical model
• Masses/springs system• Delaunay triangulation neighborhood
Biological model• Differentiation• DAP production/consumption/diffusion• Cells volume growth
Coupling both modelsCells volume growth modifies the
mechanical constraints and neighborhood
Simulations reproduce the 3 formerly predicted behaviors
Exponential growth
Stability
Red = GermlineGreen = Soma
Differentiation rate ++
Differentiation rate +
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Biochemical Kinetic model
Quantitative analysis on an ODE model Molecular levelMean concentration values on the population
Outcome of the simulation:
•Range of valid parameters
Optimization and Robustness
•Critical parameters:
• DAP excretion
• Differentiation rate
S
GG+S
Time
Po
p.
siz
e
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Exploring the impact of recombination Frequency through simulation
Differentiation by Recombination : Influence of Frequency
There is an optimum differentiation rate for growth
Gro
wth
rat
e
Differentiation rate
lox KnR lox
36% recombination rate per generation
Experimental analysis of recombination frequency
Growth onkanamycin
NO growthOn kan
lox
cre
pBAD
Time
cre
pBAD
C.F
.U /
ML
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Differentiation through Recombination:Influence of frequency
Tradeoff between:
Maximize growth
Decrease germline generation time
Increase germline proportion
Increase DAP concentration
Increase differentiation rate
Decrease differentiation rate
Trade off
germline generation time / germline proportion
G
G G S
Differentiationdivision
G G S
G G S
50% recombination per generation stability
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Differentiation through Recombination: Introducing Feedback
crerbs
dapAp
DAP
pBAD
crerbs
ara +
E coli
Differentiation
Feeding
Germline
Soma
Reproduction Reproduction
Tu
rns
ON
Tunable constant differentiationConditional differentiation
Inh
ibits
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Pop
ula
tion
siz
e
SomaGermline
Soma with retrocontrolGermline with retrocontrol
Soma withRetrocontrol
Soma
Germline with retrocontrol
Germline
time
Differentiation through Recombination: Introducing Feedback
Retrocontrol can increase robustness
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100µ
M
0µM
Differentiation through Recombination: Introducing feedback
DAP Concentration
Mea
n F
luo
resc
ence
(A
U)
rfprbs
dapA promoter
DAP?
dapA promoter can be used in the SMB to provide retro-control on differentiation
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dapA strain on limited DAP concentration
Range of limiting growth [DAP] = range of dapAp activation = 0-100µM
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Coculture
Experimental validation of DAP choice
DAP feeding supports survival
dapA- cell
dapA- cell
Prototrophcell
DAP?
Survival
dapA deletant + trp deletant strain coculture
1E+0
1E+1
1E+2
1E+3
1E+4
1E+5
1E+6
0 2 4 6 8 10
Time (h)
CFU
/ml
Coculture w ith TG1
dapA- LB
Coculture and survival
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Construction ProcessChromosomal insertion
lox71 gfp T
ftsKIn a dapA strain
DapAlox66
loxSc
ftsK
loxScar
gfp T
No replication origin
Somatic cell
dapA subtilisftsKlox71 gfp T T lox66
Germline cell
Cre
dapAp
DAP starvation >> RECOMBINATION >> Differentiation
dapA subtilis
Cre
T
cre
Differentiation control
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Perspectives & ApplicationsSMB as a tool for biological engineering.
Differentiation
DAP feeding
Tradeoff between growth & transgene expression
Partial dissociation between growth& transgene expression
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E. colight: potential application of the SMB as a “metabolic plant”
Triglyceride inclusion
Free fatty acid
DGATAcyl-coA
Triglyceride
Ph
osp
ho
lipid
Diacylglycerol
Triglycerides synthesis only in Soma Soma isolation through differentiation induction Ingestion to absorb the fatty acids as you eat
Differentiation
DAP feeding
Eat fat don’t get fat
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E. colight: experimental proof
IPTG +
DGAT +
DGAT -
- sodium oleate + sodium oleate (2mM)
IPTG - IPTG -IPTG + IPTG +
• Cloning of DGAT of acinetobacter ADP1 under pLac control
• Specific triglycerides coloration: Nile Red
E.colight makes triglycerides!
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A new synthetic organism !!
Computational proof of principleExperimental & computational analysis orienting the design processConstruction of the SMB genetic cassettes19 New Biobricks added & characterized in the registryInserting a transcription factor in both Somatic in germline cassettes enables full modularity of our deviceFull traceability of molecular biology work and full wiki documentation
Achievements
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Acknowledgements
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Who did what ?Wet Lab: David Bikard Thomas Landrain David Puyraimond Eimad Shotar
Modeling team: Gilles Vieira Aurélien Rizk
Modeling tools Biocham MGS
Interface Wet/Dry: David Guegan Nicolas Chiaruttini
Logistics: Thomas Clozel Thomas Landrain
Instructors and advisors: Samuel Botanni Franck delaplace Francois Kepes Ariel Lindner Vincent Schächter Antoine Spicher Alfonso Jaramillo
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DAP
All
ost
eric
co
ntr
ol
dapA
Lysine
Dap
A
Gen
etic
fee
db
ackpeptidoglycan